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The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes

Retrotransposons comprise a large portion of mammalian genomes. They contribute to structural changes and more importantly to gene regulation. The expansion and diversification of gene families have been implicated as sources of evolutionary novelties. Given the roles retrotransposons play in genome...

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Autores principales: Janoušek, Václav, Laukaitis, Christina M., Yanchukov, Alexey, Karn, Robert C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631067/
https://www.ncbi.nlm.nih.gov/pubmed/27503295
http://dx.doi.org/10.1093/gbe/evw192
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author Janoušek, Václav
Laukaitis, Christina M.
Yanchukov, Alexey
Karn, Robert C.
author_facet Janoušek, Václav
Laukaitis, Christina M.
Yanchukov, Alexey
Karn, Robert C.
author_sort Janoušek, Václav
collection PubMed
description Retrotransposons comprise a large portion of mammalian genomes. They contribute to structural changes and more importantly to gene regulation. The expansion and diversification of gene families have been implicated as sources of evolutionary novelties. Given the roles retrotransposons play in genomes, their contribution to the evolution of gene families warrants further exploration. In this study, we found a significant association between two major retrotransposon classes, LINEs and LTRs, and lineage-specific gene family expansions in both the human and mouse genomes. The distribution and diversity differ between LINEs and LTRs, suggesting that each has a distinct involvement in gene family expansion. LTRs are associated with open chromatin sites surrounding the gene families, supporting their involvement in gene regulation, whereas LINEs may play a structural role promoting gene duplication. Our findings also suggest that gene family expansions, especially in the mouse genome, undergo two phases. The first phase is characterized by elevated deposition of LTRs and their utilization in reshaping gene regulatory networks. The second phase is characterized by rapid gene family expansion due to continuous accumulation of LINEs and it appears that, in some instances at least, this could become a runaway process. We provide an example in which this has happened and we present a simulation supporting the possibility of the runaway process. Altogether we provide evidence of the contribution of retrotransposons to the expansion and evolution of gene families. Our findings emphasize the putative importance of these elements in diversification and adaptation in the human and mouse lineages.
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spelling pubmed-56310672017-11-01 The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes Janoušek, Václav Laukaitis, Christina M. Yanchukov, Alexey Karn, Robert C. Genome Biol Evol Research Article Retrotransposons comprise a large portion of mammalian genomes. They contribute to structural changes and more importantly to gene regulation. The expansion and diversification of gene families have been implicated as sources of evolutionary novelties. Given the roles retrotransposons play in genomes, their contribution to the evolution of gene families warrants further exploration. In this study, we found a significant association between two major retrotransposon classes, LINEs and LTRs, and lineage-specific gene family expansions in both the human and mouse genomes. The distribution and diversity differ between LINEs and LTRs, suggesting that each has a distinct involvement in gene family expansion. LTRs are associated with open chromatin sites surrounding the gene families, supporting their involvement in gene regulation, whereas LINEs may play a structural role promoting gene duplication. Our findings also suggest that gene family expansions, especially in the mouse genome, undergo two phases. The first phase is characterized by elevated deposition of LTRs and their utilization in reshaping gene regulatory networks. The second phase is characterized by rapid gene family expansion due to continuous accumulation of LINEs and it appears that, in some instances at least, this could become a runaway process. We provide an example in which this has happened and we present a simulation supporting the possibility of the runaway process. Altogether we provide evidence of the contribution of retrotransposons to the expansion and evolution of gene families. Our findings emphasize the putative importance of these elements in diversification and adaptation in the human and mouse lineages. Oxford University Press 2016-08-08 /pmc/articles/PMC5631067/ /pubmed/27503295 http://dx.doi.org/10.1093/gbe/evw192 Text en © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com (http://journals.permissions@oup.com)
spellingShingle Research Article
Janoušek, Václav
Laukaitis, Christina M.
Yanchukov, Alexey
Karn, Robert C.
The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
title The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
title_full The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
title_fullStr The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
title_full_unstemmed The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
title_short The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
title_sort role of retrotransposons in gene family expansions in the human and mouse genomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631067/
https://www.ncbi.nlm.nih.gov/pubmed/27503295
http://dx.doi.org/10.1093/gbe/evw192
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