溴尿嘧啶
SMARCA4型
脂肪生成
转录因子
染色质重塑
瑞士/瑞士法郎
化学
细胞生物学
BRD4
博士手指
组蛋白
染色质
表观遗传学
癌症研究
生物化学
生物
基因
锌指
作者
Marek Wanior,Franziska Preuß,Xiaoling Ni,Andreas Krämer,Sebastian Mathea,Tamara Göbel,David Heidenreich,Svenja Simonyi,Astrid S. Kahnt,A.C. Joerger,Stefan Knapp
标识
DOI:10.1021/acs.jmedchem.0c01242
摘要
Accessibility of the human genome is modulated by the ATP-driven SWI/SNF chromatin remodeling multiprotein complexes BAF (BRG1/BRM-associated factor) and PBAF (polybromo-associated BAF factor), which involves reading of acetylated histone tails by the bromodomain-containing proteins SMARCA2 (BRM), SMARCA4 (BRG1), and polybromo-1. Dysregulation of chromatin remodeling leads to aberrant cell proliferation and differentiation. Here, we have characterized a set of potent and cell-active bromodomain inhibitors with pan-selectivity for canonical family VIII bromodomains. Targeted SWI/SNF bromodomain inhibition blocked the expression of key genes during adipogenesis, including the transcription factors PPARγ and C/EBPα, and impaired the differentiation of 3T3-L1 murine fibroblasts into adipocytes. Our data highlight the role of SWI/SNF bromodomains in adipogenesis and provide a framework for the development of SWI/SNF bromodomain inhibitors for indirect targeting of key transcription factors regulating cell differentiation.
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