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Identification of Thymosin β4 as an effector of Hand1-mediated vascular development

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  • Nicola Smart

    (Molecular Medicine Unit, UCL-Institute of Child Health)

  • Karina N. Dubé

    (Molecular Medicine Unit, UCL-Institute of Child Health)

  • Paul R. Riley

    (Molecular Medicine Unit, UCL-Institute of Child Health)

Abstract

The bHLH transcription factor Hand1 (Heart and neural crest-derived transcript-1) has a fundamental role in cardiovascular development; however, the molecular mechanisms have not been elucidated. In this paper we identify Thymosin β4 (Tβ4/Tmsb4x), which encodes an actin monomer-binding protein implicated in cell migration and angiogenesis, as a direct target of Hand1. We demonstrate that Hand1 binds an upstream regulatory region proximal to the promoter of Tβ4 at consensus Thing1 and E-Box sites and identify both activation and repression of Tβ4 by Hand1, through direct binding within either non-canonical or canonical E-boxes, providing new insight into gene regulation by bHLH transcription factors. Hand1-mediated activation of Tβ4 is essential for yolk sac vasculogenesis and embryonic survival, and administration of synthetic TB4 partially rescues yolk sac capillary plexus formation in Hand1-null embryos. Thus, we identify an in vivo downstream target of Hand1 and reveal impaired yolk sac vasculogenesis as a primary cause of early embryonic lethality following loss of this critical bHLH factor.

Suggested Citation

  • Nicola Smart & Karina N. Dubé & Paul R. Riley, 2010. "Identification of Thymosin β4 as an effector of Hand1-mediated vascular development," Nature Communications, Nature, vol. 1(1), pages 1-10, December.
  • Handle: RePEc:nat:natcom:v:1:y:2010:i:1:d:10.1038_ncomms1041
    DOI: 10.1038/ncomms1041
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