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哺乳动物卵母细胞发育中减数分裂起始和进程的雌性特异性机制。

Female-specific mechanisms of meiotic initiation and progression in mammalian oocyte development.

机构信息

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

出版信息

Genes Cells. 2024 Oct;29(10):797-807. doi: 10.1111/gtc.13152. Epub 2024 Aug 9.

Abstract

Meiosis is regulated in sexually dimorphic manners in mammals. In females, the commitment to and entry into meiosis are coordinated with the developmental program of oocytes. Female germ cells initiate meiosis within a short time window during the fetal period and then undergo meiotic arrest until puberty. However, the genetic mechanisms underlying the orchestration of oocyte development and meiosis to maximize the reproductive lifespan of mammalian females remain largely elusive. While meiotic initiation is regulated by a sexually common mechanism, where meiosis initiator and Stimulated by Retinoic Acid Gene 8 (STRA8) activate the meiotic genes, the female-specific mode of meiotic initiation is mediated by the interaction between retinoblastoma (RB) and STRA8. This review highlights the female-specific mechanisms of meiotic initiation and meiotic prophase progression in the context of oocyte development. Furthermore, the downstream pathway of the RB-STRA8 interaction that may regulate meiotic arrest will be discussed in the context of oocyte development, highlighting a potential genetic link between the female-specific mode of meiotic entry and meiotic arrest.

摘要

减数分裂在哺乳动物中以性别二态的方式调控。在雌性中,进入减数分裂的承诺与卵母细胞的发育程序相协调。雌性生殖细胞在胎儿期的短时间窗口内启动减数分裂,然后经历减数分裂阻滞,直到青春期。然而,协调卵母细胞发育和减数分裂以最大限度地延长哺乳动物雌性生殖寿命的遗传机制在很大程度上仍未被揭示。虽然减数分裂的起始受到一种性别共同的机制的调节,即减数分裂起始因子和视黄酸基因 8 (STRA8) 激活减数分裂基因,但减数分裂起始的雌性特异性模式是由视网膜母细胞瘤 (RB) 和 STRA8 之间的相互作用介导的。本综述强调了卵母细胞发育过程中减数分裂起始和减数分裂前期进展的雌性特异性机制。此外,还将在卵母细胞发育的背景下讨论 RB-STRA8 相互作用的下游途径,该途径可能调节减数分裂阻滞,突出了减数分裂进入和减数分裂阻滞的雌性特异性模式之间的潜在遗传联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/adc8/11555627/912352eb5797/GTC-29-797-g001.jpg

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