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Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle
BACKGROUND: Quantitative Trait Loci (QTL) affecting meat tenderness have been reported on Bovine chromosome 10. Here we examine variation at the Calpain 3 (CAPN3) gene in cattle, a gene located within the confidence interval of the QTL, and which is a positional candidate gene based on the biochemic...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474649/ https://www.ncbi.nlm.nih.gov/pubmed/18590576 http://dx.doi.org/10.1186/1471-2156-9-41 |
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author | Barendse, William Harrison, Blair E Bunch, Rowan J Thomas, Merle B |
author_facet | Barendse, William Harrison, Blair E Bunch, Rowan J Thomas, Merle B |
author_sort | Barendse, William |
collection | PubMed |
description | BACKGROUND: Quantitative Trait Loci (QTL) affecting meat tenderness have been reported on Bovine chromosome 10. Here we examine variation at the Calpain 3 (CAPN3) gene in cattle, a gene located within the confidence interval of the QTL, and which is a positional candidate gene based on the biochemical activity of the protein. RESULTS: We identified single nucleotide polymorphisms (SNP) in the genomic sequence of the CAPN3 gene and tested three of these in a sample of 2189 cattle. Of the three SNP genotyped, the CAPN3:c.1538+225G>T had the largest significant additive effect, with an allele substitution effect in the Brahman of α = -0.144 kg, SE = 0.060, P = 0.016, and the polymorphism explained 1.7% of the residual phenotypic variance in that sample of the breed. Significant haplotype substitution effects were found for all three breeds, the Brahman, the Belmont Red, and the Santa Gertrudis. For the common haplotype, the haplotype substitution effect in the Brahman was α = 0.169 kg, SE = 0.056, P = 0.003. The effect of this gene was compared to Calpastatin in the same sample. The SNP show negligible frequencies in taurine breeds and low to moderate minor allele frequencies in zebu or composite animals. CONCLUSION: These associations confirm the location of a QTL for meat tenderness in this region of bovine chromosome 10. SNP in or near this gene may be responsible for part of the overall difference between taurine and zebu breeds in meat tenderness, and the greater variability in meat tenderness found in zebu and composite breeds. The evidence provided so far suggests that none of these tested SNP are causative mutations. |
format | Text |
id | pubmed-2474649 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-24746492008-07-17 Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle Barendse, William Harrison, Blair E Bunch, Rowan J Thomas, Merle B BMC Genet Research Article BACKGROUND: Quantitative Trait Loci (QTL) affecting meat tenderness have been reported on Bovine chromosome 10. Here we examine variation at the Calpain 3 (CAPN3) gene in cattle, a gene located within the confidence interval of the QTL, and which is a positional candidate gene based on the biochemical activity of the protein. RESULTS: We identified single nucleotide polymorphisms (SNP) in the genomic sequence of the CAPN3 gene and tested three of these in a sample of 2189 cattle. Of the three SNP genotyped, the CAPN3:c.1538+225G>T had the largest significant additive effect, with an allele substitution effect in the Brahman of α = -0.144 kg, SE = 0.060, P = 0.016, and the polymorphism explained 1.7% of the residual phenotypic variance in that sample of the breed. Significant haplotype substitution effects were found for all three breeds, the Brahman, the Belmont Red, and the Santa Gertrudis. For the common haplotype, the haplotype substitution effect in the Brahman was α = 0.169 kg, SE = 0.056, P = 0.003. The effect of this gene was compared to Calpastatin in the same sample. The SNP show negligible frequencies in taurine breeds and low to moderate minor allele frequencies in zebu or composite animals. CONCLUSION: These associations confirm the location of a QTL for meat tenderness in this region of bovine chromosome 10. SNP in or near this gene may be responsible for part of the overall difference between taurine and zebu breeds in meat tenderness, and the greater variability in meat tenderness found in zebu and composite breeds. The evidence provided so far suggests that none of these tested SNP are causative mutations. BioMed Central 2008-07-01 /pmc/articles/PMC2474649/ /pubmed/18590576 http://dx.doi.org/10.1186/1471-2156-9-41 Text en Copyright © 2008 Barendse et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Barendse, William Harrison, Blair E Bunch, Rowan J Thomas, Merle B Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
title | Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
title_full | Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
title_fullStr | Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
title_full_unstemmed | Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
title_short | Variation at the Calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
title_sort | variation at the calpain 3 gene is associated with meat tenderness in zebu and composite breeds of cattle |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2474649/ https://www.ncbi.nlm.nih.gov/pubmed/18590576 http://dx.doi.org/10.1186/1471-2156-9-41 |
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