A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle. Issue 1 (December 2016)
- Record Type:
- Journal Article
- Title:
- A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle. Issue 1 (December 2016)
- Main Title:
- A nonsense mutation in the COL7A1 gene causes epidermolysis bullosa in Vorderwald cattle
- Authors:
- Pausch, Hubert
Ammermüller, Simon
Wurmser, Christine
Hamann, Henning
Tetens, Jens
Drögemüller, Cord
Fries, Ruedi - Abstract:
- Abstract Background The 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. Results Pedigree 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 = 8.0 × 10−14 ). 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 theCOL7A1 gene that segregates with the disease. The same mutation was previously detected in three calves with dystrophic epidermolysis bullosa from the Rotes Höhenvieh cattle breed. We show that diseased animals from Vorderwald and Rotes Höhenvieh cattle are identical by descent for an 8.72 Mb haplotype encompassing rs876174537 indicating they inherited the deleterious allele from a recent common ancestor. ConclusionsAbstract Background The 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. Results Pedigree 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 = 8.0 × 10−14 ). 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 theCOL7A1 gene that segregates with the disease. The same mutation was previously detected in three calves with dystrophic epidermolysis bullosa from the Rotes Höhenvieh cattle breed. We show that diseased animals from Vorderwald and Rotes Höhenvieh cattle are identical by descent for an 8.72 Mb haplotype encompassing rs876174537 indicating they inherited the deleterious allele from a recent common ancestor. Conclusions Autosomal recessive epidermolysis bullosa in Vorderwald and Rotes Höhenvieh cattle is caused by a nonsense mutation in theCOL7A1 gene. Our findings demonstrate that deleterious alleles may segregate across cattle populations without apparent admixture. The identification of the causal mutation now enables the reliable detection of carrier animals. 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. … (more)
- Is Part Of:
- BMC genetics. Volume 17:Issue 1(2016)
- Journal:
- BMC genetics
- Issue:
- Volume 17:Issue 1(2016)
- Issue Display:
- Volume 17, Issue 1 (2016)
- Year:
- 2016
- Volume:
- 17
- Issue:
- 1
- Issue Sort Value:
- 2016-0017-0001-0000
- Page Start:
- 1
- Page End:
- 9
- Publication Date:
- 2016-12
- Subjects:
- Epidermolysis bullosa -- COL7A1 -- Nonsense mutation -- Skin disease -- Autosomal recessive
Genetics -- Periodicals
576.505 - Journal URLs:
- http://www.biomedcentral.com/bmcgenet/ ↗
http://www.pubmedcentral.nih.gov/tocrender.fcgi?journal=31 ↗
http://link.springer.com/ ↗ - DOI:
- 10.1186/s12863-016-0458-2 ↗
- Languages:
- English
- ISSNs:
- 1471-2156
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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