PDGFRA is a conserved HAND2 effector during early cardiac development

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.

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Publication Details

Journal
Nature Cardiovascular Research
Published
2024-12-10
DOI
https://doi.org/10.1038/s44161-024-00574-1
Citations
2
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
0.47

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article

PDGFRA is a conserved HAND2 effector during early cardiac development

Khrievono Kikhi, Dubravka Vučićević, Jeffrey E. Gretz, Samuel J. Capon et al.
2 citations
Nature Cardiovascular Research
Congenital heart defects research
0.47
article

PDGFRA is a conserved HAND2 effector during early cardiac development

Khrievono Kikhi, Dubravka Vučićević, Jeffrey E. Gretz, Samuel J. Capon, Kenny Mattonet, Anthony B. Firulli, Scott A. Lacadie, Stefan Günther, Joshua Bloomekatz, Miloslav Šanda, Deborah Yelon, Mario Looso, Sweta Talyan, Didier Y. R. Stainier, Marga Albu, Yanli Xu, Beth A. Firulli, Rupal Gehlot
article en
2 citations

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.

Nature Cardiovascular ResearchVol. 3(12)
Max Delbrück Center (DE), University of California San Diego (US), University of Mississippi (US), Max Planck Institute for Heart and Lung Research (DE), Indiana University – Purdue University Indianapolis (US)
European Commission, Max-Planck-Gesellschaft
Openalex Percentile: Top 34%
Congenital heart defects research
0.47
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