TY  - JOUR
A1  - Cui, Xiao
A1  - Lv, Yang
A1  - Chen, Miaolin
A1  - Nikoloski, Zoran
A1  - Twell, David
A1  - Zhang, Dabing
T1  - Young Genes out of the Male: An Insight from Evolutionary Age Analysis of the Pollen Transcriptome
JF  - Molecular plant
N2  - The birth of new genes in genomes is an important evolutionary event. Several studies reveal that new genes in animals tend to be preferentially expressed in male reproductive tissues such as testis (Betran et al., 2002; Begun et al., 2007; Dubruille et al., 2012), and thus an "out of testis' hypothesis for the emergence of new genes has been proposed (Vinckenbosch et al., 2006; Kaessmann, 2010). However, such phenomena have not been examined in plant species. Here, by employing a phylostratigraphic method, we dated the origin of protein-coding genes in rice and Arabidopsis thaliana and observed a number of young genes in both species. These young genes tend to encode short extracellular proteins, which may be involved in rapid evolving processes, such as reproductive barriers, species specification, and antimicrobial processes. Further analysis of transcriptome age indexes across different tissues revealed that male reproductive cells express a phylogenetically younger transcriptome than other plant tissues. Compared with sporophytic tissues, the young transcriptomes of the male gametophyte displayed greater complexity and diversity, which included a higher ratio of anti-sense and inter-genic transcripts, reflecting a pervasive transcription state that facilitated the emergence of new genes. Here, we propose that pollen may act as an "innovation incubator' for the birth of de novo genes. With cases of male-biased expression of young genes reported in animals, the "new genes out of the male' model revealed a common evolutionary force that drives reproductive barriers, species specification, and the upgrading of defensive mechanisms against pathogens.
KW  - pollen
KW  - evolution
KW  - young genes
KW  - transcriptome
Y1  - 2015
U6  - https://doi.org/10.1016/j.molp.2014.12.008
SN  - 1674-2052
SN  - 1752-9867
VL  - 8
IS  - 6
SP  - 935
EP  - 945
PB  - Cell Press
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Jetzschmann, Katharina J.
A1  - Jagerszki, Gyula
A1  - Dechtrirat, Decha
A1  - Yarman, Aysu
A1  - Gajovic-Eichelmann, Nenad
A1  - Gilsing, Hans-Detlev
A1  - Schulz, Burkhard
A1  - Gyurcsanyi, Robert E.
A1  - Scheller, Frieder W.
T1  - Vectorially Imprinted Hybrid Nanofilm for Acetylcholinesterase Recognition
JF  - Advanced functional materials
N2  - Effective recognition of enzymatically active tetrameric acetylcholinesterase (AChE) is accomplished by a hybrid nanofilm composed of a propidium-terminated self-assembled monolayer (Prop-SAM) which binds AChE via its peripheral anionic site (PAS) and an ultrathin electrosynthesized molecularly imprinted polymer (MIP) cover layer of a novel carboxylate-modified derivative of 3,4-propylenedioxythiophene. The rebinding of the AChE to the MIP/Prop-SAM nanofilm covered electrode is detected by measuring in situ the enzymatic activity. The oxidative current of the released thiocholine is dependent on the AChE concentration from approximate to 0.04 x 10(-6) to 0.4 x 10(-6)m. An imprinting factor of 9.9 is obtained for the hybrid MIP, which is among the best values reported for protein imprinting. The dissociation constant characterizing the strength of the MIP-AChE binding is 4.2 x 10(-7)m indicating the dominant role of the PAS-Prop-SAM interaction, while the benefit of the MIP nanofilm covering the Prop-SAM layer is the effective suppression of the cross-reactivity toward competing proteins as compared with the Prop-SAM. The threefold selectivity gain provided by i) the shape-specific MIP filter, ii) the propidium-SAM, iii) signal generation only by the AChE bound to the nanofilm shows promise for assessing AChE activity levels in cerebrospinal fluid.
KW  - acetylcholinesterase
KW  - biomimetic sensors
KW  - molecularly imprinted electropolymers
KW  - peripheral anionic site
KW  - propidium
Y1  - 2015
U6  - https://doi.org/10.1002/adfm.201501900
SN  - 1616-301X
SN  - 1616-3028
VL  - 25
IS  - 32
SP  - 5178
EP  - 5183
PB  - Wiley-VCH
CY  - Weinheim
ER  - 
TY  - GEN
A1  - Jones, Eppie R.
A1  - González-Fortes, Gloria M.
A1  - Connell, Sarah
A1  - Siska, Veronika
A1  - Eriksson, Anders
A1  - Martiniano, Rui
A1  - McLaughlin, Russell L.
A1  - Llorente, Marcos Gallego
A1  - Cassidy, Lara M.
A1  - Gamba, Cristina
A1  - Meshveliani, Tengiz
A1  - Bar-Yosef, Ofer
A1  - Müller, Werner
A1  - Belfer-Cohen, Anna
A1  - Matskevich, Zinovi
A1  - Jakeli, Nino
A1  - Higham, Thomas F. G.
A1  - Currat, Mathias
A1  - Lordkipanidze, David
A1  - Hofreiter, Michael
A1  - Manica, Andrea
A1  - Pinhasi, Ron
A1  - Bradley, Daniel G.
T1  - Upper Palaeolithic genomes reveal deep roots of modern Eurasians
T2  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe
N2  - We extend the scope of European palaeogenomics by sequencing the genomes of Late Upper Palaeolithic (13,300 years old, 1.4-fold coverage) and Mesolithic (9,700 years old, 15.4-fold) males from western Georgia in the Caucasus and a Late Upper Palaeolithic (13,700 years old, 9.5-fold) male from Switzerland. While we detect Late Palaeolithic–Mesolithic genomic continuity in both regions, we find that Caucasus hunter-gatherers (CHG) belong to a distinct ancient clade that split from western hunter-gatherers ∼45 kya, shortly after the expansion of anatomically modern humans into Europe and from the ancestors of Neolithic farmers ∼25 kya, around the Last Glacial Maximum. CHG genomes significantly contributed to the Yamnaya steppe herders who migrated into Europe ∼3,000 BC, supporting a formative Caucasus influence on this important Early Bronze age culture. CHG left their imprint on modern populations from the Caucasus and also central and south Asia possibly marking the arrival of Indo-Aryan languages.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 1334 
Y1  - 2015
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-439317
SN  - 1866-8372
IS  - 1334
ER  - 
TY  - JOUR
A1  - Jones, Eppie R.
A1  - González-Fortes, Gloria M.
A1  - Connell, Sarah
A1  - Siska, Veronika
A1  - Eriksson, Anders
A1  - Martiniano, Rui
A1  - McLaughlin, Russell L.
A1  - Llorente, Marcos Gallego
A1  - Cassidy, Lara M.
A1  - Gamba, Cristina
A1  - Meshveliani, Tengiz
A1  - Bar-Yosef, Ofer
A1  - Mueller, Werner
A1  - Belfer-Cohen, Anna
A1  - Matskevich, Zinovi
A1  - Jakeli, Nino
A1  - Higham, Thomas F. G.
A1  - Currat, Mathias
A1  - Lordkipanidze, David
A1  - Hofreiter, Michael
A1  - Manica, Andrea
A1  - Pinhasi, Ron
A1  - Bradley, Daniel G.
T1  - Upper Palaeolithic genomes reveal deep roots of modern Eurasians
JF  - Nature Communications
N2  - We extend the scope of European palaeogenomics by sequencing the genomes of Late Upper Palaeolithic (13,300 years old, 1.4-fold coverage) and Mesolithic (9,700 years old, 15.4-fold) males from western Georgia in the Caucasus and a Late Upper Palaeolithic (13,700 years old, 9.5-fold) male from Switzerland. While we detect Late Palaeolithic-Mesolithic genomic continuity in both regions, we find that Caucasus hunter-gatherers (CHG) belong to a distinct ancient clade that split from western hunter-gatherers similar to 45 kya, shortly after the expansion of anatomically modern humans into Europe and from the ancestors of Neolithic farmers similar to 25 kya, around the Last Glacial Maximum. CHG genomes significantly contributed to the Yamnaya steppe herders who migrated into Europe similar to 3,000 BC, supporting a formative Caucasus influence on this important Early Bronze age culture. CHG left their imprint on modern populations from the Caucasus and also central and south Asia possibly marking the arrival of Indo-Aryan languages.
Y1  - 2015
U6  - https://doi.org/10.1038/ncomms9912
SN  - 2041-1723
VL  - 6
PB  - Nature Publishing Group
CY  - London
ER  - 
TY  - JOUR
A1  - Ludwig, Arne
A1  - Reissmann, Monika
A1  - Benecke, Norbert
A1  - Bellone, Rebecca
A1  - Sandoval-Castellanos, Edson
A1  - Cieslak, Michael
A1  - González-Fortes, Gloria M.
A1  - Morales-Muniz, Arturo
A1  - Hofreiter, Michael
A1  - Pruvost, Melanie
T1  - Twenty-five thousand years of fluctuating selection on leopard complex spotting and congenital night blindness in horses
JF  - Philosophical transactions of the Royal Society of London : B, Biological sciences
N2  - Leopard complex spotting is inherited by the incompletely dominant locus, LP, which also causes congenital stationary night blindness in homozygous horses. We investigated an associated single nucleotide polymorphism in the TRPM1 gene in 96 archaeological bones from 31 localities from Late Pleistocene (approx. 17 000 YBP) to medieval times. The first genetic evidence of LP spotting in Europe dates back to the Pleistocene. We tested for temporal changes in the LP associated allele frequency and estimated coefficients of selection by means of approximate Bayesian computation analyses. Our results show that at least some of the observed frequency changes are congruent with shifts in artificial selection pressure for the leopard complex spotting phenotype. In early domestic horses from Kirklareli-Kanligecit (Turkey) dating to 2700-2200 BC, a remarkably high number of leopard spotted horses (six of 10 individuals) was detected including one adult homozygote. However, LP seems to have largely disappeared during the late Bronze Age, suggesting selection against this phenotype in early domestic horses. During the Iron Age, LP reappeared, probably by reintroduction into the domestic gene pool from wild animals. This picture of alternating selective regimes might explain how genetic diversity was maintained in domestic animals despite selection for specific traits at different times.
KW  - ancient DNA
KW  - coat colour
KW  - domestication
KW  - Equus
KW  - palaeogenetics
KW  - population
Y1  - 2015
U6  - https://doi.org/10.1098/rstb.2013.0386
SN  - 0962-8436
SN  - 1471-2970
VL  - 370
IS  - 1660
PB  - Royal Society
CY  - London
ER  - 
TY  - JOUR
A1  - Makower, A. Katharina
A1  - Schuurmans, J. Merijn
A1  - Groth, Detlef
A1  - Zilliges, Yvonne
A1  - Matthijs, Hans C. P.
A1  - Dittmann-Thünemann, Elke
T1  - Transcriptomics-Aided dissection of the intracellular and extracellular roles of microcystin in microcystis aeruginosa PCC 7806
JF  - Applied and environmental microbiology
N2  - Recent studies have provided evidence for both intracellular and extracellular roles of the potent hepatotoxin microcystin (MC) in the bloom-forming cyanobacterium Microcystis. Here, we surveyed transcriptomes of the wild-type strain M. aeruginosa PCC 7806 and the microcystin-deficient Delta mcyB mutant under low light conditions with and without the addition of external MC of the LR variant (MC-LR). Transcriptomic data acquired by microarray and quantitative PCR revealed substantial differences in the relative expression of genes of the central intermediary metabolism, photosynthesis, and energy metabolism. In particular, the data provide evidence for a lower photosystem I (PSI)-to-photosystem II (PSII) ratio and a more pronounced carbon limitation in the microcystin-deficient mutant. Interestingly, only 6% of the transcriptional differences could be complemented by external microcystin-LR addition. This MC signaling effect was seen exclusively for genes of the secondary metabolism category. The orphan polyketide synthase gene cluster IPF38-51 was specifically downregulated in response to external MC-LR under low light. Our data suggest a hierarchical and light-dependent cross talk of secondary metabolites and support both an intracellular and an extracellular role of MC in Microcystis.
Y1  - 2015
U6  - https://doi.org/10.1128/AEM.02601-14
SN  - 0099-2240
SN  - 1098-5336
VL  - 81
IS  - 2
SP  - 544
EP  - 554
PB  - American Society for Microbiology
CY  - Washington
ER  - 
TY  - JOUR
A1  - Köslin-Findeklee, Fabian
A1  - Rizi, Vajiheh Safavi
A1  - Becker, Martin A.
A1  - Parra-Londono, Sebastian
A1  - Arif, Muhammad
A1  - Balazadeh, Salma
A1  - Müller-Röber, Bernd
A1  - Kunze, Reinhard
A1  - Horst, Walter J.
T1  - Transcriptomic analysis of nitrogen starvation- and cultivar-specific leaf senescence in winter oilseed rape (Brassica napus L.)
JF  - Plant science : an international journal of experimental plant biology
N2  - High nitrogen (N) efficiency, characterized by high grain yield under N limitation, is an important agricultural trait in Brassica napus L. cultivars related to delayed senescence of older leaves during reproductive growth (a syndrome called stay-green). The aim of this study was thus to identify genes whose expression is specifically altered during N starvation-induced leaf senescence and that can be used as markers to distinguish cultivars at early stages of senescence prior to chlorophyll loss. To this end, the transcriptomes of leaves of two B. napus cultivars differing in stay-green characteristics and N efficiency were analyzed 4 days after the induction of senescence by either N starvation, leaf shading or detaching. In addition to N metabolism genes, N starvation mostly (and specifically) repressed genes related to photosynthesis, photorespiration and cell-wall structure, while genes related to mitochondrial electron transport and flavonoid biosynthesis were predominately up-regulated. A kinetic study over a period of 12 days with four B. napus cultivars differing in their stay-green characteristics confirmed the cultivar-specific regulation of six genes in agreement with their senescence behavior: the senescence regulator ANAC029, the anthocyanin synthesis-related genes ANS and DFR-like1, the ammonium transporter AMT1:4, the ureide transporter UPSS, and SPS1 involved in sucrose biosynthesis. The identified genes represent markers for the detection of cultivar-specific differences in N starvation-induced leaf senescence and can thus be employed as valuable tools in B. napus breeding. (C) 2015 Elsevier Ireland Ltd. All rights reserved.
KW  - Brassica napus
KW  - Genotypic differences
KW  - Leaf senescence
KW  - Molecular marker
KW  - N efficiency
KW  - Stay-green
Y1  - 2015
U6  - https://doi.org/10.1016/j.plantsci.2014.11.018
SN  - 0168-9452
VL  - 233
SP  - 174
EP  - 185
PB  - Elsevier
CY  - Clare
ER  - 
TY  - JOUR
A1  - Garapati, Prashanth
A1  - Xue, Gang-Ping
A1  - Munne-Bosch, Sergi
A1  - Balazadeh, Salma
T1  - Transcription Factor ATAF1 in Arabidopsis Promotes Senescence by Direct Regulation of Key Chloroplast Maintenance and Senescence Transcriptional Cascades
JF  - Plant physiology : an international journal devoted to physiology, biochemistry, cellular and molecular biology, biophysics and environmental biology of plants
N2  - Senescence represents a fundamental process of late leaf development. Transcription factors (TFs) play an important role for expression reprogramming during senescence; however, the gene regulatory networks through which they exert their functions, and their physiological integration, are still largely unknown. Here, we identify the Arabidopsis (Arabidopsis thaliana) abscisic acid (ABA)- and hydrogen peroxide-activated TF Arabidopsis thaliana ACTIVATING FACTOR1 (ATAF1) as a novel upstream regulator of senescence. ATAF1 executes its physiological role by affecting both key chloroplast maintenance and senescence-promoting TFs, namely GOLDEN2-LIKE1 (GLK1) and ORESARA1 (ARABIDOPSIS NAC092), respectively. Notably, while ATAF1 activates ORESARA1, it represses GLK1 expression by directly binding to their promoters, thereby generating a transcriptional output that shifts the physiological balance toward the progression of senescence. We furthermore demonstrate a key role of ATAF1 for ABA- and hydrogen peroxide-induced senescence, in accordance with a direct regulatory effect on ABA homeostasis genes, including NINE-CIS-EPOXYCAROTENOID DIOXYGENASE3 involved in ABA biosynthesis and ABC TRANSPORTER G FAMILY MEMBER40, encoding an ABA transport protein. Thus, ATAF1 serves as a core transcriptional activator of senescence by coupling stress-related signaling with photosynthesis- and senescence-related transcriptional cascades.
Y1  - 2015
U6  - https://doi.org/10.1104/pp.15.00567
SN  - 0032-0889
SN  - 1532-2548
VL  - 168
IS  - 3
SP  - 1122
EP  - +
PB  - American Society of Plant Physiologists
CY  - Rockville
ER  - 
TY  - JOUR
A1  - Garapati, Prashanth
A1  - Feil, Regina
A1  - Lunn, John Edward
A1  - Van Dijck, Patrick
A1  - Balazadeh, Salma
A1  - Müller-Röber, Bernd
T1  - Transcription Factor Arabidopsis Activating Factor1 Integrates Carbon Starvation Responses with Trehalose Metabolism
JF  - Plant physiology : an international journal devoted to physiology, biochemistry, cellular and molecular biology, biophysics and environmental biology of plants
N2  - Plants respond to low carbon supply by massive reprogramming of the transcriptome and metabolome. We show here that the carbon starvation-induced NAC (for NO APICAL MERISTEM/ARABIDOPSIS TRANSCRIPTION ACTIVATION FACTOR/CUP-SHAPED COTYLEDON) transcription factor Arabidopsis (Arabidopsis thaliana) Transcription Activation Factor1 (ATAF1) plays an important role in this physiological process. We identified TREHALASE1, the only trehalase-encoding gene in Arabidopsis, as a direct downstream target of ATAF1. Overexpression of ATAF1 activates TREHALASE1 expression and leads to reduced trehalose-6-phosphate levels and a sugar starvation metabolome. In accordance with changes in expression of starch biosynthesis-and breakdown-related genes, starch levels are generally reduced in ATAF1 overexpressors but elevated in ataf1 knockout plants. At the global transcriptome level, genes affected by ATAF1 are broadly associated with energy and carbon starvation responses. Furthermore, transcriptional responses triggered by ATAF1 largely overlap with expression patterns observed in plants starved for carbon or energy supply. Collectively, our data highlight the existence of a positively acting feedforward loop between ATAF1 expression, which is induced by carbon starvation, and the depletion of cellular carbon/energy pools that is triggered by the transcriptional regulation of downstream gene regulatory networks by ATAF1.
Y1  - 2015
U6  - https://doi.org/10.1104/pp.15.00917
SN  - 0032-0889
SN  - 1532-2548
VL  - 169
IS  - 1
SP  - 379
EP  - 390
PB  - American Society of Plant Physiologists
CY  - Rockville
ER  - 
TY  - JOUR
A1  - Gorochowski, Thomas E.
A1  - Ignatova, Zoya
A1  - Bovenberg, Roel A. L.
A1  - Roubos, Johannes A.
T1  - Trade-offs between tRNA abundance and mRNA secondary structure support smoothing of translation elongation rate
JF  - Nucleic acids research
N2  - Translation of protein from mRNA is a complex multi-step process that occurs at a non-uniform rate. Variability in ribosome speed along an mRNA enables refinement of the proteome and plays a critical role in protein biogenesis. Detailed single protein studies have found both tRNA abundance and mRNA secondary structure as key modulators of translation elongation rate, but recent genome-wide ribosome profiling experiments have not observed significant influence of either on translation efficiency. Here we provide evidence that this results from an inherent trade-off between these factors. We find codons pairing to high-abundance tRNAs are preferentially used in regions of high secondary structure content, while codons read by significantly less abundant tRNAs are located in lowly structured regions. By considering long stretches of high and low mRNA secondary structure in Saccharomyces cerevisiae and Escherichia coli and comparing them to randomized-gene models and experimental expression data, we were able to distinguish clear selective pressures and increased protein expression for specific codon choices. The trade-off between secondary structure and tRNA-concentration based codon choice allows for compensation of their independent effects on translation, helping to smooth overall translational speed and reducing the chance of potentially detrimental points of excessively slow or fast ribosome movement.
Y1  - 2015
U6  - https://doi.org/10.1093/nar/gkv199
SN  - 0305-1048
SN  - 1362-4962
VL  - 43
IS  - 6
SP  - 3022
EP  - 3032
PB  - Oxford Univ. Press
CY  - Oxford
ER  -