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Combinatorial Regulation of Endothelial Gene Expression by Ets and Forkhead Transcription Factors

机译:Ets和叉头转录因子对内皮基因表达的组合调控

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摘要

Vascular development begins when mesodermal cells differentiate into endothelial cells, which then form primitive vessels. It has been hypothesized that endothelial-specific gene expression may be regulated combinatorially, but the transcriptional mechanisms governing specificity in vascular gene expression remain incompletely understood. Here, we identify a 44 bp transcriptional enhancer that is sufficient to direct expression specifically and exclusively to the developing vascular endothelium. This enhancer is regulated by a composite cis-acting element, the FOX:ETS motif, which is bound and synergistically activated by Forkhead and Ets transcription factors. We demonstrate that coexpression of the Forkhead protein FoxC2 and the Ets protein Etv2 induces ectopic expression of vascular genes in Xenopus embryos, and that combinatorial knockdown of the orthologous genes in zebrafish embryos disrupts vascular development. Finally, we show that FOX: ETS motifs are present in many known endothelial-specific enhancers and that this motif is an efficient predictor of endothelial enhancers in the human genome.
机译:当中胚层细胞分化为内皮细胞,然后形成原始血管时,血管开始发育。据推测,内皮特异性基因的表达可能受到组合调节,但控制血管基因表达特异性的转录机制仍未完全了解。在这里,我们确定了一个44 bp的转录增强子,足以直接特异性地和专门地向发育中的血管内皮表达。该增强子由复合顺式作用元件FOX:ETS母体调控,该母体被Forkhead和Ets转录因子结合并协同激活。我们证明叉头蛋白FoxC2和Ets蛋白Etv2的共表达诱导非洲爪蟾胚胎中的血管基因的异位表达,并且在斑马鱼胚胎中直系同源基因的组合敲低破坏了血管的发育。最后,我们表明FOX:ETS主题存在于许多已知的内皮特异性增强子中,并且该主题是人类基因组中内皮增强子的有效预测因子。

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