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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:
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.
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页码:1272 / 1281
页数:10
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