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Gene expression profiles in testis of pigs with extreme high and low levels of androstenone

BACKGROUND: Boar taint is a major obstacle when using uncastrated male pigs for swine production. One of the main compounds causing this taint is androstenone, a pheromone produced in porcine testis. Here we use microarrays to study the expression of thousands of genes simultaneously in testis of hi...

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Autores principales: Moe, Maren, Meuwissen, Theo, Lien, Sigbjørn, Bendixen, Christian, Wang, Xuefei, Conley, Lene Nagstrup, Berget, Ingunn, Tajet, Håvard, Grindflek, Eli
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2204014/
https://www.ncbi.nlm.nih.gov/pubmed/17988377
http://dx.doi.org/10.1186/1471-2164-8-405
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author Moe, Maren
Meuwissen, Theo
Lien, Sigbjørn
Bendixen, Christian
Wang, Xuefei
Conley, Lene Nagstrup
Berget, Ingunn
Tajet, Håvard
Grindflek, Eli
author_facet Moe, Maren
Meuwissen, Theo
Lien, Sigbjørn
Bendixen, Christian
Wang, Xuefei
Conley, Lene Nagstrup
Berget, Ingunn
Tajet, Håvard
Grindflek, Eli
author_sort Moe, Maren
collection PubMed
description BACKGROUND: Boar taint is a major obstacle when using uncastrated male pigs for swine production. One of the main compounds causing this taint is androstenone, a pheromone produced in porcine testis. Here we use microarrays to study the expression of thousands of genes simultaneously in testis of high and low androstenone boars. The study allows identification of genes and pathways associated with elevated androstenone levels, which is essential for recognising potential molecular markers for breeding purposes. RESULTS: Testicular tissue was collected from 60 boars, 30 with extreme high and 30 with extreme low levels of androstenone, from each of the two breeds Duroc and Norwegian Landrace. The samples were hybridised to porcine arrays containing 26,877 cDNA clones, detecting 563 and 160 genes that were differentially expressed (p < 0.01) in Duroc and Norwegian Landrace, respectively. Of these significantly up- and down-regulated clones, 72 were found to be common for the two breeds, suggesting the possibility of both general and breed specific mechanisms in regulation of, or response to androstenone levels in boars. Ten genes were chosen for verification of expression patterns by quantitative real competitive PCR and real-time PCR. As expected, our results point towards steroid hormone metabolism and biosynthesis as important biological processes for the androstenone levels, but other potential pathways were identified as well. Among these were oxidoreductase activity, ferric iron binding, iron ion binding and electron transport activities. Genes belonging to the cytochrome P450 and hydroxysteroid dehydrogenase families were highly up-regulated, in addition to several genes encoding different families of conjugation enzymes. Furthermore, a number of genes encoding transcription factors were found both up- and down-regulated. The high number of clones belonging to ferric iron and iron ion binding suggests an importance of these genes, and the association between these pathways and androstenone levels is not previously described. CONCLUSION: This study contributes to the understanding of the complex genetic system controlling and responding to androstenone levels in pig testis. The identification of new pathways and genes involved in the biosynthesis and metabolism of androstenone is an important first step towards finding molecular markers to reduce boar taint.
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spelling pubmed-22040142008-01-17 Gene expression profiles in testis of pigs with extreme high and low levels of androstenone Moe, Maren Meuwissen, Theo Lien, Sigbjørn Bendixen, Christian Wang, Xuefei Conley, Lene Nagstrup Berget, Ingunn Tajet, Håvard Grindflek, Eli BMC Genomics Research Article BACKGROUND: Boar taint is a major obstacle when using uncastrated male pigs for swine production. One of the main compounds causing this taint is androstenone, a pheromone produced in porcine testis. Here we use microarrays to study the expression of thousands of genes simultaneously in testis of high and low androstenone boars. The study allows identification of genes and pathways associated with elevated androstenone levels, which is essential for recognising potential molecular markers for breeding purposes. RESULTS: Testicular tissue was collected from 60 boars, 30 with extreme high and 30 with extreme low levels of androstenone, from each of the two breeds Duroc and Norwegian Landrace. The samples were hybridised to porcine arrays containing 26,877 cDNA clones, detecting 563 and 160 genes that were differentially expressed (p < 0.01) in Duroc and Norwegian Landrace, respectively. Of these significantly up- and down-regulated clones, 72 were found to be common for the two breeds, suggesting the possibility of both general and breed specific mechanisms in regulation of, or response to androstenone levels in boars. Ten genes were chosen for verification of expression patterns by quantitative real competitive PCR and real-time PCR. As expected, our results point towards steroid hormone metabolism and biosynthesis as important biological processes for the androstenone levels, but other potential pathways were identified as well. Among these were oxidoreductase activity, ferric iron binding, iron ion binding and electron transport activities. Genes belonging to the cytochrome P450 and hydroxysteroid dehydrogenase families were highly up-regulated, in addition to several genes encoding different families of conjugation enzymes. Furthermore, a number of genes encoding transcription factors were found both up- and down-regulated. The high number of clones belonging to ferric iron and iron ion binding suggests an importance of these genes, and the association between these pathways and androstenone levels is not previously described. CONCLUSION: This study contributes to the understanding of the complex genetic system controlling and responding to androstenone levels in pig testis. The identification of new pathways and genes involved in the biosynthesis and metabolism of androstenone is an important first step towards finding molecular markers to reduce boar taint. BioMed Central 2007-11-07 /pmc/articles/PMC2204014/ /pubmed/17988377 http://dx.doi.org/10.1186/1471-2164-8-405 Text en Copyright © 2007 Moe 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
Moe, Maren
Meuwissen, Theo
Lien, Sigbjørn
Bendixen, Christian
Wang, Xuefei
Conley, Lene Nagstrup
Berget, Ingunn
Tajet, Håvard
Grindflek, Eli
Gene expression profiles in testis of pigs with extreme high and low levels of androstenone
title Gene expression profiles in testis of pigs with extreme high and low levels of androstenone
title_full Gene expression profiles in testis of pigs with extreme high and low levels of androstenone
title_fullStr Gene expression profiles in testis of pigs with extreme high and low levels of androstenone
title_full_unstemmed Gene expression profiles in testis of pigs with extreme high and low levels of androstenone
title_short Gene expression profiles in testis of pigs with extreme high and low levels of androstenone
title_sort gene expression profiles in testis of pigs with extreme high and low levels of androstenone
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2204014/
https://www.ncbi.nlm.nih.gov/pubmed/17988377
http://dx.doi.org/10.1186/1471-2164-8-405
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