<script type="text/javascript">
<!--
document.write('<div id="oa_widget"></div>');
document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=undefined&type=result"></script>');
-->
</script>Interactions between Cdx genes and retinoic acid modulate early cardiogenesis
 Copyright policy )
 Copyright policy )Interactions between Cdx genes and retinoic acid modulate early cardiogenesis
Cdx transcription factors regulate embryonic positional identities and have crucial roles in anteroposterior patterning (AP) processes of all three germ layers. Previously we have shown that the zebrafish homologues cdx1a and cdx4 redundantly regulate posterior mesodermal derivatives inducing embryonic blood cell fate specification and patterning of the embryonic kidney. Here we hypothesize that cdx factors restrict formation of anterior mesodermal derivatives such as cardiac cells by imposing posterior identity to developing mesodermal cells. We show that ectopic expression of Cdx1 or Cdx4 applied during the brief window of mesoderm patterning in differentiating murine embryonic stem cell (ESC) strongly suppresses cardiac development as assayed by expression of cardiac genes and formation of embryoid bodies (EB) containing "beating" cell clusters. Conversely, in loss-of-function studies performed in cdx-deficient zebrafish embryos, we observed a dose-dependent expansion of tbx5a(+) anterior-lateral plate mesoderm giving rise to cardiac progenitors. However, further cardiac development of these mesodermal cells required additional suppression of the retinoic acid (RA) pathway, possibly due to differential activity of inhibitory RA signals in cdx mutants. Together, our data suggest that cdx proteins affect cardiogenesis by regulating the formation of cardiogenic mesoderm and together with the RA pathway control the early development of cardiac precursor cells.
-  University of Tübingen Germany
-  Massachusetts General Hospital United States
-  Boston Children's Hospital United States
-  University of Auckland New Zealand
-  Howard Hughes Medical Institute United States
Male, Embryonic stem cells, Embryo, Nonmammalian, Cdx, Mesoderm, Mice, Retinoic acid, Basic Helix-Loop-Helix Transcription Factors, Animals, Myocytes, Cardiac, Molecular Biology, Zebrafish, Cells, Cultured, Embryoid Bodies, Embryonic Stem Cells, In Situ Hybridization, Homeodomain Proteins, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Regulation, Developmental, Cell Differentiation, Cell Biology, Embryo, Mammalian, Mutation, Female, T-Box Domain Proteins, Cardiac, Developmental Biology, Signal Transduction
Male, Embryonic stem cells, Embryo, Nonmammalian, Cdx, Mesoderm, Mice, Retinoic acid, Basic Helix-Loop-Helix Transcription Factors, Animals, Myocytes, Cardiac, Molecular Biology, Zebrafish, Cells, Cultured, Embryoid Bodies, Embryonic Stem Cells, In Situ Hybridization, Homeodomain Proteins, Reverse Transcriptase Polymerase Chain Reaction, Gene Expression Regulation, Developmental, Cell Differentiation, Cell Biology, Embryo, Mammalian, Mutation, Female, T-Box Domain Proteins, Cardiac, Developmental Biology, Signal Transduction
3 Research products, page 1 of 1
- 2017IsRelatedTo
- citations This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).- 47 - popularity This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.- Top 10% - influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).- Top 10% - impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.- Top 10% 
