Abrieu A, Magnaghi-Jaulin L, Kahana J A, Peter M, Castro A, Vigneron S, Lorca T, Cleveland D W, Labbé J C
Ludwig Institute for Cancer Research, University of California, San Diego, 9500 Gilman Drive, La Jolla, CA 92093, USA.
Cell. 2001 Jul 13;106(1):83-93. doi: 10.1016/s0092-8674(01)00410-x.
The mitotic checkpoint acts to inhibit entry into anaphase until all chromosomes have successfully attached to spindle microtubules. Unattached kinetochores are believed to release an activated form of Mad2 that inhibits APC/C-dependent ubiquitination and subsequent proteolysis of components needed for anaphase onset. Using Xenopus egg extracts, a vertebrate homolog of yeast Mps1p is shown here to be a kinetochore-associated kinase, whose activity is necessary to establish and maintain the checkpoint. Since high levels of Mad2 overcome checkpoint loss in Mps1-depleted extracts, Mps1 acts upstream of Mad2-mediated inhibition of APC/C. Mps1 is essential for the checkpoint because it is required for recruitment and retention of active CENP-E at kinetochores, which in turn is necessary for kinetochore association of Mad1 and Mad2.
有丝分裂检查点的作用是抑制细胞进入后期,直到所有染色体都成功附着在纺锤体微管上。未附着的动粒被认为会释放一种活化形式的Mad2,它会抑制后期促进复合物/细胞周期体(APC/C)依赖性泛素化以及后期起始所需成分的后续蛋白水解。利用非洲爪蟾卵提取物,本文显示酵母Mps1p的一种脊椎动物同源物是一种与动粒相关的激酶,其活性对于建立和维持该检查点是必需的。由于高水平的Mad2能克服Mps1缺失提取物中的检查点丧失,所以Mps1在Mad2介导的对APC/C的抑制作用上游发挥作用。Mps1对该检查点至关重要,因为它是在动粒处募集和保留活性CENP - E所必需的,而这反过来又是Mad1和Mad2与动粒结合所必需的。