Epigenomic Regulation of PPARgamma and Adipogenesis

我们对组蛋白H3（分别为H3K4、H3K9、H3K27、H3K36和H3K79）的K4、K9、K27、H3K36和H3K79)位点特异性甲基化在脂肪形成和PPARgamma调控中的作用感兴趣。我们之前报道过增强子H3K4me1甲基转移酶MLL3/MLL4和相关的PTIP控制PPARgamma和C/EBPa的诱导，并且是脂肪形成所必需的(Cho YW, Cell Metab 2009; Lee JE, eLife 2013；Jang Y, NAR 2019)， H3K9甲基转移酶G9a抑制PPARgamma表达和脂肪形成（Wang L, EMBO J 2013）， H3K27甲基转移酶Ezh2组成性抑制Wnt基因促进脂肪形成（Wang L, PNAS 2010），并且在前细胞中，组蛋白H3.3突变体H3.3 k36m缺失nsd2介导的H3K36甲基化会损害脂肪组织的发育和功能（Zhuang L, Nat Comm 2018）。我们还发现，表观基因组读取器Brd4控制细胞身份基因诱导，对体内脂肪形成至关重要（Lee JE, Nat Comm 2017）。总之，这些发现表明，表观基因组因素在脂肪形成的调控中起着关键作用（Lee JE， MCB 2019综述）。

We are interested in the roles of site-specific methylations on K4, K9, K27, K36 and K79 of histone H3 (H3K4, H3K9, H3K27, H3K36 and H3K79, respectively) in regulation of adipogenesis and PPARgamma. We reported previously that enhancer H3K4me1 methyltransferases MLL3/MLL4 and associated PTIP control the induction of PPARgamma and C/EBPa and are essential for adipogenesis (Cho YW, Cell Metab 2009; Lee JE, eLife 2013; Jang Y, NAR 2019), that H3K9 methyltransferase G9a represses PPARgamma expression and adipogenesis (Wang L, EMBO J 2013), that H3K27 methyltransferase Ezh2 constitutively represses Wnt genes to facilitate adipogenesis (Wang L, PNAS 2010), and that depletion of Nsd2-mediated H3K36 methylation by histone H3.3 mutant H3.3K36M in progenitor cells impairs adipose tissue development and function (Zhuang L, Nat Comm 2018). We also showed that the epigenomic reader Brd4 controls cell identity gene induction and is essential for adipogenesis in vivo (Lee JE, Nat Comm 2017). Together, these findings indicate that epigenomic factors play critical roles in the regulation of adipogenesis (reviewed in Lee JE, MCB 2019). Using conditional knockout mice and preadipocytes, we found surprisingly that although ligand-bound glucocorticoid receptor (GR) accelerates adipogenesis in culture, endogenous GR is dispensable for adipogenesis in culture and in mice (Park Y, MCB 2017a). We also found that KLF4 and Krox20 are dispensable for adipogenesis in culture and in mice (Park Y, MCB 2017b). These unexpected results prompted us to study adipogenesis in vivo. We previously profiled genomic binding of enhancer epigenomic writers (MLL4, CBP), adipogenic TFs (EBF2, C/EBPa, C/EBPb, PPARgamma), coactivator MED1, RNA Polymerase II, as well as epigenome (H3K4me1/2/3, H3K9me2, H3K27me3, H3K36me3, H3K27ac), transcriptome, and chromatin opening during adipogenesis of immortalized preadipocytes derived from mouse BAT. Our data provide a rich resource for understanding epigenomic regulation of brown adipogenesis in culture (Lai B, NAR 2017). We are profiling enhancers and gene expression during adipogenesis in vivo.