Cooperative interaction of Etv2 and Gata2 regulates the development of endothelial and hematopoietic lineages.

TitleCooperative interaction of Etv2 and Gata2 regulates the development of endothelial and hematopoietic lineages.
Publication TypeJournal Article
Year of Publication2014
AuthorsShi X, Richard J, Zirbes KM, Gong W, Lin G, Kyba M, Thomson JA, Koyano-Nakagawa N, Garry DJ
JournalDev Biol
Volume389
Issue2
Pagination208-18
Date Published2014 May 15
ISSN1095-564X
KeywordsAnimals, Cell Differentiation, Cell Line, Cell Lineage, Embryoid Bodies, Embryonic Development, Endothelial Cells, GATA2 Transcription Factor, Gene Expression Regulation, Developmental, Hematopoietic Stem Cells, Mice, Protein Binding, Protein Interaction Domains and Motifs, Proto-Oncogene Proteins, Trans-Activators, Transcription Factors, Transcriptional Activation
Abstract

Regulatory mechanisms that govern lineage specification of the mesodermal progenitors to become endothelial and hematopoietic cells remain an area of intense interest. Both Ets and Gata factors have been shown to have important roles in the transcriptional regulation in endothelial and hematopoietic cells. We previously reported Etv2 as an essential regulator of vasculogenesis and hematopoiesis. In the present study, we demonstrate that Gata2 is co-expressed and interacts with Etv2 in the endothelial and hematopoietic cells in the early stages of embryogenesis. Our studies reveal that Etv2 interacts with Gata2 in vitro and in vivo. The protein-protein interaction between Etv2 and Gata2 is mediated by the Ets and Gata domains. Using the embryoid body differentiation system, we demonstrate that co-expression of Gata2 augments the activity of Etv2 in promoting endothelial and hematopoietic lineage differentiation. We also identify Spi1 as a common downstream target gene of Etv2 and Gata2. We provide evidence that Etv2 and Gata2 bind to the Spi1 promoter in vitro and in vivo. In summary, we propose that Gata2 functions as a cofactor of Etv2 in the transcriptional regulation of mesodermal progenitors during embryogenesis.

DOI10.1016/j.ydbio.2014.02.018
Alternate JournalDev. Biol.
PubMed ID24583263
PubMed Central IDPMC4099474
Grant ListR01 HL085729 / HL / NHLBI NIH HHS / United States
R01HL085729 / HL / NHLBI NIH HHS / United States
U01 HL100407 / HL / NHLBI NIH HHS / United States
U01HL100407 / HL / NHLBI NIH HHS / United States