Department of Genetics and Reproduction, Veterinary Research Institute, 621 00 Brno, Czech Republic.
Institute of Animal Physiology and Genetics, Czech Academy of Science, 277 21 Libechov, Czech Republic.
Int J Mol Sci. 2023 Feb 27;24(5):4604. doi: 10.3390/ijms24054604.
Receiving complete and undamaged genetic information is vital for the survival of daughter cells after chromosome segregation. The most critical steps in this process are accurate DNA replication during S phase and a faithful chromosome segregation during anaphase. Any errors in DNA replication or chromosome segregation have dire consequences, since cells arising after division might have either changed or incomplete genetic information. Accurate chromosome segregation during anaphase requires a protein complex called cohesin, which holds together sister chromatids. This complex unifies sister chromatids from their synthesis during S phase, until separation in anaphase. Upon entry into mitosis, the spindle apparatus is assembled, which eventually engages kinetochores of all chromosomes. Additionally, when kinetochores of sister chromatids assume amphitelic attachment to the spindle microtubules, cells are finally ready for the separation of sister chromatids. This is achieved by the enzymatic cleavage of cohesin subunits Scc1 or Rec8 by an enzyme called Separase. After cohesin cleavage, sister chromatids remain attached to the spindle apparatus and their poleward movement on the spindle is initiated. The removal of cohesion between sister chromatids is an irreversible step and therefore it must be synchronized with assembly of the spindle apparatus, since precocious separation of sister chromatids might lead into aneuploidy and tumorigenesis. In this review, we focus on recent discoveries concerning the regulation of Separase activity during the cell cycle.
接收完整且未受损的遗传信息对于染色体分离后子细胞的存活至关重要。在这个过程中,最关键的步骤是 S 期准确的 DNA 复制和后期的染色体正确分离。任何 DNA 复制或染色体分离的错误都会带来严重的后果,因为分裂后产生的细胞可能会有改变或不完整的遗传信息。后期染色体的正确分离需要一种称为黏合蛋白的蛋白质复合物,它将姐妹染色单体结合在一起。这个复合物将姐妹染色单体从 S 期的合成开始结合在一起,直到后期分离。当进入有丝分裂时,纺锤体装置被组装,最终与所有染色体的动粒结合。此外,当姐妹染色单体的动粒呈双中心附着于纺锤体微管时,细胞最终准备好分离姐妹染色单体。这是通过酶分离酶将黏合蛋白亚基 Scc1 或 Rec8 切割来实现的。黏合蛋白切割后,姐妹染色单体仍附着于纺锤体装置,并开始向纺锤体的极移动。姐妹染色单体之间的黏合的去除是一个不可逆的步骤,因此它必须与纺锤体装置的组装同步,因为姐妹染色单体过早分离可能导致非整倍体和肿瘤发生。在这篇综述中,我们将重点介绍细胞周期中分离酶活性调节的最新发现。