BRG1 promotes COUP-TFII expression and venous specification during embryonic vascular development

被引:55
|
作者
Davis, Reema B. [1 ,2 ]
Curtis, Carol D. [1 ]
Griffin, Courtney T. [1 ,2 ]
机构
[1] Oklahoma Med Res Fdn, Cardiovasc Biol Res Program, Oklahoma City, OK 73104 USA
[2] Univ Oklahoma, Hlth Sci Ctr, Dept Cell Biol, Oklahoma City, OK 73126 USA
来源
DEVELOPMENT | 2013年 / 140卷 / 06期
基金
美国国家卫生研究院;
关键词
SWI/SNF; Chromatin remodeling; Veins; Mouse; NR2F2; CHROMATIN-REMODELING ENZYMES; NOTCH SIGNALING PATHWAYS; ENDOTHELIAL-CELLS; ARTERIOVENOUS-MALFORMATIONS; CARDIOVASCULAR DEVELOPMENT; YOLK-SAC; DIFFERENTIATION; ANGIOGENESIS; GRIDLOCK; ARTERY;
D O I
10.1242/dev.087379
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Arteries and veins acquire distinct molecular identities prior to the onset of embryonic blood circulation, and their specification is crucial for vascular development. The transcription factor COUP-TFII currently functions at the top of a signaling pathway governing venous fate. It promotes venous identity by inhibiting Notch signaling and subsequent arterialization of endothelial cells, yet nothing is known about what regulates COUP-TFII expression in veins. We now report that the chromatin-remodeling enzyme BRG1 promotes COUP-TFII expression in venous endothelial cells during murine embryonic development. Conditional deletion of Brg1 from vascular endothelial cells resulted in downregulated COUP-TFII expression and aberrant expression of arterial markers on veins. BRG1 promotes COUP-TFII expression by binding conserved regulatory elements within the COUP-TFII promoter and remodeling chromatin to make the promoter accessible to transcriptional machinery. This study provides the first description of a factor promoting COUP-TFII expression in vascular endothelium and highlights a novel role for chromatin remodeling in venous specification.
引用
收藏
页码:1272 / 1281
页数:10
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