Back to Search Start Over

Molecular basis for Flk1 expression in hemato-cardiovascular progenitors in the mouse

Authors :
Satoru Takahashi
Masatsugu Ema
Hiroshi Kataoka
Kyunghee Choi
Fang Liu
Asami Wakamatsu
Makoto Kobayashi
Shin-Ichi Nishikawa
Michito Hamada
Hiroyuki Ishitobi
Takuya Azami
Ken Matsumoto
Source :
Development. 138:5357-5368
Publication Year :
2011
Publisher :
The Company of Biologists, 2011.

Abstract

The mouse Flk1 gene is expressed in various mesodermal progenitor cells of developing embryos. Recent studies have shown that Flk1 expression marks multipotent mesodermal progenitors, giving rise to various hemato-cardiovascular cell lineages during development. Flk1 expression also marks hemato-cardiovascular cell lineages in differentiating embryonic stem (ES) cells, which may be used in transplantation decisions to treat cardiovascular diseases. Despite its developmental and clinical importance in cardiovascular tissues, the transcriptional regulatory system of Flk1 has remained unclear. Here, we report a novel enhancer of the mouse Flk1 gene directing early mesodermal expression during development as well as ES differentiation. The enhancer enriches various mesodermal progenitors, such as primitive erythropoietic progenitors, hemangioblast (BL-CFC) and cardiovascular progenitors (CV-CFC). The enhancer is activated by Bmp, Wnt and Fgf, and it contains Gata-, Cdx-, Tcf/Lef-, ER71/Etv2- and Fox-binding sites, some of which are bound specifically by each of these transcription factors. As these transcription factors are known to act under the control of the Bmp, Wnt and Fgf families, early Flk1 expression may be induced by cooperative interactions between Gata, Tcf/Lef, Cdx and ER71/Etv2 under the control of Bmp, Wnt and Fgf signaling. The enhancer is required for early Flk1 expression and for hemangioblast development during ES differentiation.

Details

ISSN :
14779129 and 09501991
Volume :
138
Database :
OpenAIRE
Journal :
Development
Accession number :
edsair.doi.dedup.....a51c88178592f14024a2b962f319f769
Full Text :
https://doi.org/10.1242/dev.065565