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DMRT1:人类性腺发生所需的古老性调节因子。

DMRT1: An Ancient Sexual Regulator Required for Human Gonadogenesis.

机构信息

Department of Genetics, Cell Biology, and Development, University of Minnesota, Minneapolis, Minnesota, USA.

出版信息

Sex Dev. 2022;16(2-3):112-125. doi: 10.1159/000518272. Epub 2021 Sep 1.

Abstract

Transcriptional regulators related to the invertebrate sexual regulators doublesex and mab-3 occur throughout metazoans and control sex in most animal groups. Seven of these DMRT genes are found in mammals, and mouse genetics has shown that one, Dmrt1, plays a crucial role in testis differentiation, both in germ cells and somatic cells. Deletions and, more recently, point mutations affecting human DMRT1 have demonstrated that its heterozygosity is associated with 46,XY complete gonadal dysgenesis. Most of our detailed knowledge of DMRT1 function in the testis, the focus of this review, derives from mouse studies, which have revealed that DMRT1 is essential for male somatic and germ cell differentiation and maintenance of male somatic cell fate after differentiation. Moreover, ectopic DMRT1 can reprogram differentiated female granulosa cells into male Sertoli-like cells. The ability of DMRT1 to control sexual cell fate likely derives from at least 3 properties. First, DMRT1 functionally collaborates with another key male sex regulator, SOX9, and possibly other proteins to maintain and reprogram sexual cell fate. Second, and related, DMRT1 appears to function as a pioneer transcription factor, binding "closed" inaccessible chromatin and promoting its opening to allow binding by other regulators including SOX9. Third, DMRT1 binds DNA by a highly unusual form of interaction and can bind with different stoichiometries.

摘要

与无脊椎动物性调节因子 doublesex 和 mab-3 相关的转录调节因子存在于后生动物中,并控制大多数动物群体的性别。这些 DMRT 基因中有 7 个存在于哺乳动物中,小鼠遗传学表明,其中一个 Dmrt1 在生殖细胞和体细胞的睾丸分化中起着至关重要的作用。缺失,以及最近的点突变,影响人类 DMRT1 表明其杂合性与 46,XY 完全性腺发育不良有关。我们对 DMRT1 在睾丸中的功能的大部分详细了解,即本综述的重点,源自小鼠研究,这些研究表明 DMRT1 对于雄性体细胞和生殖细胞分化以及分化后雄性体细胞命运的维持是必不可少的。此外,异位 DMRT1 可以将分化的雌性颗粒细胞重编程为雄性 Sertoli 样细胞。DMRT1 控制性细胞命运的能力可能至少源于 3 种特性。首先,DMRT1 与另一个关键的雄性性调节因子 SOX9 具有功能上的协作关系,并且可能与其他蛋白质一起维持和重编程性细胞命运。其次,相关的是,DMRT1 似乎作为一种先驱转录因子发挥作用,结合“封闭的”不可接近的染色质并促进其开放,以允许其他调节剂(包括 SOX9)结合。第三,DMRT1 通过一种非常特殊的相互作用形式结合 DNA,并且可以以不同的化学计量结合。

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