TBX5 is required for embryonic cardiac cell cycle progression.

Journal Article (Journal Article)

Despite the critical importance of TBX5 in normal development and disease, relatively little is known about the mechanisms by which TBX5 functions in the embryonic heart. Our present studies demonstrate that TBX5 is necessary to control the length of the embryonic cardiac cell cycle, with depletion of TBX5 leading to cardiac cell cycle arrest in late G(1)- or early S-phase. Blocking cell cycle progression by TBX5 depletion leads to a decrease in cardiac cell number, an alteration in the timing of the cardiac differentiation program, defects in cardiac sarcomere formation, and ultimately, to cardiac programmed cell death. In these studies we have also established that terminally differentiated cardiomyocytes retain the capacity to undergo cell division. We further show that TBX5 is sufficient to determine the length of the embryonic cardiac cell cycle and the timing of the cardiac differentiation program. Thus, these studies establish a role for TBX5 in regulating the progression of the cardiac cell cycle.

Full Text

Duke Authors

Cited Authors

  • Goetz, SC; Brown, DD; Conlon, FL

Published Date

  • July 2006

Published In

Volume / Issue

  • 133 / 13

Start / End Page

  • 2575 - 2584

PubMed ID

  • 16728474

Pubmed Central ID

  • PMC1635805

International Standard Serial Number (ISSN)

  • 0950-1991

Digital Object Identifier (DOI)

  • 10.1242/dev.02420


  • eng

Conference Location

  • England