Vong Queenie P, Cao Kan, Li Hoi Y, Iglesias Pablo A, Zheng Yixian
Department of Embryology, Carnegie Institution of Washington and Howard Hughes Medical Institute, 3520 San Martin Drive, Baltimore, MD 21218, USA.
Science. 2005 Dec 2;310(5753):1499-504. doi: 10.1126/science.1120160.
Proper chromosome segregation requires the attachment of sister kinetochores to microtubules from opposite spindle poles to form bi-oriented chromosomes on the metaphase spindle. The chromosome passenger complex containing Survivin and the kinase Aurora B regulates this process from the centromeres. We report that a de-ubiquitinating enzyme, hFAM, regulates chromosome alignment and segregation by controlling both the dynamic association of Survivin with centromeres and the proper targeting of Survivin and Aurora B to centromeres. Survivin is ubiquitinated in mitosis through both Lys(48) and Lys(63) ubiquitin linkages. Lys(63) de-ubiquitination mediated by hFAM is required for the dissociation of Survivin from centromeres, whereas Lys(63) ubiquitination mediated by the ubiquitin binding protein Ufd1 is required for the association of Survivin with centromeres. Thus, ubiquitinaton regulates dynamic protein-protein interactions and chromosome segregation independently of protein degradation.
正确的染色体分离需要姐妹动粒附着于来自纺锤体两极的微管,从而在中期纺锤体上形成双定向染色体。包含生存素(Survivin)和激酶Aurora B的染色体乘客复合体从着丝粒调控这一过程。我们报告称,一种去泛素化酶hFAM通过控制生存素与着丝粒的动态结合以及生存素和Aurora B向着丝粒的正确靶向,来调控染色体排列和分离。生存素在有丝分裂过程中通过赖氨酸48(Lys(48))和赖氨酸63(Lys(63))泛素连接被泛素化。hFAM介导的赖氨酸63去泛素化是生存素从着丝粒解离所必需的,而泛素结合蛋白Ufd1介导的赖氨酸63泛素化是生存素与着丝粒结合所必需的。因此,泛素化独立于蛋白质降解来调控动态的蛋白质 - 蛋白质相互作用和染色体分离。