| Literature DB >> 17395646 |
Melin Khandekar1, William Brandt, Yinghui Zhou, Susan Dagenais, Thomas W Glover, Norio Suzuki, Ritsuko Shimizu, Masayuki Yamamoto, Kim-Chew Lim, James Douglas Engel.
Abstract
GATA-2, a transcription factor that has been shown to play important roles in multiple organ systems during embryogenesis, has been ascribed the property of regulating the expression of numerous endothelium-specific genes. However, the transcriptional regulatory hierarchy governing Gata2 activation in endothelial cells has not been fully explored. Here, we document GATA-2 endothelial expression during embryogenesis by following GFP expression in Gata2-GFP knock-in embryos. Using founder transgenic analyses, we identified a Gata2 endothelium enhancer in the fourth intron and found that Gata2 regulation by this enhancer is restricted to the endocardial, lymphatic and vascular endothelium. Whereas disruption of three ETS-binding motifs within the enhancer diminished its activity, the ablation of its single E box extinguished endothelial enhancer-directed expression in transgenic mice. Development of the endothelium is known to require SCL (TAL1), and an SCL-E12 (SCL-Tcfe2a) heterodimer can bind the crucial E box in the enhancer in vitro. Thus, GATA-2 is expressed early in lymphatic, cardiac and blood vascular endothelial cells, and the pan-endothelium-specific expression of Gata2 is controlled by a discrete intronic enhancer.Entities:
Mesh:
Substances:
Year: 2007 PMID: 17395646 DOI: 10.1242/dev.001297
Source DB: PubMed Journal: Development ISSN: 0950-1991 Impact factor: 6.868