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基于 MPF 的减数分裂细胞周期调控:海星卵母细胞半个世纪的经验教训。

MPF-based meiotic cell cycle control: Half a century of lessons from starfish oocytes.

机构信息

Professor Emeritus of Tokyo Institute of Technology.

Visiting Professor of Ochanomizu University.

出版信息

Proc Jpn Acad Ser B Phys Biol Sci. 2018;94(4):180-203. doi: 10.2183/pjab.94.013.

Abstract

In metazoans that undergo sexual reproduction, genomic inheritance is ensured by two distinct types of cell cycle, mitosis and meiosis. Mitosis maintains the genomic ploidy in somatic cells reproducing within a generation, whereas meiosis reduces by half the ploidy in germ cells to prepare for successive generations. The meiotic cell cycle is believed to be a derived form of the mitotic cell cycle; however, the molecular mechanisms underlying both of these processes remain elusive. My laboratory has long studied the meiotic cell cycle in starfish oocytes, particularly the control of meiotic M-phase by maturation- or M phase-promoting factor (MPF) and the kinase cyclin B-associated Cdk1 (cyclin B-Cdk1). Using this system, we have unraveled the molecular principles conserved in metazoans that modify M-phase progression from the mitotic type to the meiotic type needed to produce a haploid genome. Furthermore, we have solved a long-standing enigma concerning the molecular identity of MPF, a universal inducer of M-phase both in mitosis and meiosis of eukaryotic cells.

摘要

在进行有性生殖的后生动物中,基因组的遗传通过两种不同类型的细胞周期——有丝分裂和减数分裂来保证。有丝分裂维持着在同一代内进行繁殖的体细胞中的基因组ploidy,而减数分裂将生殖细胞的ploidy 减半,为连续几代的繁殖做准备。减数分裂细胞周期被认为是有丝分裂细胞周期的衍生形式;然而,这两个过程的分子机制仍然难以捉摸。我的实验室长期以来一直在研究海星卵母细胞的减数分裂细胞周期,特别是成熟促进因子或 M 期促进因子 (MPF) 和与激酶 cyclin B 相关的 Cdk1(cyclin B-Cdk1)对减数分裂 M 期的控制。使用这个系统,我们已经揭示了后生动物中保守的分子原理,这些原理将 M 期的进程从有丝分裂类型修改为减数分裂类型,以产生单倍体基因组。此外,我们还解决了一个长期以来关于 MPF 的分子身份的谜团,MPF 是真核细胞有丝分裂和减数分裂中 M 期的普遍诱导物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/08cf/5968197/80c716180733/pjab-94-180-g001.jpg

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