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雄性单细胞核神经元转录图谱揭示性别特异性和性别共享行为的调节因子。

Single-Nucleus Neuronal Transcriptional Profiling of Male Uncovers Regulators of Sex-Specific and Sex-Shared Behaviors.

作者信息

Morillo Katherine S, St Ange Jonathan, Weng Yifei, Kaletsky Rachel, Murphy Coleen T

出版信息

bioRxiv. 2025 Jun 25:2024.12.12.628226. doi: 10.1101/2024.12.12.628226.

Abstract

Sexual differentiation of the nervous system drives profound neurobiological and behavioral differences between the sexes across various organisms, including . Using single-nucleus RNA sequencing, we profiled and compared adult male and hermaphrodite neurons, generating an atlas of adult male-specific and sex-shared neurons. We expanded the molecular map of male-specific neurons, and identified highly dimorphic expression of GPCRs, neuropeptides, and ion channels. Our data demonstrate sex-shared neurons exhibit substantial heterogeneity between the sexes, while sex-specific neurons repurpose conserved molecular pathways to regulate dimorphic behaviors. We show that the PHD neurons display remarkable similarity to sex-shared AWA neurons, suggesting partial repurposing of conserved pathways, and that they and the GPCR SRT-18 may play a role in pheromone sensing. We further demonstrate that the ubiquitously expressed MAPK phosphatase regulates both sex-specific and sex-shared behaviors. Our data provide a rich resource for discovering sex-specific transcriptomic differences and the molecular basis of sex-specific behaviors.

摘要

神经系统的性别分化驱动了包括人类在内的各种生物体中两性之间深刻的神经生物学和行为差异。通过单核RNA测序,我们对成年雄性和雌雄同体的神经元进行了分析和比较,生成了成年雄性特异性和性别共享神经元的图谱。我们扩展了雄性特异性神经元的分子图谱,并鉴定了GPCR、神经肽和离子通道的高度二态性表达。我们的数据表明,性别共享的神经元在两性之间表现出显著的异质性,而性别特异性的神经元则重新利用保守的分子途径来调节二态性行为。我们发现PHD神经元与性别共享的AWA神经元表现出显著的相似性,这表明保守途径的部分重新利用,并且它们和GPCR SRT-18可能在信息素感知中发挥作用。我们进一步证明,普遍表达的MAPK磷酸酶调节性别特异性和性别共享的行为。我们的数据为发现性别特异性转录组差异和性别特异性行为的分子基础提供了丰富的资源。

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