Laboratory of Chromosome Dynamics, Institute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi, Tokyo 113-0032, Japan.
Laboratory of Chromosome Dynamics, Institute of Molecular and Cellular Biosciences, University of Tokyo, Yayoi, Tokyo 113-0032, Japan. Department of Biological Sciences, Graduate School of Science, University of Tokyo, Yayoi, Tokyo 113-0032, Japan.
Science. 2015 Sep 11;349(6253):1237-40. doi: 10.1126/science.aaa2655.
Chromosomal instability (CIN) is a major trait of cancer cells and a potent driver of tumor progression. However, the molecular mechanisms underlying CIN still remain elusive. We found that a number of CIN(+) cell lines have impairments in the integrity of the conserved inner centromere-shugoshin (ICS) network, which coordinates sister chromatid cohesion and kinetochore-microtubule attachment. These defects are caused mostly by the loss of histone H3 lysine 9 trimethylation at centromeres and sometimes by a reduction in chromatin-associated cohesin; both pathways separately sustain centromeric shugoshin stability. Artificial restoration of the ICS network suppresses chromosome segregation errors in a wide range of CIN(+) cells, including RB- and BRCA1-deficient cells. Thus, dysfunction of the ICS network might be a key mechanism underlying CIN in human tumorigenesis.
染色体不稳定(CIN)是癌细胞的主要特征,也是肿瘤进展的有力驱动因素。然而,CIN 的分子机制仍然难以捉摸。我们发现,许多 CIN(+)细胞系的内着丝粒-保护蛋白(ICS)网络完整性受损,该网络协调着姐妹染色单体的黏合以及动粒-微管的连接。这些缺陷主要是由于着丝粒处组蛋白 H3 赖氨酸 9 三甲基化的丢失,有时则是由于染色质相关黏合蛋白的减少;这两种途径分别维持着着丝粒保护蛋白的稳定性。ICS 网络的人工重建可抑制广泛的 CIN(+)细胞中的染色体分离错误,包括 RB 和 BRCA1 缺陷细胞。因此,ICS 网络的功能障碍可能是人类肿瘤发生中 CIN 的关键机制。