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Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens

BACKGROUND: In chickens, three mutant alleles have been reported at the C locus, including the albino mutation, and the recessive white mutation, which is characterized by white plumage and pigmented eyes. The albino mutation was found to be a 6 bp deletion in the tyrosinase (TYR) gene. The present...

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Autores principales: Chang, Chung-Ming, Coville, Jean-Luc, Coquerelle, Gérard, Gourichon, David, Oulmouden, Ahmad, Tixier-Boichard, Michèle
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2006
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1373650/
https://www.ncbi.nlm.nih.gov/pubmed/16457736
http://dx.doi.org/10.1186/1471-2164-7-19
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author Chang, Chung-Ming
Coville, Jean-Luc
Coquerelle, Gérard
Gourichon, David
Oulmouden, Ahmad
Tixier-Boichard, Michèle
author_facet Chang, Chung-Ming
Coville, Jean-Luc
Coquerelle, Gérard
Gourichon, David
Oulmouden, Ahmad
Tixier-Boichard, Michèle
author_sort Chang, Chung-Ming
collection PubMed
description BACKGROUND: In chickens, three mutant alleles have been reported at the C locus, including the albino mutation, and the recessive white mutation, which is characterized by white plumage and pigmented eyes. The albino mutation was found to be a 6 bp deletion in the tyrosinase (TYR) gene. The present work describes an approach to identify the structural rearrangement in the TYR gene associated with the recessive white mutation. RESULTS: Molecular analysis of the chicken TYR gene has revealed a major structural difference (Restriction Fragment Length Polymorphism, RFLP) in the genomic DNA of the recessive white chicken. A major size difference of 7.7 kb was found in intron 4 of the TYR gene by long-range PCR. Molecular cloning and sequencing results showed the insertion of a complete avian retroviral sequence of the Avian Leukosis Virus (ALV) family. Several aberrant transcripts of the tyrosinase gene were found in 10 week old recessive white chickens but not in the homozygous wild type colored chicken. We established a rapid genotyping diagnostic test based on the discovery of this retroviral insertion. It shows that all homozygous carriers of this insertion had a white plumage in various chicken strains. Furthermore, it was possible to distinguish heterozygous carriers from homozygous normal chickens in a segregating line. CONCLUSION: In this study, we conclude that the insertion of a complete avian retroviral sequence in intron 4 of the tyrosinase gene is diagnostic of the recessive white mutation in chickens. This insertion causes aberrant transcripts lacking exon 5, and we propose that this insertion is the causal mutation for the recessive white allele in the chicken.
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spelling pubmed-13736502006-02-18 Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens Chang, Chung-Ming Coville, Jean-Luc Coquerelle, Gérard Gourichon, David Oulmouden, Ahmad Tixier-Boichard, Michèle BMC Genomics Research Article BACKGROUND: In chickens, three mutant alleles have been reported at the C locus, including the albino mutation, and the recessive white mutation, which is characterized by white plumage and pigmented eyes. The albino mutation was found to be a 6 bp deletion in the tyrosinase (TYR) gene. The present work describes an approach to identify the structural rearrangement in the TYR gene associated with the recessive white mutation. RESULTS: Molecular analysis of the chicken TYR gene has revealed a major structural difference (Restriction Fragment Length Polymorphism, RFLP) in the genomic DNA of the recessive white chicken. A major size difference of 7.7 kb was found in intron 4 of the TYR gene by long-range PCR. Molecular cloning and sequencing results showed the insertion of a complete avian retroviral sequence of the Avian Leukosis Virus (ALV) family. Several aberrant transcripts of the tyrosinase gene were found in 10 week old recessive white chickens but not in the homozygous wild type colored chicken. We established a rapid genotyping diagnostic test based on the discovery of this retroviral insertion. It shows that all homozygous carriers of this insertion had a white plumage in various chicken strains. Furthermore, it was possible to distinguish heterozygous carriers from homozygous normal chickens in a segregating line. CONCLUSION: In this study, we conclude that the insertion of a complete avian retroviral sequence in intron 4 of the tyrosinase gene is diagnostic of the recessive white mutation in chickens. This insertion causes aberrant transcripts lacking exon 5, and we propose that this insertion is the causal mutation for the recessive white allele in the chicken. BioMed Central 2006-02-05 /pmc/articles/PMC1373650/ /pubmed/16457736 http://dx.doi.org/10.1186/1471-2164-7-19 Text en Copyright © 2006 Chang et al; licensee BioMed Central Ltd.
spellingShingle Research Article
Chang, Chung-Ming
Coville, Jean-Luc
Coquerelle, Gérard
Gourichon, David
Oulmouden, Ahmad
Tixier-Boichard, Michèle
Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
title Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
title_full Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
title_fullStr Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
title_full_unstemmed Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
title_short Complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
title_sort complete association between a retroviral insertion in the tyrosinase gene and the recessive white mutation in chickens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1373650/
https://www.ncbi.nlm.nih.gov/pubmed/16457736
http://dx.doi.org/10.1186/1471-2164-7-19
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