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Transcriptome architecture across tissues in the pig

BACKGROUND: Artificial selection has resulted in animal breeds with extreme phenotypes. As an organism is made up of many different tissues and organs, each with its own genetic programme, it is pertinent to ask: How relevant is tissue in terms of total transcriptome variability? Which are the genes...

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Autores principales: Ferraz, André LJ, Ojeda, Ana, López-Béjar, Manel, Fernandes, Lana T, Castelló, Anna, Folch, Josep M, Pérez-Enciso, Miguel
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2008
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2335121/
https://www.ncbi.nlm.nih.gov/pubmed/18416811
http://dx.doi.org/10.1186/1471-2164-9-173
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author Ferraz, André LJ
Ojeda, Ana
López-Béjar, Manel
Fernandes, Lana T
Castelló, Anna
Folch, Josep M
Pérez-Enciso, Miguel
author_facet Ferraz, André LJ
Ojeda, Ana
López-Béjar, Manel
Fernandes, Lana T
Castelló, Anna
Folch, Josep M
Pérez-Enciso, Miguel
author_sort Ferraz, André LJ
collection PubMed
description BACKGROUND: Artificial selection has resulted in animal breeds with extreme phenotypes. As an organism is made up of many different tissues and organs, each with its own genetic programme, it is pertinent to ask: How relevant is tissue in terms of total transcriptome variability? Which are the genes most distinctly expressed between tissues? Does breed or sex equally affect the transcriptome across tissues? RESULTS: In order to gain insight on these issues, we conducted microarray expression profiling of 16 different tissues from four animals of two extreme pig breeds, Large White and Iberian, two males and two females. Mixed model analysis and neighbor – joining trees showed that tissues with similar developmental origin clustered closer than those with different embryonic origins. Often a sound biological interpretation was possible for overrepresented gene ontology categories within differentially expressed genes between groups of tissues. For instance, an excess of nervous system or muscle development genes were found among tissues of ectoderm or mesoderm origins, respectively. Tissue accounted for ~11 times more variability than sex or breed. Nevertheless, we were able to confidently identify genes with differential expression across tissues between breeds (33 genes) and between sexes (19 genes). The genes primarily affected by sex were overall different than those affected by breed or tissue. Interaction with tissue can be important for differentially expressed genes between breeds but not so much for genes whose expression differ between sexes. CONCLUSION: Embryonic development leaves an enduring footprint on the transcriptome. The interaction in gene × tissue for differentially expressed genes between breeds suggests that animal breeding has targeted differentially each tissue's transcriptome.
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spelling pubmed-23351212008-04-25 Transcriptome architecture across tissues in the pig Ferraz, André LJ Ojeda, Ana López-Béjar, Manel Fernandes, Lana T Castelló, Anna Folch, Josep M Pérez-Enciso, Miguel BMC Genomics Research Article BACKGROUND: Artificial selection has resulted in animal breeds with extreme phenotypes. As an organism is made up of many different tissues and organs, each with its own genetic programme, it is pertinent to ask: How relevant is tissue in terms of total transcriptome variability? Which are the genes most distinctly expressed between tissues? Does breed or sex equally affect the transcriptome across tissues? RESULTS: In order to gain insight on these issues, we conducted microarray expression profiling of 16 different tissues from four animals of two extreme pig breeds, Large White and Iberian, two males and two females. Mixed model analysis and neighbor – joining trees showed that tissues with similar developmental origin clustered closer than those with different embryonic origins. Often a sound biological interpretation was possible for overrepresented gene ontology categories within differentially expressed genes between groups of tissues. For instance, an excess of nervous system or muscle development genes were found among tissues of ectoderm or mesoderm origins, respectively. Tissue accounted for ~11 times more variability than sex or breed. Nevertheless, we were able to confidently identify genes with differential expression across tissues between breeds (33 genes) and between sexes (19 genes). The genes primarily affected by sex were overall different than those affected by breed or tissue. Interaction with tissue can be important for differentially expressed genes between breeds but not so much for genes whose expression differ between sexes. CONCLUSION: Embryonic development leaves an enduring footprint on the transcriptome. The interaction in gene × tissue for differentially expressed genes between breeds suggests that animal breeding has targeted differentially each tissue's transcriptome. BioMed Central 2008-04-16 /pmc/articles/PMC2335121/ /pubmed/18416811 http://dx.doi.org/10.1186/1471-2164-9-173 Text en Copyright © 2008 Ferraz 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
Ferraz, André LJ
Ojeda, Ana
López-Béjar, Manel
Fernandes, Lana T
Castelló, Anna
Folch, Josep M
Pérez-Enciso, Miguel
Transcriptome architecture across tissues in the pig
title Transcriptome architecture across tissues in the pig
title_full Transcriptome architecture across tissues in the pig
title_fullStr Transcriptome architecture across tissues in the pig
title_full_unstemmed Transcriptome architecture across tissues in the pig
title_short Transcriptome architecture across tissues in the pig
title_sort transcriptome architecture across tissues in the pig
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2335121/
https://www.ncbi.nlm.nih.gov/pubmed/18416811
http://dx.doi.org/10.1186/1471-2164-9-173
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