Mandibulofacial dysostosis attributed to a recessive mutation of CYP26C1 in hereford cattle

Renae L. Sieck, Anna M. Fuller, Patrick S. Bedwell, Jack A. Ward, Stacy K. Sanders, Shi Hua Xiang, Sichong Peng, Jessica L. Petersen, David J. Steffen

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

In spring 2020, six Hereford calves presented with congenital facial deformities attributed to a condition we termed mandibulofacial dysostosis (MD). Affected calves shared hallmark features of a variably shortened and/or asymmetric lower mandible and bilateral skin tags present 2–10 cm caudal to the commissure of the lips. Pedigree analysis revealed a single common ancestor shared by the sire and dam of each affected calf. Whole-genome sequencing (WGS) of 20 animals led to the discovery of a variant (Chr26 g. 14404993T>C) in Exon 3 of CYP26C1 associated with MD. This missense mutation (p.L188P), is located in an α helix of the protein, which the identified amino acid substitution is predicted to break. The implication of this mutation was further validated through genotyping 2 additional affected calves, 760 other Herefords, and by evaluation of available WGS data from over 2500 other individuals. Only the affected individuals were homozygous for the variant and all heterozygotes had at least one pedigree tie to the suspect founder. CYP26C1 plays a vital role in tissue-specific regulation of retinoic acid (RA) during embryonic development. Dysregulation of RA can result in teratogenesis by altering the endothelin-1 signaling pathway affecting the expression of Dlx genes, critical to mandibulofacial development. We postulate that this recessive missense mutation in CYP26C1 impacts the catalytic activity of the encoded enzyme, leading to excess RA resulting in the observed MD phenotype.

Original languageEnglish (US)
Article number1246
Pages (from-to)1-14
Number of pages14
JournalGenes
Volume11
Issue number11
DOIs
StatePublished - Nov 2020

Keywords

  • Animal models
  • Bos taurus
  • Congenital defect
  • De novo mutation
  • First pharyngeal arch
  • Retinoic acid signaling

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Fingerprint

Dive into the research topics of 'Mandibulofacial dysostosis attributed to a recessive mutation of CYP26C1 in hereford cattle'. Together they form a unique fingerprint.

Cite this