Delta-interacting protein A, a new inhibitory partner of CCAAT/enhancer-binding protein β, implicated in adipocyte differentiation

被引:31
|
作者
Bezy, O
Elabd, C
Cochet, O
Petersen, RK
Kristiansen, K
Dani, C
Ailhaud, R
Amri, EZ
机构
[1] Fac Sci, Inst Signaling Dev Biol & Canc Res, Ctr Biochim, UMR 6543 CNRS, F-06108 Nice, France
[2] Univ So Denmark, Dept Biochem & Mol Biol, DK-5230 Odense, Denmark
关键词
D O I
10.1074/jbc.M411741200
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
CCAAT/enhancer-binding protein beta (C/EBP beta) is expressed early during the adipocyte differentiation program and plays an important role in this process. In an attempt to identify novel proteins that interact with C/EBP beta, we performed a yeast two-hybrid screen with a preadipocyte cDNA library and identified a new co-regulator, delta-interacting protein A (DIPA). DIPA mRNA is expressed during adipocyte differentiation of clonal cell lines. DIPA interacts with C/EBP beta and -delta proteins in intact cells and inhibits their transcriptional activity but not that of C/EBP alpha. Stable overexpression of DIPA in preadipocytes partially inhibits adipocyte differentiation, whereas its gene silencing enhances this process. DIPA and C/EBP beta co-localize in the nucleus, and overexpression of DIPA in preadipocytes results in a partial inhibition of the mitotic clonal expansion which is critical for differentiation. Thus, DIPA is a novel partner of C/EBP beta that down-regulates early events of adipogenesis.
引用
收藏
页码:11432 / 11438
页数:7
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