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Global regulatory architecture of human, mouse and rat tissue transcriptomes

BACKGROUND: Predicting molecular responses in human by extrapolating results from model organisms requires a precise understanding of the architecture and regulation of biological mechanisms across species. RESULTS: Here, we present a large-scale comparative analysis of organ and tissue transcriptom...

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Autores principales: Prasad, Ajay, Kumar, Suchitra Suresh, Dessimoz, Christophe, Bleuler, Stefan, Laule, Oliver, Hruz, Tomas, Gruissem, Wilhelm, Zimmermann, Philip
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008137/
https://www.ncbi.nlm.nih.gov/pubmed/24138449
http://dx.doi.org/10.1186/1471-2164-14-716
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author Prasad, Ajay
Kumar, Suchitra Suresh
Dessimoz, Christophe
Bleuler, Stefan
Laule, Oliver
Hruz, Tomas
Gruissem, Wilhelm
Zimmermann, Philip
author_facet Prasad, Ajay
Kumar, Suchitra Suresh
Dessimoz, Christophe
Bleuler, Stefan
Laule, Oliver
Hruz, Tomas
Gruissem, Wilhelm
Zimmermann, Philip
author_sort Prasad, Ajay
collection PubMed
description BACKGROUND: Predicting molecular responses in human by extrapolating results from model organisms requires a precise understanding of the architecture and regulation of biological mechanisms across species. RESULTS: Here, we present a large-scale comparative analysis of organ and tissue transcriptomes involving the three mammalian species human, mouse and rat. To this end, we created a unique, highly standardized compendium of tissue expression. Representative tissue specific datasets were aggregated from more than 33,900 Affymetrix expression microarrays. For each organism, we created two expression datasets covering over 55 distinct tissue types with curated data from two independent microarray platforms. Principal component analysis (PCA) revealed that the tissue-specific architecture of transcriptomes is highly conserved between human, mouse and rat. Moreover, tissues with related biological function clustered tightly together, even if the underlying data originated from different labs and experimental settings. Overall, the expression variance caused by tissue type was approximately 10 times higher than the variance caused by perturbations or diseases, except for a subset of cancers and chemicals. Pairs of gene orthologs exhibited higher expression correlation between mouse and rat than with human. Finally, we show evidence that tissue expression profiles, if combined with sequence similarity, can improve the correct assignment of functionally related homologs across species. CONCLUSION: The results demonstrate that tissue-specific regulation is the main determinant of transcriptome composition and is highly conserved across mammalian species.
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spelling pubmed-40081372014-05-03 Global regulatory architecture of human, mouse and rat tissue transcriptomes Prasad, Ajay Kumar, Suchitra Suresh Dessimoz, Christophe Bleuler, Stefan Laule, Oliver Hruz, Tomas Gruissem, Wilhelm Zimmermann, Philip BMC Genomics Research Article BACKGROUND: Predicting molecular responses in human by extrapolating results from model organisms requires a precise understanding of the architecture and regulation of biological mechanisms across species. RESULTS: Here, we present a large-scale comparative analysis of organ and tissue transcriptomes involving the three mammalian species human, mouse and rat. To this end, we created a unique, highly standardized compendium of tissue expression. Representative tissue specific datasets were aggregated from more than 33,900 Affymetrix expression microarrays. For each organism, we created two expression datasets covering over 55 distinct tissue types with curated data from two independent microarray platforms. Principal component analysis (PCA) revealed that the tissue-specific architecture of transcriptomes is highly conserved between human, mouse and rat. Moreover, tissues with related biological function clustered tightly together, even if the underlying data originated from different labs and experimental settings. Overall, the expression variance caused by tissue type was approximately 10 times higher than the variance caused by perturbations or diseases, except for a subset of cancers and chemicals. Pairs of gene orthologs exhibited higher expression correlation between mouse and rat than with human. Finally, we show evidence that tissue expression profiles, if combined with sequence similarity, can improve the correct assignment of functionally related homologs across species. CONCLUSION: The results demonstrate that tissue-specific regulation is the main determinant of transcriptome composition and is highly conserved across mammalian species. BioMed Central 2013-10-20 /pmc/articles/PMC4008137/ /pubmed/24138449 http://dx.doi.org/10.1186/1471-2164-14-716 Text en Copyright © 2013 Prasad 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
Prasad, Ajay
Kumar, Suchitra Suresh
Dessimoz, Christophe
Bleuler, Stefan
Laule, Oliver
Hruz, Tomas
Gruissem, Wilhelm
Zimmermann, Philip
Global regulatory architecture of human, mouse and rat tissue transcriptomes
title Global regulatory architecture of human, mouse and rat tissue transcriptomes
title_full Global regulatory architecture of human, mouse and rat tissue transcriptomes
title_fullStr Global regulatory architecture of human, mouse and rat tissue transcriptomes
title_full_unstemmed Global regulatory architecture of human, mouse and rat tissue transcriptomes
title_short Global regulatory architecture of human, mouse and rat tissue transcriptomes
title_sort global regulatory architecture of human, mouse and rat tissue transcriptomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4008137/
https://www.ncbi.nlm.nih.gov/pubmed/24138449
http://dx.doi.org/10.1186/1471-2164-14-716
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