XB-ART-54584
J Cardiovasc Dev Dis
2016 Jun 04;32:. doi: 10.3390/jcdd3020021.
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A Matter of the Heart: The African Clawed Frog Xenopus as a Model for Studying Vertebrate Cardiogenesis and Congenital Heart Defects.
Hempel A
,
Kühl M
.
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The African clawed frog, Xenopus, is a valuable non-mammalian model organism to investigate vertebrate heart development and to explore the underlying molecular mechanisms of human congenital heart defects (CHDs). In this review, we outline the similarities between Xenopus and mammalian cardiogenesis, and provide an overview of well-studied cardiac genes in Xenopus, which have been associated with congenital heart conditions. Additionally, we highlight advantages of modeling candidate genes derived from genome wide association studies (GWAS) in Xenopus and discuss commonly used techniques.
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Genes referenced: frzb2
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Figure 1. Early cardiogenesis in mouse (upper panel) and Xenopus (lower panel). During gastrulation myocardial progenitor cells arise from the mesoderm and migrate to the ventral midline to the anterior part of the embryo. The progenitor cells form the cardiac crescent (first heart field), which already includes differentiated cardiomyocytes. The primary heart tube is formed at the ventral midline, starts to beat and undergoes looping and further morphological remodeling. Subsequently, the different cardiac chambers are formed. Cr-Ca/D-V/A-P and R-L axes are indicated. A: anterior; Ca, caudal; Cr: cranial; D: dorsal; L: left; LA: left atrium; LV: left ventricle; OFT: outflow tract; PLA: primitive left atrium; P: posterior; PRA: primitive right atrium; R: right; RA: right atrium; RV: right ventricle; V: ventral. |
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