MEIOSIN Directs the Switch from Mitosis to Meiosis in Mammalian Germ Cells

Dev Cell. 2020 Feb 24;52(4):429-445.e10. doi: 10.1016/j.devcel.2020.01.010. Epub 2020 Feb 6.

Abstract

The mechanisms regulating meiotic initiation in mammals are enigmatic. It is known that retinoic acid (RA) signaling plays a pivotal role during meiotic initiation. STRA8, which is expressed in response to RA, is thought to be a key factor promoting meiotic initiation. However, the specific role of STRA8 in meiotic initiation has remained elusive. Here, we identified MEIOSIN as a germ-cell-specific factor that associates with STRA8. MEIOSIN, like STRA8, is expressed in response to RA and plays an essential role in meiotic initiation in both males and females. Functional analyses revealed that MEIOSIN acts as a transcription factor together with STRA8, and that both factors are critical for driving meiotic gene activation. Furthermore, temporally restricted expression of MEIOSIN leads to meiotic entry decision during spermatogenesis. The present study demonstrates that MEIOSIN, in collaboration with STRA8, plays a central role in regulating the mitosis to meiosis germ cell fate decision in mammals.

Keywords: STRA8; cell cycle; germ cell; meiosis; meiotic recombination; retinoic acid; retinoic acid chromosome; spermatogenesis; synaptonemal complex.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adaptor Proteins, Signal Transducing / physiology*
  • Animals
  • Cell Cycle*
  • Cell Differentiation
  • Female
  • Gene Expression Regulation*
  • Germ Cells / cytology
  • Germ Cells / physiology*
  • Male
  • Meiosis*
  • Mice
  • Mice, Inbred C57BL
  • Mice, Knockout
  • Mitosis*
  • Signal Transduction
  • Spermatogenesis
  • Transcription Factors / physiology*

Substances

  • Adaptor Proteins, Signal Transducing
  • Stra8 protein, mouse
  • Transcription Factors