The Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes
AffiliationUniv Arizona, Coll Med, Dept Med
MetadataShow full item record
PublisherOXFORD UNIV PRESS
CitationThe Role of Retrotransposons in Gene Family Expansions in the Human and Mouse Genomes 2016, 8 (9):2632 Genome Biology and Evolution
JournalGenome Biology and Evolution
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/).
Collection InformationThis 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 email@example.com.
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.
VersionFinal published version
SponsorsNextGenProject [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]
- The role of retrotransposons in gene family expansions: insights from the mouse Abp gene family.
- Authors: Janoušek V, Karn RC, Laukaitis CM
- Issue date: 2013 May 29
- Long terminal repeat retrotransposons of Mus musculus.
- Authors: McCarthy EM, McDonald JF
- Issue date: 2004
- LTR-retrotransposons in plants: Engines of evolution.
- Authors: Galindo-González L, Mhiri C, Deyholos MK, Grandbastien MA
- Issue date: 2017 Aug 30
- Long terminal repeats power evolution of genes and gene expression programs in mammalian oocytes and zygotes.
- Authors: Franke V, Ganesh S, Karlic R, Malik R, Pasulka J, Horvat F, Kuzman M, Fulka H, Cernohorska M, Urbanova J, Svobodova E, Ma J, Suzuki Y, Aoki F, Schultz RM, Vlahovicek K, Svoboda P
- Issue date: 2017 Aug
- Comparative genomic analysis reveals multiple long terminal repeats, lineage-specific amplification, and frequent interelement recombination for Cassandra retrotransposon in pear (Pyrus bretschneideri Rehd.).
- Authors: Yin H, Du J, Li L, Jin C, Fan L, Li M, Wu J, Zhang S
- Issue date: 2014 Jun 4