Professor Emeritus of Tokyo Institute of Technology.
Visiting Professor of Ochanomizu University.
Proc Jpn Acad Ser B Phys Biol Sci. 2018;94(4):180-203. doi: 10.2183/pjab.94.013.
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.
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。