4.7 Article

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

Journal

DEVELOPMENT
Volume 138, Issue 24, Pages 5357-5368

Publisher

COMPANY OF BIOLOGISTS LTD
DOI: 10.1242/dev.065565

Keywords

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

Funding

  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

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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.

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