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苗勒管抑制物质导致大脑和行为中的性别关联偏向。

Müllerian inhibiting substance contributes to sex-linked biases in the brain and behavior.

作者信息

Wang Pei-Yu, Protheroe Anna, Clarkson Andrew N, Imhoff Floriane, Koishi Kyoko, McLennan Ian S

机构信息

Department of Anatomy, University of Otago, Dunedin, New Zealand.

出版信息

Proc Natl Acad Sci U S A. 2009 Apr 28;106(17):7203-8. doi: 10.1073/pnas.0902253106. Epub 2009 Apr 9.

DOI:10.1073/pnas.0902253106
PMID:19359476
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2678437/
Abstract

Many behavioral traits and most brain disorders are common to males and females but are more evident in one sex than the other. The control of these subtle sex-linked biases is largely unstudied and has been presumed to mirror that of the highly dimorphic reproductive nuclei. Sexual dimorphism in the reproductive tract is a product of Müllerian inhibiting substance (MIS), as well as the sex steroids. Males with a genetic deficiency in MIS signaling are sexually males, leading to the presumption that MIS is not a neural regulator. We challenge this presumption by reporting that most immature neurons in mice express the MIS-specific receptor (MISRII) and that male Mis(-/-) and Misrii(-/-) mice exhibit subtle feminization of their spinal motor neurons and of their exploratory behavior. Consequently, MIS may be a broad regulator of the subtle sex-linked biases in the nervous system.

摘要

许多行为特征和大多数脑部疾病在男性和女性中都很常见,但在某一性别中比另一性别更为明显。对这些微妙的性别关联偏差的控制在很大程度上尚未得到研究,并且一直被认为与高度二态性的生殖核的控制情况相似。生殖道中的性别二态性是苗勒氏管抑制物质(MIS)以及性类固醇的产物。MIS信号通路存在基因缺陷的雄性在性别上为雄性,这导致人们推测MIS不是一种神经调节因子。我们通过报告小鼠中大多数未成熟神经元表达MIS特异性受体(MISRII),以及雄性Mis(-/-)和Misrii(-/-)小鼠的脊髓运动神经元及其探索行为表现出微妙的女性化特征,对这一推测提出了质疑。因此,MIS可能是神经系统中微妙的性别关联偏差的广泛调节因子。

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