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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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Formato: | Texto |
Lenguaje: | English |
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Public Library of Science
2010
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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. |
format | Text |
id | pubmed-2908688 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT yangruolin characterizationandcomparisonofthetissuerelatedmodulesinhumanandmouse AT subing characterizationandcomparisonofthetissuerelatedmodulesinhumanandmouse |