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hCDC14A与BRAP2相互作用的初步研究

Primary analysis on interaction between hCDC14A and BRAP2

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【作者】 胡海英张烁何敏胡仁明

【Author】 HU Hai-ying, ZHANG Shuo, HE Ming, HU Ren-ming(Department of Endocrinology and Metabolism, Huashan Hospital, Institute of Endocrinology and Diabetology at Fudan University, Shanghai 200040, China. )

【机构】 复旦大学附属华山医院内分泌科复旦大学内分泌糖尿病研究所复旦大学附属华山医院内分泌科复旦大学内分泌糖尿病研究所 上海200040上海200040

【摘要】 目的:筛选hCDC14A(human cell division cycle gene14A)的相互作用蛋白,探索功能联系。方法:酵母双杂交筛选hCDC14A的可能相互作用蛋白,Pulldown实验和免疫共沉淀实验验证蛋白质间相互作用,免疫荧光显微镜观察目的基因在细胞中的表达和定位,体内泛素化实验提示可能的相互作用机制。结果:酵母双杂交筛查到BRAP2(BRCA1 associated protein2)为hCDC14A的可能相互作用蛋白,两者有共同定位,BRAP2可以增强hCDC14A的泛素化修饰。结论:BRAP2可以与hCDC14A相互作用,可能是hCDC14A的泛素连接酶。

【Abstract】 AIM: To search for new candidate partners of human cell division cycle gene 14A (hCDC 14A) and explore their functional relationships.METHODS: Yeast two-hybrid screening was employed to find hCDC 14A new partners. Physical interaction between two proteins was verified using Pulldown and co-immunoprecipitation assays. Subcellular localizations were revealed by immunofluorescence. In vivo ubiquitination test implied their potential functional relationship.RESULTS: BRAP2 (BRCA1 associated protein 2) was found to be a new candidate partner of hCDC 14A. hCDC 14A was modified by ubiquitination, and BRAP2 increased this modification in vivo. As expected, hCDC 14A and BRAP2 co-localized on mitotic spindles in HeLa cells.CONCLUSION: BRAP2 may be an ubiquitin E3 ligase of hCDC 14A.

【基金】 国家“973”子课题资助项目(No.2002CB713703);国家自然科学基金重点资助项目(No.30230380)
  • 【文献出处】 中国病理生理杂志 ,Chinese Journal of Pathophysiology , 编辑部邮箱 ,2007年06期
  • 【分类号】Q25
  • 【被引频次】1
  • 【下载频次】149
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