Cardiovascular Biology Research Program, Oklahoma Medical Research Foundation, Oklahoma City, OK 73104, USA.
Development. 2013 Mar;140(6):1272-81. doi: 10.1242/dev.087379. Epub 2013 Feb 13.
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.
动脉和静脉在胚胎血液循环开始之前获得独特的分子特征,它们的特化对于血管发育至关重要。转录因子 COUP-TFII 目前在调控静脉命运的信号通路中处于顶端。它通过抑制 Notch 信号通路和随后的内皮细胞动脉化来促进静脉特征,但关于什么调节静脉中的 COUP-TFII 表达尚不清楚。我们现在报告说,染色质重塑酶 BRG1 在小鼠胚胎发育过程中促进静脉内皮细胞中 COUP-TFII 的表达。血管内皮细胞中 Brg1 的条件性缺失导致 COUP-TFII 表达下调和静脉上动脉标记物的异常表达。BRG1 通过结合 COUP-TFII 启动子内保守的调节元件并重塑染色质以使启动子可被转录机制利用,从而促进 COUP-TFII 的表达。本研究首次描述了促进血管内皮中 COUP-TFII 表达的因子,并强调了染色质重塑在静脉特化中的新作用。