| Literature DB >> 25267199 |
Ju Young Kim1, Ra Ham Lee2, Tae Min Kim3, Dong-Wook Kim2, Young-Joo Jeon2, Sung-Ho Huh4, Se-Yeong Oh5, Michael Kyba6, Hiroshi Kataoka7, Kyunghee Choi8, David M Ornitz4, Jung-Il Chae2, Changwon Park1.
Abstract
In this study, we report that OVOL2, a C2H2 zinc finger protein, is a novel binding protein of ER71, which is a critical transcription factor for blood and vessel development. OVOL2 directly interacted with ER71, but not with ETS1 or ETS2, in the nucleus. ER71-mediated activation of the Flk1 promoter was further enhanced by OVOL2, although OVOL2 alone failed to activate it. Consistently, coexpression of ER71 and OVOL2 in differentiating embryonic stem cells led to a significant augmentation of FLK1(+), endothelial, and hematopoietic cells. Such cooperative effects were impaired by the short hairpin RNA-mediated inhibition of Ovol2. Collectively, we show that ER71 directly interacts with OVOL2 and that such interaction is critical for FLK1(+) cell generation and their differentiation into downstream cell lineages.Entities:
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Year: 2014 PMID: 25267199 PMCID: PMC4224193 DOI: 10.1182/blood-2014-03-556332
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113