脂肪生成
过氧化物酶体增殖物激活受体
核受体
转录因子
染色质免疫沉淀
细胞生物学
生物
核受体辅活化子1
视黄醇X受体
交易激励
化学
内分泌学
受体
内科学
基因表达
生物化学
脂肪组织
基因
发起人
医学
作者
Olivier van Beekum,Arjan B. Brenkman,Lars Grøntved,Nicole Hamers,Niels J. F. van den Broek,Ruud Berger,Susanne Mandrup,Eric Kalkhoven
出处
期刊:Endocrinology
[The Endocrine Society]
日期:2007-12-20
卷期号:149 (4): 1840-1849
被引量:64
摘要
The transcription factor peroxisome proliferator-activated receptor gamma (PPARgamma) plays a key role in the regulation of lipid and glucose metabolism in adipocytes, by regulating their differentiation, maintenance, and function. The transcriptional activity of PPARgamma is dictated by the set of proteins with which this nuclear receptor interacts under specific conditions. Here we identify the HIV-1 Tat-interacting protein 60 (Tip60) as a novel positive regulator of PPARgamma transcriptional activity. Using tandem mass spectrometry, we found that PPARgamma and the acetyltransferase Tip60 interact in cells, and through use of chimeric proteins, we established that coactivation by Tip60 critically depends on the N-terminal activation function 1 of PPARgamma, a domain involved in isotype-specific gene expression and adipogenesis. Chromatin immunoprecipitation experiments showed that the endogenous Tip60 protein is recruited to PPARgamma target genes in mature 3T3-L1 adipocytes but not in preadipocytes, indicating that Tip60 requires PPARgamma for its recruitment to PPARgamma target genes. Importantly, we show that in common with disruption of PPARgamma function, small interfering RNA-mediated reduction of Tip60 protein impairs differentiation of 3T3-L1 preadipocytes. Taken together, these findings qualify the acetyltransferase Tip60 as a novel adipogenic factor.
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