Adipocyte Biology and Gene Regulation Section, National Institute of Diabetes and Digestive and Kidney Diseases, National Institutes of Health (NIH), Bethesda, MD, USA.
Laboratory of Genetics and Genomics, National Institute on Aging, NIH, Baltimore, MD, USA.
Nat Commun. 2021 Mar 12;12(1):1630. doi: 10.1038/s41467-021-21893-y.
Cell type-specific enhancers are activated by coordinated actions of lineage-determining transcription factors (LDTFs) and chromatin regulators. The SWI/SNF chromatin remodeling complex BAF and the histone H3K4 methyltransferase MLL4 (KMT2D) are both implicated in enhancer activation. However, the interplay between BAF and MLL4 in enhancer activation remains unclear. Using adipogenesis as a model system, we identify BAF as the major SWI/SNF complex that colocalizes with MLL4 and LDTFs on active enhancers and is required for cell differentiation. In contrast, the promoter enriched SWI/SNF complex PBAF is dispensable for adipogenesis. By depleting BAF subunits SMARCA4 (BRG1) and SMARCB1 (SNF5) as well as MLL4 in cells, we show that BAF and MLL4 reciprocally regulate each other's binding on active enhancers before and during adipogenesis. By focusing on enhancer activation by the adipogenic pioneer transcription factor C/EBPβ without inducing cell differentiation, we provide direct evidence for an interdependent relationship between BAF and MLL4 in activating cell type-specific enhancers. Together, these findings reveal a positive feedback between BAF and MLL4 in promoting LDTF-dependent activation of cell type-specific enhancers.
细胞类型特异性增强子是由谱系决定转录因子(LDTFs)和染色质调节剂的协调作用激活的。SWI/SNF 染色质重塑复合物 BAF 和组蛋白 H3K4 甲基转移酶 MLL4(KMT2D)都与增强子激活有关。然而,BAF 和 MLL4 在增强子激活中的相互作用尚不清楚。我们以脂肪生成作为模型系统,确定 BAF 是与 MLL4 和 LDTFs 共定位在活性增强子上并需要细胞分化的主要 SWI/SNF 复合物。相比之下,富含启动子的 SWI/SNF 复合物 PBAF 对于脂肪生成是可有可无的。通过在细胞中耗尽 BAF 亚基 SMARCA4(BRG1)和 SMARCB1(SNF5)以及 MLL4,我们表明 BAF 和 MLL4 在脂肪生成之前和期间相互调节彼此在活性增强子上的结合。通过专注于脂肪生成先驱转录因子 C/EBPβ 激活增强子而不诱导细胞分化,我们为 BAF 和 MLL4 在激活细胞类型特异性增强子中的相互依赖关系提供了直接证据。总之,这些发现揭示了 BAF 和 MLL4 在促进 LDTF 依赖性激活细胞类型特异性增强子中的正反馈关系。