Reactivation of an embryonic cardiac neural crest transcriptional profile during zebrafish heart regeneration

During vertebrate development, the heart primarily arises from mesoderm, with crucial contributions from cardiac neural crest (CdNC) cells that migrate to the heart and form a variety of cardiovascular derivatives. Here, by integrating bulk and single cell RNA-seq with ATAC-seq, we identify a gene regulatory subcircuit specific to migratory cardiac crest cells composed of key transcription factors <i>egr1, sox9a, tfap2a,</i> and <i>ets1.</i> Notably, we show that cells expressing the canonical neural crest gene <i>sox10</i> are essential for proper cardiac regeneration in adult zebrafish. Furthermore, expression of all transcription factors from the migratory cardiac crest gene subcircuit are reactivated after injury at the wound edge. Together, our results uncover a developmental gene regulatory network that is important for CdNC fate determination, with key factors of the program reexpressed during regeneration.

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Publication Details

Journal
Proceedings of the National Academy of Sciences
Published
2025-06-18
DOI
https://doi.org/10.1073/pnas.2423697122
Citations
5
Primary Topic
Congenital heart defects research
Type
article
Field-Weighted Citation Impact
4.03

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article

Reactivation of an embryonic cardiac neural crest transcriptional profile during zebrafish heart regeneration

Rekha M. Dhillon-Richardson, Marianne E. Bronner-Fraser, Joseph K. McKenna, Alexandra K. Haugan et al.
5 citations
Proceedings of the National Academy of Sciences
Congenital heart defects research
4.03
article

Reactivation of an embryonic cardiac neural crest transcriptional profile during zebrafish heart regeneration

Rekha M. Dhillon-Richardson, Marianne E. Bronner-Fraser, Joseph K. McKenna, Alexandra K. Haugan, Megan L. Martik, Luke Lyons
article en
5 citations

Abstract

During vertebrate development, the heart primarily arises from mesoderm, with crucial contributions from cardiac neural crest (CdNC) cells that migrate to the heart and form a variety of cardiovascular derivatives. Here, by integrating bulk and single cell RNA-seq with ATAC-seq, we identify a gene regulatory subcircuit specific to migratory cardiac crest cells composed of key transcription factors <i>egr1, sox9a, tfap2a,</i> and <i>ets1.</i> Notably, we show that cells expressing the canonical neural crest gene <i>sox10</i> are essential for proper cardiac regeneration in adult zebrafish. Furthermore, expression of all transcription factors from the migratory cardiac crest gene subcircuit are reactivated after injury at the wound edge. Together, our results uncover a developmental gene regulatory network that is important for CdNC fate determination, with key factors of the program reexpressed during regeneration.

Proceedings of the National Academy of SciencesVol. 122(25)
California Institute of Technology (US), University of California, Berkeley (US)
American Heart Association, Shurl and Kay Curci Foundation, National Institutes of Health, National Heart, Lung, and Blood Institute
Openalex Percentile: Top 6%
Congenital heart defects research
4.03
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Reactivation of an embryonic cardiac neural crest transcriptional profile during zebrafish heart regeneration — Rekha M. Dhillon-Richardson, Marianne E. Bronner-Fraser, et al. · Proceedings of the National Academy of Sciences (2025) | TGRS Research Map | TGRS