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卵母细胞中的黏连蛋白——足以应对哺乳动物减数分裂?

Cohesin in oocytes-tough enough for Mammalian meiosis?

机构信息

Department of Developmental and Regenerative Biology, Mount Sinai School of Medicine, One Gustave L. Levy Place, Box 1020, New York, NY 10029, USA.

Institute of Physiological Chemistry, Faculty of Medicine Carl Gustav Carus, Dresden University of Technology, Fiedlerstr. 42, MTZ, D-01307 Dresden, Germany.

出版信息

Genes (Basel). 2010 Dec 13;1(3):495-504. doi: 10.3390/genes1030495.

Abstract

Sister chromatid cohesion is essential for cell division. During meiosis, it is also required for proper synapsis of pairs of sister chromatids and for chiasma formation and maintenance. Since mammalian oocytes remain arrested in late prophase for a very long period-up to five decades in humans-the preservation of cohesion throughout this period is a formidable challenge. Mouse models with cohesin deficiencies and aging wild-type mice showed that this challenge is not fully met: cohesion weakens and deteriorates with increasing age. These recent findings have highly significant implications for our comprehension of the genesis of aneuploidies.

摘要

姐妹染色单体黏合对于细胞分裂是必需的。在减数分裂过程中,它对于姐妹染色单体的正确联会以及交叉结构的形成和维持也是必需的。由于哺乳动物卵母细胞在很长一段时间内(人类长达五十年)停留在早前期的后期,因此在整个过程中保持黏合是一个巨大的挑战。具有黏合蛋白缺陷的小鼠模型和衰老的野生型小鼠的研究表明,这一挑战并未完全得到满足:随着年龄的增长,黏合逐渐减弱和恶化。这些最新发现对我们理解非整倍体的发生具有非常重要的意义。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d47d/3966221/2f294ab57182/genes-01-00495-g001.jpg

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