Abe Yusuke, Sako Kosuke, Takagaki Kentaro, Hirayama Youko, Uchida Kazuhiko S K, Herman Jacob A, DeLuca Jennifer G, Hirota Toru
Division of Experimental Pathology, Cancer Institute of the Japanese Foundation for Cancer Research (JFCR), Tokyo 135-8550, Japan.
Department of Biochemistry and Molecular Biology, Colorado State University, Fort Collins, CO 80523, USA.
Dev Cell. 2016 Mar 7;36(5):487-97. doi: 10.1016/j.devcel.2016.02.008.
Incorrect attachment of kinetochore microtubules is the leading cause of chromosome missegregation in cancers. The highly conserved chromosomal passenger complex (CPC), containing mitotic kinase Aurora B as a catalytic subunit, ensures faithful chromosome segregation through destabilizing incorrect microtubule attachments and promoting biorientation of chromosomes on the mitotic spindle. It is unknown whether CPC dysfunction affects chromosome segregation fidelity in cancers and, if so, how. Here, we show that heterochromatin protein 1 (HP1) is an essential CPC component required for full Aurora B activity. HP1 binding to the CPC becomes particularly important when Aurora B phosphorylates kinetochore targets to eliminate erroneous microtubule attachments. Remarkably, a reduced proportion of HP1 bound to CPC is widespread in cancers, which causes an impairment in Aurora B activity. These results indicate that HP1 is an essential modulator for CPC function and identify a molecular basis for chromosome segregation errors in cancer cells.
动粒微管附着错误是癌症中染色体错误分离的主要原因。高度保守的染色体乘客复合体(CPC),以有丝分裂激酶Aurora B作为催化亚基,通过破坏不正确的微管附着并促进染色体在有丝分裂纺锤体上的双定向排列,确保染色体的准确分离。目前尚不清楚CPC功能障碍是否会影响癌症中的染色体分离保真度,如果会,又是如何影响的。在这里,我们表明异染色质蛋白1(HP1)是Aurora B充分发挥活性所必需的CPC成分。当Aurora B磷酸化动粒靶点以消除错误的微管附着时,HP1与CPC的结合变得尤为重要。值得注意的是,与CPC结合的HP1比例降低在癌症中广泛存在,这导致Aurora B活性受损。这些结果表明,HP1是CPC功能的必需调节因子,并确定了癌细胞中染色体分离错误的分子基础。