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Evolution of orthologous tandemly arrayed gene clusters
BACKGROUND: Tandemly Arrayed Gene (TAG) clusters are groups of paralogous genes that are found adjacent on a chromosome. TAGs represent an important repertoire of genes in eukaryotes. In addition to tandem duplication events, TAG clusters are affected during their evolution by other mechanisms, such...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283317/ https://www.ncbi.nlm.nih.gov/pubmed/22152029 http://dx.doi.org/10.1186/1471-2105-12-S9-S2 |
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author | Tremblay Savard, Olivier Bertrand, Denis El-Mabrouk, Nadia |
author_facet | Tremblay Savard, Olivier Bertrand, Denis El-Mabrouk, Nadia |
author_sort | Tremblay Savard, Olivier |
collection | PubMed |
description | BACKGROUND: Tandemly Arrayed Gene (TAG) clusters are groups of paralogous genes that are found adjacent on a chromosome. TAGs represent an important repertoire of genes in eukaryotes. In addition to tandem duplication events, TAG clusters are affected during their evolution by other mechanisms, such as inversion and deletion events, that affect the order and orientation of genes. The DILTAG algorithm developed in [1] makes it possible to infer a set of optimal evolutionary histories explaining the evolution of a single TAG cluster, from an ancestral single gene, through tandem duplications (simple or multiple, direct or inverted), deletions and inversion events. RESULTS: We present a general methodology, which is an extension of DILTAG, for the study of the evolutionary history of a set of orthologous TAG clusters in multiple species. In addition to the speciation events reflected by the phylogenetic tree of the considered species, the evolutionary events that are taken into account are simple or multiple tandem duplications, direct or inverted, simple or multiple deletions, and inversions. We analysed the performance of our algorithm on simulated data sets and we applied it to the protocadherin gene clusters of human, chimpanzee, mouse and rat. CONCLUSIONS: Our results obtained on simulated data sets showed a good performance in inferring the total number and size distribution of duplication events. A limitation of the algorithm is however in dealing with multiple gene deletions, as the algorithm is highly exponential in this case, and becomes quickly intractable. |
format | Online Article Text |
id | pubmed-3283317 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-32833172012-02-22 Evolution of orthologous tandemly arrayed gene clusters Tremblay Savard, Olivier Bertrand, Denis El-Mabrouk, Nadia BMC Bioinformatics Proceedings BACKGROUND: Tandemly Arrayed Gene (TAG) clusters are groups of paralogous genes that are found adjacent on a chromosome. TAGs represent an important repertoire of genes in eukaryotes. In addition to tandem duplication events, TAG clusters are affected during their evolution by other mechanisms, such as inversion and deletion events, that affect the order and orientation of genes. The DILTAG algorithm developed in [1] makes it possible to infer a set of optimal evolutionary histories explaining the evolution of a single TAG cluster, from an ancestral single gene, through tandem duplications (simple or multiple, direct or inverted), deletions and inversion events. RESULTS: We present a general methodology, which is an extension of DILTAG, for the study of the evolutionary history of a set of orthologous TAG clusters in multiple species. In addition to the speciation events reflected by the phylogenetic tree of the considered species, the evolutionary events that are taken into account are simple or multiple tandem duplications, direct or inverted, simple or multiple deletions, and inversions. We analysed the performance of our algorithm on simulated data sets and we applied it to the protocadherin gene clusters of human, chimpanzee, mouse and rat. CONCLUSIONS: Our results obtained on simulated data sets showed a good performance in inferring the total number and size distribution of duplication events. A limitation of the algorithm is however in dealing with multiple gene deletions, as the algorithm is highly exponential in this case, and becomes quickly intractable. BioMed Central 2011-10-05 /pmc/articles/PMC3283317/ /pubmed/22152029 http://dx.doi.org/10.1186/1471-2105-12-S9-S2 Text en Copyright ©2011 Tremblay Savard 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 | Proceedings Tremblay Savard, Olivier Bertrand, Denis El-Mabrouk, Nadia Evolution of orthologous tandemly arrayed gene clusters |
title | Evolution of orthologous tandemly arrayed gene clusters |
title_full | Evolution of orthologous tandemly arrayed gene clusters |
title_fullStr | Evolution of orthologous tandemly arrayed gene clusters |
title_full_unstemmed | Evolution of orthologous tandemly arrayed gene clusters |
title_short | Evolution of orthologous tandemly arrayed gene clusters |
title_sort | evolution of orthologous tandemly arrayed gene clusters |
topic | Proceedings |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3283317/ https://www.ncbi.nlm.nih.gov/pubmed/22152029 http://dx.doi.org/10.1186/1471-2105-12-S9-S2 |
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