PUBLICATION

Cfdp1 Is Essential for Cardiac Development and Function

Authors
Giardoglou, P., Deloukas, P., Dedoussis, G., Beis, D.
ID
ZDB-PUB-230812-44
Date
2023
Source
Cells   12(15): (Journal)
Registered Authors
Beis, Dimitris
Keywords
arrythmias, bradycardia, cardiovascular development, cfdp1, coronary artery disease, zebrafish models of human disease
MeSH Terms
  • Zebrafish*/metabolism
  • Humans
  • Nuclear Proteins*/metabolism
  • Heart
  • Cardiovascular Diseases*
  • Animals
  • Phenotype
  • Wnt Signaling Pathway
(all 8)
PubMed
37566073 Full text @ Cells
Abstract
Cardiovascular diseases (CVDs) are the prevalent cause of mortality worldwide. A combination of environmental and genetic effectors modulates the risk of developing them. Thus, it is vital to identify candidate genes and elucidate their role in the manifestation of the disease. Large-scale human studies have revealed the implication of Craniofacial Development Protein 1 (CFDP1) in Coronary Artery Disease (CAD). CFDP1 belongs to the evolutionary conserved Bucentaur (BCNT) family, and to date, its function and mechanism of action in Cardiovascular Development are still unclear. We utilized zebrafish to investigate the role of cfdp1 in the developing heart due to the high genomic homology, similarity in heart physiology, and ease of experimental manipulations. We showed that cfdp1 was expressed during development, and we tested two morpholinos and generated a cfdp1 mutant line. The cfdp1-/- embryos developed arrhythmic hearts and exhibited defective cardiac performance, which led to a lethal phenotype. Findings from both knockdown and knockout experiments showed that abrogation of cfdp1 leads to downregulation of Wnt signaling in embryonic hearts during valve development but without affecting Notch activation in this process. The cfdp1 zebrafish mutant line provides a valuable tool for unveiling the novel mechanism of regulating cardiac physiology and function. cfdp1 is essential for cardiac development, a previously unreported phenotype most likely due to early lethality in mice. The detected phenotype of bradycardia and arrhythmias is an observation with potential clinical relevance for humans carrying heterozygous CFDP1 mutations and their risk of developing CAD.
Genes / Markers
Figures
Figure Gallery (8 images)
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Expression
Phenotype
Mutations / Transgenics
Allele Construct Type Affected Genomic Region
aa106
    Small Deletion
    ia5TgTransgenic Insertion
      s939TgTransgenic Insertion
        twu34TgTransgenic Insertion
          y1TgTransgenic Insertion
            1 - 5 of 5
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            Human Disease / Model
            No data available
            Sequence Targeting Reagents
            Target Reagent Reagent Type
            cfdp1CRISPR2-cfdp1CRISPR
            cfdp1MO2-cfdp1MRPHLNO
            cfdp1MO3-cfdp1MRPHLNO
            1 - 3 of 3
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            Fish
            Antibodies
            No data available
            Orthology
            No data available
            Engineered Foreign Genes
            Marker Marker Type Name
            EGFPEFGEGFP
            mCherryEFGmCherry
            1 - 2 of 2
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            Mapping
            No data available