Acetyl-coenzyme A acyltransferase 2 attenuates the apoptotic effects of BNIP3 in two human cell lines

被引:49
作者
Cao, Wei [1 ]
Liu, Nansong [1 ]
Tang, Shuai [1 ]
Bao, Lei [1 ]
Shen, Li [1 ]
Yuan, Hanying [1 ]
Zhao, Xin [2 ]
Lu, Hong [1 ]
机构
[1] Fudan Univ, Sch Life Sci, Inst Genet, State Key Lab Genet Engn, Shanghai 200433, Peoples R China
[2] McGill Univ, Dept Anim Sci, Ste Anne De Bellevue H9X3V9, PQ, Canada
来源
BIOCHIMICA ET BIOPHYSICA ACTA-GENERAL SUBJECTS | 2008年 / 1780卷 / 06期
基金
中国国家自然科学基金;
关键词
BNIP3; ACAA2; split-ubiquitin membrane yeast two-hybrid system; apoptosis; mitochondrial membrane potential;
D O I
10.1016/j.bbagen.2008.02.007
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
BNIP3 is a unique pro-apoptotic protein which belongs to the BH3-only subset of the Bcl-2 family and localizes on mitochondrial membrane. Despite the inherent difficulty of identifying binding partners for membrane proteins, several binding partners for BNIP3 have been identified. In this study, a modified split-ubiquitin membrane yeast two-hybrid system was constructed and used to identify acetyl-Coenzyme A acyltransferase 2 (ACAA2) as a new BNIP3 binding partner. The interaction between BNIP3 and ACAA2 was confirmed by pull-down and co-immunoprecipitation assays. ACAA2 was also found to co-localize with BNIP3 in mitochondria. Furthermore, the apoptosis induced by over-expressed BNIP3 via transfection OF hypoxia treatment was abolished by ACAA2 in human hepatocellular carcinoma HepG2 cells and osteosarcoma U-2 OS cells. These results strongly suggest that ACAA2 be a functional BNIP3 binding partner and provide a possible linkage between fatty acid metabolism and apoptosis of cells. (c) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:873 / 880
页数:8
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