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New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs
BACKGROUND: Previously, in boars with extreme androstenone levels, differential expression of the CYP11A1 gene in the testes has been characterised. CYP11A1 is located in a region where a QTL influencing boar fat androstenone levels has been detected in a Large White pig population. Clarifying the r...
Autores principales: | , , , , |
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Formato: | Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098772/ https://www.ncbi.nlm.nih.gov/pubmed/21504607 http://dx.doi.org/10.1186/1297-9686-43-15 |
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author | Robic, Annie Le Mignon, Guillaume Fève, Katia Larzul, Catherine Riquet, Juliette |
author_facet | Robic, Annie Le Mignon, Guillaume Fève, Katia Larzul, Catherine Riquet, Juliette |
author_sort | Robic, Annie |
collection | PubMed |
description | BACKGROUND: Previously, in boars with extreme androstenone levels, differential expression of the CYP11A1 gene in the testes has been characterised. CYP11A1 is located in a region where a QTL influencing boar fat androstenone levels has been detected in a Large White pig population. Clarifying the role of CYP11A1 in boar taint is important because it catalyses the initial step of androstenone synthesis and also of steroid synthesis. RESULTS: A genome-wide association study located CYP11A1 at approximately 1300 kb upstream from SNP H3GA0021967, defining the centre of the region containing the QTL for androstenone variation. In this study, we partially sequenced the CYP11A1 gene and identified several new single nucleotide polymorphisms (SNP) within it. Characterisation of one animal, heterozygous for CYP11A1 testicular expression but homozygous for a haplotype of a large region containing CYP11A1, revealed that variation of CYP11A1 expression is probably regulated by a mutation located downstream from the SNP H3GA0021967. We analysed CYP11A1 expression in LW families according to haplotypes of the QTL region's centre. Effects of haplotypes on CYP11A1 expression and on androstenone accumulation were not concordant. CONCLUSION: This study shows that testicular expression of CYP11A1 is not solely responsible for the QTL influencing boar fat androstenone levels. As a conclusion, we propose to refute the hypothesis that a single mutation located near the centre of the QTL region could control androstenone accumulation in fat by regulating the CYP11A1 expression. |
format | Text |
id | pubmed-3098772 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-30987722011-05-21 New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs Robic, Annie Le Mignon, Guillaume Fève, Katia Larzul, Catherine Riquet, Juliette Genet Sel Evol Research BACKGROUND: Previously, in boars with extreme androstenone levels, differential expression of the CYP11A1 gene in the testes has been characterised. CYP11A1 is located in a region where a QTL influencing boar fat androstenone levels has been detected in a Large White pig population. Clarifying the role of CYP11A1 in boar taint is important because it catalyses the initial step of androstenone synthesis and also of steroid synthesis. RESULTS: A genome-wide association study located CYP11A1 at approximately 1300 kb upstream from SNP H3GA0021967, defining the centre of the region containing the QTL for androstenone variation. In this study, we partially sequenced the CYP11A1 gene and identified several new single nucleotide polymorphisms (SNP) within it. Characterisation of one animal, heterozygous for CYP11A1 testicular expression but homozygous for a haplotype of a large region containing CYP11A1, revealed that variation of CYP11A1 expression is probably regulated by a mutation located downstream from the SNP H3GA0021967. We analysed CYP11A1 expression in LW families according to haplotypes of the QTL region's centre. Effects of haplotypes on CYP11A1 expression and on androstenone accumulation were not concordant. CONCLUSION: This study shows that testicular expression of CYP11A1 is not solely responsible for the QTL influencing boar fat androstenone levels. As a conclusion, we propose to refute the hypothesis that a single mutation located near the centre of the QTL region could control androstenone accumulation in fat by regulating the CYP11A1 expression. BioMed Central 2011-04-19 /pmc/articles/PMC3098772/ /pubmed/21504607 http://dx.doi.org/10.1186/1297-9686-43-15 Text en Copyright ©2011 Robic 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 Robic, Annie Le Mignon, Guillaume Fève, Katia Larzul, Catherine Riquet, Juliette New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs |
title | New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs |
title_full | New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs |
title_fullStr | New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs |
title_full_unstemmed | New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs |
title_short | New investigations around CYP11A1 and its possible involvement in an androstenone QTL characterised in Large White pigs |
title_sort | new investigations around cyp11a1 and its possible involvement in an androstenone qtl characterised in large white pigs |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3098772/ https://www.ncbi.nlm.nih.gov/pubmed/21504607 http://dx.doi.org/10.1186/1297-9686-43-15 |
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