@article{TsukayaByrneHoriguchietal.2013, author = {Tsukaya, Hirokazu and Byrne, Mary E. and Horiguchi, Gorou and Sugiyama, Munetaka and Van Lijsebettens, Mieke and Lenhard, Michael}, title = {How do 'housekeeping' genes control organogenesis?-unexpected new findings on the role of housekeeping genes in cell and organ differentiation}, series = {Journal of plant research}, volume = {126}, journal = {Journal of plant research}, number = {1}, publisher = {Springer}, address = {Tokyo}, issn = {0918-9440}, doi = {10.1007/s10265-012-0518-2}, pages = {3 -- 15}, year = {2013}, abstract = {In recent years, an increasing number of mutations in what would appear to be 'housekeeping genes' have been identified as having unexpectedly specific defects in multicellular organogenesis. This is also the case for organogenesis in seed plants. Although it is not surprising that loss-of-function mutations in 'housekeeping' genes result in lethality or growth retardation, it is surprising when (1) the mutant phenotype results from the loss of function of a 'housekeeping' gene and (2) the mutant phenotype is specific. In this review, by defining housekeeping genes as those encoding proteins that work in basic metabolic and cellular functions, we discuss unexpected links between housekeeping genes and specific developmental processes. In a surprising number of cases housekeeping genes coding for enzymes or proteins with functions in basic cellular processes such as transcription, post-transcriptional modification, and translation affect plant development.}, language = {en} } @article{JunemannWinterhoffNordholzetal.2013, author = {Junemann, Alexander and Winterhoff, Moritz and Nordholz, Benjamin and Rottner, Klemens and Eichinger, Ludwig and Gr{\"a}f, Ralph and Faix, Jan}, title = {ForC lacks canonical formin activity but bundles actin filaments and is required for multicellular development of Dictyostelium cells}, series = {European journal of cell biology}, volume = {92}, journal = {European journal of cell biology}, number = {6-7}, publisher = {Elsevier}, address = {Jena}, issn = {0171-9335}, doi = {10.1016/j.ejcb.2013.07.001}, pages = {201 -- 212}, year = {2013}, abstract = {Diaphanous-related formins (DRFs) drive the nucleation and elongation of linear actin filaments downstream of Rho GTPase signalling pathways. Dictyostelium formin C (ForC) resembles a DRF, except that it lacks a genuine formin homology domain 1 (FH1), raising the questions whether or not ForC can nucleate and elongate actin filaments. We found that a recombinant ForC-FH2 fragment does not nucleate actin polymerization, but moderately decreases the rate of spontaneous actin assembly and disassembly, although the barbed-end elongation rate in the presence of the formin was not markedly changed. However, the protein bound to and crosslinked actin filaments into loose bundles of mixed polarity. Furthermore, ForC is an important regulator of morphogenesis since ForC-null cells are severely impaired in development resulting in the formation of aberrant fruiting bodies. Immunoblotting revealed that ForC is absent during growth, but becomes detectable at the onset of early aggregation when cells chemotactically stream together to form a multicellular organism, and peaks around the culmination stage. Fluorescence microscopy of cells ectopically expressing a GFP-tagged, N-terminal ForC fragment showed its prominent accumulation in the leading edge, suggesting that ForC may play a role in cell migration. In agreement with its expression profile, no defects were observed in random migration of vegetative mutant cells. Notably, chemotaxis of starved cells towards a source of cAMP was severely impaired as opposed to control. This was, however, largely due to a marked developmental delay of the mutant, as evidenced by the expression profile of the early developmental marker csA. In line with this, chemotaxis was almost restored to wild type levels after prolonged starvation. Finally, we observed a complete failure of phototaxis due to abolished slug formation and a massive reduction of spores consistent with forC promoter-driven expression of beta-galactosidase in prespore cells. Together, these findings demonstrate ForC to be critically involved in signalling of the cytoskeleton during various stages of development.}, language = {en} } @article{MuellerMuellerBauretal.2013, author = {M{\"u}ller, Juliane and M{\"u}ller, Steffen and Baur, Heiner and Mayer, Frank}, title = {Intra-individual gait speed variability in healthy children aged 1-15 years}, series = {Gait \& posture}, volume = {38}, journal = {Gait \& posture}, number = {4}, publisher = {Elsevier}, address = {Clare}, issn = {0966-6362}, doi = {10.1016/j.gaitpost.2013.02.011}, pages = {631 -- 636}, year = {2013}, abstract = {Introduction: Gait speed is one of the most commonly and frequently used parameters to evaluate gait development. It is characterized by high variability when comparing different steps in children. The objective of this study was to determine intra-individual gait speed variability in children. Methods: Gait speed measurements (6-10 trials across a 3 m walkway) were performed and analyzed in 8263 children, aged 1-15 years. The coefficient of variation (CV) served as a measure for intra-individual gait speed variability measured in 6.6 +/- 1.0 trials per child. Multiple linear regression analysis was conducted to evaluate the influence of age and body height on changes in variability. Additionally, a subgroup analysis for height within the group of 6-year-old children was applied. Results: A successive reduction in gait speed variability (CV) was observed for age groups (age: 1-15 years) and body height groups (height: 0.70-1.90 m). The CV in the oldest subjects was only one third of the CV (CV 6.25 +/- 3.52\%) in the youngest subjects (CV 16.58 +/- 10.01\%). Up to the age of 8 years (or 1.40 m height) there was a significant reduction in CV over time, compared to a leveling off for the older (taller) children. Discussion: The straightforward approach measuring gait speed variability in repeated trials might serve as a fundamental indicator for gait development in children. Walking velocity seems to increase to age 8. Enhanced gait speed consistency of repeated trials develops up to age 15.}, language = {en} } @article{MehnertAkhrifTelkemeyeretal.2013, author = {Mehnert, Jan and Akhrif, Atae and Telkemeyer, Silke and Rossi, Sonja and Schmitz, Christoph H. and Steinbrink, Jens and Wartenburger, Isabell and Obrig, Hellmuth and Neufang, Susanne}, title = {Developmental changes in brain activation and functional connectivity during response inhibition in the early childhood brain}, series = {Brain and development : official journal of the Japanese Society of Child Neurology}, volume = {35}, journal = {Brain and development : official journal of the Japanese Society of Child Neurology}, number = {10}, publisher = {Elsevier}, address = {Amsterdam}, issn = {0387-7604}, doi = {10.1016/j.braindev.2012.11.006}, pages = {894 -- 904}, year = {2013}, abstract = {Response inhibition is an attention function which develops relatively early during childhood. Behavioral data suggest that by the age of 3, children master the basic task requirements for the assessment of response inhibition but performance improves substantially until the age of 7. The neuronal mechanisms underlying these developmental processes, however, are not well understood. In this study, we examined brain activation patterns and behavioral performance of children aged between 4 and 6 years compared to adults by applying a go/no-go paradigm during near-infrared spectroscopy (NIRS) brain imaging. We furthermore applied task-independent functional connectivity measures to the imaging data to identify maturation of intrinsic neural functional networks. We found a significant group x condition related interaction in terms of inhibition-related reduced right fronto-parietal activation in children compared to adults. In contrast, motor-related activation did not differ between age groups. Functional connectivity analysis revealed that in the children's group, short-range coherence within frontal areas was stronger, and long-range coherence between frontal and parietal areas was weaker, compared to adults. Our findings show that in children aged from 4 to 6 years fronto-parietal brain maturation plays a crucial part in the cognitive development of response inhibition.}, language = {en} }