DMRT1 promotes oogenesis by transcriptional activation of Stra8 in the mammalian fetal ovary

Anthony D. Krentz, Mark W Murphy, Aaron L Sarver, Michael D. Griswold, Vivian J Bardwell, David A Zarkower

Research output: Contribution to journalArticlepeer-review

78 Scopus citations

Abstract

Dmrt1 belongs to the DM domain gene family of conserved sexual regulators. In the mouse Dmrt1 is expressed in the genital ridge (the gonadal primordium) in both sexes and then becomes testis-specific shortly after sex determination. The essential role of DMRT1 in testicular differentiation is well established, and includes transcriptional repression of the meiotic inducer Stra8. However Dmrt1 mutant females are fertile and the role of Dmrt1 in the ovary has not been studied. Here we show in the mouse that most Dmrt1 mutant germ cells in the fetal ovary have greatly reduced expression of STRA8, and fail to properly localize SYCP3 and γH2AX during meiotic prophase. Lack of DMRT1 in the fetal ovary results in the formation of many fewer primordial follicles in the juvenile ovary, although these are sufficient for fertility. Genome-wide chromatin immunoprecipitiation (ChIP-chip) and quantitative ChIP (qChIP) combined with mRNA expression profiling suggests that transcriptional activation of Stra8 in fetal germ cells is the main function of DMRT1 in females, and that this regulation likely is direct. Thus DMRT1 controls Stra8 sex-specifically, activating it in the fetal ovary and repressing it in the adult testis.

Original languageEnglish (US)
Pages (from-to)63-70
Number of pages8
JournalDevelopmental Biology
Volume356
Issue number1
DOIs
StatePublished - Aug 1 2011

Bibliographical note

Funding Information:
We thank Chris Small for technical assistance, Pierre Chambon for STRA8 antibody, Jon Hennebold and Eli Adashi for H1FOO antibody, George Enders for GCNA and Patricia Hunt and members of the Zarkower and Bardwell laboratories for helpful discussions. This work was funded by the NIH ( GM059152 and T32HD007480 ), the Minnesota Medical Foundation, and by a Doctoral Dissertation Fellowship from the University of Minnesota Graduate School.

Keywords

  • DM domain
  • Dmrt1
  • Meiosis
  • Ovary
  • Stra8

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