SWI/SNF chromatin-remodeling complexes in cardiovascular development and disease

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• 作者：Ariana Bevilacqua ; Monte S. Willis ; Scott J. Bultman
• 关键词：BAF ; BRG1/BRM-associated factor ; BRG1 ; brahma-related gene 1 ; BRM ; brahma ; SMC ; smooth muscle cell ; SWI/SNF ; mating type switching/sucrose non-fermenting ; VEC ; vascular endothelial cell
• 刊名：Cardiovascular Pathology
• 出版年：March-April, 2014
• 年：2014
• 卷：23
• 期：2
• 页码：85-91
• 全文大小：1523 K

文摘

Our understanding of congenital heart defects has been recently advanced by whole exome sequencing projects, which have identified de novo mutations in many genes encoding epigenetic regulators. Notably, multiple subunits of switching defective/sucrose non-fermenting (SWI/SNF) chromatin-remodeling complexes have been identified as strong candidates underlying these defects because they physically and functionally interact with cardiogenic transcription factors critical to cardiac development, such as TBX5, GATA-4, and NKX2-5. While these studies indicate a critical role of SWI/SNF complexes in cardiac development and congenital heart disease, many exciting new discoveries have identified their critical role in the adult heart in both physiological and pathological conditions involving multiple cell types in the heart, including cardiomyocytes, vascular endothelial cells, pericytes, and neural crest cells. This review summarizes the role of SWI/SNF chromatin-remodeling complexes in cardiac development, congenital heart disease, cardiac hypertrophy, and vascular endothelial cell survival. Although the clinical relevance of SWI/SNF mutations has traditionally been focused primarily on their role in tumor suppression, these recent studies illustrate their critical role in the heart whereby they regulate cell proliferation, differentiation, and apoptosis of cardiac derived cell lines.