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哺乳动物卵母细胞减数分裂细胞周期调控中的分子参与者。

Molecular participants in regulation of the meiotic cell cycle in mammalian oocytes.

作者信息

Pomerantz Yael, Dekel Nava

机构信息

Department of Biological Regulation, The Weizmann Institute of Science, 234 Herzl St, Rehovot 76100, Israel.

出版信息

Reprod Fertil Dev. 2013;25(3):484-94. doi: 10.1071/RD12242.

Abstract

Meiosis in oocytes consists of two consecutive asymmetric cell divisions, each completed by the extrusion of one set of chromosomes into a small polar body. First polar body (PBI) extrusion is triggered by the inactivation of cyclin-dependent kinase 1 (CDK1), following the degradation of its regulatory subunit cyclin B1 by the ubiquitin proteasome pathway. The present review covers the sequence of events leading to PBI extrusion, and compares them to the corresponding events in mitotic cell division. The latest findings regarding the contribution of ubiquitin chain topology, separase, securin, cyclin B1, CDK1, Polo-like kinase 1 and mitogen-activated protein kinase kinase 1/2 to the regulation of meiosis are discussed.

摘要

卵母细胞中的减数分裂由两个连续的不对称细胞分裂组成,每次分裂通过将一组染色体挤压到一个小的极体中来完成。第一极体(PBI)的挤出是由细胞周期蛋白依赖性激酶1(CDK1)失活触发的,其调节亚基细胞周期蛋白B1通过泛素蛋白酶体途径降解。本综述涵盖了导致PBI挤出的一系列事件,并将它们与有丝分裂细胞分裂中的相应事件进行了比较。讨论了关于泛素链拓扑结构、分离酶、securin、细胞周期蛋白B1、CDK1、Polo样激酶1和丝裂原活化蛋白激酶激酶1/2对减数分裂调节作用的最新发现。

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