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Secured cutting: controlling separase at the metaphase to anaphase transition

机译:安全切割:控制分离酶在中期到后期的过渡

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摘要

The final irreversible step in the duplication and distribution of genomes to daughter cells takes place at the metaphase to anaphase transition. At this point aligned sister chromatid pairs split and separate. During metaphase, cohesion between sister chromatids is maintained by the chromosomal multi-subunit cohesin complex. Here, I review recent findings as to how anaphase is initiated by proteolytic cleavage of the Scc1 subunit of cohesin. Scc1 is cleaved by a site-specific protease that is conserved in all eukaryotes, and is now called ‘separase’. As a result of this cleavage, the cohesin complex is destroyed, allowing the spindle to pull sister chromatids into opposite halves of the cell. Because of the final and irreversible nature of Scc1 cleavage, this reaction is tightly controlled. Several independent mechanisms seem to impose regulation on Scc1 cleavage, acting on both the activity of separase and the susceptibility of the substrate.
机译:基因组向子细胞的复制和分布中不可逆的最后一步发生在中期到后期的转变。此时对齐的姐妹染色单体对分裂并分离。在中期,姐妹染色单体之间的凝聚力通过染色体多亚基凝聚素复合物维持。在这里,我回顾了最近的发现,涉及到如何通过黏附素Scc1亚基的蛋白水解切割引发后期反应。 Scc1被所有真核生物中保守的位点特异性蛋白酶裂解,现在称为“分离酶”。这种切割的结果是,粘着蛋白复合物被破坏,使纺锤体将姐妹染色单体拉入细胞的相对两半。由于Scc1裂解的最终和不可逆的性质,该反应受到严格控制。几个独立的机制似乎对Scc1的切割施加了调控,既作用于Separase的活性,又作用于底物的敏感性。

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