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dc.contributor.authorJanoušek, Václav
dc.contributor.authorLaukaitis, Christina M.
dc.contributor.authorYanchukov, Alexey
dc.contributor.authorKarn, Robert C.
dc.date.accessioned2016-12-12T22:19:27Z
dc.date.available2016-12-12T22:19:27Z
dc.date.issued2016-09
dc.identifier.citationThe Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes 2016, 8 (9):2632 Genome Biology and Evolutionen
dc.identifier.issn1759-6653
dc.identifier.pmid27503295
dc.identifier.doi10.1093/gbe/evw192
dc.identifier.urihttp://hdl.handle.net/10150/621594
dc.description.abstractRetrotransposons 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.
dc.description.sponsorshipNextGenProject [CZ.1.07/2.3.00/20.0303]; Charles University in Prague Institutional Research Support [SVV 260 208/2015]; National Cancer Institute at the National Institutes of Health [U54 CA143924, P30 CA23074]; American Cancer Society [74-001-34-IRG]; Czech National Grid Infrastructure MetaCentrum running under the program "Projects of Large Research, Development, and Innovations Infrastructures" [CESNET LM2015042]en
dc.language.isoenen
dc.publisherOXFORD UNIV PRESSen
dc.relation.urlhttp://gbe.oxfordjournals.org/lookup/doi/10.1093/gbe/evw192en
dc.rights© The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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/).en
dc.rights.urihttps://creativecommons.org/licenses/by-nc/4.0/
dc.subjectgene familiesen
dc.subjecttransposable elementsen
dc.subjectretrotransposonsen
dc.subjectLINEen
dc.subjectLTRen
dc.subjectSINEen
dc.titleThe Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomesen
dc.typeArticleen
dc.contributor.departmentUniv Arizona, Coll Med, Dept Meden
dc.identifier.journalGenome Biology and Evolutionen
dc.description.collectioninformationThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at repository@u.library.arizona.edu.en
dc.eprint.versionFinal published versionen
refterms.dateFOA2018-07-02T07:56:49Z
html.description.abstractRetrotransposons 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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© The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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/).
Except where otherwise noted, this item's license is described as © The Author 2016. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution. 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/).