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Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles

BACKGROUND: Microarray profiling has the potential to illuminate the molecular processes that govern the phenotypic characteristics of porcine skeletal muscles, such as hypertrophy or atrophy, and the expression of specific fibre types. This information is not only important for understanding basic...

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Autores principales: Bai, Qianfan, McGillivray, Christine, da Costa, Nuno, Dornan, Saffron, Evans, Gary, Stear, Michael James, Chang, Kin-Chow
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2003
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC152649/
https://www.ncbi.nlm.nih.gov/pubmed/12611633
http://dx.doi.org/10.1186/1471-2164-4-8
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author Bai, Qianfan
McGillivray, Christine
da Costa, Nuno
Dornan, Saffron
Evans, Gary
Stear, Michael James
Chang, Kin-Chow
author_facet Bai, Qianfan
McGillivray, Christine
da Costa, Nuno
Dornan, Saffron
Evans, Gary
Stear, Michael James
Chang, Kin-Chow
author_sort Bai, Qianfan
collection PubMed
description BACKGROUND: Microarray profiling has the potential to illuminate the molecular processes that govern the phenotypic characteristics of porcine skeletal muscles, such as hypertrophy or atrophy, and the expression of specific fibre types. This information is not only important for understanding basic muscle biology but also provides underpinning knowledge for enhancing the efficiency of livestock production. RESULTS: We report on the de novo development of a composite skeletal muscle cDNA microarray, comprising 5500 clones from two developmentally distinct cDNA libraries (longissimus dorsi of a 50-day porcine foetus and the gastrocnemius of a 3-day-old pig). Clones selected for the microarray assembly were of low to moderate abundance, as indicated by colony hybridisation. We profiled the differential expression of genes between the psoas (red muscle) and the longissimus dorsi (white muscle), by co-hybridisation of Cy3 and Cy5 labelled cDNA derived from these two muscles. Results from seven microarray slides (replicates) correctly identified genes that were expected to be differentially expressed, as well as a number of novel candidate regulatory genes. Quantitative real-time RT-PCR on selected genes was used to confirm the results from the microarray. CONCLUSION: We have developed a porcine skeletal muscle cDNA microarray and have identified a number of candidate genes that could be involved in muscle phenotype determination, including several members of the casein kinase 2 signalling pathway.
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spelling pubmed-1526492003-04-05 Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles Bai, Qianfan McGillivray, Christine da Costa, Nuno Dornan, Saffron Evans, Gary Stear, Michael James Chang, Kin-Chow BMC Genomics Research Article BACKGROUND: Microarray profiling has the potential to illuminate the molecular processes that govern the phenotypic characteristics of porcine skeletal muscles, such as hypertrophy or atrophy, and the expression of specific fibre types. This information is not only important for understanding basic muscle biology but also provides underpinning knowledge for enhancing the efficiency of livestock production. RESULTS: We report on the de novo development of a composite skeletal muscle cDNA microarray, comprising 5500 clones from two developmentally distinct cDNA libraries (longissimus dorsi of a 50-day porcine foetus and the gastrocnemius of a 3-day-old pig). Clones selected for the microarray assembly were of low to moderate abundance, as indicated by colony hybridisation. We profiled the differential expression of genes between the psoas (red muscle) and the longissimus dorsi (white muscle), by co-hybridisation of Cy3 and Cy5 labelled cDNA derived from these two muscles. Results from seven microarray slides (replicates) correctly identified genes that were expected to be differentially expressed, as well as a number of novel candidate regulatory genes. Quantitative real-time RT-PCR on selected genes was used to confirm the results from the microarray. CONCLUSION: We have developed a porcine skeletal muscle cDNA microarray and have identified a number of candidate genes that could be involved in muscle phenotype determination, including several members of the casein kinase 2 signalling pathway. BioMed Central 2003-03-01 /pmc/articles/PMC152649/ /pubmed/12611633 http://dx.doi.org/10.1186/1471-2164-4-8 Text en Copyright © 2003 Bai et al; licensee BioMed Central Ltd. This is an Open Access article: verbatim copying and redistribution of this article are permitted in all media for any purpose, provided this notice is preserved along with the article's original URL.
spellingShingle Research Article
Bai, Qianfan
McGillivray, Christine
da Costa, Nuno
Dornan, Saffron
Evans, Gary
Stear, Michael James
Chang, Kin-Chow
Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles
title Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles
title_full Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles
title_fullStr Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles
title_full_unstemmed Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles
title_short Development of a porcine skeletal muscle cDNA microarray: analysis of differential transcript expression in phenotypically distinct muscles
title_sort development of a porcine skeletal muscle cdna microarray: analysis of differential transcript expression in phenotypically distinct muscles
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC152649/
https://www.ncbi.nlm.nih.gov/pubmed/12611633
http://dx.doi.org/10.1186/1471-2164-4-8
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