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哺乳动物生殖细胞减数分裂的细胞周期调控。

Cell cycle regulation for meiosis in mammalian germ cells.

机构信息

Department of Chromosome Biology, Institute of Molecular Embryology and Genetics (IMEG), Kumamoto University, Kumamoto 860-0811, Japan.

出版信息

J Reprod Dev. 2023 Jun 6;69(3):139-146. doi: 10.1262/jrd.2023-010. Epub 2023 Mar 17.

Abstract

In mouse fetal gonads, germ cell development is accompanied by changes in cell cycle mode in response to external signals and intrinsic mechanisms of cells. During fetal development, male germ cells undergo G0/G1 arrest, while female germ cells exit the mitotic cell cycle and enter meiosis. In fetal testes, NANOS2 and CYP26B1 force germ cells to stay in G0/G1 arrest phase, preventing them from entering the meiotic cell cycle. In the fetal ovary, external signals, such as RA, BMP, and WNT, promote the competency of female germ cells to enter the meiotic cell cycle. MEIOSIN and STRA8 ensure the establishment of the meiotic cell cycle by activating meiotic genes, such that meiotic entry coincides with the S phase. This review discusses germ cell development from the viewpoint of cell cycle regulation and highlights the mechanism of the entry of germ cells into meiosis.

摘要

在小鼠胎儿生殖腺中,细胞周期模式的变化伴随着生殖细胞的发育,这是对外界信号和细胞内在机制的响应。在胎儿发育过程中,雄性生殖细胞经历 G0/G1 期阻滞,而雌性生殖细胞退出有丝分裂细胞周期并进入减数分裂。在胎儿睾丸中,NANOS2 和 CYP26B1 迫使生殖细胞停留在 G0/G1 期阻滞阶段,防止它们进入减数分裂细胞周期。在胎儿卵巢中,RA、BMP 和 WNT 等外部信号促进雌性生殖细胞进入减数分裂细胞周期的能力。MEIOSIN 和 STRA8 通过激活减数分裂基因来确保减数分裂细胞周期的建立,使得减数分裂的进入与 S 期一致。本综述从细胞周期调控的角度讨论了生殖细胞的发育,并强调了生殖细胞进入减数分裂的机制。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a231/10267585/07a64c61ce14/jrd-69-139-g001.jpg

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