Clift Dean, Bizzari Farid, Marston Adele L
The Wellcome Trust Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.
Genes Dev. 2009 Mar 15;23(6):766-80. doi: 10.1101/gad.507509.
Chromosome segregation is triggered by separase, an enzyme that cleaves cohesin, the protein complex that holds sister chromatids together. Separase activation requires the destruction of its inhibitor, securin, which occurs only upon the correct attachment of chromosomes to the spindle. However, other mechanisms restrict separase activity to the appropriate window in the cell cycle because cohesin is cleaved in a timely manner in securin-deficient cells. We investigated the mechanism by which the protector protein Shugoshin counteracts cohesin cleavage in budding yeast. We show that Shugoshin can prevent separase activation independently of securin. Instead, PP2A(Cdc55) is essential for Shugoshin-mediated inhibition of separase. Loss of both securin and Cdc55 leads to premature sister chromatid separation, resulting in aneuploidy. We propose that Cdc55 is a separase inhibitor that acts downstream from Shugoshin under conditions where sister chromatids are not under tension.
染色体分离由分离酶触发,分离酶是一种切割黏连蛋白的酶,黏连蛋白是将姐妹染色单体结合在一起的蛋白质复合物。分离酶的激活需要破坏其抑制剂securin,而securin只有在染色体正确附着到纺锤体上时才会被降解。然而,其他机制将分离酶的活性限制在细胞周期的适当窗口内,因为在securin缺陷型细胞中,黏连蛋白会被及时切割。我们研究了保护蛋白守护蛋白在芽殖酵母中对抗黏连蛋白切割的机制。我们发现,守护蛋白可以独立于securin阻止分离酶的激活。相反,蛋白磷酸酶2A(Cdc55)对于守护蛋白介导的分离酶抑制至关重要。securin和Cdc55的缺失都会导致姐妹染色单体过早分离,从而导致非整倍体。我们提出,在姐妹染色单体没有受到张力的情况下,Cdc55是一种在守护蛋白下游起作用的分离酶抑制剂。