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证明肿瘤抑制蛋白 BRCA2 不会调节人类细胞的胞质分裂。

Evidence that the tumor-suppressor protein BRCA2 does not regulate cytokinesis in human cells.

机构信息

Cell Division and Aneuploidy Laboratory, Cancer Research UK London Research Institute, Clare Hall Laboratories, Blanche Lane, South Mimms, Hertfordshire EN6 3LD, UK.

出版信息

J Cell Sci. 2010 May 1;123(Pt 9):1395-400. doi: 10.1242/jcs.068015. Epub 2010 Mar 31.

Abstract

Germline mutations in the tumor-suppressor gene BRCA2 predispose to breast and ovarian cancer. BRCA2 plays a well-established role in maintaining genome stability by regulating homologous recombination. BRCA2 has more recently been implicated in cytokinesis, the final step of cell division, but the molecular basis for this remains unknown. We have used time-lapse microscopy, recently developed cytokinesis assays and BAC recombineering (bacterial artificial chromosome recombinogenic engineering) to investigate the function and localization of BRCA2 during cell division. Our analysis suggests that BRCA2 does not regulate cytokinesis in human cells. Thus, cytokinesis defects are unlikely to contribute to chromosomal instability and tumorigenesis in BRCA2-related cancers.

摘要

种系突变的肿瘤抑制基因 BRCA2 易患乳腺癌和卵巢癌。BRCA2 在维持基因组稳定性方面发挥着重要作用,通过调节同源重组来实现。BRCA2 最近也被牵连到胞质分裂中,即细胞分裂的最后一步,但分子基础尚不清楚。我们使用延时显微镜、新开发的胞质分裂检测和 BAC 重组(细菌人工染色体重组工程)来研究 BRCA2 在细胞分裂过程中的功能和定位。我们的分析表明,BRCA2 并不调节人类细胞的胞质分裂。因此,胞质分裂缺陷不太可能导致 BRCA2 相关癌症中的染色体不稳定性和肿瘤发生。

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