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DMRT1: An Ancient Sexual Regulator Required for Human Gonadogenesis

期刊

SEXUAL DEVELOPMENT
卷 16, 期 2-3, 页码 112-125

出版社

KARGER
DOI: 10.1159/000518272

关键词

DM domain; DMRT1; DSD; Testis

资金

  1. NIH [GM059152, GM127379]
  2. University of Minnesota Foundation
  3. University of Minnesota Medical School

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DMRT1 has been found to play a crucial role in testis differentiation in mice, with its control over sexual cell fate likely stemming from multiple properties, such as its functional collaboration with SOX9, function as a pioneer transcription factor, and highly unusual DNA binding interactions.
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.

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