Uhlmann Frank
Lincoln's Inn Fields Laboratories, Cancer Research UK, 44 Lincoln's Inn Fields, London WC2A 3PX, UK.
Biochem Soc Symp. 2003(70):243-51. doi: 10.1042/bss0700243.
The final, irreversible step in the duplication and distribution of genomes to daughter cells takes place when chromosomes split at the metaphase-to-anaphase transition. A protease of the CD clan, separase (C50 family), is the key regulator of this transition. During metaphase, cohesion between sister chromatids is maintained by a chromosomal protein complex, cohesin. Anaphase is triggered when separase cleaves the Scc1 subunit of cohesin at two specific recognition sequences. 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 impose regulation on separase activity, as well as on the susceptibility of the cleavage target Scc1 to cleavage by separase. This chapter provides an overview of these multiple levels of regulation.
当染色体在中期到后期的转变过程中分裂时,基因组复制并分配到子细胞的最后一个不可逆步骤就发生了。CD家族的一种蛋白酶,分离酶(C50家族),是这一转变的关键调节因子。在中期,姐妹染色单体之间的黏连由一种染色体蛋白复合体黏连蛋白维持。当分离酶在两个特定识别序列处切割黏连蛋白的Scc1亚基时,后期就被触发了。这种切割的结果是,黏连蛋白复合体被破坏,使得纺锤体能够将姐妹染色单体拉到细胞的相对两半。由于Scc1切割的最终性和不可逆性,这个反应受到严格控制。有几种独立的机制对分离酶的活性以及切割靶点Scc1对分离酶切割的敏感性进行调节。本章将概述这些多层次的调节。