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PDGFRA is a conserved HAND2 effector during early cardiac development

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Item Type:Article
Title:PDGFRA is a conserved HAND2 effector during early cardiac development
Creators Name:Xu, Y., Gehlot, R., Capon, S.J., Albu, M., Gretz, J., Bloomekatz, J., Mattonet, K., Vucicevic, D., Talyan, S., Kikhi, K., Günther, S., Looso, M., Firulli, B.A., Sanda, M., Firulli, A.B., Lacadie, S.A., Yelon, D. and Stainier, D.Y.R.
Abstract:The basic helix–loop–helix transcription factor HAND2 has multiple roles during vertebrate organogenesis, including cardiogenesis. However, much remains to be uncovered about its mechanism of action. Here, we show the generation of several hand2 mutant alleles in zebrafish and demonstrate that dimerization-deficient mutants display the null phenotype but DNA-binding-deficient mutants do not. Rescue experiments with Hand2 variants using a newly identified hand2 enhancer confirmed these observations. To identify Hand2 effectors critical for cardiogenesis, we analyzed the transcriptomes of hand2 loss- and gain-of-function embryonic cardiomyocytes and tested the function of eight candidate genes in vivo; pdgfra was most effective in rescuing myocardial migration in hand2 mutants. Accordingly, we identified a putative Hand2-binding region in the zebrafish pdgfra locus that is important for its expression. In addition, Hand2 loss- and gain-of-function experiments in mouse embryonic stem cell-derived cardiac cells decreased and increased Pdgfra expression, respectively. Altogether, these results further our mechanistic understanding of HAND2 function during early cardiogenesis.
Keywords:Basic Helix-Loop-Helix Transcription Factors, Binding Sites, Cardiac Myocytes, Cell Movement, Developmental Gene Expression Regulation, Genetically Modified Animals, Heart, Mouse Embryonic Stem Cells, Mutation, Organogenesis, Phenotype, Platelet-Derived Growth Factor alpha Receptor, Signal Transduction, Zebrafish Proteins, Animals, Mice, Zebrafish
Source:Nature Cardiovascular Research
ISSN:2731-0590
Publisher:Springer Nature
Volume:3
Number:12
Page Range:1531-1548
Date:December 2024
Official Publication:https://doi.org/10.1038/s44161-024-00574-1
PubMed:View item in PubMed

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