Case Cardiovascular Research Institute, Department of Medicine, Case Western Reserve University School of Medicine, and Harrington Heart & Vascular Institute, University Hospitals Case Medical Center, Cleveland, OH 44106, USA.
Cell. 2013 Aug 1;154(3):569-82. doi: 10.1016/j.cell.2013.07.013.
Heart failure (HF) is driven by the interplay between regulatory transcription factors and dynamic alterations in chromatin structure. Pathologic gene transactivation in HF is associated with recruitment of histone acetyl-transferases and local chromatin hyperacetylation. We therefore assessed the role of acetyl-lysine reader proteins, or bromodomains, in HF. Using a chemical genetic approach, we establish a central role for BET family bromodomain proteins in gene control during HF pathogenesis. BET inhibition potently suppresses cardiomyocyte hypertrophy in vitro and pathologic cardiac remodeling in vivo. Integrative transcriptional and epigenomic analyses reveal that BET proteins function mechanistically as pause-release factors critical to expression of genes that are central to HF pathogenesis and relevant to the pathobiology of failing human hearts. This study implicates epigenetic readers as essential effectors of transcriptional pause release during HF pathogenesis and identifies BET coactivator proteins as therapeutic targets in the heart.
心力衰竭(HF)是由调节转录因子和染色质结构的动态变化之间的相互作用驱动的。HF 中的病理性基因转录激活与组蛋白乙酰转移酶的募集和局部染色质超乙酰化有关。因此,我们评估了乙酰赖氨酸读蛋白或溴结构域在 HF 中的作用。我们使用化学遗传学方法,确定 BET 家族溴结构域蛋白在 HF 发病机制中的基因控制中的核心作用。BET 抑制在体外强烈抑制心肌细胞肥大和体内病理性心脏重塑。综合转录组学和表观基因组学分析表明,BET 蛋白作为暂停释放因子发挥作用,对于与 HF 发病机制相关的关键基因的表达至关重要,并且与衰竭人类心脏的病理生物学相关。这项研究表明,表观遗传读蛋白是 HF 发病机制中转录暂停释放的必要效应因子,并确定 BET 共激活蛋白是心脏的治疗靶点。