Department of Molecular Carcinogenesis, Center for Cancer Epigenetics, The University of Texas M. D. Anderson Cancer Center, Smithville, Texas, USA Laboratory of Endocrinology and Receptor Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Laboratory of Endocrinology and Receptor Biology, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health, Bethesda, Maryland, USA.
Mol Cell Biol. 2014 Oct 1;34(19):3746-53. doi: 10.1128/MCB.00622-14. Epub 2014 Jul 28.
The acetyltransferase Gcn5 is critical for embryogenesis and shows partial functional redundancy with its homolog PCAF. However, the tissue- and cell lineage-specific functions of Gcn5 and PCAF are still not well defined. Here we probe the functions of Gcn5 and PCAF in adipogenesis. We found that the double knockout (DKO) of Gcn5/PCAF inhibits expression of the master adipogenic transcription factor gene PPARγ, thereby preventing adipocyte differentiation. The adipogenesis defects in Gcn5/PCAF DKO cells are rescued by ectopic expression of peroxisome proliferator-activated receptor γ (PPARγ), suggesting Gcn5/PCAF act upstream of PPARγ to facilitate adipogenesis. The requirement of Gcn5/PCAF for PPARγ expression was unexpectedly bypassed by prolonged treatment with an adipogenic inducer, 3-isobutyl-1-methylxanthine (IBMX). However, neither PPARγ ectopic expression nor prolonged IBMX treatment rescued defects in Prdm16 expression in DKO cells, indicating that Gcn5/PCAF are essential for normal Prdm16 expression. Gcn5/PCAF regulate PPARγ and Prdm16 expression at different steps in the transcription process, facilitating RNA polymerase II recruitment to Prdm16 and elongation of PPARγ transcripts. Overall, our study reveals that Gcn5/PCAF facilitate adipogenesis through regulation of PPARγ expression and regulate brown adipogenesis by influencing Prdm16 expression.
乙酰转移酶 Gcn5 对于胚胎发生至关重要,并且与它的同源物 PCAF 表现出部分功能冗余。然而,Gcn5 和 PCAF 的组织和细胞谱系特异性功能仍未得到很好的定义。在这里,我们探讨了 Gcn5 和 PCAF 在脂肪生成中的功能。我们发现 Gcn5/PCAF 的双敲除 (DKO) 抑制了主脂肪生成转录因子基因 PPARγ 的表达,从而阻止了脂肪细胞分化。在 Gcn5/PCAF DKO 细胞中,过表达过氧化物酶体增殖物激活受体 γ (PPARγ) 挽救了脂肪生成缺陷,表明 Gcn5/PCAF 在 PPARγ 上游发挥作用,促进脂肪生成。出乎意料的是,长时间用脂肪生成诱导剂 3-异丁基-1-甲基黄嘌呤 (IBMX) 处理可以绕过 Gcn5/PCAF 对 PPARγ 表达的需求。然而,PPARγ 过表达或长时间 IBMX 处理都不能挽救 DKO 细胞中 Prdm16 表达的缺陷,表明 Gcn5/PCAF 对于正常的 Prdm16 表达是必需的。Gcn5/PCAF 在转录过程的不同步骤调节 PPARγ 和 Prdm16 的表达,促进 RNA 聚合酶 II 募集到 Prdm16 并延长 PPARγ 转录物的延伸。总的来说,我们的研究揭示了 Gcn5/PCAF 通过调节 PPARγ 表达促进脂肪生成,并通过影响 Prdm16 表达来调节棕色脂肪生成。