Key Laboratory of Systems Biology, Institute of Biochemistry and Cell Biology, Shanghai Institutes for Biological Sciences, Chinese Academy of Sciences, 320 Yue-Yang Road, Shanghai, China.
Cell Death Differ. 2011 Feb;18(2):315-27. doi: 10.1038/cdd.2010.100. Epub 2010 Aug 20.
Krüppel-like factors (KLFs) as a family of zinc-finger transcription factors involve in the regulation of many physiological processes. In these studies, KLF9 was characterized for its role in adipogenesis. The expression of KLF9 was markedly upregulated during the middle stage of 3T3-L1 adipocyte differentiation, and inhibition of KLF9 by RNAi impaired adipogenesis. Using promoter deletion and mutation analysis, we identified two KLF9-binding sites within the 0.6-kb region of the PPARγ2 proximal promoter, indicating that KLF9 interacts with the PPARγ2 promoter. Furthermore, we found that KLF9 could synergistically activate PPARγ2 promoter by directly interacting with C/EBPα. In addition, overexpression of PPARγ2 rescued the impairment of adipocyte differentiation induced by KLF9 knockdown, which supports that PPARγ2 is a downstream target of KLF9. Collectively, our results indicate KLF9 as a key pro-adipogenic transcription factor through regulation of PPARγ2 expression with C/EBPα at the middle stage of adipogenesis.
Krüppel 样因子 (KLFs) 作为一类锌指转录因子,参与许多生理过程的调节。在这些研究中,KLF9 的作用在脂肪生成中得到了表征。在 3T3-L1 脂肪细胞分化的中期,KLF9 的表达明显上调,而 RNAi 抑制 KLF9 则损害脂肪生成。通过启动子缺失和突变分析,我们在 PPARγ2 近端启动子的 0.6kb 区域内鉴定出两个 KLF9 结合位点,表明 KLF9 与 PPARγ2 启动子相互作用。此外,我们发现 KLF9 可以通过与 C/EBPα 直接相互作用协同激活 PPARγ2 启动子。此外,过表达 PPARγ2 挽救了由 KLF9 敲低引起的脂肪细胞分化受损,这支持 PPARγ2 是 KLF9 的下游靶标。总之,我们的结果表明 KLF9 是一种关键的促脂肪生成转录因子,通过与 C/EBPα 在脂肪生成的中期调节 PPARγ2 的表达。