A fate map of Tbx1 expressing cells reveals heterogeneity in the second cardiac field

Tuong Huynh, Li Chen, Phillip Terrell, Antonio Baldini

Research output: Contribution to journalArticlepeer-review


Tbx1 is required for the expansion of second heart field (SHF) cardiac progenitors destined to the outflow tract of the heart. Loss of Tbx1 causes heart defects in humans and mice. We report a novel Tbx1Cre knock-in allele that we use to fate map Tbx1-expressing cells during development in conjunction with a reporter and 3D image reconstruction. Tbx1 descendants constitute a mesodermal cell population that surrounds the primitive pharynx and approaches the arterial pole of the heart from lateral and posterior, but not anterior directions. These cells populate most of the outflow tract with the exception of the anterior portion, thus identifying a population of the SHF of distinct origin. Both myocardial and underlying endocardial layers were labeled, suggesting a common origin of these cell types. Finally, we show that Tbx1 Cre-positive and Tbx1Cre-negative cell descendants occupy discrete domains in the outflow tract throughout development.

Original languageEnglish
Pages (from-to)470-475
Number of pages6
Issue number7
Publication statusPublished - Jul 2007


  • Cardiovascular development
  • Cre-based cell fate mapping
  • Outflow tract of the heart
  • Second heart field
  • Tbx1

ASJC Scopus subject areas

  • Genetics


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