Daniels Matthew J, Wang Yunmei, Lee Miyoung, Venkitaraman Ashok R
University of Cambridge, Cancer Research UK, Department of Oncology and the Medical Research Council (MRC) Cancer Cell Unit, Hutchison/MRC Research Centre, Hills Road, Cambridge CB2 2XZ, UK.
Science. 2004 Oct 29;306(5697):876-9. doi: 10.1126/science.1102574. Epub 2004 Sep 16.
Germ-line mutations inactivating BRCA2 predispose to cancer. BRCA2-deficient cells exhibit alterations in chromosome number (aneuploidy), as well as structurally aberrant chromosomes. Here, we show that BRCA2 deficiency impairs the completion of cell division by cytokinesis. BRCA2 inactivation in murine embryo fibroblasts (MEFs) and HeLa cells by targeted gene disruption or RNA interference delays and prevents cell cleavage. Impeded cell separation is accompanied by abnormalities in myosin II organization during the late stages in cytokinesis. BRCA2 may have a role in regulating these events, as it localizes to the cytokinetic midbody. Our findings thus link cytokinetic abnormalities to a hereditary cancer syndrome characterized by chromosomal instability and may help to explain why BRCA2-deficient tumors are frequently aneuploid.
使BRCA2失活的种系突变易患癌症。BRCA2缺陷细胞表现出染色体数目改变(非整倍体)以及结构异常的染色体。在此,我们表明BRCA2缺陷会损害细胞分裂通过胞质分裂的完成。通过靶向基因破坏或RNA干扰使小鼠胚胎成纤维细胞(MEF)和HeLa细胞中的BRCA2失活会延迟并阻止细胞分裂。细胞分离受阻伴随着胞质分裂后期肌球蛋白II组织的异常。BRCA2可能在调节这些事件中起作用,因为它定位于胞质分裂中间体。因此,我们的发现将胞质分裂异常与以染色体不稳定为特征的遗传性癌症综合征联系起来,并可能有助于解释为什么BRCA2缺陷肿瘤经常是非整倍体。