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哺乳动物性别决定的分子基础:SRY对缪勒氏管抑制物质基因表达的激活

Molecular basis of mammalian sexual determination: activation of Müllerian inhibiting substance gene expression by SRY.

作者信息

Haqq C M, King C Y, Ukiyama E, Falsafi S, Haqq T N, Donahoe P K, Weiss M A

机构信息

Pediatric Surgical Research Laboratory, Massachusetts General Hospital, Boston 02114.

出版信息

Science. 1994 Dec 2;266(5190):1494-500. doi: 10.1126/science.7985018.

Abstract

The pathway of male sexual development in mammals is initiated by SRY, a gene on the short arm of the Y chromosome. Its expression in the differentiating gonadal ridge directs testicular morphogenesis, characterized by elaboration of Müllerian inhibiting substance (MIS) and testosterone. SRY and MIS each belong to conserved gene families that function in the control of growth and differentiation. Structural and biochemical studies of the DNA binding domain of SRY (the HMG box) revealed a protein-DNA interaction consisting of partial side chain intercalation into a widened minor groove. Functional studies of SRY in a cell line from embryonic gonadal ridge demonstrated activation of a gene-regulatory pathway leading to expression of MIS. SRY molecules containing mutations associated with human sex reversal have altered structural interactions with DNA and failed to induce transcription of MIS.

摘要

哺乳动物雄性性发育途径由SRY启动,SRY是Y染色体短臂上的一个基因。它在分化中的性腺嵴中的表达引导睾丸形态发生,其特征是产生苗勒氏管抑制物质(MIS)和睾酮。SRY和MIS各自属于在生长和分化控制中起作用的保守基因家族。对SRY的DNA结合结构域(HMG盒)的结构和生化研究揭示了一种蛋白质-DNA相互作用,该相互作用由部分侧链插入变宽的小沟组成。在来自胚胎性腺嵴的细胞系中对SRY的功能研究表明,一种基因调节途径被激活,导致MIS表达。含有与人类性反转相关突变的SRY分子改变了与DNA的结构相互作用,并且未能诱导MIS转录。

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