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Embryonic transcription factor expression in mice predicts medial amygdala neuronal identity and sex-specific responses to innate behavioral cues

机译:小鼠中的胚胎转录因子表达预测内侧杏仁核神经元身份和对先天行为提示的性别特异性反应

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摘要

The medial subnucleus of the amygdala (MeA) plays a central role in processing sensory cues required for innate behaviors. However, whether there is a link between developmental programs and the emergence of inborn behaviors remains unknown. Our previous studies revealed that the telencephalic preoptic area (POA) embryonic niche is a novel source of MeA destined progenitors. Here, we show that the POA is comprised of distinct progenitor pools complementarily marked by the transcription factors Dbx1 and Foxp2. As determined by molecular and electrophysiological criteria this embryonic parcellation predicts postnatal MeA inhibitory neuronal subtype identity. We further find that Dbx1-derived and Foxp2+ cells in the MeA are differentially activated in response to innate behavioral cues in a sex-specific manner. Thus, developmental transcription factor expression is predictive of MeA neuronal identity and sex-specific neuronal responses, providing a potential developmental logic for how innate behaviors could be processed by different MeA neuronal subtypes.>DOI:
机译:杏仁核(MeA)的内侧亚核在处理先天行为所需的感觉线索中起着核心作用。然而,发展计划与先天行为的出现之间是否存在联系仍然未知。我们以前的研究表明,远脑视前区(POA)的胚胎位是MeA致祖细胞的新来源。在这里,我们显示POA由转录因子Dbx1和Foxp2互补标记的不同祖细胞组成。如通过分子和电生理标准所确定的,该胚胎分裂预测了产后MeA抑制性神经元亚型的同一性。我们进一步发现,MeA中的Dbx1衍生和Foxp2 +细胞在以性别特异性方式响应先天行为提示时被差异激活。因此,发育转录因子的表达可预测MeA神经元身份和性别特异性神经元反应,为不同MeA神经元亚型如何处理先天行为提供了潜在的发展逻辑。> DOI:

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