A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle
Hubert PauschiD, Simon Ammermueller, Christine WurmseriD, Henning Hamann, Jens TetensiD, Cord Droegemueller, Ruedi FriesiD
Abstract
BackgroundThe widespread use of individual sires for artificial insemination promotes the propagation of recessive conditions. Inadvertent matings between unnoticed carriers of deleterious alleles may result in the manifestation of fatal phenotypes in their progeny. Breeding consultants and farmers reported on Vorderwald calves with a congenital skin disease. The clinical findings in affected calves were compatible with epidermolysis bullosa.\n\nResultsPedigree analysis indicated autosomal recessive inheritance of epidermolysis bullosa in Vorderwald cattle. We genotyped two diseased and 41 healthy animals at 41,436 single nucleotide polymorphisms and performed whole-genome haplotype-based association testing, which allowed us to map the locus responsible for the skin disease to the distal end of bovine chromosome 22 (P=8.0x10-14). The analysis of whole-genome re-sequencing data of one diseased calf, three obligate mutation carriers and 1682 healthy animals from various bovine breeds revealed a nonsense mutation (rs876174537, p.Arg1588X) in the COL7A1 gene that segregates with the disease. The same mutation was previously detected in three calves with dystrophic epidermolysis bullosa from the Rotes H[o]ehenvieh cattle breed. We show that diseased animals from Vorderwald and Rotes H[o]ehenvieh cattle are identical by descent for an 8.72 Mb haplotype encompassing rs876174537 indicating they inherited the deleterious allele from a recent common ancestor.\n\nConclusionsAutosomal recessive epidermolysis bullosa in Vorderwald and Rotes H[o]ehenvieh cattle is caused by a nonsense mutation in the COL7A1 gene. Our findings demonstrate that recessive deleterious alleles may segregate across cattle populations without apparent admixture. The identification of the causal mutation now enables the reliable detection of carriers of the defective allele. Genome-based mating strategies can avoid inadvertent matings of carrier animals thereby preventing the birth of homozygous calves that suffer from a painful skin disease.
02 /Specification & Classification
Click any tag to browse matching papers- Assay
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A missense mutation in TUBD1 is associated with high juvenile mortality in Braunvieh and Fleckvieh cattle
Hermann Schwarzenbacher, Johann Burgstaller, … Hubert Pausch·bioRxiv·May 3, 2016
- Identification of two independent COL5A1 variants in dogs with Ehlers Danlos syndrome
Anina Bauer, John F. Bateman, … Fiona L. Bateman·GenesPeer-reviewed·Sep 21, 2019
- An endogenous retrovirus insertion disrupting bovine ALKBH8 causes a failure-to-thrive syndrome with immunodeficiency associated with juvenile mortality in Brown Swiss cattle
S. Glatthard, Naveen Kumar Kadri, … Joana G. P. Jacinto·bioRxiv·Jul 10, 2026
- A frameshift mutation in GON4L is associated with proportionate dwarfism in Fleckvieh cattle
Hermann Schwarzenbacher, Christine Wurmser, … Hubert Pausch·Genetics Selection EvolutionPeer-reviewed·Mar 31, 2016
- Therapeutic base and prime editing of COL7A1 mutations in recessive dystrophic epidermolysis bullosa
S.-a. Hong, S.-E. Kim, … S. E. Lee·bioRxiv·Jul 12, 2021
- Inheritance of a Single Edited CD46 Allele Is Associated with Reduced Ex Vivo Susceptibility to Bovine Viral Diarrhea Virus
Aspen M. Workman, Alexandria C Krueger, … Brian L. Vander Ley·bioRxiv·Sep 1, 2026