| Literature DB >> 32032549 |
Kei-Ichiro Ishiguro1, Kumi Matsuura2, Naoki Tani3, Naoki Takeda4, Shingo Usuki3, Mariko Yamane2, Michihiko Sugimoto4, Sayoko Fujimura3, Mihoko Hosokawa5, Shinichiro Chuma5, Minoru S H Ko6, Kimi Araki4, Hitoshi Niwa2.
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.Entities:
Keywords: STRA8; cell cycle; germ cell; meiosis; meiotic recombination; retinoic acid; retinoic acid chromosome; spermatogenesis; synaptonemal complex
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Year: 2020 PMID: 32032549 DOI: 10.1016/j.devcel.2020.01.010
Source DB: PubMed Journal: Dev Cell ISSN: 1534-5807 Impact factor: 12.270