4.4 Article

Pitx2 regulates cardiac left-right asymmetry by patterning second cardiac lineage-derived myocardium

Journal

DEVELOPMENTAL BIOLOGY
Volume 296, Issue 2, Pages 437-449

Publisher

ACADEMIC PRESS INC ELSEVIER SCIENCE
DOI: 10.1016/j.ydbio.2006.06.009

Keywords

left-right asymmetry; secondary heart field; homeobox

Funding

  1. NEI NIH HHS [R01 EY014126, R01 EY 014126] Funding Source: Medline
  2. NHLBI NIH HHS [HL 64658, R01 HL074066, 1R01 HL 074066-01, UM1 HL128773, R01 HL064658, DP1 HL117649] Funding Source: Medline
  3. NIDCR NIH HHS [R01 DE 016329-01, R01 DE016329] Funding Source: Medline
  4. NIH HHS [DP1 OD006428] Funding Source: Medline

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Current models of left-right asymmetry hold that an early asymmetric signal is generated at the node and transduced to lateral plate mesoderm in a linear signal transduction cascade through the function of the Nodal signaling molecule. The Pitx2 homeobox gene functions at the final stages of this cascade to direct asymmetric morphogenesis of selected organs including the heart. We previously showed that Pitx2 regulated an asymmetric pathway that was independent of cardiac looping suggesting a second asymmetric cardiac pathway. It has been proposed that in the cardiac outflow tract Pitx2 functions in both cardiac neural crest, as a target of canonical Wnt-signaling, and in the mesoderm-derived cardiac second lineage. We used fate mapping, conditional loss of function, and chimera analysis in mice to investigate the role of Pitx2 in outflow tract morphogenesis. Our findings reveal that Pitx2 is dispensable in the cardiac neural crest but functions in second lineage myocardium revealing that this cardiac progenitor field is patterned asymmetrically. (c) 2006 Elsevier Inc. All rights reserved.

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