Lei Wen-Long, Qian Wei-Ping, Sun Qing-Yuan
Department of Reproductive Medicine, Peking University Shenzhen Hospital, Shenzhen, China.
Fertility Preservation Lab, Reproductive Medicine Center, Guangdong Second Provincial General Hospital, Guangzhou, China.
Front Cell Dev Biol. 2021 Feb 25;9:638559. doi: 10.3389/fcell.2021.638559. eCollection 2021.
Meiosis is essential to the continuity of life in sexually-reproducing organisms through the formation of haploid gametes. Unlike somatic cells, the germ cells undergo two successive rounds of meiotic divisions after a single cycle of DNA replication, resulting in the decrease in ploidy. In humans, errors in meiotic progression can cause infertility and birth defects. Post-translational modifications, such as phosphorylation, ubiquitylation and sumoylation have emerged as important regulatory events in meiosis. There are dynamic equilibrium of protein phosphorylation and protein dephosphorylation in meiotic cell cycle process, regulated by a conservative series of protein kinases and protein phosphatases. Among these protein phosphatases, PP2A, PP4, and PP6 constitute the PP2A-like subfamily within the serine/threonine protein phosphatase family. Herein, we review recent discoveries and explore the role of PP2A-like protein phosphatases during meiotic progression.
减数分裂对于有性生殖生物的生命延续至关重要,它通过形成单倍体配子来实现。与体细胞不同,生殖细胞在DNA复制的单个周期后经历两轮连续的减数分裂,导致倍性降低。在人类中,减数分裂过程中的错误会导致不孕和出生缺陷。翻译后修饰,如磷酸化、泛素化和类泛素化,已成为减数分裂中的重要调控事件。在减数分裂细胞周期过程中,蛋白质磷酸化和蛋白质去磷酸化存在动态平衡,这由一系列保守的蛋白激酶和蛋白磷酸酶调节。在这些蛋白磷酸酶中,PP2A、PP4和PP6在丝氨酸/苏氨酸蛋白磷酸酶家族中构成了PP2A样亚家族。在此,我们综述了最近的发现,并探讨了PP2A样蛋白磷酸酶在减数分裂过程中的作用。