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Combinatorial regulation of endothelial gene expression by ets and forkhead transcription factors.

Cell | 2008

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.

Pubmed ID: 19070576 RIS Download

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Associated grants

  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL089707
  • Agency: NHLBI NIH HHS, United States
    Id: P01 HL089707-01A1
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR052130
  • Agency: NHLBI NIH HHS, United States
    Id: HL54737
  • Agency: NHLBI NIH HHS, United States
    Id: K08 HL089330
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL064658-08
  • Agency: NHLBI NIH HHS, United States
    Id: HL64658
  • Agency: NIAMS NIH HHS, United States
    Id: R01 AR052130-04
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL064658
  • Agency: NHLBI NIH HHS, United States
    Id: R01 HL054737

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RRID:SCR_003496

Collection of curated, non-redundant genomic DNA, transcript RNA, and protein sequences produced by NCBI. Provides a reference for genome annotation, gene identification and characterization, mutation and polymorphism analysis, expression studies, and comparative analyses. Accessed through the Nucleotide and Protein databases.

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