4.7 Article

Atrial Identity Is Determined by a COUP-TFII Regulatory Network

期刊

DEVELOPMENTAL CELL
卷 25, 期 4, 页码 417-426

出版社

CELL PRESS
DOI: 10.1016/j.devcel.2013.04.017

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资金

  1. National Institutes of Health [HL76448, DK45641, DK62434, DK59820]
  2. Diabetes Research Center grant [P30 DK079638]

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Atria and ventricles exhibit distinct molecular profiles that produce structural and functional differences between the two cardiac compartments. However, the factors that determine these differences remain largely undefined. Cardiomyocyte-specific COUP-TFII ablation produces ventricularized atria that exhibit ventricle-like action potentials, increased cardiomyocyte size, and development of extensive T tubules. Changes in atrial characteristics are accompanied by alterations of 2,584 genes, of which 81% were differentially expressed between atria and ventricles, suggesting that a major function of myocardial COUP-TFII is to determine atrial identity. Chromatin immunoprecipitation assays using E13.5 atria identified classic atrial-ventricular identity genes Tbx5, Hey2, Irx4, MLC2v, MLC2a, and MLC1a, among many other cardiac genes, as potential COUP-TFII direct targets. Collectively, our results reveal that COUP-TFII confers atrial identity through direct binding and by modulating expression of a broad spectrum of genes that have an impact on atrial development and function.

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