4.7 Article

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

期刊

DEVELOPMENT
卷 138, 期 24, 页码 5357-5368

出版社

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.065565

关键词

Cardiogenesis; Flk1 (Kdr); Hemangioblasts; Hematopoiesis; VEGF; Vasculogenesis; Mouse

资金

  1. Special Coordination Funds for Promoting Science and Technology
  2. PRESTO
  3. Japan Science and Technology Agency (JST)
  4. Ministry of Education, Culture, Sports, Science, and Technology, Japan [23122503]
  5. American Heart Association
  6. Grants-in-Aid for Scientific Research [21659043, 23122503] Funding Source: KAKEN

向作者/读者索取更多资源

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.

作者

我是这篇论文的作者
点击您的名字以认领此论文并将其添加到您的个人资料中。

评论

主要评分

4.7
评分不足

次要评分

新颖性
-
重要性
-
科学严谨性
-
评价这篇论文

推荐

暂无数据
暂无数据