Department of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto university, Honjo 2-2-1, Chuo-ku, Kumamoto, Kumamoto, 860-0811, Japan.
Mammalian Development Laboratory, Department of Gene Function and Phenomics, National Institute of Genetics, Mishima, Shizuoka, 411-8540, Japan.
Nat Commun. 2023 Oct 25;14(1):6443. doi: 10.1038/s41467-023-42259-6.
Meiosis is differently regulated in males and females. In females, germ cells initiate meiosis within a limited time period in the fetal ovary and undergo a prolonged meiotic arrest until puberty. However, how meiosis initiation is coordinated with the cell cycle to coincide with S phase remains elusive. Here, we demonstrate that STRA8 binds to RB via the LXCXE motif. Mutation of the RB-binding site of STRA8 in female mice delays meiotic entry, which consequently delays progression of meiotic prophase and leads to precocious depletion of the oocyte pool. Single-cell RNA-sequencing analysis reveals that the STRA8-RB interaction is required for S phase entry and meiotic gene activation, ensuring precise timing of meiosis initiation in oocytes. Strikingly, the results suggest STRA8 could sequester RB from E2F during pre-meiotic G1/S transition. This study highlights the gene regulatory mechanisms underlying the female-specific mode of meiotic initiation in mice.
减数分裂在男性和女性中的调控方式不同。在女性中,生殖细胞在胎儿期的卵巢中在有限的时间内启动减数分裂,并经历长时间的减数分裂停滞,直到青春期。然而,减数分裂起始如何与细胞周期协调,以与 S 期重合,仍然难以捉摸。在这里,我们证明 STRA8 通过 LXCXE 基序与 RB 结合。在雌性小鼠中突变 STRA8 的 RB 结合位点会延迟减数分裂的进入,这会导致减数分裂前期的进展延迟,并导致卵母细胞池过早耗尽。单细胞 RNA 测序分析表明,STRA8-RB 相互作用对于 S 期进入和减数分裂基因激活是必需的,确保卵母细胞减数分裂起始的精确定时。引人注目的是,结果表明 STRA8 可以在减数分裂前的 G1/S 转换期间将 RB 从 E2F 中隔离出来。这项研究强调了小鼠中减数分裂起始的女性特异性模式的基因调控机制。