Baarends W M, van der Laan R, Grootegoed J A
Department of Endocrinology and Reproduction, Erasmus University, Rotterdam, The Netherlands.
J Endocrinol Invest. 2000 Oct;23(9):597-604. doi: 10.1007/BF03343782.
The ubiquitin system is involved in numerous cellular processes, regulating the amounts and/or activities of specific proteins through posttranslational coupling with ubiquitin or ubiquitin-like proteins. In spermatogenesis, there appears to be a special requirement for certain components of the ubiquitin system, as exemplified in human and mouse by mutation of USP9Y and HR6B, respectively. Both genes encode proteins which take part in the ubiquitin system and are ubiquitously expressed, but their mutation generates no apparent phenotype other than male infertility. Different phases of mammalian spermatogenesis probably require different specialized activities of the ubiquitin system. It is anticipated that ubiquitination activities similar to those required during mitotic cell cycle regulation will play some role in control of the meiotic divisions. In spermatocytes, there is an intricate link among DNA repair, the ubiquitin system, and regulation of meiotic chromatin structure, as indicated by the co-localization of proteins involved in these processes on meiotic recombination complexes. HR6B and its nearly identical homolog HR6A are multiple function proteins, with ubiquitin-conjugating activity and essential roles in post-replication DNA repair. HR6B, possibly together with the ubiquitin-ligating enzyme mRAD1 8Sc, is most likely involved in chromatin re-organization during the meiotic and post-meiotic phases of spermatogenesis. Biochemical data indicate that, in particular during spermiogenesis, the general activity of the ubiquitin system is high, which most likely is related to the high requirement for massive breakdown of cytoplasmatic and nuclear proteins during this last phase of spermatogenesis.
泛素系统参与众多细胞过程,通过与泛素或类泛素蛋白进行翻译后偶联来调节特定蛋白质的数量和/或活性。在精子发生过程中,泛素系统的某些成分似乎有特殊需求,例如在人类和小鼠中分别由USP9Y和HR6B的突变所例证。这两个基因编码参与泛素系统且广泛表达的蛋白质,但它们的突变除了导致雄性不育外没有产生明显的表型。哺乳动物精子发生的不同阶段可能需要泛素系统的不同特殊活性。预计与有丝分裂细胞周期调控所需的泛素化活性类似的活性将在减数分裂的控制中发挥一定作用。在精母细胞中,DNA修复、泛素系统和减数分裂染色质结构调控之间存在复杂的联系,这些过程中涉及的蛋白质在减数分裂重组复合体上的共定位表明了这一点。HR6B及其几乎相同的同源物HR6A是多功能蛋白质,具有泛素结合活性且在复制后DNA修复中起关键作用。HR6B可能与泛素连接酶mRAD1 8Sc一起,最有可能参与精子发生的减数分裂和减数分裂后阶段的染色质重组。生化数据表明,特别是在精子形成过程中,泛素系统的总体活性很高,这很可能与精子发生最后阶段对细胞质和核蛋白大量分解的高需求有关。