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哺乳动物生殖细胞进入减数分裂的调控。

Control of mammalian germ cell entry into meiosis.

机构信息

Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.

Institute for Molecular Bioscience, The University of Queensland, Brisbane, QLD 4072, Australia.

出版信息

Mol Cell Endocrinol. 2014 Jan 25;382(1):488-497. doi: 10.1016/j.mce.2013.09.026. Epub 2013 Sep 27.

Abstract

Germ cells are unique in undergoing meiosis to generate oocytes and sperm. In mammals, meiosis onset is before birth in females, or at puberty in males, and recent studies have uncovered several regulatory steps involved in initiating meiosis in each sex. Evidence suggests that retinoic acid (RA) induces expression of the critical pre-meiosis gene Stra8 in germ cells of the fetal ovary, pubertal testis and adult testis. In the fetal testis, CYP26B1 degrades RA, while FGF9 further antagonises RA signalling to suppress meiosis. Failsafe mechanisms involving Nanos2 may further suppress meiosis in the fetal testis. Here, we draw together the growing knowledge relating to these meiotic control mechanisms, and present evidence that they are co-ordinately regulated and that additional factors remain to be identified. Understanding this regulatory network will illuminate not only how the foundations of mammalian reproduction are laid, but also how mis-regulation of these steps can result in infertility or germline tumours.

摘要

生殖细胞的独特之处在于通过减数分裂产生卵子和精子。在哺乳动物中,女性的减数分裂起始于出生前,而男性的减数分裂起始于青春期,最近的研究揭示了涉及两性中启动减数分裂的几个调节步骤。有证据表明,视黄酸(RA)诱导胎儿卵巢、青春期睾丸和成年睾丸生殖细胞中关键的减数分裂前基因 Stra8 的表达。在胎儿睾丸中,CYP26B1 降解 RA,而 FGF9 进一步拮抗 RA 信号以抑制减数分裂。涉及 Nanos2 的故障安全机制可能进一步抑制胎儿睾丸中的减数分裂。在这里,我们汇集了与这些减数分裂控制机制相关的不断增长的知识,并提供了证据表明它们是协调调节的,并且还有其他因素有待确定。了解这个调节网络不仅将阐明哺乳动物生殖基础的建立方式,还将阐明这些步骤的失调如何导致不育或生殖细胞肿瘤。

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