| Literature DB >> 27830782 |
Bulent Ataman1, Gabriella L Boulting1, David A Harmin1, Marty G Yang1, Mollie Baker-Salisbury1, Ee-Lynn Yap1, Athar N Malik1, Kevin Mei1, Alex A Rubin1, Ivo Spiegel1, Ershela Durresi1, Nikhil Sharma1, Linda S Hu1, Mihovil Pletikos2, Eric C Griffith1, Jennifer N Partlow3, Christine R Stevens4, Mazhar Adli5, Maria Chahrour6, Nenad Sestan2, Christopher A Walsh3, Vladimir K Berezovskii1, Margaret S Livingstone1, Michael E Greenberg1.
Abstract
Sensory stimuli drive the maturation and function of the mammalian nervous system in part through the activation of gene expression networks that regulate synapse development and plasticity. These networks have primarily been studied in mice, and it is not known whether there are species- or clade-specific activity-regulated genes that control features of brain development and function. Here we use transcriptional profiling of human fetal brain cultures to identify an activity-dependent secreted factor, Osteocrin (OSTN), that is induced by membrane depolarization of human but not mouse neurons. We find that OSTN has been repurposed in primates through the evolutionary acquisition of DNA regulatory elements that bind the activity-regulated transcription factor MEF2. In addition, we demonstrate that OSTN is expressed in primate neocortex and restricts activity-dependent dendritic growth in human neurons. These findings suggest that, in response to sensory input, OSTN regulates features of neuronal structure and function that are unique to primates.Entities:
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Year: 2016 PMID: 27830782 PMCID: PMC5499253 DOI: 10.1038/nature20111
Source DB: PubMed Journal: Nature ISSN: 0028-0836 Impact factor: 49.962