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Characterization and Comparison of the Tissue-Related Modules in Human and Mouse

BACKGROUND: Due to the advances of high throughput technology and data-collection approaches, we are now in an unprecedented position to understand the evolution of organisms. Great efforts have characterized many individual genes responsible for the interspecies divergence, yet little is known abou...

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Detalles Bibliográficos
Autores principales: Yang, Ruolin, Su, Bing
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908688/
https://www.ncbi.nlm.nih.gov/pubmed/20661448
http://dx.doi.org/10.1371/journal.pone.0011730
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author Yang, Ruolin
Su, Bing
author_facet Yang, Ruolin
Su, Bing
author_sort Yang, Ruolin
collection PubMed
description BACKGROUND: Due to the advances of high throughput technology and data-collection approaches, we are now in an unprecedented position to understand the evolution of organisms. Great efforts have characterized many individual genes responsible for the interspecies divergence, yet little is known about the genome-wide divergence at a higher level. Modules, serving as the building blocks and operational units of biological systems, provide more information than individual genes. Hence, the comparative analysis between species at the module level would shed more light on the mechanisms underlying the evolution of organisms than the traditional comparative genomics approaches. RESULTS: We systematically identified the tissue-related modules using the iterative signature algorithm (ISA), and we detected 52 and 65 modules in the human and mouse genomes, respectively. The gene expression patterns indicate that all of these predicted modules have a high possibility of serving as real biological modules. In addition, we defined a novel quantity, “total constraint intensity,” a proxy of multiple constraints (of co-regulated genes and tissues where the co-regulation occurs) on the evolution of genes in module context. We demonstrate that the evolutionary rate of a gene is negatively correlated with its total constraint intensity. Furthermore, there are modules coding the same essential biological processes, while their gene contents have diverged extensively between human and mouse. CONCLUSIONS: Our results suggest that unlike the composition of module, which exhibits a great difference between human and mouse, the functional organization of the corresponding modules may evolve in a more conservative manner. Most importantly, our findings imply that similar biological processes can be carried out by different sets of genes from human and mouse, therefore, the functional data of individual genes from mouse may not apply to human in certain occasions.
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spelling pubmed-29086882010-07-26 Characterization and Comparison of the Tissue-Related Modules in Human and Mouse Yang, Ruolin Su, Bing PLoS One Research Article BACKGROUND: Due to the advances of high throughput technology and data-collection approaches, we are now in an unprecedented position to understand the evolution of organisms. Great efforts have characterized many individual genes responsible for the interspecies divergence, yet little is known about the genome-wide divergence at a higher level. Modules, serving as the building blocks and operational units of biological systems, provide more information than individual genes. Hence, the comparative analysis between species at the module level would shed more light on the mechanisms underlying the evolution of organisms than the traditional comparative genomics approaches. RESULTS: We systematically identified the tissue-related modules using the iterative signature algorithm (ISA), and we detected 52 and 65 modules in the human and mouse genomes, respectively. The gene expression patterns indicate that all of these predicted modules have a high possibility of serving as real biological modules. In addition, we defined a novel quantity, “total constraint intensity,” a proxy of multiple constraints (of co-regulated genes and tissues where the co-regulation occurs) on the evolution of genes in module context. We demonstrate that the evolutionary rate of a gene is negatively correlated with its total constraint intensity. Furthermore, there are modules coding the same essential biological processes, while their gene contents have diverged extensively between human and mouse. CONCLUSIONS: Our results suggest that unlike the composition of module, which exhibits a great difference between human and mouse, the functional organization of the corresponding modules may evolve in a more conservative manner. Most importantly, our findings imply that similar biological processes can be carried out by different sets of genes from human and mouse, therefore, the functional data of individual genes from mouse may not apply to human in certain occasions. Public Library of Science 2010-07-22 /pmc/articles/PMC2908688/ /pubmed/20661448 http://dx.doi.org/10.1371/journal.pone.0011730 Text en Yang, Su. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Yang, Ruolin
Su, Bing
Characterization and Comparison of the Tissue-Related Modules in Human and Mouse
title Characterization and Comparison of the Tissue-Related Modules in Human and Mouse
title_full Characterization and Comparison of the Tissue-Related Modules in Human and Mouse
title_fullStr Characterization and Comparison of the Tissue-Related Modules in Human and Mouse
title_full_unstemmed Characterization and Comparison of the Tissue-Related Modules in Human and Mouse
title_short Characterization and Comparison of the Tissue-Related Modules in Human and Mouse
title_sort characterization and comparison of the tissue-related modules in human and mouse
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2908688/
https://www.ncbi.nlm.nih.gov/pubmed/20661448
http://dx.doi.org/10.1371/journal.pone.0011730
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