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Evolution of Osteocrin as an activity-regulated factor in the primate brain

机译:灵长类动物脑中Osteocrin作为活性调节因子的演变

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摘要

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.
机译:感觉刺激部分通过调节突触发育和可塑性的基因表达网络的激活来驱动哺乳动物神经系统的成熟和功能。这些网络主要是在小鼠中进行研究的,尚不清楚是否存在控制大脑发育和功能特征的物种或进化枝特异性活动调节基因。在这里,我们使用人类胎儿脑培养物的转录概况分析来鉴定活性依赖性分泌因子Osteocrin(OSTN),其是由人而非小鼠神经元的膜去极化诱导的。我们发现OSTN已通过进化收购结合活性调节转录因子MEF2的DNA调节元件而被重新用于灵长类动物。此外,我们证明了OSTN在灵长类动物新皮层中表达,并限制了人类神经元中活动依赖性树突的生长。这些发现表明,响应于感觉输入,OSTN调节了灵长类独有的神经元结构和功能特征。

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  • 来源
    《Nature》 |2016年第7628期|242-247|共6页
  • 作者单位

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Yale Sch Med, Dept Neurosci, New Haven, CT 06510 USA|Yale Sch Med, Kavli Inst Neurosci, New Haven, CT 06510 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA;

    Broad Inst & Harvard, Cambridge, MA 02142 USA;

    Univ Virginia, Sch Med, Dept Biochem & Mol Genet, Charlottesville, VA 22903 USA;

    Univ Texas Southwestern Med Ctr Dallas, Dept Neurosci, MvDermott Ctr Human Growth & Dev, Dallas, TX 75390 USA;

    Yale Sch Med, Dept Neurosci, New Haven, CT 06510 USA|Yale Sch Med, Kavli Inst Neurosci, New Haven, CT 06510 USA;

    Harvard Med Sch, Boston Childrens Hosp, Div Genet & Genom, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

    Harvard Med Sch, Dept Neurobiol, Boston, MA 02115 USA;

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