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乳腺癌易感基因BRCA2的产物与DSS1之间的相互作用,DSS1是一种从酵母到哺乳动物功能保守的蛋白质。

Interaction between the product of the breast cancer susceptibility gene BRCA2 and DSS1, a protein functionally conserved from yeast to mammals.

作者信息

Marston N J, Richards W J, Hughes D, Bertwistle D, Marshall C J, Ashworth A

机构信息

Section of Gene Function and Regulation, Institute of Cancer Research, Chester Beatty Laboratories, London, United Kingdom SW3 6JB.

出版信息

Mol Cell Biol. 1999 Jul;19(7):4633-42. doi: 10.1128/MCB.19.7.4633.

Abstract

Germ line mutations in the breast cancer susceptibility gene BRCA2 predispose to early-onset breast cancer, but the function of the nuclear protein encoded by the gene is ill defined. Using the yeast two-hybrid system with fragments of human BRCA2, we identified an interaction with the human DSS1 (deleted in split hand/split foot) gene. Yeast and mammalian two-hybrid assays showed that DSS1 can associate with BRCA2 in the region of amino acids 2472 to 2957 in the C terminus of the protein. Using coimmunoprecipitation of epitope-tagged BRCA2 and DSS1 cDNA constructs transiently expressed in COS cells, we were able to demonstrate an association. Furthermore, endogenous BRCA2 could be coimmunoprecipitated with endogenous DSS1 in MCF7 cells, demonstrating an in vivo association. Apparent orthologues of the mammalian DSS1 gene were identified in the genome of the yeasts Schizosaccharomyces pombe and Saccharomyces cerevisiae. Yeast strains in which these DSS1-like genes were deleted showed a temperature-sensitive growth phenotype, which was analyzed by flow cytometry. This provides evidence for a link between the BRCA2 tumor suppressor gene and a gene required for completion of the cell cycle.

摘要

乳腺癌易感基因BRCA2中的种系突变易导致早发性乳腺癌,但该基因编码的核蛋白功能尚不明确。利用含有人BRCA2片段的酵母双杂交系统,我们鉴定出它与人类DSS1(手足裂缺综合征缺失基因)存在相互作用。酵母和哺乳动物双杂交试验表明,DSS1可在该蛋白C端氨基酸2472至2957区域与BRCA2结合。通过对在COS细胞中瞬时表达的表位标记BRCA2和DSS1 cDNA构建体进行共免疫沉淀,我们证实了二者之间的结合。此外,内源性BRCA2可与MCF7细胞中的内源性DSS1共免疫沉淀,证明了二者在体内的结合。在粟酒裂殖酵母和酿酒酵母的基因组中鉴定出了哺乳动物DSS1基因明显的直系同源基因。缺失这些类DSS1基因的酵母菌株表现出温度敏感的生长表型,并通过流式细胞术进行了分析。这为BRCA2肿瘤抑制基因与细胞周期完成所需基因之间的联系提供了证据。

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