TY - THES A1 - Kersting, Katerina T1 - Development of a CRISPR/Cas gene editing technique for the coccolithophore Chrysotila carterae Y1 - 2024 ER - TY - THES A1 - You, Lili T1 - Chloroplast engineering for recombinant protein production and stress protection Y1 - 2024 ER - TY - THES A1 - Székely, András Csaba T1 - Long-distance circadian coordination via a phloem-delivered mobile transcript Y1 - 2024 ER - TY - THES A1 - Apodiakou, Anastasia T1 - Analysis of the regulation of SDI genes, unravelling the role of the SLIM1 transcription factor, and the SNRK3.15 kinase in Arabidopsis under sulfur deprivation Y1 - 2024 ER - TY - THES A1 - Montulet, Orianne T1 - Functional characterization of putative interactors of the Cellulose Synthase Complex Y1 - 2024 ER - TY - JOUR A1 - Ogunkola, Moses Olalekan A1 - Guiraudie-Capraz, Gaelle A1 - Féron, François A1 - Leimkühler, Silke T1 - The Human Mercaptopyruvate Sulfurtransferase TUM1 Is Involved in Moco Biosynthesis, Cytosolic tRNA Thiolation and Cellular Bioenergetics in Human Embryonic Kidney Cells JF - Biomolecules N2 - Sulfur is an important element that is incorporated into many biomolecules in humans. The incorporation and transfer of sulfur into biomolecules is, however, facilitated by a series of different sulfurtransferases. Among these sulfurtransferases is the human mercaptopyruvate sulfurtransferase (MPST) also designated as tRNA thiouridine modification protein (TUM1). The role of the human TUM1 protein has been suggested in a wide range of physiological processes in the cell among which are but not limited to involvement in Molybdenum cofactor (Moco) biosynthesis, cytosolic tRNA thiolation and generation of H2S as signaling molecule both in mitochondria and the cytosol. Previous interaction studies showed that TUM1 interacts with the L-cysteine desulfurase NFS1 and the Molybdenum cofactor biosynthesis protein 3 (MOCS3). Here, we show the roles of TUM1 in human cells using CRISPR/Cas9 genetically modified Human Embryonic Kidney cells. Here, we show that TUM1 is involved in the sulfur transfer for Molybdenum cofactor synthesis and tRNA thiomodification by spectrophotometric measurement of the activity of sulfite oxidase and liquid chromatography quantification of the level of sulfur-modified tRNA. Further, we show that TUM1 has a role in hydrogen sulfide production and cellular bioenergetics. KW - Moco biosynthesis KW - sulfite oxidase KW - cytosolic tRNA thiolation KW - 5-methoxycarbonylmethyl-2-thiouridine KW - H2S biosynthesis KW - cellular bioenergetics Y1 - 2023 U6 - https://doi.org/10.3390/biom13010144 SN - 2218-273X VL - 13 SP - 1 EP - 23 PB - MDPI CY - Basel, Schweiz ET - 1 ER - TY - JOUR A1 - Marggraf, Lara Christin A1 - Lindecke, Oliver A1 - Voigt, Christian C. A1 - Pētersons, Gunārs A1 - Voigt-Heucke, Silke Luise T1 - Nathusius’ bats, Pipistrellus nathusii, bypass mating opportunities of their own species, but respond to foraging heterospecifics on migratory transit flights JF - Frontiers in Ecology and Evolution N2 - In late summer, migratory bats of the temperate zone face the challenge of accomplishing two energy-demanding tasks almost at the same time: migration and mating. Both require information and involve search efforts, such as localizing prey or finding potential mates. In non-migrating bat species, playback studies showed that listening to vocalizations of other bats, both con-and heterospecifics, may help a recipient bat to find foraging patches and mating sites. However, we are still unaware of the degree to which migrating bats depend on con-or heterospecific vocalizations for identifying potential feeding or mating opportunities during nightly transit flights. Here, we investigated the vocal responses of Nathusius’ pipistrelle bats, Pipistrellus nathusii, to simulated feeding and courtship aggregations at a coastal migration corridor. We presented migrating bats either feeding buzzes or courtship calls of their own or a heterospecific migratory species, the common noctule, Nyctalus noctula. We expected that during migratory transit flights, simulated feeding opportunities would be particularly attractive to bats, as well as simulated mating opportunities which may indicate suitable roosts for a stopover. However, we found that when compared to the natural silence of both pre-and post-playback phases, bats called indifferently during the playback of conspecific feeding sounds, whereas P. nathusii echolocation call activity increased during simulated feeding of N. noctula. In contrast, the call activity of P. nathusii decreased during the playback of conspecific courtship calls, while no response could be detected when heterospecific call types were broadcasted. Our results suggest that while on migratory transits, P. nathusii circumnavigate conspecific mating aggregations, possibly to save time or to reduce the risks associated with social interactions where aggression due to territoriality might be expected. This avoidance behavior could be a result of optimization strategies by P. nathusii when performing long-distance migratory flights, and it could also explain the lack of a response to simulated conspecific feeding. However, the observed increase of activity in response to simulated feeding of N. noctula, suggests that P. nathusii individuals may be eavesdropping on other aerial hawking insectivorous species during migration, especially if these occupy a slightly different foraging niche. KW - playback KW - phonotaxis KW - bats KW - acoustic communication KW - animal migration KW - eavesdropping KW - echolocation KW - Pipistrellus nathusii Y1 - 2023 U6 - https://doi.org/10.3389/fevo.2022.908560 SN - 2296-701X SP - 1 EP - 10 PB - Frontiers CY - Lausanne, Schweiz ER - TY - THES A1 - Artins, Anthony T1 - Crosstalk between Target Of Rapamycin (TOR) and sugar signaling in Arabidopsis thaliana Y1 - 2023 ER - TY - THES A1 - Amen, Rahma T1 - Adaptive radiation in African weakly electric fish genus Campylomormyrus BT - a behavior, ecological and morphological perspective N2 - The African weakly electric fish genus Campylomormyrus includes 15 described species mostly native to the Congo River and its tributaries. They are considered sympatric species, because their distribution area overlaps. These species generate species-specific electric organ discharges (EODs) varying in waveform characteristics, including duration, polarity, and phase number. They exhibit also pronounced divergence in their snout, i.e. the length, thickness, and curvature. The diversifications in these two phenotypical traits (EOD and snout) have been proposed as key factors promoting adaptive radiation in Campylomormyrus. The role of EODs as a pre-zygotic isolation mechanism driving sympatric speciation by promoting assortative mating has been examined using behavioral, genetical, and histological approaches. However, the evolutionary effects of the snout morphology and its link to species divergence have not been closely examined. Hence, the main objective of this study is to investigate the effect of snout morphology diversification and its correlated EOD to better understand their sympatric speciation and evolutionary drivers. Moreover, I aim to utilize the intragenus and intergenus hybrids of Campylomormyrus to better understand trait divergence as well as underlying molecular/genetic mechanisms involved in the radiation scenario. To this end, I utilized three different approaches: feeding behavior analysis, diet assessment, and geometric morphometrics analysis. I performed feeding behavior experiments to evaluate the concept of the phenotype-environment correlation by testing whether Campylomormyrus species show substrate preferences. The behavioral experiments showed that the short snout species exhibits preference to sandy substrate, the long snout species prefers a stone substrate, and the species with intermediate snout size does not exhibit any substrate preference. The experiments suggest that the diverse feeding apparatus in the genus Campylomormyrus may have evolved in adaptation to their microhabitats. I also performed diet assessments of sympatric Campylomormyrus species and a sister genus species (Gnathonemus petersii) with markedly different snout morphologies and EOD using NGS-based DNA metabarcoding of their stomach contents. The diet of each species was documented showing that aquatic insects such as dipterans, coleopterans and trichopterans represent the major diet component. The results showed also that all species are able to exploit diverse food niches in their habitats. However, comparing the diet overlap indices showed that different snout morphologies and the associated divergence in the EOD translated into different prey spectra. These results further support the idea that the EOD could be a ‘magic trait’ triggering both adaptation and reproductive isolation. Geometric morphometrics method was also used to compare the phenotypical shape traits of the F1 intragenus (Campylomormyrus) and intergenus (Campylomormyrus species and Gnathonemus petersii) hybrids relative to their parents. The hybrids of these species were well separated based on the morphological traits, however the hybrid phenotypic traits were closer to the short-snouted species. In addition, the likelihood that the short snout expressed in the hybrids increases with increasing the genetic distance of the parental species. The results confirmed that additive effects produce intermediate phenotypes in F1-hybrids. It seems, therefore, that morphological shape traits in hybrids, unlike the physiological traits, were not expressed straightforward. KW - adaptive radiation KW - ecological speciation KW - African weakly electric fish KW - trophic apparatus KW - DNA metabarcoding KW - geometric morphometric Y1 - 2023 ER - TY - THES A1 - Gonzalez Duran, Enrique T1 - Genetic control of intracellular gene transfer by DNA repair in N. tabacum N2 - Mitochondria and plastids are organelles with an endosymbiotic origin. During evolution, many genes are lost from the organellar genomes and get integrated in the nuclear genome, in what is known as intracellular/endosymbiotic gene transfer (IGT/EGT). IGT has been reproduced experimentally in Nicotiana tabacum at a gene transfer rate (GTR) of 1 event in 5 million cells, but, despite its centrality to eukaryotic evolution, there are no genetic factors known to influence the frequency of IGT in higher eukaryotes. The focus of this work was to determine the role of different DNA repair pathways of double strand break repair (DSBR) in the integration step of organellar DNA in the nuclear genome during IGT. Here, a CRISPR/Cas9 mutagenesis strategy was implemented in N. tabacum, with the aim of generating mutants in nuclear genes without expected visible phenotypes. This strategy led to the generation of a collection of independent mutants in the LIG4 (necessary for non-homologous end joining, NHEJ) and POLQ genes (necessary for microhomology mediated end joining, MMEJ). Targeting of other DSBR genes (KU70, KU80, RPA1C) generated mutants with unexpectedly strong developmental phenotypes.. These factors have telomeric roles, hinting towards a possible relationship between telomere length, and strength of developmental disruption upon loss of telomere structure in plants. The mutants were made in a genetic background encoding a plastid-encoded IGT reporter, that confers kanamycin resistance upon transfer to the nucleus. Through large scale independent experiments, increased IGT from the chloroplast to the nucleus was observed in lig4 mutants, as well as lines encoding a POLQ gene with a defective polymerase domain (polqΔPol). This shows that NHEJ or MMEJ have a double-sided relationship with IGT: while transferred genes may integrate using either pathway, the presence of both pathways suppresses IGT in wild-type somatic cells, thus demonstrating for the first time the extent on which nuclear genes control IGT frequency in plants. The IGT frequency increases in the mutants are likely mediated by increased availability of double strand breaks for integration. Additionally, kinetic analysis reveals that gene transfer (GT) events accumulate linearly as a function of time spent under antibiotic selection in the experiment, demonstrating that, contrary to what was previously thought, there is no such thing as a single GTR in somatic IGT experiments. Furthermore, IGT in tissue culture experiments appears to be the result of a "race against the clock" for integration in the nuclear genome, that starts when the organellar DNA arrives to the nucleus granting transient antibiotic resistance. GT events and escapes of kanamycin selection may be two possible outcomes from this race: those instances where the organellar DNA gets to integrate are recovered as GT events, and in those cases where timely integration fails, antibiotic resistance cannot be sustained, and end up considered as escapes. In the mutants, increased opportunities for integration in the nuclear genome change the overall ratio between IGT and escape events. The resources generated here are promising starting points for future research: (1) the mutant collection, for the further study of processes that depend on DNA repair in plants (2) the collection of GT lines obtained from these experiments, for the study of the effect of DSBR pathways over integration patterns and stability of transferred genes and (3) the developed CRISPR/Cas9 workflow for mutant generation, to make N. tabacum meet its potential as an attractive model for answering complex biological questions. N2 - Mitochondrien und Plastiden sind beides Organellen endosymbiotischen Ursprungs. Im Laufe der Evolution gehen viele Gene aus den Organellengenomen verloren und werden in das Kerngenom integriert, was als intrazellulärer/endosymbiotischer Gentransfer (IGT/EGT) bezeichnet wird. IGT konnte experimentell in Nicotiana tabacum mit einer Gentransferrate (GTR) von einem Ereignis in fünf Millionen Zellen nachgestellt werden, aber trotz seiner zentralen Bedeutung für die eukaryotische Evolution sind keine genetischen Faktoren bekannt, die die Häufigkeit von IGT in höheren Eukaryoten beeinflussen. Der Schwerpunkt dieser Arbeit lag auf der Bestimmung der Rolle verschiedener DNA-Reparaturwege der Doppelstrangbruchreparatur (DSBR) bei der Integration von Organellen-DNA in das Kerngenom während des IGT. Dazu wurde in N. tabacum eine CRISPR/Cas9-basierte Mutagenesestrategie angewandt, mit dem Ziel, Mutanten in Kerngenen zu erzeugen, für die keine sichtbaren Phänotypen zu erwarten sind. Diese Strategie führte zur Erzeugung einer Reihe unabhängiger Mutanten im LIG4-Gen (notwendig für „non-homologous end joining“, die nicht-homologe Verbindung von Enden, NHEJ) und POLQ (notwendig für „microhomology mediated end joining“, die Mikrohomologie-vermittelte Verbindung von Enden, MMEJ). Die gezielte Beeinflussung anderer DSBR-Gene (KU70, KU80, RPA1C) führte zu Mutanten mit unerwartet starken Entwicklungsphänotypen. Diese Gene spielen eine Rolle beim Erhalt der Telomere, was auf einen möglichen Zusammenhang zwischen der Telomerlänge und der Stärke der Entwicklungsstörung bei Verlust der Telomerstruktur in Pflanzen hindeutet. Die Mutanten wurden in einem genetischen Hintergrund erzeugt, der über einen in den Plastiden lokalisierten IGT-Reporter verfügt, der nach Übertragung in den Zellkern Kanamycin-Resistenz vermittelt. In groß angelegten unabhängigen Experimenten wurde in lig4-Mutanten sowie in Linien, die für ein POLQ-Gen mit einer defekten Polymerase-Domäne (polqΔPol) kodieren, eine erhöhte GTR vom Chloroplasten zum Zellkern beobachtet. Dies zeigt, dass NHEJ oder MMEJ eine zweischneidige Beziehung zum IGT haben: Während übertragene Gene folglich über jeden der beiden Mechanismen integriert werden können, unterdrückt das gleichzeitige Vorhandensein beider Wege IGT in somatischen Wildtyp-Zellen, wodurch zum ersten Mal gezeigt wird, in welchem Ausmaß Kerngene die IGT-Häufigkeit in Pflanzen kontrollieren. Die erhöhte Verfügbarkeit von Doppelstrangbrüchen für die Integration könnte für die erhöhte IGT-Häufigkeit in den Mutanten verantwortlich sein. Darüber hinaus zeigt die Analyse des Zeitverlaufs, dass Gentransferereignisse (GT) in Abhängigkeit von der Zeit, die im Experiment unter Antibiotikaselektion verbracht wurde, linear akkumulieren, was beweist, dass es, anders als bisher angenommen, in somatischen IGT-Experimenten keine statische GTR gibt. Darüber hinaus scheint IGT in Gewebekulturexperimenten das Ergebnis eines Wettlaufs mit der Zeit um die Integration in das Kerngenom zu sein, der beginnt, wenn die Organellen-DNA in den Zellkern gelangt und eine vorübergehende Antibiotikaresistenz gewährt. Echte GT-Ereignisse und „Escapes“ (scheinbare Resistenz, ein vorläufiges Ausweichen vor der Kanamycin-Selektion) können zwei mögliche Ergebnisse dieses Wettlaufs sein: Die Fälle, in denen die Organellen-DNA integriert wird, werden als GT-Ereignisse gewertet, und in den Fällen, in denen die rechtzeitige Integration scheitert, kann die Antibiotikaresistenz nicht aufrechterhalten werden und sie werden als „Escape“ betrachtet. In den Mutanten verändern sich die Möglichkeiten zur Integration in das Kerngenom, wodurch sich das Gesamtverhältnis zwischen IGT- und „Escape“-Ereignissen ändert. Die hier erzeugten Ressourcen sind vielversprechende Ausgangspunkte für künftige Forschungen: (1) die Mutantensammlung, für die Untersuchung von weiteren Prozessen, die von der DNA-Reparatur in Pflanzen abhängen, (2) die Sammlung von GT-Linien, die aus den hier beschriebenen Experimenten gewonnen wurden, für die Untersuchung der Auswirkungen von DSBR-Mechanismen auf Integrationsmuster und Stabilität übertragener Gene und (3) der hier entwickelte Arbeitsablauf für die Mutantenerzeugung mittels CRISPR/Cas9, damit N. tabacum sein Potenzial als attraktives Modell für die Beantwortung komplexer biologischer Fragestellungen erfüllen kann. T2 - Genetische Kontrolle des intrazellulären Gentransfers durch DNA-Reparatur in N. tabacum KW - endosymbiosis KW - organelles KW - gene KW - transfer KW - DNA KW - repair KW - genome KW - editing KW - evolution KW - plant Y1 - 2023 ER - TY - THES A1 - Bühler, Miriam T1 - The role of (xeno)hormone-activated GPER1 for centrosome amplification and whole chromosomal instability in colon cell lines N2 - The G protein-coupled estrogen receptor (GPER1) is acknowledged as an important mediator of estrogen signaling. Given the ubiquitous expression of GPER1, it is likely that the receptor plays a role in a variety of malignancies, not only in the classic hormonally regulated tissues (e.g., breast, ovary, and prostate), but also in the colon. As colorectal cancer (CRC) is the third most common cancer in both men and women worldwide and environmental factors and dietary habits are important risk factors, it is increasingly recognized that natural and synthetic hormones and their associated receptors might play a role in CRC. Through oral consumption, environmental contaminants with endocrine activity are in contact with the gastrointestinal mucosa, where they might exert their toxic effects. Although GPER1 has been shown to be engaged in physiological and pathophysiological processes, its role in CRC remains poorly understood. Thus, pro- as well as anti-tumorigenic effects are described in the literature. This thesis has uncovered novel roles of GPER1 in mediating major CRC-associated phenotypes in transformed and non-transformed colon cell lines. Exposure to the estrogens 17β-estradiol (E2), bisphenol-A (BPA) and diethylstilbestrol (DES) but also the androgen dihydrotestosterone (DHT) resulted in GPER1-dependent induction of supernumerary centrosomes, whole chromosomal instability (w-CIN) and aneuploidy. Indeed, both knockdown and inhibition of GPER1 attenuated the generation of (xeno)hormone-driven supernumerary centrosomes and karyotype instability. Mechanistically, (xeno)hormone-induced centrosome amplification was associated with transient multipolar mitosis and the generation of so called anaphase “lagging” chromosomes. The results of this thesis propose a GPER1/PKA/AKAP9-pathway in regulating centrosome numbers in colorectal cancer cells and the involvement of the centriolar protein centrin. Remarkably, exposure to (xeno)hormones resulted in atypical enlargement and unexpected phosphorylation of the centriole marker centrin in interphase. These findings provide a novel role for GPER1 in key CRC-prone lesions and shed light on underlying mechanisms that involve GPER1 function in the colon. Elucidating to what extent centrosomal proteins are involved in the GPER1-mediated aneugenic effect will be an important task for future studies. The present study was intended to lay a first foundation to understand the molecular basis and potential risk factors of CRC which might help to reduce the use of laboratory animals. Since numerous animal experiments are conducted in biomedical research, the development of alternative methods is indispensable. The Federal Institute for Risk Assessment (BfR) as the German Center for the Protection of Laboratory Animals (Bf3R) addresses this issue by uncovering underlying mechanisms leading to colorectal cancer as necessary prerequisite in order to develop alternative methods. N2 - Der G-Protein-gekoppelte Östrogenrezeptor (GPER1) ist als wichtiger Vermittler von Östrogensignalen bekannt. Angesichts der ubiquitären Expression von GPER1 ist es wahrscheinlich, dass der Rezeptor bei einer Vielzahl von Krebserkrankungen eine Rolle spielt, nicht nur in den klassischen hormonell regulierten Geweben (z. B. Brust, Eierstöcke und Prostata), sondern auch im Darm. Da Darmkrebs (Colorectal cancer, CRC) weltweit die dritthäufigste Krebserkrankung sowohl bei Männern als auch bei Frauen ist und Umweltfaktoren und Ernährungsgewohnheiten wichtige Risikofaktoren darstellen, geht man zunehmend davon aus, dass natürliche und synthetische Hormone und ihre zugehörigen Rezeptoren eine Rolle im Darmkrebs spielen könnten. Durch orale Aufnahme kommen Umweltschadstoffe mit endokriner Aktivität mit der Magen-Darm-Schleimhaut in Kontakt, wo sie ihre toxischen Wirkungen entfalten könnten. Obwohl gezeigt wurde, dass GPER1 an physiologischen und pathophysiologischen Prozessen beteiligt ist, ist seine Rolle im Darmkrebs nach wie vor unzureichend geklärt. So werden in der Literatur sowohl Tumor-fördernde als auch -hemmende Wirkungen beschrieben werden. In dieser Arbeit wurden neue Rollen von GPER1 bei der Vermittlung wichtiger Darmkrebs-assoziierter Phänotypen in transformierten und nicht-transformierten Kolonzelllinien aufgedeckt. Die Exposition gegenüber den Östrogenen 17β-Östradiol (E2), Bisphenol-A (BPA) und Diethylstilbestrol (DES), aber auch dem Androgen Dihydrotestosteron (DHT) führte zu einer GPER1-abhängigen Induktion von überzähligen Zentrosomen, chromosomaler Instabilität (w-CIN) und Aneuploidie. Sowohl der Knockdown, als auch die Inhibierung von GPER1 verringerten die Entstehung von (xeno)hormon-bedingten überzähligen Zentrosomen und Karyotyp Instabilität. Mechanistisch gesehen war die (Xeno-)Hormon-induzierte Zentrosomen Amplifikation mit einer vorübergehenden multipolaren Mitose und der Bildung von sogenannten Anaphasen „lagging“ Chromosomen verbunden. Die Ergebnisse dieser Arbeit deuten auf einen GPER1/PKA/AKAP9-Weg zur Regulierung der Zentrosomenzahl in Darmkrebszellen und eine Beteiligung des zentriolären Proteins Zentrin hin. Bemerkenswerterweise führte die Exposition gegenüber (Xeno-)Hormonen zu einer atypischen Vergrößerung und unerwarteten Phosphorylierung des Zentriolen Markers Centrin in der Interphase. Diese Ergebnisse enthüllen eine neue Rolle für GPER1 in wichtigen, mit Darmkrebs assoziierten Läsionen und geben Aufschluss auf die zugrundeliegenden Mechanismen der GPER1-Funktion im Darm. Die Aufklärung zu welchem Ausmaßes zentrosomale Proteine an der GPER1-vermittelten aneugenischen Wirkung beteiligt sind, wird eine wichtige Aufgabe für zukünftige Studien sein. Mit der vorliegenden Studie sollte eine erste Grundlage für das Verständnis der molekularen Grundlagen und potenziellen Risikofaktoren von Darmkrebs geschaffen werden, was dazu beitragen könnte, den Einsatz von Versuchstieren zu reduzieren. Da in der biomedizinischen Forschung zahlreiche Tierversuche durchgeführt werden, ist die Entwicklung von Alternativmethoden unerlässlich. Das Bundesinstitut für Risikobewertung (BfR) als Deutsches Zentrum zum Schutz von Versuchstieren (Bf3R) widmet sich diesem Thema, indem es die zugrundeliegenden Mechanismen, die zu Darmkrebs führen, als notwendige Voraussetzung für die Entwicklung alternativer Methoden aufdeckt. KW - centrosome amplification KW - colon cancer KW - G protein-coupled estrogen receptor KW - whole chromosomal instability KW - (xeno)hormones KW - Zentrosomen Amplifikation KW - Darmkrebs KW - G protein-gekoppelter Östrogen Rezeptor KW - chromosomale Instabilität KW - (Xeno)Hormone Y1 - 2023 ER - TY - THES A1 - von Bismarck, Thekla T1 - The influence of long-term light acclimation on photosynthesis in dynamic light N2 - Photosynthesis converts light into metabolic energy which fuels plant growth. In nature, many factors influence light availability for photosynthesis on different time scales, from shading by leaves within seconds up to seasonal changes over months. Variability of light energy supply for photosynthesis can limit a plant´s biomass accumulation. Plants have evolved multiple strategies to cope with strongly fluctuation light (FL). These range from long-term optimization of leaf morphology and physiology and levels of pigments and proteins in a process called light acclimation, to rapid changes in protein activity within seconds. Therefore, uncovering how plants deal with FL on different time scales may provide key ideas for improving crop yield. Photosynthesis is not an isolated process but tightly integrates with metabolism through mutual regulatory interactions. We thus require mechanistic understanding of how long-term light acclimation shapes both, dynamic photosynthesis and its interactions with downstream metabolism. To approach this, we analyzed the influence of growth light on i) the function of known rapid photosynthesis regulators KEA3 and VCCN1 in dynamic photosynthesis (Chapter 2-3) and ii) the interconnection of photosynthesis with photorespiration (PR; Chapter 4). We approached topic (i) by quantifying the effect of different growth light regimes on photosynthesis and photoprotection by using kea3 and vccn1 mutants. Firstly, we found that, besides photosynthetic capacity, the activities of VCCN1 and KEA3 during a sudden high light phase also correlated with growth light intensity. This finding suggests regulation of both proteins by the capacity of downstream metabolism. Secondly, we showed that KEA3 accelerated photoprotective non-photochemical quenching (NPQ) kinetics in two ways: Directly via downregulating the lumen proton concentration and thereby de-activating pH-dependent NPQ, and indirectly via suppressing accumulation of the photoprotective pigment zeaxanthin. For topic (ii), we analyzed the role of PR, a process which recycles a toxic byproduct of the carbon fixation reactions, in metabolic flexibility in a dynamically changing light environment. For this we employed the mutants hpr1 and ggt1 with a partial block in PR. We characterized the function of PR during light acclimation by tracking molecular and physiological changes of the two mutants. Our data, in contrast to previous reports, disprove a generally stronger physiological relevance of PR under dynamic light conditions. Additionally, the two different mutants showed pronounced and distinct metabolic changes during acclimation to a condition inducing higher photosynthetic activity. This underlines that PR cannot be regarded purely as a cyclic detoxification pathway for 2PG. Instead, PR is highly interconnected with plant metabolism, with GGT1 and HPR1 representing distinct metabolic modulators. In summary, the presented work provides further insight into how energetic and metabolic flexibility is ensured by short-term regulators and PR during long-term light acclimation. N2 - Photosynthese wandelt Lichtenergie in metabolische Energie um, welche das Pflanzenwachstum antreibt. In der Natur wird die Verfügbarkeit von Licht von vielerlei Faktoren auf unterschiedlichen Zeitskalen beeinflusst, z. B. von der Beschattung durch Blätter innerhalb von Sekunden bis hin zu jahreszeitlichen Veränderungen über Monate. Fluktuationen in der Lichtenergieverfügbarkeit in der Natur kann die Biomasseakkumulation der Pflanzen limitieren. Pflanzen haben verschiedene Strategien entwickelt, um stark fluktuierendes Licht nutzen zu können. Diese reichen von der langfristigen Optimierung der Blattmorphologie und Physiologie und des Gehalts an Pigmenten und Proteinen in dem Prozess der Lichtakklimatisierung bis hin zu schnellen Veränderungen der Proteinaktivität innerhalb von Sekunden. Daher kann die Aufdeckung der Art und Weise, wie Pflanzen mit FL auf verschiedenen Zeitskalen umgehen, wichtige Ideen zur Verbesserung der Ernteerträge liefern. Die Photosynthese ist kein isolierter Prozess, sondern steht in enger Interaktion mit den nachgeschalteten Stoffwechselwegen. Daher benötigen wir mechanistisches Verständnis, wie Lichtakklimatisierung die dynamische Photosynthese als auch deren Interaktion mit Downstream-Metabolismus moduliert. Dafür haben wir den Einfluss von Lichtakklimatisierung auf i) die Funktion der schnellen Photosyntheseregulatoren KEA3 und VCCN1 in der dynamischen Photosynthese und ii) die flexible Interaktion von Photorespiration mit Photosynthese analysiert. Im ersten Themenkomplex (i) wurden die Auswirkungen verschiedener Wachstumslicht-bedingungen auf Photosynthese und Photoprotektion anhand von kea3- und vccn1-Mutanten quantifiziert. Zum einen konnten wir zeigen, dass neben der photosynthetischen Kapazität auch die Aktivitäten von VCCN1 und KEA3 während eines Hochlichtpulses mit der Wachstumslichtintensität korrelierten. Dies deutet auf eine Regulierung beider Proteine durch die Kapazität des Downstream-Metabolismus hin. Zum anderen beschleunigte KEA3 die Kinetik des photoprotektiven nicht-photochemischen Quenchings (NPQ) auf zweifache Weise: Direkt über die Herabregulierung der lumenalen Protonenkonzentration, was den pH-abhängigen NPQ deaktivierte, und indirekt über die Unterdrückung der Akkumulation des photoprotektiven Pigments Zeaxanthin. Für das zweite Thema (ii) untersuchten wir die Rolle des photorespiratorischen Metabolismus (PR), welcher ein toxisches Nebenprodukt der Kohlenstofffixierungsreaktionen recycelt, in der metabolischen Flexibilität in einer sich dynamisch verändernden Lichtumgebung. Dazu verwendeten wir die Mutanten hpr1 und ggt1 mit teilweise blockiertem PR Flux. Unsere Daten widerlegen, im Gegensatz zu früheren Berichten, eine allgemein größere physiologische Bedeutung von PR unter dynamischen Lichtbedingungen. Die beiden Mutanten zeigten ausgeprägte und distinkte metabolische Veränderungen während der Akklimatisierung an eine Bedingung mit höherer photosynthetischer Aktivität. Dies zeigt, dass PR nicht ausschließlich als zyklischer Entgiftungsweg für 2PG angesehen werden kann. Vielmehr ist PR tief in den pflanzlichen Stoffwechsel eingebettet, wobei GGT1 und HPR1 als distinkte Stellschrauben des Downstream-Metabolismus agieren. Zusammenfassend liefert die vorliegende Arbeit weitere Erkenntnisse darüber, wie die energetische und metabolische Flexibilität durch kurzfristige Regulatoren und den photorespiratorischen Metabolismus während der langfristigen Lichtakklimatisierung gewährleistet wird. KW - photosynthesis KW - fluctuating light KW - Arabidopsis thaliana KW - Photosynthese KW - fluktuierendes Licht Y1 - 2023 ER - TY - THES A1 - Rolo, David T1 - Assembly of photosystem I in thylakoid membranes T1 - Die Assemblierung des Photosystems I in der Thylakoidmembran N2 - The light reactions of photosynthesis are carried out by a series of multiprotein complexes embedded in thylakoid membranes. Among them, photosystem I (PSI), acting as plastocyanin-ferderoxin oxidoreductase, catalyzes the final reaction. Together with light-harvesting antenna I, PSI forms a high-molecular-weight supercomplex of ~600 kDa, consisting of eighteen subunits and nearly two hundred co-factors. Assembly of the various components into a functional thylakoid membrane complex requires precise coordination, which is provided by the assembly machinery. Although this includes a small number of proteins (PSI assembly factors) that have been shown to play a role in the formation of PSI, the process as a whole, as well as the intricacy of its members, remains largely unexplored. In the present work, two approaches were used to find candidate PSI assembly factors. First, EnsembleNet was used to select proteins thought to be functionally related to known PSI assembly factors in Arabidopsis thaliana (approach I), and second, co-immunoprecipitation (Co-IP) of tagged PSI assembly factors in Nicotiana tabacum was performed (approach II). Here, the novel PSI assembly factors designated CO-EXPRESSED WITH PSI ASSEMBLY 1 (CEPA1) and Ycf4-INTERACTING PROTEIN 1 (Y4IP1) were identified. A. thaliana null mutants for CEPA1 and Y4IP1 showed a growth phenotype and pale leaves compared with the wild type. Biophysical experiments using pulse amplitude modulation (PAM) revealed insufficient electron transport on the PSII acceptor side. Biochemical analyses revealed that both CEPA1 and Y4IP1 are specifically involved in PSI accumulation in A. thaliana at the post-translational level but are not essential. Consistent with their roles as factors in the assembly of a thylakoid membrane protein complex, the two proteins localize to thylakoid membranes. Remarkably, cepa1 y4ip1 double mutants exhibited lethal phenotypes in early developmental stages under photoautotrophic growth. Finally, co-IP and native gel experiments supported a possible role for CEPA1 and Y4IP1 in mediating PSI assembly in conjunction with other PSI assembly factors (e.g., PPD1- and PSA3-CEPA1 and Ycf4-Y4IP1). The fact that CEPA1 and Y4IP1 are found exclusively in green algae and higher plants suggests eukaryote-specific functions. Although the specific mechanisms need further investigation, CEPA1 and Y4IP1 are two novel assembly factors that contribute to PSI formation. N2 - Die Lichtreaktionen der Photosynthese werden von einer Reihe von Multiproteinkomplexen durchgeführt, die in Thylakoidmembranen eingebettet sind. Hier katalysiert das Photosystem I (PSI), das als Plastocyanin-Ferderoxin-Oxidoreduktase fungiert, die letzte Reaktion. Zusammen mit der lichtsammelnden Antenne I bildet PSI einen hochmolekularen Superkomplex von etwa 600 kDa, der aus achtzehn Untereinheiten und fast zweihundert Co-Faktoren besteht. Der Zusammenbau der verschiedenen Komponenten zu einem funktionsfähigen Thylakoidmembrankomplex erfordert eine präzise Koordination, die durch den Assemblierungsapparat gewährleistet wird. Obwohl dieser eine kleine Anzahl von Proteinen (PSI-Assemblierungsfaktoren) umfasst, die nachweislich eine Rolle bei der Bildung des PSI spielen, ist der Prozess als Ganzes sowie die Komplexität seiner Mitglieder noch weitgehend unerforscht. In der vorliegenden Arbeit wurden zwei Ansätze verwendet, um Kandidaten für PSI-Assemblierungsfaktoren zu finden. Erstens wurde EnsembleNet verwendet, um Proteine auszuwählen, von denen angenommen wird, dass sie funktionell mit bekannten PSI-Assemblierungsfaktoren in Arabidopsis thaliana verwandt sind (Ansatz I), und zweitens wurde eine Co-Immunopräzipitation (Co-IP) von markierten PSI-Assemblierungsfaktoren in Nicotiana tabacum durchgeführt (Ansatz II). Dabei wurden die neuartigen PSI-Assemblierungsfaktoren mit der Bezeichnung CO-EXPRESSED WITH PSI ASSEMBLY 1 (CEPA1) und Ycf4-INTERACTING PROTEIN 1 (Y4IP1) identifiziert. A. thaliana Nullmutanten für CEPA1 und Y4IP1 zeigten einen Wachstumsphänotyp und blasse Blätter im Vergleich zum Wildtyp. Biophysikalische Experimente unter Verwendung der Pulsamplitudenmodulation (PAM) zeigten einen unzureichenden Elektronentransport auf der PSII-Akzeptorseite. Biochemische Analysen ergaben, dass sowohl CEPA1 als auch Y4IP1 spezifisch an der PSI-Akkumulation in A. thaliana auf posttranslationaler Ebene beteiligt, jedoch nicht essentiell sind. Entsprechend ihrer Rolle als Faktoren für den Aufbau eines Thylakoidmembran-Proteinkomplexes sind die beiden Proteine an Thylakoidmembranen lokalisiert. Bemerkenswerterweise wiesen cepa1 y4ip1-Doppelmutanten in frühen Entwicklungsstadien unter photoautotrophem Wachstum tödliche Phänotypen auf. Schließlich untermauerten Co-IP- und native Gelexperimente eine mögliche Rolle von CEPA1 und Y4IP1 bei der Vermittlung des PSI-Aufbaus in Verbindung mit anderen PSI-Aufbaufaktoren (z. B. PPD1- und PSA3-CEPA1, und Ycf4-Y4IP1). Die Tatsache, dass CEPA1 und Y4IP1 ausschließlich in Grünalgen und höheren Pflanzen vorkommen, lässt auf eukaryontenspezifische Funktionen schließen. Obwohl die spezifischen Mechanismen noch weiter untersucht werden müssen, sind CEPA1 und Y4IP1 zwei neuartige Assemblierungsfaktoren, die zur PSI-Bildung beitragen. KW - photosynthesis KW - photosystem I KW - biogenesis KW - thylakoid membranes KW - assembly factor KW - Photosynthese KW - Photosystem I KW - Biogenese KW - Thylakoidmembran KW - Assemblierungsfaktor Y1 - 2023 ER - TY - THES A1 - Leer, Marina T1 - Computational analysis of the effects of ageing and diet on stem cell function and ectopic fat accumulation in the musculoskeletal system N2 - The musculoskeletal system provides support and enables movement to the body, and its deterioration is a crucial aspect of age-related functional decline. Mesenchymal stromal cells (MSCs) play an important role in musculoskeletal homeostasis due to their broad differentiation potentials and their ability to support osteogenic and myogenic tissue maintenance and regeneration. In the bone, MSCs differentiate either into osteochondrogenic progenitors to form osteocytes and chondrocytes, or increasingly with age into adipogenic progenitors which give rise to bone-resident adipocytes. In skeletal muscle, during healthy regeneration MSCs provide regulatory signals that activate local, tissue-specific stem cells, known as satellite cells, which regenerate contractile myofibres. This process involves a significant cross-talk to immune cells stemming from both lymphoid and myeloid lineages. During ageing, muscle-resident MSCs undergo increased adipogenic lineage commitment, causing niche changes that contribute to fatty infiltration in muscles. These shifts in cell populations in bone lead to the loss of osteogenic cells and subsequently osteoporosis, or in muscle to impaired regeneration and to the development of sarcopenia. However, the signals that drive transition of MSCs into their respective cellular fates remain elusive. This thesis aims to elucidate the transcriptional shifts modulating cell states and cell types in musculoskeletal MSC fate determination. Single-cell RNA-sequencing (scRNA-seq) was used to characterise cell type-specific transcript regulation. State-of-the-art bioinformatics tools were combined with different analytical platforms that include both droplet-based scRNA-seq for large heterogeneous populations, and microfluidics-based scRNA-seq to assess small, rare subpopulations. For each platform, distinct computational pipelines were established including filtering steps to exclude low-quality cells, and data visualisation was performed by dimensionality reduction. Downstream analysis included clustering, cell type annotation, and differential gene expression to investigate transcriptional states in defined cell types during ageing and injury in the muscle and bone. Finally, a novel tool to assess publication activities in defined areas of research for the identified marker genes was developed. The results in the bone indicate that ageing MSCs increasingly commit towards an adipogenic fate at the expense of osteogenic specialisation. The data also suggests that significant cell population shifts of MSC-type fibro-adipogenic progenitors during muscle ageing underlie the pathologies observed in homeostatic and post-injury regenerative conditions. High-throughput visualisation of publication activity for candidate genes enabled more effective biological evaluation of scRNA-seq data. These results expose critical age-related changes in the stem cell niches of skeletal muscle and bone, highlight their respective sensitivity to nutrition and pathology, and elucidate novel factors that modulate stem cell-based regeneration. Targeting these processes might improve musculoskeletal health in the context of ageing and prevent the negative effects of pathological lineage determination. N2 - Der Stütz- und Bewegungsapparat durchläuft eine altersbedingte gesundheitliche Verschlechterung, welche mit voranschreitendem Funktionsverlust einhergeht. Mesenchymale Stromazellen (MSCs) spielen aufgrund ihres breiten Differenzierungspotenzials und ihrer Fähigkeit, myogene bzw. osteogene Regenerationsprozesse zu unterstützen, eine wichtige Rolle in der muskuloskelettalen Homöostase. Im Knochen differenzieren MSCs entweder zu osteochondrogenen Vorläufern, um Knochen- bzw. Knorpelzellen zu bilden. Oder mit zunehmendem Alter werden vermehrt adipogene Vorläufer gebildet, aus denen Knochen-Fettzellen entstehen. Im Skelettmuskel sezernieren MSCs während der Muskelregeneration beispielsweise regulatorische Signale, die lokale, gewebespezifische Stammzellen, sogenannte Satellitenzellen, aktivieren, und diese daraufhin die kontraktilen Muskelfasern regenerieren. Dieser Prozess umfasst bedeutsame Wechselwirkung von Stammzellen mit Immunzellen sowohl der lymphoiden als auch aus myeloischen Abstammungslinien. Während des Alterns erhalten muskelresidente MSCs jedoch ein erhöhtes adipogenenes Potential, welches Nischenveränderung verursacht und damit zu einer Fettinfiltration in den Muskeln beitragen kann. Die Verschiebungen der Zellpopulationen verursachen einerseits den Verlust von osteogenen Vorläufern und fördern degenerative Prozesse im Knochengewebe, die Osteoporose zur Folge haben, oder beeinträchtigen die Regeneration im Muskel sowie dessen Funktionalität, und können damit zur altersbedingten Sarkopenie beitragen. MSCs durchlaufen einen Entscheidungsprozess um final zu differenzieren, der jedoch bislang nur unzureichend charakterisiert ist. Um diesen Aspekt zu beleuchten, untersucht diese Dissertation die diesem Prozess zugrundeliegende Veränderung der Transkriptionsprofile, welche die Zellzustände und Zelltypen bei der Differenzierung von muskuloskelettalen MSCs steuern. Einzelzell-RNA-Sequenzierung (scRNA-Seq) wurde verwendet, um die zelltyp-spezifische Transkriptionsregulation zu charakterisieren. Moderne bioinformatische Analyse-Tools und -Plattformen wurden kombiniert, die sowohl droplet-basierte (für große heterogene Populationen) als auch mikrofluidik-basierte scRNA-seq (für kleine, seltene Subpopulationen), umfassten. Es wurden plattform-spezifische Datenverarbeitungs-Pipelines generiert, einschließlich des Herausfilterns von Zellen geringer Qualität und Datenvisualisierung mit verschiedenen Dimensionsreduktions-Methoden. Die anschließende Analyse umfasste Clustering von Subpopulationen, Zelltyp-Annotation und differenzielle Genexpression, um die Transkriptionszustände in den definierten Zelltypen während des Alterns und bei Regeneration im Muskel und Knochen zu untersuchen. Abschließend wurde eine Software zur Bewertung der Publikationsaktivitäten in definierten Forschungsgebieten für die identifizierten Markergene entwickelt. Die Ergebnisse deuten im Knochen darauf hin, dass alternde MSCs auf Kosten der osteogenen Spezialisierung zunehmend adipogener werden. Weiterhin deuten unsere Daten darauf hin, dass im alternden Muskel eine signifikante Zellpopulationsanreicherung von MSCs zu fibro-adipogenen Vorläuferzellen stattfindet, welche den Pathologien in den Prozessen der Homöostase und Muskelregeneration nach Verletzung unterliegen. Die Visualisierung der Publikationsaktivität für Kandidatengene ermöglicht eine effektivere biologische Bewertung von scRNA-seq-Daten. Diese Ergebnisse offenbaren kritische altersbedingte Veränderungen innerhalb der Stammzellnischen von Skelettmuskeln und Knochen, und identifizieren neue Faktoren, die an stammzell-basierten Regeneration beteiligt sind. Diese Prozesse gezielt zu beeinflussen, könnte die muskuloskelettale Gesundheit im Alter verbessern und negative Effekte einer pathologischen Differenzierung verhindern. KW - single-cell RNA-sequencing KW - single-cell analysis KW - transcriptomics KW - mesenchymal stromal cells KW - musculoskeletal system KW - stem cell differentiation KW - mesenchymale stromale Zellen KW - Muskel-Skelett-System / Bewegungsapparat KW - Einzelzell-Sequenzierung KW - Einzelzell-Analyse KW - Stammzelldifferenzierung KW - Transkriptomik Y1 - 2023 ER - TY - THES A1 - Gätjen, Dominic T1 - A Pichia pastoris surface display system for the efficient screening of high-producing antibody clones N2 - Pichia pastoris (syn. Komagataella phaffi) is a distinguished expression system widely used in industrial production processes. Recent molecular research has focused on numerous approaches to increase recombinant protein yield in P. pastoris. For example, the design of expression vectors and synthetic genetic elements, gene copy number optimization, or co-expression of helper proteins (transcription factors, chaperones, etc.). However, high clonal variability of transformants and low screening throughput have hampered significant success. To enhance screening capacities, display-based methodologies inherit the potential for efficient isolation of producer clones via fluorescence-activated cell sorting (FACS). Therefore, this study focused on developing a novel clone selection method that is based on the non-covalent attachment of Fab fragments on the P. pastoris cell surface to be applicable for FACS. Initially, a P. pastoris display system was developed, which is a prerequisite for the surface capture of secreted Fabs. A Design of Experiments approach was applied to analyze the influence of various genetic elements on antibody fragment display. The combined P. pastoris formaldehyde dehydrogenase promoter (PFLD1), Saccharomyces cerevisiae invertase 2 signal peptide (ScSUC2), - agglutinin (ScSAG1) anchor protein, and the ARS of Kluyveromyces lactis (panARS) conferred highest display levels. Subsequently, eight single-chain variable fragments (scFv) specific for the constant part of the Fab heavy or light chain were individually displayed in P. pastoris. Among the tested scFvs, the anti-human CH1 IgG domain scFv allowed the most efficient Fab capture detected by flow cytometry. Irrespective of the Fab sequence, exogenously added as well as simultaneously secreted Fabs were successfully captured on the cell surface. Furthermore, Fab secretion capacities were shown to correlate to the level of surface-bound Fabs as demonstrated for characterized producer clones. Flow-sorted clones presenting high amounts of Fabs showed an increase in median Fab titers (factor of 21 to 49) compared to unsorted clones when screened in deep-well plates. For selected candidates, improved functional Fab yields of sorted cells vs. unsorted cells were confirmed in an upscaled shake flask production. Since the scFv capture matrix was encoded on an episomal plasmid with inherently unstable autonomously replicating sequences (ARS), efficient plasmid curing was observed after removing the selective pressure. Hence, sorted clones could be immediately used for production without the need to modify the expression host or vector. The resulting switchable display/secretion system provides a streamlined approach for the isolation of Fab producers and subsequent Fab production. KW - Pichia pastoris KW - Antibody Y1 - 2023 ER - TY - JOUR A1 - Taguchi, Mioko A1 - Goto, Mutsuo A1 - Matsuoka, Koji A1 - Tiedemann, Ralph A1 - Pastene, Luis A. T1 - Population genetic structure of Bryde's whales (Balaenoptera brydei) on the central and western North Pacific feeding grounds JF - Canadian Journal of Fisheries and Aquatic Sciences N2 - The genetic structure of Bryde's whale (Balaenoptera brydei) on the central and western North Pacific feeding grounds was investigated using a total of 1195 mitochondrial control region sequences and 1182 microsatellite genotypes at 17 loci in specimens collected from three longitudinal areas, 1W (135 degrees E-165 degrees E), 1E (165 degrees E-180 degrees), and 2 (180 degrees-155 degrees W). Genetic diversities were similar among areas and a haplotype network did not show any geographic structure, while an analysis of molecular variance found evidence of genetic structure in this species. Pairwise FST and G'ST estimates and heterogeneity tests attributed this structure to weak but significant differentiation between areas 1W/1E and 2. A Mantel test and a high-resolution analysis of genetic diversity statistics showed a weak spatial cline of genetic differentiation. These findings could be reconciled by two possible stock structure scenarios: (1) a single population with kin-association affecting feeding ground preference and (2) two populations with feeding ground preference for either area 1W or area 2. An estimated dispersal rate between areas 1W and 2 indicates that both scenarios should be considered as a precautionary principle in stock assessments. KW - stock structure KW - stock assessment KW - fisheries management KW - conservation KW - cetacean Y1 - 2023 U6 - https://doi.org/10.1139/cjfas-2022-0005 SN - 0706-652X SN - 1205-7533 VL - 80 IS - 1 SP - 142 EP - 155 PB - Canadian science publishing CY - Ottawa ER - TY - THES A1 - Gramma, Vladislav T1 - Potato FLC-like and SVP-like proteins jointly control growth and distinct developmental processes N2 - Based on worldwide consumption, Solanum tuberosum L. (potato) is the most important non-grain food crop. Potato has two ways of stable propagation: sexually via flowering and vegetatively via tuberization. Remarkably, these two developmental processes are controlled by similar molecular regulators and mechanisms. Given that FLC and SVP genes act as key flowering regulators in the model species Arabidopsis and in various other crop species, this study aimed at identifying FLC and SVP homologs in potato and investigating their roles in the regulation of plant development, with a particular focus on flowering and tuberization. Our analysis demonstrated that there are five FLC-like and three SVP like proteins encoded in the potato genome. The expression profiles of StFLCs and StSVPs throughout potato development and the detected interactions between their proteins indicate tissue specificity of the individual genes and distinct roles of a variety of putative protein complexes. In particular, we discovered that StFLC-D, as well as StFLC-B, StSVP-A, and StSVP-B play a complex role in the regulation of flowering time, as not only increased but also decreased levels of their transcripts promote earlier flowering. Most importantly, StFLC-D has a marked impact on tuberization under non-inductive conditions and susceptibility to temperature-induced tuber malformation, also known as second growth. Plants with decreased levels of StFLC-D demonstrated a strong ability to produce tubers under long days and appeared to be insensitive to temperature-induced second growth. Lastly, our data also suggests that StFLCs and StSVPs may be involved in the nitrogen-dependent regulation of potato development. Taken together, this study highlights the functional importance of StFLC and StSVP genes in the regulation of distinct developmental processes in potato. KW - potato KW - Solanum tuberosum KW - tuberization KW - flowering KW - FLOWERING LOCUS C KW - FLC KW - short vegetative phase KW - SVP KW - tuber second growth Y1 - 2023 ER - TY - THES A1 - Agarwal, Pallavi T1 - Functional characterization of ROS-responsive genes, ANAC085 and ATR7, in Arabidopsis thaliana Y1 - 2023 ER - TY - THES A1 - Rasul, Fiaz T1 - Biostimulant SuperFifty based molecular priming to increase plant strength and stress tolerance Y1 - 2023 ER - TY - THES A1 - Mariette, Alban T1 - Building a wall: Developing small molecule biosensors to visualize cell wall biosynthesis and untangling mechanismus underlying nucleotide sugar transport Y1 - 2023 ER - TY - THES A1 - Kiemel, Katrin T1 - Zooplankton adaptations and community dynamics in space and time N2 - In times of ongoing biodiversity loss, understanding how communities are structured and what mechanisms and local adaptations underlie the patterns we observe in nature is crucial for predicting how future ecological and anthropogenic changes might affect local and regional biodiversity. Aquatic zooplankton are a group of primary consumers that represent a critical link in the food chain, providing nutrients for the entire food web. Thus, understanding the adaptability and structure of zooplankton communities is essential. In this work, the genetic basis for the different temperature adaptations of two seasonally shifted (i.e., temperature-dependent) occurring freshwater rotifers of a formerly cryptic species complex (Brachionus calyciflorus) was investigated to understand the overall genetic diversity and evolutionary scenario for putative adaptations to different temperature regimes. Furthermore, this work aimed to clarify to what extent the different temperature adaptations may represent a niche partitioning process thus enabling co-existence. The findings were then embedded in a metacommunity context to understand how zooplankton communities assemble in a kettle hole metacommunity located in the northeastern German "Uckermark" and which underlying processes contribute to the biodiversity patterns we observe. Using a combined approach of newly generated mitochondrial resources (genomes/cds) and the analysis of a candidate gene (Heat Shock Protein 40kDa) for temperature adaptation, I showed that the global representatives of B. calyciflorus s.s.. are genetically more similar than B. fernandoi (average pairwise nucleotide diversity: 0.079 intraspecific vs. 0.257 interspecific) indicating that both species carry different standing genetic variation. In addition to differential expression in the thermotolerant B. calyciflorus s.s. and thermosensitive B. fernandoi, the HSP 40kDa also showed structural variation with eleven fixed and six positively selected sites, some of which are located in functional areas of the protein. The estimated divergence time of ~ 25-29 Myr combined with the fixed sites and a prevalence of ancestral amino acids in B. calyciflorus s.s. indicate that B. calyciflorus s.s. remained in the ancestral niche, while B. fernandoi partitioned into a new niche. The comparison of mitochondrial and nuclear markers (HPS 40kDa, ITS1, COI) revealed a hybridisation event between the two species. However, as hybridisation between the two species is rare, it can be concluded that the temporally isolated niches (i.e., seasonal-shifted occurrence) they inhabit based on their different temperature preferences most likely represent a pre-zygotic isolation mechanism that allows sympatric occurrence while maintaining species boundaries. To determine the processes underlying zooplankton community assembly, a zooplankton metacommunity comprising 24 kettle holes was sampled over a two-year period. Active (i.e., water samples) and dormant communities (i.e., dormant eggs hatched from sediment) were identified using a two-fragment DNA metabarcoding approach (COI and 18S). Species richness and diversity as well as community composition were analysed considering spatial, temporal and environmental parameters. The analysis revealed that environmental filtering based on parameters such as pH, size and location of the habitat patch (i.e., kettle hole) and surrounding field crops largely determined zooplankton community composition (explained variance: Bray-Curtis dissimilarities: 10.5%; Jaccard dissimilarities: 12.9%), indicating that adaptation to a particular habitat is a key feature of zooplankton species in this system. While the spatial configuration of the kettle holes played a minor role (explained variance: Bray-Curtis dissimilarities: 2.8% and Jaccard dissimilarities: 5.5%), the individual kettle hole sites had a significant influence on the community composition. This suggests monopolisation/priority effects (i.e., dormant communities) of certain species in individual kettle holes. As environmental filtering is the dominating process structuring zooplankton communities, this system could be significantly influenced by future land-use change, pollution and climate change. N2 - In Zeiten des fortschreitenden Verlusts biologischer Vielfalt ist es von entscheidender Bedeutung zu verstehen, wie natürliche Gemeinschaften strukturiert sind und welche Mechanismen und lokalen Anpassungen den beobachteten Biodiversitätsmustern zugrunde liegen, um eine wissenschaftliche Grundlage für die Vorhersage künftiger Veränderungen der lokalen und regionalen biologische Vielfalt zu schaffen. Aquatisches Zooplankton ist eine artenreiche Gruppe Primärkonsumenten, die ein entscheidendes Glied in der Nahrungskette darstellen, indem sie Nährstoffe für das gesamte Nahrungsnetz bereitstellen. Daher ist es von entscheidender Bedeutung, die Anpassungsfähigkeit und Struktur von Zooplanktongemeinschaften zu verstehen. In dieser Arbeit wurden die genetischen Grundlagen für die unterschiedliche Temperaturanpassung zweier saisonal-versetzt (d.h. temperaturabhängig) vorkommender limnischen Rädertierarten eines ehemals kryptischen Artenkomplexes (Brachionus calyciflorus) untersucht, um die genetische Variation und das evolutionäre Divergenz-Szenario sowie Grundlagen für die mutmaßliche Anpassungen an unterschiedliche Temperaturregime zu verstehen. Weiterhin sollte untersucht werden, ob die Temperaturanpassungen als Prozess der Nischenaufteilung verstanden werden können die die Koexistenz der Arten ermöglicht. Diese Ergebnisse wurden dann in einen Metagemeinschaftskontext eingebettet, um zu verstehen, wie sich Zooplanktongemeinschaften in einer Soll-Metagemeinschaft, welche sich in der nordostdeutschen Region "Uckermark" befindet, zusammensetzen und welche zugrundeliegenden Prozesse zu den beobachteten Biodiversitätsmustern führen. Eine Kombination aus neu generierten mitochondrialen Ressourcen (Genome/codierende Sequenzen) und der Analyse eines Kandidatengens (HSP 40kDa Gen) für die Temperaturanpassung ergab zum einen, dass die globalen Vertreter von B. calyciflorus s.s. einander genetisch ähnlicher sind als B. fernandoi (Nukleotiddiversität: 0,079 intraspezifisch vs. 0,257 interspezifisch) und beide Arten somit eine unterschiedliche genetische Variation besitzen. Zum anderen wird das HSP 40kDa wird nicht nur in dem wärmetoleranten B. calyciflorus s.s. und wärmeempfindlichen B. fernandoi unterschiedlich exprimiert, sondern weist auch strukturelle Variationen mit elf fixierten und sechs positiv selektierten Positionen auf, von denen einige in funktionellen Regionen des HSP 40kDa liegen. Die geschätzte Divergenzzeit von ca. 25-29 Millionen Jahren sowie die fixierten Positionen und die Dominanz anzestraler Aminosäuren in B. calyciflorus s.s. legen nahe, dass B. calyciflorus s.s. in der anzestralen Nische verblieb, während B. fernandoi eine neue Nische besetzte. Der Vergleich von mitochondrialen und nukleären Markern (HSP 40kDa, ITS1, COI) ergab ein Hybridisierungsereignis zwischen beiden Arten. Da Hybridisierung jedoch selten ist, können die zeitlich isolierten Nischen (d.h. saisonal-versetztes Auftreten), die sie aufgrund ihrer unterschiedlichen Temperaturpräferenzen bewohnen, als prä-zygotischer Isolationsmechanismus verstanden werden, der ein sympatrisches Vorkommen der Arten unter Aufrechterhaltung der Artgrenzen ermöglicht. Um die Prozesse zu bestimmen, die der Strukturierung von Zooplanktongemeinschaften zugrunde liegen, wurde über einen Zeitraum von zwei Jahren eine Zooplankton-Metagemeinschaft, bestehend aus 24 Söllen beprobt. Aktive (d.h. Wasserproben) und ruhende Gemeinschaften (d.h. aus dem Sediment geschlüpfte Gemeinschaften) wurden mit einem Zwei-Fragment-DNA-Metabarcoding-Ansatz (COI und 18S) bestimmt. Die Artenzahl und Abundanz sowie die Zusammensetzung der Gemeinschaften wurden unter Berücksichtigung räumlicher, zeitlicher und umweltbezogener Parameter analysiert. Die Analyse ergab, dass Umweltfilterung basierend auf Parametern wie pH-Wert, Größe, Lage und Typ des Habitats (d.h. des Solls) und der umgebenden Feldfrüchte die Zusammensetzung der Zooplanktongemeinschaft weitgehend bestimmt (erklärte Varianz: Bray-Curtis-Dissimilaritäten: 10,5%; Jaccard-Dissimilaritäten: 12,9%), was darauf hindeutet, dass die Anpassung an einen bestimmten Lebensraum ein wichtiges Merkmal der Zooplanktonarten in diesem System ist. Während die räumliche Struktur der Sölle eine geringe Rolle spielte (erklärte Varianz: Bray-Curtis-Dissimilaritäten: 2,8% und Jaccard-Dissimilaritäten: 5,5%), hatten die einzelnen Standorte einen erheblichen Einfluss auf die Zusammensetzung der Gemeinschaft. Dies deutet auf Monopolisierung/Prioritätseffekte (d.h. ruhende Gemeinschaften) bestimmter Arten in einzelnen Söllen hin. Da Umweltfilterung der dominierende Prozess für die Strukturierung der Zooplanktongemeinschaften ist, könnte dieses System durch künftige Landnutzungsänderungen, Verschmutzung und Klimawandel erheblich beeinflusst werden. KW - Zooplankton KW - Metacommunity KW - B. calyciflorus species complex KW - adaptation KW - hybridization KW - Metagemeinschaft KW - Anpassung KW - Hybridisierung Y1 - 2023 ER - TY - JOUR A1 - Pandey, Yogesh T1 - Enriched cell-free and cell-based native membrane derived vesicles (nMV) enabling rapid in-vitro electrophysiological analysis of the voltage-gated sodium channel 1.5. JF - Biochimica et Biophysica Acta (BBA) - Biomembranes N2 - Here, we demonstrate the utility of native membrane derived vesicles (nMVs) as tools for expeditious electrophysiological analysis of membrane proteins. We used a cell-free (CF) and a cell-based (CB) approach for preparing protein-enriched nMVs. We utilized the Chinese Hamster Ovary (CHO) lysate-based cell-free protein synthesis (CFPS) system to enrich ER-derived microsomes in the lysate with the primary human cardiac voltage-gated sodium channel 1.5 (hNaV1.5; SCN5A) in 3 h. Subsequently, CB-nMVs were isolated from fractions of nitrogen-cavitated CHO cells overexpressing the hNaV1.5. In an integrative approach, nMVs were micro-transplanted into Xenopus laevis oocytes. CB-nMVs expressed native lidocaine-sensitive hNaV1.5 currents within 24 h; CF-nMVs did not elicit any response. Both the CB- and CF-nMV preparations evoked single-channel activity on the planar lipid bilayer while retaining sensitivity to lidocaine application. Our findings suggest a high usability of the quick-synthesis CF-nMVs and maintenance-free CB-nMVs as ready-to-use tools for in-vitro analysis of electrogenic membrane proteins and large, voltage-gated ion channels. KW - Cell-free protein synthesis KW - Electrophysiology KW - Membrane proteins KW - Micro-translantation KW - Protein expression Y1 - 2023 U6 - https://doi.org/10.1016/j.bbamem.2023.184144 SN - 1879-2642 SN - 0005-2736 VL - 1865 IS - 5 PB - Elsevier CY - Amsterdam ER - TY - THES A1 - John, Sheeba T1 - Characterizing the role of Heat Shock Factor HSFA 7b in regulating thermomemory at the SAM in Arabidopsis thaliana N2 - Heat stress (HS) is one of the major abiotic stresses which adversely affects the survival and growth of plants due to their sessile nature. To combat the detrimental effects of HS and develop thermotolerance, plants have evolved several defense mechanisms. Thermomemory is one such molecular mechanism whereby plants that have been acclimated (or primed/P) by a moderate HS can respond more efficiently and continue their growth after exposure to a severe or lethal HS (called triggering/T), while unprimed plants cannot survive. Thermomemory is known to be regulated by several transcription factors (TFs), epigenetic changes, chromatin remodellers, post-transcriptional changes and it also involves protein stability control and primary metabolism adjustment. Recent research has suggested that the shoot apical meristem (SAM) in Arabidopsis thaliana has a distinct transcriptional thermomemory which is possibly regulated by eight TFs called HEAT SHOCK FACTORS (HSFs). The main objective of this PhD thesis is to investigate the role of HSFA7b (one of the eight HSFs), in regulating thermomemory at the SAM by identifying the molecular networks it regulates. HSFA7a, a close homolog of HSFA7b, is also one of the eight HSFs that are involved in regulating thermomemory at the SAM. Thermomemory was found to be defective in the hsfa7b and hsfa7a hsfa7b mutants; the percentage survival of these seedlings was significantly lower than in wild-type (WT) seedlings after the priming and triggering (PT) treatment. Transcriptome and ChIP analyses were performed to identify the molecular networks controlled by HSFA7b and its close homolog HSFA7a, in regulating thermomemory at the SAM. The chromatin regulator SPLAYED (SYD) was found to be regulated by both HSFA7a and HSFA7b at the SAM during thermomemory. SYD is directly involved in SAM maintenance by directly regulating WUSCHEL (WUS), a master regulator of stem cell maintenance. WUS expression was down-regulated at the SAM of PT treated hsfa7a/b mutants compared to WT-Col-0 seedlings. HSFA7a and HSFA7b also jointly regulate the expression of orphan gene QUA QUINE STARCH (QQS) during thermomemory. Starch accumulation negatively correlates with QQS expression and this trend was observed in WT plants in response to thermopriming. The remobilization of starch was affected in the hsfa7a/b mutants compared to WT plants during the recovery period after T treatment. These findings indicate that defects in SAM maintenance and starch remobilization could possibly contribute to the reduced thermomemory in the hsfa7a/b mutants. Moreover, transcriptome and ChIP analysis indicate that ethylene signaling genes are directly regulated by HSFA7b during thermomemory. Transcriptome analysis of the HSFA7b-IOE line indicates that HSFA7b positively regulates the expression of HEAT STRESS ASSOCIATED 32 (HSA32), an important thermomemory gene, and HSFA7b strongly suppresses the expression of the reactive oxygen species (ROS) responsive REDOX RESPONSIVE TRANSCRIPTION FACTOR 1 (RRTF1) gene, which is also a repressed target of SYD. In Arabidopsis, the HSFA7b transcript undergoes alternative splicing at high temperatures to form two splice variants: one correctly/constitutively spliced variant which is functional and codes for the HSFA7b protein and one intron retained splice variant. Higher accumulation of the functional HSFA7b splice variant was found at the SAM compared to other tissues. Moreover, accumulation of the functional splice variant was higher in P and PT plants compared to control plants, whereas higher levels of the intron retained splice variant is found in plants subjected directly to the T treatment. The intron retained HSFA7b splice variant is degraded by the non-sense mediated decay (NMD) pathway as a means of regulating transcript level essential for protein synthesis at high temperatures. Importantly, HSFA7b protein accumulation was observed in plants subjected to PT treatment that survive and continue growth, but not in plants subjected directly to T treatment that do not survive, indicating that constitutive/ correct splicing of the HSFA7b transcript is a component of thermomemory. Taken together, these findings suggest that HSFA7a and HSFA7b jointly regulate SAM maintenance via the chromatin remodeller SYD and starch remobilization via QQS. In addition to them, HSFA7b also regulates the expression of ethylene signaling genes, heat responsive genes and the ROS responsive RRTF1. Furthermore, constitutive/correct splicing in the HSFA7b transcript is also an essential component of thermomemory. Y1 - 2023 ER - TY - THES A1 - Machani, Fridah Gechemba T1 - Functional analysis of ATAF1 and ANAC032 NAC transcription factors in response to nitrogen Supply in Arabidopsis thaliana Y1 - 2023 ER - TY - THES A1 - Romero Prada, Lorena Margarita T1 - Crop improvement towards oxidative stress Y1 - 2023 ER - TY - THES A1 - Sarlet, Adrien T1 - Tuning the viscoelasticity of Escherichia coli biofilms T1 - Abstimmung der Viskoelastizität von Escherichia coli-Biofilmen BT - interplay between extrinsic and intrinsic factors BT - Wechselspiel zwischen extrinsischen und intrinsischen Faktoren N2 - Biofilms are heterogeneous structures made of microorganisms embedded in a self-secreted extracellular matrix. Recently, biofilms have been studied as sustainable living materials with a focus on the tuning of their mechanical properties. One way of doing so is to use metal ions. In particular biofilms have been shown to stiffen in presence of some metal cations and to soften in presence of others. However, the specificity and the determinants of those interactions vary between species. While Escherichia coli is a widely studied model organism, little is known concerning the response of its biofilms to metal ions. In this work, we aimed at tuning the mechanics of E. coli biofilms by acting on the interplay between matrix composition and metal cations. To do so, we worked with E. coli strains producing a matrix composed of curli amyloid fibres or phosphoethanolamine-cellulose (pEtN-cellulose) fibres or both. The viscoelastic behaviour of the resulting biofilms was investigated with rheology after incubation with one of the following metal ion solutions: FeCl3, AlCl3, ZnCl2 and CaCl2 or ultrapure water. We observed that the strain producing both fibres stiffen by a factor of two when exposed to the trivalent metal cations Al(III) and Fe(III) while no such response is observed for the bivalent cations Zn(II) and Ca(II). Strains producing only one matrix component did not show any stiffening in response to either cation, but even a small softening. In order to investigate further the contribution of each matrix component to the mechanical properties, we introduced additional bacterial strains producing curli fibres in combination with non-modified cellulose, non-modified cellulose only or neither component. We measured biofilms produced by those different strains with rheology and without any solution. Since rheology does not preserve the architecture of the matrix, we compared those results to the mechanical properties of biofilms probed with the non-destructive microindentation. The microindentation results showed that biofilm stiffness is mainly determined by the presence of curli amyloid fibres in the matrix. However, this clear distinction between biofilm matrices containing or not containing curli is absent from the rheology results, i.e. following partial destruction of the matrix architecture. In addition, rheology also indicated a negative impact of curli on biofilm yield stress and flow stress. This suggests that curli fibres are more brittle and therefore more affected by the mechanical treatments. Finally, to examine the molecular interactions between the biofilms and the metal cations, we used Attenuated total reflectance - Fourier transform infrared spectroscopy (ATR-FTIR) to study the three E.coli strains producing a matrix composed of curli amyloid fibres, pEtN-cellulose fibres or both. We measured biofilms produced by those strains in presence of each of the aforementioned metal cation solutions or ultrapure water. We showed that the three strains cannot be distinguished based on their FTIR spectra and that metal cations seem to have a non-specific effect on bacterial membranes in absence of pEtN-cellulose. We subsequently conducted similar experiments on purified curli or pEtN-cellulose fibres. The spectra of the pEtN-cellulose fibres revealed a non-valence-specific interaction between metal cations and the phosphate of the pEtN-modification. Altogether, these results demonstrate that the mechanical properties of E. coli biofilms can be tuned via incubation with metal ions. While the mechanism involving curli fibres remains to be determined, metal cations seem to adsorb onto pEtN-cellulose and this is not valence-specific. This work also underlines the importance of matrix architecture to biofilm mechanics and emphasises the specificity of each matrix composition. N2 - Biofilme sind heterogene Strukturen aus Mikroorganismen, die in eine selbst-abgesonderte extrazelluläre Matrix eingebettet sind. In letzter Zeit wurden Biofilme als nachhaltige lebende Materialien untersucht, mit dem Ziel ihre mechanischen Eigenschaften zu modifizieren. Eine Möglichkeit, dies zu tun, ist die Verwendung von Metallionen. Es hat sich gezeigt, dass Biofilme in Gegenwart einiger Metallkationen steifer und in Gegenwart anderer weicher werden. Die Spezifität und die Bestimmungsfaktoren dieser Wechselwirkungen sind jedoch je nach Spezies unterschiedlich. Obwohl Escherichia coli ein weithin untersuchter Modellorganismus ist, ist wenig über den Einfluss von Metallionen auf die Eigenschaften von E. coli-Biofilmen bekannt. Ziel dieser Arbeit war, die mechanischen Eigenschaften von E. coli-Biofilmen durch Beeinflussung des Zusammenspiels von Matrixzusammensetzung und Metallkationen zu untersuchen und zu verändern. Zu diesem Zweck wurden E. coli-Stämme verwendet, die eine Matrix aus Curli-Fasern oder Phosphoethanolamin-modifizierter Zellulose (pEtN-Zellulose) oder aus beiden produzieren. Das viskoelastische Verhalten der resultierenden Biofilme wurde nach Inkubation mit einer der folgenden Metallsalzlösungen (oder Reinstwasser) rheologisch untersucht: FeCl3, AlCl3, ZnCl2 und CaCl2. Es zeigte sich, dass die Steifigkeit von Biofilmen des Stammes, der beide Fasern produziert, um das Doppelte höher ist, wenn sie den dreiwertigen Metallkationen Al(III) und Fe(III) ausgesetzt werden. Im Gegensatz dazu konnte keine derartige Veränderung der Steifigkeit beobachtet werden, wenn stattdessen die zweiwertigen Kationen Zn(II) und Ca(II) zugesetzt wurden. Stämme, die nur eine Matrixkomponente produzieren, zeigten keine Versteifung in Gegenwart von Kationen, sondern sogar eine geringe Erweichung. Um den Beitrag der einzelnen Matrixkomponenten zu den mechanischen Eigenschaften weiter zu untersuchen, wurden weitere Bakterienstämme mit den bereits genannten verglichen. Diese Stämme produzieren entweder Curli-Fasern in Kombination mit nicht modifizierter Zellulose, ausschließlich nicht modifizierte Zellulose oder keine der beiden Komponenten. Die resultierenden Biofilme wurden ohne den Zusatz von Salzlösung rheologisch charakterisiert. Da die Matrixarchitektur bei Rheologiemessungen zerstört wird, wurden die Biofilme ebenfalls mit Mikroindentation untersucht, welche mit intakten Biofilmen durchgeführt werden kann. Die Ergebnisse der Mikroindentation zeigen, dass die Steifigkeit der Biofilme hauptsächlich durch das Vorhandensein von Curli-Fasern bestimmt wird. Diese klare Unterscheidung der mechanischen Eigenschaften zwischen Biofilmmatrices mit und ohne Curli ist jedoch in den rheologischen Ergebnissen nicht erkennbar, d. h. nach teilweiser Zerstörung der Matrixarchitektur. Darüber hinaus zeigte die Rheologie eine niedrigere Fließspannung für Biofilme, die Curli enthalten. In der Kombination deuten diese Ergebnisse darauf hin, dass Curli-Fasern spröder und daher stärker von der mechanischen Behandlung betroffen sind. Um die molekularen Wechselwirkungen zwischen der Biofilm-Matrix und Metallkationen zu untersuchen, wurden die drei E. coli-Stämme, die eine Matrix aus Curli-Fasern, pEtN-Zellulose oder beidem bilden, mit abgeschwächter Totalreflexions-Fourier-Transformations-Infrarot-Spektroskopie (ATR-FTIR) charakterisiert. Die von diesen Stämmen produzierten Biofilme wurden in Gegenwart jeder der oben genannten Metallsalzlösungen und in Reinstwasser untersucht. Es wurde gezeigt, dass die drei Stämme anhand ihrer FTIR-Spektren nicht unterschieden werden können und dass in Abwesenheit von pEtN-Zellulose eine mögliche unspezifische Wirkung auf bakterielle Membranen besteht. Ähnliche Experimente mit gereinigten Curli-Fasern oder pEtN-Zellulose deuten darauf hin, dass Metallkationen in erster Linie eine nicht-valenzspezifische Wechselwirkung mit der Phosphatgruppe der pEtN-Modifikation eingehen. Insgesamt zeigen diese Ergebnisse, dass die mechanischen Eigenschaften von E. coli-Biofilmen durch Inkubation mit Metallkationen modifiziert werden können. Während die Mechanismen, an denen Curli-Fasern beteiligt sind, noch nicht aufgeklärt sind, scheinen Metallkationen an pEtN-Zellulose zu adsorbieren. Diese Arbeit unterstreicht auch die Bedeutung der Matrixarchitektur für die Mechanik von Biofilmen und verdeutlicht die Wichtigkeit der jeweiligen Matrixzusammensetzung für die Spezifität und das Ausmaß der beobachteten Effekte. KW - E. coli KW - biofilm KW - metal cation KW - matrix KW - viscoelasticity KW - E. coli KW - Biofilm KW - Metallkation KW - Matrix KW - Viskoelastizität Y1 - 2023 ER - TY - JOUR A1 - Hermanussen, Michael A1 - Scheffler, Christiane A1 - Pulungan, Aman B. A1 - Bandyopadhyay, Arup Ratan A1 - Ghosh, Jyoti Ratan A1 - Özdemir, Ayşegül A1 - Koca Özer, Başak A1 - Musalek, Martin A1 - Lebedeva, Lidia A1 - Godina, Elena A1 - Bogin, Barry A1 - Tutkuviene, Janina A1 - Budrytė, Milda A1 - Gervickaite, Simona A1 - Limony, Yehuda A1 - Kirchengast, Sylvia A1 - Buston, Peter A1 - Groth, Detlef A1 - Rösler, Antonia A1 - Gasparatos, Nikolaos A1 - Erofeev, Sergei A1 - Novine, Masiar A1 - Navazo, Bárbara A1 - Dahinten, Silvia A1 - Gomuła, Aleksandra A1 - Nowak-Szczepańska, Natalia A1 - Kozieł, Sławomir T1 - Environment, social behavior, and growth BT - Proceedings of the 30th Aschauer Soiree, held at Krobielowice, Poland, June 18th 2022 JF - Human biology and public health N2 - Twenty-four scientists met for the annual Auxological conference held at Krobielowice castle, Poland, to discuss the diverse influences of the environment and of social behavior on growth following last year’s focus on growth and public health concerns (Hermanussen et al., 2022b). Growth and final body size exhibit marked plastic responses to ecological conditions. Among the shortest are the pygmoid people of Rampasasa, Flores, Indonesia, who still live under most secluded insular conditions. Genetics and nutrition are usually considered responsible for the poor growth in many parts of this world, but evidence is accumulating on the prominent impact of social embedding on child growth. Secular trends not only in the growth of height, but also in body proportions, accompany the secular changes in the social, economic and political conditions, with major influences on the emotional and educational circumstances under which the children grow up (Bogin, 2021). Aspects of developmental tempo and aspects of sports were discussed, and the impact of migration by the example of women from Bangladesh who grew up in the UK. Child growth was considered in particular from the point of view of strategic adjustments of individual size within the network of its social group. Theoretical considerations on network characteristics were presented and related to the evolutionary conservation of growth regulating hypothalamic neuropeptides that have been shown to link behavior and physical growth in the vertebrate species. New statistical approaches were presented for the evaluation of short term growth measurements that permit monitoring child growth at intervals of a few days and weeks. KW - St. Nicolas House Analysis KW - child growth KW - body proportions KW - social network KW - public health KW - migration Y1 - 2023 U6 - https://doi.org/10.52905/hbph2023.1.59 SN - 2748-9957 VL - 1 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Gasparatos, Nikolaos A1 - Scheffler, Christiane A1 - Hermanussen, Michael T1 - Assessing the applicability of changepoint analysis to analyse short-term growth JF - Human biology and public health N2 - Background: Assessing short-term growth in humans is still fraught with difficulties. Especially when looking for small variations and increments, such as mini growth spurts, high precision instruments or frequent measurements are necessary. Daily measurements however require a lot of effort, both for anthropologists and for the subjects. Therefore, new sophisticated approaches are needed that reduce fluctuations and reveal underlying patterns. Objectives: Changepoints are abrupt variations in the properties of time series data. In the context of growth, such variations could be variation in mean height. By adjusting the variance and using different growth models, we assessed the ability of changepoint analysis to analyse short-term growth and detect mini growth spurts. Sample and Methods: We performed Bayesian changepoint analysis on simulated growth data using the bcp package in R. Simulated growth patterns included stasis, linear growth, catch-up growth, and mini growth spurts. Specificity and a normalised variant of the Matthews correlation coefficient (MCC) were used to assess the algorithm’s performance. Welch’s t-test was used to compare differences of the mean. Results: First results show that changepoint analysis can detect mini growth spurts. However, the ability to detect mini growth spurts is highly dependent on measurement error. Data preparation, such as ranking and rotating time series data, showed negligible improvements. Missing data was an issue and may affect the prediction quality of the classification metrics. Conclusion: Changepoint analysis is a promising tool to analyse short-term growth. However, further optimisation and analysis of real growth data is needed to make broader generalisations. KW - changepoint analysis KW - changepoint detection KW - performance evaluation KW - mini growth spurt KW - short-term growth Y1 - 2023 U6 - https://doi.org/10.52905/hbph2023.1.62 SN - 2748-9957 VL - 1 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Groth, Detlef A1 - Scheffler, Christiane A1 - Hermanussen, Michael T1 - Human growth data analysis and statistics – the 5th Gülpe International Student Summer School JF - Human biology and public health N2 - The Summer School in Gülpe (Ecological Station of the University of Potsdam) offers an exceptional learning opportunity for students to apply their knowledge and skills to real-world problems. With the guidance of experienced human biologists, statisticians, and programmers, students have the unique chance to analyze their own data and gain valuable insights. This interdisciplinary setting not only bridges different research areas but also leads to highly valuable outputs. The progress of students within just a few days is truly remarkable, especially when they are motivated and receive immediate feedback on their questions, problems, and results. The Summer School covers a wide range of topics, with this year’s focus mainly on two areas: understanding the impact of socioeconomic and physiological factors on human development and mastering statistical techniques for analyzing data such as changepoint analysis and the St. Nicolas House Analysis (SNHA) to visualize interacting variables. The latter technique, born out of the Summer School’s emphasis on gaining comprehensive data insights and understanding major relationships, has proven to be a valuable tool for researchers in the field. The articles in this special issue demonstrate that the Summer School in Gülpe stands as a testament to the power of practical learning and collaboration. Students who attend not only gain hands-on experience but also benefit from the expertise of professionals and the opportunity to engage with peers from diverse disciplines. KW - Summer Schools KW - Statistical Exercise KW - Repetition Y1 - 2023 U6 - https://doi.org/10.52905/hbph2023.1.70 SN - 2748-9957 VL - 1 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Rösler, Antonia A1 - Scheffler, Christiane A1 - Hermanussen, Michael T1 - No evidence of growth impairment after forced migration in Polish school children after World War II JF - Human biology and public health N2 - Background: Migration is omnipresent. It can come hand in hand with emotional stress which is known to influence the growth of children. Objective: The aim of this study was to analyse whether type of migration (forced or voluntary) and the geographic direction had influenced the growth of Polish children after World War II. Sample and Methods: A sub dataset of 2,208 individuals between the ages of 2-20, created from data of the 2nd Polish Anthropological Survey carried out in 1966–1969, including anthropometrical data and social and demographic information based on questionnaire, was used to analyse migration effects. Results: No association could be found between the direction of migration and the height of the children. The confidence intervals of the means of all classified migration categories overlap significantly and the effect size of the influence of migration category on height is ds=.140, which is too low to see any effects, even if there were one. Conclusion: Neither forced nor voluntary migration in Poland after World War II led to a change in height in children of migrating families. KW - nutrition KW - stunting KW - socioeconomy KW - education KW - secular changes KW - pubertal timing Y1 - 2023 U6 - https://doi.org/10.52905/hbph2023.1.68 SN - 2748-9957 VL - 1 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Hermanussen, Michael A1 - Scheffler, Christiane T1 - Nutrition, size, and tempo JF - Human biology and public health N2 - Nutrition is a prerequisite, but not a regulator of growth. Growth is defined as increase in size over time. The understanding of growth includes an understanding of the binary concept of physical time and individual tempo. Excess food causes tempo acceleration. Food restriction delays tempo. Tempo reflects the pace of life. It is a dynamic physical response to a broad spectrum of social, economic, political, and emotional (SEPE) factors and can affect life expectancy. Variations in tempo create distortions of the z-score patterns of height and weight. Illness or intermediate food shortage lead to intermediate halts in development and create short dips in the z-score patterns. Children who develop throughout life at delayed pace usually run at lower z-scores for height and weight, and show a characteristic adolescent trough; children who develop throughout life at faster than average pace usually run at higher z-scores and show a characteristic adolescent peak in their z-score patterns. During adolescence, almost half of the height variance is due to tempo variation. There is not one tempo for the whole body. Different organ systems grow and mature at different pace. KW - food access KW - physical time KW - SEPS factors KW - pace of life KW - catch-up-growth Y1 - 2023 U6 - https://doi.org/10.52905/hbph2022.3.37 SN - 2748-9957 VL - 2022 IS - 3 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - JOUR A1 - Scheffler, Christiane A1 - Hermanussen, Michael T1 - What does stunting tell us? JF - Human biology and public health N2 - Stunting is commonly linked with undernutrition. Yet, already after World War I, German pediatricians questioned this link and stated that no association exists between nutrition and height. Recent analyses within different populations of Low- and middle-income countries with high rates of stunted children failed to support the assumption that stunted children have a low BMI and skinfold sickness as signs of severe caloric deficiency. So, stunting is not a synonym of malnutrition. Parental education level has a positive influence on body height in stunted populations, e.g., in India and in Indonesia. Socially disadvantaged children tend to be shorter and lighter than children from affluent families. Humans are social mammals; they regulate growth similar to other social mammals. Also in humans, body height is strongly associated with the position within the social hierarchy, reflecting the personal and group-specific social, economic, political, and emotional environment. These non-nutritional impact factors on growth are summarized by the concept of SEPE (Social-Economic-Political-Emotional) factors. SEPE reflects on prestige, dominance-subordination, social identity, and ego motivation of individuals and social groups. KW - SEPE Factors KW - physical fitness KW - height in history KW - malnutrition Y1 - 2023 U6 - https://doi.org/10.52905/hbph2022.3.36 SN - 2748-9957 VL - 2022 IS - 3 SP - 1 EP - 15 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - THES A1 - Kappel, Sandrine T1 - Photosynthesis in fluctuating light BT - pgr5 suppressor mutant screen : low NPQ mutant identification and characterization N2 - Light is the essential energy source for plants to drive photosynthesis. In nature, light availability is highly variable and often fluctuates on very short time scales. As a result, plants developed mechanisms to cope with these fluctuations. Understanding how to improve light use efficiency in natural fluctuating light (FL) conditions is a major target for agronomy. In the first project, we identified an Arabidopsis thaliana plant that showed reduced levels of rapidly inducible non-photochemical quenching (NPQ). This plant was devoid of any T-DNA insertion. Using a mapping-by-sequencing approach, we successfully located the causal genomic region near the end of chromosome 4. Through variant investigations in that region, we identified a deletion of about 20 kb encompassing 9 genes. By complementation analysis, we confirmed that one of the deleted genes, VTC2, is the causal gene responsible for the low NPQ. Loss of VTC2 decreased NPQ particularly in old leaves, with young leaves being only slightly affected. Additionally, ascorbate levels were almost abolished in old leaves, likely causing the NPQ decrease by reducing the activity of the xanthophyll cycle. Although ascorbate levels in younger leaves were reduced compared to wild-type plants, they remained at a comparably higher level. This difference may be due to the VTC2 paralog VTC5, which is expressed at a higher level in young leaves than in old ones. Plants require the PROTON GRADIENT REGULATION 5 (PGR5) protein for survival in FL. pgr5 mutants die because they fail to increase the luminal proton concentration in response to high light (HL) phases. A rapid elevation in ∆pH is needed to slow down electron transport through the Cytochrome b6 f complex (photosynthetic control). In FL, such lack of control in the pgr5 mutants results in photosystem I (PSI) overreduction, reactive oxygen species (ROS) production, and cell death. Decreases in photosystem II (PSII) activity introduced by crossing pgr5 with PSII deficient mutants rescued the lethality of pgr5 in FL. PGR5 was suggested to act as part of the ferredoxin-plastoquinone reductase (FQR), involved in cyclic electron transfer around PSI. However, the proposed molecular role of PGR5 remains highly debated. To learn more about PGR5 function, we performed a forward genetic screen in Arabidopsis thaliana to identify EMS-induced suppressor mutants surviving longer when grown in FL compared to pgr5 mutants (referred to as ”suppressor of pgr5 lethality in fluctuating light”, splf ). 11 different candidate genes were identified in a total of 22 splf plants. Mutants of seven of these genes in the pgr5 background showed low Fv/Fm values when grown in non-fluctuating low light (LL). Five of these 4genes were previously reported to have a role in PSII biogenesis or function. Two others, RPH1 and a DEAD/DEAH box helicase (AT3G02060), have not been linked to PSII function before. Three of splf candidate genes link to primary metabolism, fructose-2,6-bisphosphatase (F2KP ), udp-glucose pyrophosphorylase 1 (UGP1 ) and ferredoxin-dependent glutamate synthase (Fd-GOGAT ). They are characterized by the fact that they survive longer in FL than pgr5 mutants but do not procede beyond the early vegetative phase and then die. N2 - Pflanzen wandeln Sonnenlicht durch die Photosynthese in chemische Energie um. In der Natur unterliegt die Verfügbarkeit von Licht jedoch starken Schwankungen, beispielsweise durch kurzzeitige Wolkenverdeckungen. Um mit diesen Veränderungen umzugehen, haben Pflanzen spezielle Mechanismen entwickelt. Das Verständnis, wie die Lichtnutzung unter diesen fluktuierenden Bedingungen optimiert werden kann, stellt eines der Hauptziele in der Landwirtschaft dar. Ziel dieser Arbeit ist es, zu diesem Verständnis beizutragen. Wir haben eine neue Mutante der Ackerschmalwand identifiziert, die reduzierte Levels des schnell induzierbaren nicht-photochemischen Quenchings (NPQ) aufwies. NPQ ist ein wichtiger Mechanismus, mit dem Pflanzen auf schnelle Wechsel zu stärkerem Licht reagieren können. Die Untersuchung ergab, dass das Fehlen des Gens VTC2 die Ursache für die Reduzierung des NPQ war, mit Auswirkungen auf den Vitamin-C-Spiegel und die Aktivität des Xanthophyllzyklus. Besonders interessant war, dass der Verlust des Gens hauptsächlich ältere Blätter beeinflusste. Das Gen PGR5 ist für das Überleben von Pflanzen in schwankenden Lichtverhältnissen notwendig. Obwohl viele wissenschaftliche Arbeiten diesem Gen gewidmet sind, sind seine genauen Funktionen nur im Ansatz bekannt. In unserer Studie haben wir Ackerschmalwand Pflanzen ohne dieses Gen mit Chemikalien mutagenisiert und sie dann in schwankenden Lichtverhältnissen wachsen lassen. Dabei konnten wir Suppressormutanten finden, die überlebt haben. Durch diese Herangehensweise haben wir 11 Kandidatengene identifiziert, die eine mögliche Verbindung zum PGR5-Mechanismus aufweisen könnten. Einige dieser Mutanten hemmen das Photosystem II, das für das Einfangen der Lichtenergie verantwortlich ist, während andere Teile den Primärmetabolismus für Zucker und Stickstoff verändern. Zusammenfassend bietet die Arbeit Einsichten in die Mechanismen, mit denen Pflanzen auf schwankende Lichtbedingungen reagieren, und identifiziert spezifische Gene, die in diesen Prozessen eine Rolle spielen. KW - photosynthesis KW - fluctuating light KW - PGR5 KW - suppressor mutant screen KW - low NPQ Y1 - 2023 ER - TY - JOUR A1 - Hake, Tim A1 - Bodenberger, Bernhard A1 - Groth, Detlef T1 - In Python available: St. Nicolas House Algorithm (SNHA) with bootstrap support for improved performance in dense networks JF - Human biology and public health N2 - The St. Nicolas House Algorithm (SNHA) finds association chains of direct dependent variables in a data set. The dependency is based on the correlation coefficient, which is visualized as an undirected graph. The network prediction is improved by a bootstrap routine. It enables the computation of the empirical p-value, which is used to evaluate the significance of the predicted edges. Synthetic data generated with the Monte Carlo method were used to firstly compare the Python package with the original R package, and secondly to evaluate the predicted network using the sensitivity, specificity, balanced classification rate and the Matthew's correlation coefficient (MCC). The Python implementation yields the same results as the R package. Hence, the algorithm was correctly ported into Python. The SNHA scores high specificity values for all tested graphs. For graphs with high edge densities, the other evaluation metrics decrease due to lower sensitivity, which could be partially improved by using bootstrap,while for graphs with low edge densities the algorithm achieves high evaluation scores. The empirical p-values indicated that the predicted edges indeed are significant. KW - Python KW - correlation KW - network reconstruction KW - bootstrap KW - St. Nicolas House Algorithm Y1 - 2023 U6 - https://doi.org/10.52905/hbph2023.1.63 SN - 2748-9957 VL - 1 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - THES A1 - Hashemi Ranjbar, Seirana T1 - Plasticity and trade-offs in plant metabolic networks N2 - A biological trade-off situation denotes the dependence between traits whereby an increase in the value of one of the traits leads to a decrease in the value of at least one of the others. Understanding trade-offs in cellular systems is relevant to understanding the limits and constraints to tuning desired phenotypes. Therefore, it is mainly the case for rates (i.e. fluxes) of biochemical reactions that shape not only molecular traits, like metabolite concentrations but also determine physiological traits, like growth. Intracellular fluxes are the final phenotype from transcriptional and (post)translational regulation. Quantifying intracellular fluxes provides insights into cellular physiology under particular growth conditions and can be used to characterize the metabolic activity of different pathways. However, estimating fluxes from labelling experiments is labour-intensive; therefore, developing approaches to accurately and precisely predict intracellular fluxes is essential. This thesis addresses two main problems: (i) identifying flux trade-offs and (ii) predicting accurate and precise reaction flux at a genome-scale level. To this end, the concept of an absolute flux trade-off is defined, and a constraint-based approach, termed FluTO, was developed to identify absolute flux trade-offs. FluTO is cast as a mixed integer programming approach applied to genome-scale metabolic models of E. coli, S. cerevisiae, and A. thaliana, imposing realistic constraints on growth and nutrient uptake.. The findings showed that trade-offs are not only species-specific but also specific to carbon sources. In addition, we found that different models of a single species have a different number of reactions in trade-offs. We also showed that absolute flux trade-offs depend on the biomass reaction used to model the growth of A. thaliana under different carbon and nitrogen conditions. Findings reflect the strong relation between nitrogen, carbon, and sulphur metabolisms in the leaves of C3 plants. The concept of relative trade-offs was introduced to further study trade-offs in metabolic networks. A constraint-based approach, FluTOr, was proposed to identify reactions whose fluxes are in relative trade-off concerning an optimized fitness-related cellular task, like growth. FluTOr was employed to find the relative flux trade-offsin the genome-scale metabolic networks of E. coli, S. cerevisiae, and A. thaliana. The results showed that in contrast to the A. thaliana model, the relative trade-offs in the two microorganisms depend on the carbon source, reflecting the differences in the underlying metabolic network. Furthermore, applying FluTOr also showed that reactions that participated in relative trade-offs were implicated in cofactor biosynthesis in the two microorganisms. Prediction of reaction fluxes in the constraint-based metabolic framework is usually performed by parsimonious flux balance analysis (pFBA), employing the principle of efficient usage of protein resources. However, we argued that principles related to the coordination of flux values, neglected in previous studies, provide other means to predict intracellular fluxes. To this end, we designed a constraint-based approach, termed complex-balanced FBA (cbFBA), to predict steady-state flux distributions that maximize the number of balanced complexes in a flux distribution, whereby multi-reaction dependencies are maximized. The comparative analysis showed a better agreement of the flux distributions resulting from cbFBA compared to pFBA with experimentally measured fluxes from 17 E. coli strains and 26 S. cerevisiae knock-out mutants. The results also showed that the predictions from cbFBA are more precise than those from pFBA since cbFBA results in a smaller space of alternative solutions than pFBA. N2 - Eine biologische Abwägungssituation bezeichnet die Abhängigkeit zwischen Merkmalen, wobei ein Anstieg des Wertes eines der Merkmale zu einer Abnahme des Wertes mindestens eines der anderen Merkmale führt. Das Verständnis von Abwägungen in zellulären Systemen ist relevant, um die Grenzen und Einschränkungen bei der Differenzierung gewünschter Phänotypen zu verstehen. Dieses ist häufig der Fall bei Fließgeschwindigkeiten (d.h. Ströme) biochemischer Reaktionen, die nicht nur molekulare Merkmale wie Metabolitkonzentrationen beschreiben, sondern auch physiologische Merkmale wie Wachstum bestimmen. Intrazelluläre Ströme sind der endgültige Phänotyp der transkriptionellen und (post)translationalen Regulation. Die Quantifizierung intrazellulärer Ströme liefert Einblicke in die Zellphysiologie unter bestimmten Wachstumsbedingungen und kann verwendet werden, um die Stoffwechselaktivität verschiedener Wege zu charakterisieren. Die Schätzung von Strömen aus Markierungsexperimenten ist jedoch arbeitsintensiv. Daher ist die Entwicklung von Ansätzen zur genauen und präzisen Vorhersage intrazellulärer Ströme unerlässlich. Diese Dissertation befasst sich mit zwei Hauptproblemen: (i) Identifizierung von Abwägungspunkten (Trade-offs) zwischen Strömen und (ii) Vorhersage des genauen und präzisen Reaktionsflusses auf Genomebene. Zu diesem Zweck wird das Konzept eines absoluten Trade-offs von Strömen definiert und ein Constraint-basierter Ansatz namens FluTO entwickelt, um absolute Trade-offs von Strömen zu identifizieren. FluTO ist als gemischter ganzzahliger Programmieransatz konzipiert, der auf genomweite Stoffwechselmodelle von E. coli, S. cerevisiae und A. thaliana angewendet wird und realistische Einschränkungen für Wachstum und Nährstoffaufnahme auferlegt. Die Ergebnisse zeigten, dass Trade-offs nicht nur artspezifisch, sondern auch spezifisch für Kohlenstoffquellen sind. Darüber hinaus haben wir festgestellt, dass verschiedene Modelle einer einzelnen Art eine unterschiedliche Anzahl von Reaktionen in Trade-offs aufweisen. Wir haben auch gezeigt, dass absolute Trade-offs von Strömen von der Biomassereaktion abhängen, die verwendet wird, um das Wachstum von A. thaliana unter verschiedenen Kohlenstoff- und Stickstoffbedingungen zu modellieren. Die Ergebnisse spiegeln die starke Beziehung zwischen dem Stickstoff-, Kohlenstoff- und Schwefelstoffwechsel in den Blättern von C3-Pflanzen wieder. Das Konzept der relativen Trade-Offs wurde eingeführt, um Trade-Offs in metabolischen Netzwerken weiter zu untersuchen. Ein Constraint-basierter Ansatz, FluTOr, wurde entwickelt, um Reaktionen zu identifizieren, deren Ströme in einem relativen Trade-off bezüglich einer optimierten fitnessbezogenen zellulären Aufgabe wie Wachstum stehen. FluTOr wurde eingesetzt, um die relativen Trade-offs von Strömen in den metabolischen Netzwerken von E. coli, S. cerevisiae und A. thaliana auf Genomebene zu finden. Die Ergebnisse zeigten, dass im Gegensatz zum A. Thaliana Modell die relativen Trade-offs in den beiden Mikroorganismen von der Kohlenstoffquelle abhängen, was die Unterschiede im zugrunde liegenden metabolischen Netzwerk wiederspiegelt. Darüber hinaus zeigte die Anwendung von FluTOr auch, dass Reaktionen, die an relativen Trade-offs teilnahmen, an der Cofaktor-Biosynthese in den beiden Mikroorganismen beteiligt waren. Die Vorhersage von Reaktionsflüssen mittels Constraint-basierten metabolischen Methoden wird normalerweise durch eine überschaubare Flussbilanzanalyse (pFBA) durchgeführt, die das Prinzip der effizienten Nutzung von Proteinressourcen anwendet. Wir argumentierten jedoch, dass Prinzipien im Zusammenhang mit der Koordination von Flusswerten, die in früheren Studien vernachlässigt wurden, andere Mittel zur Vorhersage intrazellulärer Ströme bieten. Zu diesem Zweck haben wir einen Constraint-basierten Ansatz entwickelt, der als Complex-Balanced FBA (cbFBA) bezeichnet wird, um Steady-State-Verteilungen von Strömen vorherzusagen, die die Anzahl der ausgewogenen Komplexe in einer Verteilung von Strömen maximieren, wodurch Abhängigkeiten von mehreren Reaktionen maximiert werden. Die vergleichende Analyse zeigte eine bessere Übereinstimmung der Verteilungen von Strömen, die sich aus cbFBA im Vergleich zu pFBA ergaben, mit experimentell gemessenen Strömen von 17 E. coli Stämmen und 26 S. cerevisiae Knock-out-Mutanten. Die Ergebnisse zeigten auch, dass die Vorhersagen von cbFBA genauer sind als die von pFBA, da cbFBA zu weniger alternativen Lösungen führt als pFBA. T2 - Plastizität und Kompromisse in pflanzlichen Stoffwechselnetzwerken KW - trade-off KW - cbFBA KW - metabolic network KW - balanced complex KW - reaction rate KW - Kompromiss KW - cbFBA KW - metabolisches Netzwerk KW - ausgewogener Komplex KW - Reaktionsgeschwindigkeit Y1 - 2023 ER - TY - THES A1 - Stephan, Mareike Sophia T1 - A bacterial mimetic system to study bacterial inactivation and infection N2 - The emerging threat of antibiotic-resistant bacteria has become a global challenge in the last decades, leading to a rising demand for alternative treatments for bacterial infections. One approach is to target the bacterial cell envelope, making understanding its biophysical properties crucial. Specifically, bacteriophages use the bacterial envelope as an entry point to initiate infection, and they are considered important building blocks of new antibiotic strategies against drug-resistant bacteria.. Depending on the structure of the cell wall, bacteria are classified as Gram-negative and Gram-positive. Gram-negative bacteria are equipped with a complex cell envelope composed of two lipid membranes enclosing a rigid peptidoglycan layer. The synthesis machinery of the Gram-negative cell envelope is the target of antimicrobial agents, including new physical sanitizing procedures addressing the outer membrane (OM). It is therefore very important to study the biophysical properties of the Gram-negative bacterial cell envelope. The high complexity of the Gram-negative OM sets the demand for a model system in which the contribution of individual components can be evaluated separately. In this respect, giant unilamellar vesicles (GUVs) are promising membrane systems to study membrane properties while controlling parameters such as membrane composition and surrounding medium conditions. The aim of this work was to develop methods and approaches for the preparation and characterization of a GUV-based membrane model that mimics the OM of the Gram-negative cell envelope. A major component of the OM is the lipopolysaccharide (LPS) on the outside of the OM heterobilayer. The vesicle model was designed to contain LPS in the outer leaflet and lipids in the inner leaflet. Furthermore, the interaction of the prepared LPS-GUVs with bacteriophages was tested. LPS containing GUVs were prepared by adapting the inverted emulsion technique to meet the challenging properties of LPS, namely their high self-aggregation rate in aqueous solutions. Notably, an additional emulsification step together with the adaption of solution conditions was employed to asymmetrically incorporate LPS containing long polysaccharide chains into the artificial membranes. GUV membrane asymmetry was verified with a fluorescence quenching assay. Since the necessary precautions for handling the quenching agent sodium dithionite are often underestimated and poorly described, important parameters were tested and identified to obtain a stable and reproducible assay. In the context of varied LPS incorporation, a microscopy-based technique was introduced to determine the LPS content on individual GUVs and to directly compare vesicle properties and LPS coverage. Diffusion coefficient measurements in the obtained GUVs showed that increasing LPS concentrations in the membranes resulted in decreased diffusivity. Employing LPS-GUVs we could demonstrate that a Salmonella bacteriophage bound with high specificity to its LPS receptor when presented at the GUV surface, and that the number of bound bacteriophages scaled with the amount of presented LPS receptor. In addition to binding, the bacteriophages were able to eject their DNA into the vesicle lumen. LPS-GUVs thus provide a starting platform for bottom-up approaches for the generation of more complex membranes, in which the effects of individual components on the membrane properties and the interaction with antimicrobial agents such as bacteriophages could be explored. N2 - Die wachsende Bedrohung durch antibiotikaresistente Bakterien ist in den letzten Jahrzehnten zu einer globalen Herausforderung geworden, was zu einer steigenden Nachfrage nach alternativen Behandlungsmethoden für bakterielle Infektionen geführt hat. Ein Ansatz besteht darin, die bakterielle Zellhülle anzugreifen, weshalb das Verständnis ihrer biophysikalischen Eigenschaften entscheidend ist. Insbesondere Bakteriophagen, Viren, die Bakterien infizieren, nutzen die Bakterienhülle als ersten Angriffspunkt für die Infektion und gelten als wichtige Bausteine für neue Antibiotikastrategien gegen arzneimittelresistente Bakterien. Je nach Struktur der Zellwand werden Bakterien in gramnegative und grampositive Bakterien eingeteilt. Gramnegative Bakterien sind mit einer komplexen Zellhülle ausgestattet. Daher ist es sehr wichtig, ihre biophysikalischen Eigenschaften zu untersuchen. Die hohe Komplexität der äußeren Zellhülle, auch äußere Membran genannt, erfordert ein Modellsystem, in dem der Beitrag jeder einzelnen Komponente separat bewertet werden kann. In dieser Hinsicht sind Vesikel-basierte Modellsysteme sehr vielversprechend, da sie wichtige Eigenschaften der äußeren Membran simulieren können, aber in ihrer Komplexität stark reduziert und kontrollierbar sind. Ziel dieser Arbeit war es, Methoden und Ansätze für die Herstellung und Charakterisierung eines Vesikel-basierten Modells zu entwickeln, das die äußere Membran der gramnegativen bakteriellen Zellhülle nachahmt. Ein Hauptbestandteil der äußeren Membran ist Lipopolysaccharid (LPS), das asymmetrisch auf der Außenseite der äußeren Membran vorhanden ist. Das Vesikelmodell wurde so konzipiert, dass es außen LPS und innen Phospholipide enthält. Die Herstellung des beschriebenen Modellsystems erforderte einige Anpassungen, da die Hüllkomponente LPS eine hohe Tendenz zur Bildung von Selbstaggregaten aufweist. Durch die Einführung eines zusätzlichen Schrittes in das Standardprotokoll konnten Vesikel mit LPS-Inkorporation erzeugt werden. Es wurde sowohl die Menge als auch die asymmetrische Verteilung des LPS-Einbaus bestimmt. Mit Hilfe von Bakteriophagen sollte die biologische Wirkung des Modellsystems getestet werden. Es wurde gezeigt, dass Bakteriophagen, die spezifisch LPS erkennen und binden, nach Zugabe zum Modellsystem die Vesikel binden und ihr genetisches Material in das Vesikel-Innere injizieren. Die hier beschriebenen LPS-haltigen Vesikel können als Ausgangsplattform für Bottom-up-Ansätze zur Herstellung komplexerer Membranen verwendet werden. Mit diesen komplexeren, aber kontrollierbaren Systemen lassen sich die Auswirkungen einzelner Komponenten der bakteriellen Zellhülle auf die Eigenschaften der Zellhülle sowie ihre Wechselwirkung mit antimikrobiellen Wirkstoffen wie Bakteriophagen untersuchen. KW - Bakterien KW - Bakteriophagen KW - Zellmembran KW - Vesikel KW - Konfokale Mikroskopie KW - Lipopolysaccharid KW - gramnegativ KW - bacteria KW - bacteriophage KW - cell membrane KW - vesicle KW - confocal microscopy KW - lipopolysaccharide KW - gram-negative Y1 - 2023 ER - TY - THES A1 - Bastos Lima, Rita T1 - Seed coat-derived brassnosteroids non-cell autonomously regulate endosperm development Y1 - 2023 ER - TY - THES A1 - Kulshreshtha, Ritika T1 - Dissecting the functional of role of microtubule and cellulose microfibril patterning during flower development in Arabidopsis Y1 - 2023 ER - TY - THES A1 - Li, Xiaoping T1 - Regulation of starch granule number and morphology in arabidopsis thaliana Y1 - 2023 ER - TY - THES A1 - Apriyanto, Ardha T1 - Analysis of starch metabolism in source and sink tissue of plants T1 - Analyse des Stärkestoffwechsels im Source und Sink Gewebe von Pflanzen N2 - Starch is an essential biopolymer produced by plants. Starch can be made inside source tissue (such as leaves) and sink tissue (such as fruits and tubers). Nevertheless, understanding how starch metabolism is regulated in source and sink tissues is fundamental for improving crop production. Despite recent advances in the understanding of starch and its metabolism, there is still a knowledge gap in the source and sink metabolism. Therefore, this study aimed to summarize the state of the art regarding starch structure and metabolism inside plants. In addition, this study aimed to elucidate the regulation of starch metabolism in the source tissue using the leaves of a model organism, Arabidopsis thaliana, and the sink tissue of oil palm (Elaeis guineensis) fruit as a commercial crop. The research regarding the source tissue will focus on the effect of the blockage of starch degradation on the starch parameter in leaves, especially in those of A. thaliana, which lack both disproportionating enzyme 2 (DPE2) and plastidial glucan phosphorylase 1 (PHS1) (dpe2/phs1). The additional elimination of phosphoglucan water dikinase (PWD), starch excess 4 (SEX4), isoamylase 3 (ISA3), and disproportionating enzyme 1 (DPE1) in the dpe2/phs1 mutant background demonstrates the alteration of starch granule number per chloroplast. This study provides insights into the control mechanism of granule number regulation in the chloroplast. The research regarding the sink tissue will emphasize the relationship between starch metabolism and the lipid metabolism pathway in oil palm fruits. This study was conducted to observe the alteration of starch parameters, metabolite abundance, and gene expression during oil palm fruit development with different oil yields. This study shows that starch and sucrose can be used as biomarkers for oil yield in oil palms. In addition, it is revealed that the enzyme isoforms related to starch metabolism influence the oil production in oil palm fruit. Overall, this thesis presents novel information regarding starch metabolism in the source tissue of A.thaliana and the sink tissue of E.guineensis. The results shown in this thesis can be applied to many applications, such as modifying the starch parameter in other plants for specific needs. N2 - Stärke ist ein unverzichtbares Biopolymer, das von Pflanzen sowohl in den Quellgeweben (sources, z. B. Blätter) als auch in den Senkengeweben (sinks, z. B. Früchten und Knollen) gebildet wird. Daher ist ein profundes Wissen über die Regulation des Stärkestoffwechsel in den source und sink Organen von grundlegender Bedeutung für die Verbesserung der Pflanzenproduktion. Trotz der jüngsten Fortschritte im Verständnis des Stärkestoffwechsels bleiben weiterhin viele Fragen über den detaillierten source und sink Metabolismus offen. Ziel dieser Studie war es daher, den aktuellen Forschungsstand über die Struktur und den Stoffwechsel von Stärke in Pflanzen aufzuzeigen. Darüber hinaus sollte in dieser Studie die Regulierung des Stärkestoffwechsels in den Blättern (source) des Modellorganismus Arabidopsis thaliana und in den Ölpalmfrüchten (sink) von Elaeis guineensis, einer Nutzpflanze, aufgeklärt werden. Die Analyse des source Gewebes konzentrierte sich dabei auf die Auswirkungen auf Stärkeparamter wie beispielsweise die Granulazahl durch die Blockierung des Stärkeabbaus in Blättern. Dazu wurde die Arabidopsis Mutante, der das cytosolische Disproportionating Enzym 2 (DPE2) und die plastidiale Glucanphosphorylase 1 (PHS1) fehlen (dpe2/phs1), untersucht. Ebenfalls wurden Dreifachmutanten im Hintergund von dpe2/phs1, denen Starch excess 4 (SEX4), Isoamylase 3, Phosphoglucan-Wasser-Dikinase (PWD) oder das Disproportionating Enzym 1 (DPE1) fehlen, erzeugt. Die Analyse zeigt, dass die Anzahl der Stärkegranula pro Chloroplast nicht festgelegt ist und während des gesamten Wachstums der Pflanze reguliert wird. Diese Daten liefern ein verbessertes Verständnis über die Komplexität der Kontrollmechanismen der Granulazahlregulation in Chloroplasten. Die Untersuchung des sink Gewebes soll die Beziehung zwischen dem Stärkestoffwechsel und dem Lipidstoffwechselweg in Ölpalmenfrüchten verdeutlichen. Diese Studie wurde durchgeführt, um die Veränderung von Stärkeparametern, die Häufigkeit von Metaboliten und die Genexpression während der Entwicklung von Ölpalmenfrüchten mit unterschiedlichen Ölausbeuten zu erforschen. Die Analyse zeigt, dass sowohl Stärke als auch Saccharose als reliable Biomarker für den Ölertrag von Ölpalmen verwendet werden können. Darüber hinaus konnte bewiesen werden, dass die mit dem Stärkestoffwechsel verbundenen Enzymisoformen die Ölproduktion in Ölpalmenfrüchten beeinflussen. Insgesamt liefert diese Arbeit neue Informationen über den Stärkestoffwechsel im source Gewebe von A.thaliana und im sink von E.guineensis. Die in dieser Arbeit gezeigten Ergebnisse können für viele Anwendungen genutzt werden, z. B. für die Veränderung der Stärkeparameter in anderen Pflanzen für spezifische Bedürfnisse. KW - starch KW - oil palm KW - Arabidopsis thaliana KW - source and sink KW - Arabidopsis thaliana KW - Palmöl KW - Source und Sink KW - Stärke Y1 - 2023 ER - TY - THES A1 - Peng, Maolin T1 - The role of prion-like domains in plant temperatur sensing Y1 - 2023 ER - TY - JOUR A1 - Petrich, Annett A1 - Aji, Amit Koikkarah A1 - Dunsing, Valentin A1 - Chiantia, Salvatore T1 - Benchmarking of novel green fluorescent proteins for the quantification of protein oligomerization in living cells JF - PLoS one N2 - Protein-protein-interactions play an important role in many cellular functions. Quantitative non-invasive techniques are applied in living cells to evaluate such interactions, thereby providing a broader understanding of complex biological processes. Fluorescence fluctuation spectroscopy describes a group of quantitative microscopy approaches for the characterization of molecular interactions at single cell resolution. Through the obtained molecular brightness, it is possible to determine the oligomeric state of proteins. This is usually achieved by fusing fluorescent proteins (FPs) to the protein of interest. Recently, the number of novel green FPs has increased, with consequent improvements to the quality of fluctuation-based measurements. The photophysical behavior of FPs is influenced by multiple factors (including photobleaching, protonation-induced "blinking" and long-lived dark states). Assessing these factors is critical for selecting the appropriate fluorescent tag for live cell imaging applications. In this work, we focus on novel green FPs that are extensively used in live cell imaging. A systematic performance comparison of several green FPs in living cells under different pH conditions using Number & Brightness (N & B) analysis and scanning fluorescence correlation spectroscopy was performed. Our results show that the new FP Gamillus exhibits higher brightness at the cost of lower photostability and fluorescence probability (pf), especially at lower pH. mGreenLantern, on the other hand, thanks to a very high pf, is best suited for multimerization quantification at neutral pH. At lower pH, mEGFP remains apparently the best choice for multimerization investigation. These guidelines provide the information needed to plan quantitative fluorescence microscopy involving these FPs, both for general imaging or for protein-protein-interactions quantification via fluorescence fluctuation-based methods. Y1 - 2023 U6 - https://doi.org/10.1371/journal.pone.0285486 SN - 1932-6203 VL - 18 IS - 8 PB - PLoS CY - San Fransisco ER - TY - JOUR A1 - Kappel, Christian A1 - Friedrich, Thomas A1 - Oberkofler, Vicky A1 - Jiang, Li A1 - Crawford, Tim A1 - Lenhard, Michael A1 - Bäurle, Isabel T1 - Genomic and epigenomic determinants of heat stress-induced transcriptional memory in Arabidopsis JF - Genome biology : biology for the post-genomic era N2 - Background Transcriptional regulation is a key aspect of environmental stress responses. Heat stress induces transcriptional memory, i.e., sustained induction or enhanced re-induction of transcription, that allows plants to respond more efficiently to a recurrent HS. In light of more frequent temperature extremes due to climate change, improving heat tolerance in crop plants is an important breeding goal. However, not all heat stress-inducible genes show transcriptional memory, and it is unclear what distinguishes memory from non-memory genes. To address this issue and understand the genome and epigenome architecture of transcriptional memory after heat stress, we identify the global target genes of two key memory heat shock transcription factors, HSFA2 and HSFA3, using time course ChIP-seq. Results HSFA2 and HSFA3 show near identical binding patterns. In vitro and in vivo binding strength is highly correlated, indicating the importance of DNA sequence elements. In particular, genes with transcriptional memory are strongly enriched for a tripartite heat shock element, and are hallmarked by several features: low expression levels in the absence of heat stress, accessible chromatin environment, and heat stress-induced enrichment of H3K4 trimethylation. These results are confirmed by an orthogonal transcriptomic data set using both de novo clustering and an established definition of memory genes. Conclusions Our findings provide an integrated view of HSF-dependent transcriptional memory and shed light on its sequence and chromatin determinants, enabling the prediction and engineering of genes with transcriptional memory behavior. KW - Transcriptional memory KW - Priming KW - Heat stress KW - HSFA2 KW - HSFA3 KW - Arabidopsis thaliana KW - Histone H3K4 trimethylation KW - ChIP-seq Y1 - 2023 U6 - https://doi.org/10.1186/s13059-023-02970-5 SN - 1474-760X VL - 24 IS - 1 PB - BioMed Central CY - London ER - TY - JOUR A1 - Ferreira, Clara Mendes A1 - Dammhahn, Melanie A1 - Eccard, Jana T1 - So many choices, so little time BT - food preference and movement vary with the landscape of fear JF - Ecology and evolution N2 - Spatial and temporal variation in perceived predation risk is an important determinant of movement and foraging activity of animals. Foraging in this landscape of fear, individuals need to decide where and when to move, and what resources to choose. Foraging theory predicts the outcome of these decisions based on energetic trade-offs, but complex interactions between perceived predation risk and preferences of foragers for certain functional traits of their resources are rarely considered. Here, we studied the interactive effects of perceived predation risk on food trait preferences and foraging behavior in bank voles (Myodes glareolus) in experimental landscapes. Individuals (n = 19) were subjected for periods of 24 h to two extreme, risk-uniform landscapes (either risky or safe), containing 25 discrete food patches, filled with seeds of four plant species in even amounts. Seeds varied in functional traits: size, nutrients, and shape. We evaluated whether and how risk modifies forager preference for functional traits. We also investigated whether perceived risk and distance from shelter affected giving-up density (GUD), time in patches, and number of patch visits. In safe landscapes, individuals increased time spent in patches, lowered GUD and visited distant patches more often compared to risky landscapes. Individuals preferred bigger seeds independent of risk, but in the safe treatment they preferred fat-rich over carb-rich seeds. Thus, higher densities of resource levels remained in risky landscapes, while in safe landscapes resource density was lower and less diverse due to selective foraging. Our results suggest that the interaction of perceived risk and dietary preference adds an additional layer to the cascading effects of a landscape of fear which affects biodiversity at resource level. KW - foraging behavior KW - functional traits KW - giving-up density KW - myodes glareolus KW - perceived predation risk KW - seed ecology Y1 - 2023 U6 - https://doi.org/10.1002/ece3.10330 SN - 2045-7758 VL - 13 IS - 7 PB - Wiley CY - Hoboken ER - TY - JOUR A1 - Apriyanto, Ardha A1 - Compart, Julia A1 - Fettke, Jörg T1 - Transcriptomic analysis of mesocarp tissue during fruit development of the oil palm revealed specific isozymes related to starch metabolism that control oil yield JF - Frontiers in plant science N2 - The oil palm (Elaeis guineensis Jacq.) produces a large amount of oil from the fruit. However, increasing the oil production in this fruit is still challenging. A recent study has shown that starch metabolism is essential for oil synthesis in fruit-producing species. Therefore, the transcriptomic analysis by RNA-seq was performed to observe gene expression alteration related to starch metabolism genes throughout the maturity stages of oil palm fruit with different oil yields. Gene expression profiles were examined with three different oil yields group (low, medium, and high) at six fruit development phases (4, 8, 12, 16, 20, and 22 weeks after pollination). We successfully identified and analyzed differentially expressed genes in oil palm mesocarps during development. The results showed that the transcriptome profile for each developmental phase was unique. Sucrose flux to the mesocarp tissue, rapid starch turnover, and high glycolytic activity have been identified as critical factors for oil production in oil palms. For starch metabolism and the glycolytic pathway, we identified specific gene expressions of enzyme isoforms (isozymes) that correlated with oil production, which may determine the oil content. This study provides valuable information for creating new high-oil-yielding palm varieties via breeding programs or genome editing approaches. KW - starch KW - oil yield KW - fruit development KW - gene expression KW - RNA-seq KW - and palm KW - oil KW - Elaeis guineensis Jacq Y1 - 2023 U6 - https://doi.org/10.3389/fpls.2023.1220237 SN - 1664-462X VL - 14 PB - Frontiers Media CY - Lausanne ER - TY - JOUR A1 - Compart, Julia A1 - Singh, Aakanksha A1 - Fettke, Jörg A1 - Apriyanto, Ardha T1 - Customizing starch properties BT - a review of starch modifications and their applications JF - Polymers N2 - Starch has been a convenient, economically important polymer with substantial applications in the food and processing industry. However, native starches present restricted applications, which hinder their industrial usage. Therefore, modification of starch is carried out to augment the positive characteristics and eliminate the limitations of the native starches. Modifications of starch can result in generating novel polymers with numerous functional and value-added properties that suit the needs of the industry. Here, we summarize the possible starch modifications in planta and outside the plant system (physical, chemical, and enzymatic) and their corresponding applications. In addition, this review will highlight the implications of each starch property adjustment. KW - starch KW - starch modification KW - in planta modification KW - physical modification KW - chemical modification KW - enzymatic modification KW - starch application Y1 - 2023 U6 - https://doi.org/10.3390/polym15163491 SN - 2073-4360 VL - 15 IS - 16 PB - MDPI CY - Basel ER - TY - JOUR A1 - Berry, Paul E. A1 - Dammhahn, Melanie A1 - Blaum, Niels T1 - Keeping cool on hot days BT - activity responses of African antelope to heat extremes JF - Frontiers in ecology and evolution N2 - Long-lived organisms are likely to respond to a rapidly changing climate with behavioral flexibility. Animals inhabiting the arid parts of southern Africa face a particularly rapid rise in temperature which in combination with food and water scarcity places substantial constraints on the ability of animals to tolerate heat. We investigated how three species of African antelope-springbok Antidorcas marsupialis, kudu Tragelaphus strepsiceros and eland T. oryx-differing in body size, habitat preference and movement ecology, change their activity in response to extreme heat in an arid savanna. Serving as a proxy for activity, dynamic body acceleration data recorded every five minutes were analyzed for seven to eight individuals per species for the three hottest months of the year. Activity responses to heat during the hottest time of day (the afternoons) were investigated and diel activity patterns were compared between hot and cool days. Springbok, which prefer open habitat, are highly mobile and the smallest of the species studied, showed the greatest decrease in activity with rising temperature. Furthermore, springbok showed reduced mean activity over the 24 h cycle on hot days compared to cool days. Large-bodied eland seemed less affected by afternoon heat than springbok. While eland also reduced diurnal activity on hot days compared to cool days, they compensated for this by increasing nocturnal activity, possibly because their predation risk is lower. Kudu, which are comparatively sedentary and typically occupy shady habitat, seemed least affected during the hottest time of day and showed no appreciable difference in diel activity patterns between hot and cool days. The interplay between habitat preference, body size, movement patterns, and other factors seems complex and even sub-lethal levels of heat stress have been shown to impact an animal's long-term survival and reproduction. Thus, differing heat tolerances among species could result in a shift in the composition of African herbivore communities as temperatures continue to rise, with significant implications for economically important wildlife-based land use and conservation. KW - springbok KW - kudu KW - eland KW - dynamic body acceleration KW - tri-axial accelerometers KW - behavioral flexibility KW - climate change KW - savanna ecology Y1 - 2023 U6 - https://doi.org/10.3389/fevo.2023.1172303 SN - 2296-701X VL - 11 PB - Frontiers Media CY - Lausanne ER - TY - JOUR A1 - Stiegler, Jonas A1 - Pahl, Janice A1 - Guillen, Rafael Arce A1 - Ullmann, Wiebke A1 - Blaum, Niels T1 - The heat is on BT - impacts of rising temperature on the activity of a common European mammal JF - Frontiers in Ecology and Evolution N2 - Climate conditions severely impact the activity and, consequently, the fitness of wildlife species across the globe. Wildlife can respond to new climatic conditions, but the pace of human-induced change limits opportunities for adaptation or migration. Thus, how these changes affect behavior, movement patterns, and activity levels remains unclear. In this study, we investigate how extreme weather conditions affect the activity of European hares (Lepus europaeus) during their peak reproduction period. When hares must additionally invest energy in mating, prevailing against competitors, or lactating, we investigated their sensitivities to rising temperatures, wind speed, and humidity. To quantify their activity, we used the overall dynamic body acceleration (ODBA) calculated from tri-axial acceleration measurements of 33 GPS-collared hares. Our analysis revealed that temperature, humidity, and wind speed are important in explaining changes in activity, with a strong response for high temperatures above 25 & DEG;C and the highest change in activity during temperature extremes of over 35 & DEG;C during their inactive period. Further, we found a non-linear relationship between temperature and activity and an interaction of activity changes between day and night. Activity increased at higher temperatures during the inactive period (day) and decreased during the active period (night). This decrease was strongest during hot tropical nights. At a stage of life when mammals such as hares must substantially invest in reproduction, the sensitivity of females to extreme temperatures was particularly pronounced. Similarly, both sexes increased their activity at high humidity levels during the day and low wind speeds, irrespective of the time of day, while the effect of humidity was stronger for males. Our findings highlight the importance of understanding the complex relationships between extreme weather conditions and mammal behavior, critical for conservation and management. With ongoing climate change, extreme weather events such as heat waves and heavy rainfall are predicted to occur more often and last longer. These events will directly impact the fitness of hares and other wildlife species and hence the population dynamics of already declining populations across Europe. KW - activity KW - ODBA KW - animal tracking KW - European hare KW - extreme weather events KW - climate change Y1 - 2023 U6 - https://doi.org/10.3389/fevo.2023.1193861 SN - 2296-701X VL - 11 PB - Frontiers Media CY - Lausanne ER - TY - THES A1 - Pankaj, Rishabh T1 - Epigenetic reprogramming of seed development BT - exploring the role of histone demethylases and DNA methylation in arabidopsis N2 - The development of seeds in angiosperms starts with a complex process of double fertilization, involving the fusion of the maternal egg cell and central cell with two paternal sperm cells. This gives rise to the embryo and the nourishing endosperm, which are then enclosed by the seed coat, derived from the maternal integuments. The growth of the seed coat in Arabidopsis thaliana (Arabidopsis) is actively inhibited before fertilization by epigenetic regulators known as Polycomb Group (PcG) proteins. These proteins deposit a repressive histone mark called H3K27me3, which must be removed to enable seed coat formation. In this thesis, I explored the mechanism of removal of H3K27me3 marks from the integument cells following fertilization, which allows for seed coat formation. We hypothesized that this removal should be primarily facilitated by histone demethylases from the JMJ family and potentially influenced by the plant hormones Brassinosteroids (BRs). This hypothesis was supported by the expression patterns of the JMJ protein REF6 and of BR related genes, which are specifically expressed in the integuments and in the seed coat. Moreover, mutations in both these pathways lead to developmental defects, such as reduced ovule viability and delayed seed coat growth. Our research provides evidence suggesting that BR signalling is likely involved in recruiting JMJ-type histone demethylases to target loci responsible for seed coat growth. Moreover, we have discovered an additional pathway through which BRs regulate seed coat development, independent of their influence on H3K27me3 marks. This finding emphasizes the diverse roles of BRs in coordinating seed development, extending beyond their well-known involvement in plant growth and development. Furthermore, I explored the role of another epigenetic mark, DNA methylation, in fertilization-independent (or autonomous) seed formation in Arabidopsis. For this, we utilized epigenetic Recombinant Inbred Lines (epiRILs) and thus identified an epigenetic Quantitative Trait Locus (epiQTL) on chromosome II, potentially responsible for the larger autonomous seed size observed in DNA methylation mutants. Overall, this thesis significantly enhances our comprehension of the intricate relationship between epigenetic modifications, hormonal signaling, and plant reproductive processes. It offers valuable insights into the genetic mechanisms governing both sexual and asexual seed formation, while also presenting potential avenues for the engineer of advantageous traits in agricultural crops. KW - Epigenetics KW - Seed development KW - Seed Coat Development KW - H3K27me3 Methylation KW - Auxin KW - Brassinosteriods KW - DNA Methylation KW - JUMONJI KW - Histone Modification Y1 - 2023 ER - TY - THES A1 - Jiang, Li T1 - Analysis of the role of Heat shock factors and Mediator subunits in heat stress memory in Arabidopsis thaliana N2 - In nature, plants often encounter biotic and abiotic stresses, which can cause reduced crop yield and quality, and threaten the nutrition of a growing human population. As heat stress (HS) is one of the main abiotic stresses, and is projected to increase due to global warming, it is necessary to better understand how plants respond and survive under HS. In Arabidopsis thaliana, plants can survive under severe HS if primed by a non-lethal HS, a process called acquisition of thermotolerance. This primed stated can be maintained for several days, and the ability of plants to maintain the primed state is called maintenance of acquired thermotolerance (mATT) or HS memory. According to current research, two Heat shock factors (HSFs) HSFA2 and HSFA3 are known to account for the majority of mATT capability, and there are other HSFs e.g. HSFA1b and HSFA6b in HSF complexes containing HSFA2 and/or HSFA3, however, the roles of these HSFs in HS memory is not clearly understood. Moreover, the mechanism of these HSFs in regulating HS memory is unclear, whether transcriptional machinery e.g. the Mediator complex contributes to transcriptional memory. This work investigates the role of HSFs and Mediator subunits in HS memory in A. thaliana. For the role of HSFs, the interaction between HSFA1b and HSFA2 during HS memory phase was confirmed by in vivo co- immunoprecipitation (Co-IP). HSFA1b, HSFA2, HSFA3 and HSFA6b targeted HS memory-related genes according to DNA affinity purification sequencing (DAP-seq) data, and targets of HSFA1b were confirmed in vivo by chromatin immunoprecipitation qPCR (ChIP-qPCR). The mutant of hsfa6b showed an HS memory deficiency phenotype in mATT survival assay. These data confirmed the role for HSFA2 and HSFA3 in HS memory, and suggest that HSFA1b and HSFA6b also function in HS memory. The Mediator complex functions as an RNA Polymerase II (RNA Pol II) co-regulator, and includes Head, Middle, Tail and Kinase modules. Both MED23 and MED32 belong to the Tail module, and they have a positive role in HS memory. MED23 interacted with HSFA3, as determined by yeast two hybrid (Y2H) and in vivo Co-IP assays. The med23 mutant showed a decreased HS memory phenotype, reduced expression of Type I (sustained expression) memory genes following HS, and reduced accumulation of the memory-associated Tri-methylation of histone H3 lysine 4 (H3K4me3)histone modification at HS memory-related gene loci after HS. MED23 was recruited to HS-inducible memory and non-memory genes after HS, as determined by ChIP-qPCR. The med32 mutant showed a reduced HS memory phenotype, decreased expression of Type I and Type II (hyper-induction) memory genes, and lower accumulation of H3K4me3 at memory gene lociafter HS. However, MED32 did not show interaction with any tested HSF in Y2H or in vivo Co-IP. MED32 regulated the recruitment of RNA Pol II at HS-inducible genes after HS, but was not itself recruited to HS memory genes after HS. These results provided more evidence that the Mediator subunits MED23 and MED32 regulate HS memory on transcriptional and epigenetic levels. In general, this work provides a better insight into the molecular mechanism of how HSFs and Mediator subunits regulate HS memory in plants and will provide new perspectives to breed crops with improved thermotolerance. N2 - In der Natur sind Pflanzen häufig mit biotischen und abiotischen Stressfaktoren konfrontiert, die zu Ertrags- und Qualitätsmängeln führen können und die Ernährung der wachsenden Weltbevölkerung gefährden. Da Hitzestress (HS) einer der wichtigsten abiotischen Stressfaktoren ist und aufgrund der globalen Erwärmung voraussichtlich noch zunehmen wird, steigt die Notwendigkeit zu verstehen wie Pflanzen auf HS reagieren und überleben. Arabidopsis thaliana können unter schwerem Hitzestress überleben, wenn sie durch einen nicht-tödlichen Hitzestress vorbereitet werden, diesen Prozess bezeichnet man als Erwerb von Thermotoleranz. Die Fähigkeit der Pflanzen, diesen Zustand aufrechtzuerhalten, wird als Aufrechterhaltung der erworbenen Thermotoleranz (mATT) oder HS-Gedächtnis bezeichnet. Nach dem derzeitigen Stand der Forschung sind zwei Hitzeschockfaktoren (HSFs), HSFA2 und HSFA3, für den Großteil der mATT-Fähigkeit verantwortlich. Außerdem gibt es weitere HSFs z.B. HSFA1b und HSFA6b, die ebenfalls im HSF-Komplex neben HSFA2 und/oder HSFA3 enthalten sind. Jedoch ist ihre Rolle im HS-Gedächtnis noch nicht eindeutig geklärt. Darüber hinaus ist der Mechanismus dieser HSFs bei der Regulierung des HS-Gedächtnisses unklar, ob z. B. die Transkriptionsmaschinerie, unter anderem der Mediator-Komplex, zum Transkriptionsgedächtnis beiträgt. In dieser Arbeit wird die Rolle der HSFs und der Mediator-Untereinheiten beim HS-Gedächtnis in A. thaliana untersucht. Bezüglich der Rolle der HSFs, wurde die Interaktion zwischen HSFA1b und HSFA2, während der HS-Gedächtnisphase, durch in vivo Co-Immunopräzipitation (Co-IP) bestätigt. HSFA1b, HSFA2, HSFA3 und HSFA6b binden, laut DNA-Affinitätsreinigungs-Sequenzierung (DAP-seq), zielgerichtet an HS-Gedächtnis-verwandte Gene. Die Ziele von HSFA1b wurden in vivo durch Chromatin-Immunpräzipitation qPCR (ChIP-qPCR) bestätigt. Die hsfa6b-Mutante zeigte im mATT-Überlebenstest einen Phänotypen für HS-Gedächtnisdefizit. Diese Daten bestätigten die Rolle von HSFA2 und HSFA3 im HS-Gedächtnis und legen nahe, dass HSFA1b und HSFA6b ebenfalls eine Funktion im HS-Gedächtnis haben. Der Mediator-Komplex fungiert als Co-Regulator der RNA-Polymerase II (RNA Pol II) und umfasst die Module Head, Middle, Tail und Kinase. Sowohl MED23 als auch MED32 gehören zum Tail-Modul und spielen eine positive Rolle im HS-Gedächtnis. MED23 interagiert mit HSFA3, wie durch Hefe-Zwei-Hybrid- (Y2H) und In-vivo-Co-IP-Assays festgestellt wurde. Die med23-Mutante zeigte einen verminderten HS-Gedächtnisphänotyp, eine verringerte Expression von Gedächtnisgenen des Typ I (anhaltende Expression) nach HS und eine verringerte Akkumulation der gedächtnisassoziierten Histonmodifikation Tri-Methylierung von Histon H3 Lysin 4 (H3K4me3) an HS-Gedächtnis-bezogenen Genorten nach HS. MED23 wurde nach HS an HS-induzierbaren Gedächtnis- und Nicht-Gedächtnis-Genen rekrutiert, wie durch ChIP-qPCR festgestellt wurde. Die med32-Mutante zeigte einen reduzierten HS-Gedächtnisphänotyp, eine verringerte Expression von Typ-I- und Typ-II-Gedächtnisgenen (Hyperinduktion) und eine geringere Anhäufung von H3K4me3 an Gedächtnisgenloci nach HS. MED32 zeigte jedoch keine Interaktion mit einem der getesteten HSFs in Y2H oder in vivo Co-IP. MED32 regulierte die Rekrutierung von RNA Pol II an HS-induzierbaren Genen nach HS, wurde aber selbst nicht an HS-Gedächtnisgenen nach HS rekrutiert. Diese Ergebnisse liefern weitere Beweise dafür, dass die Mediator-Untereinheiten MED23 und MED32 das HS-Gedächtnis auf transkriptioneller und epigenetischer Ebene regulieren. Im Allgemeinen bietet diese Arbeit einen besseren Einblick in den molekularen Mechanismus, wie HSFs und Mediator-Untereinheiten das HS-Gedächtnis in Pflanzen regulieren und wird neue Perspektiven für die Züchtung von Pflanzen mit verbesserter Thermotoleranz eröffnen. KW - Heat stress memory, Heat shock factors, Mediator subunits, MED23, MED32, Arabidopsis thaliana Y1 - 2023 ER -