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Tracing the history of LINE and SINE extinction in sigmodontine rodents

BACKGROUND: L1 retrotransposons have co-evolved with their mammalian hosts for the entire history of mammals and currently compose ~ 20% of a mammalian genome. B1 retrotransposons are dependent on L1 for retrotransposition and span the evolutionary history of rodents since their radiation. L1s were...

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Autores principales: Yang, Lei, Scott, LuAnn, Wichman, Holly A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6530004/
https://www.ncbi.nlm.nih.gov/pubmed/31139266
http://dx.doi.org/10.1186/s13100-019-0164-5
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author Yang, Lei
Scott, LuAnn
Wichman, Holly A.
author_facet Yang, Lei
Scott, LuAnn
Wichman, Holly A.
author_sort Yang, Lei
collection PubMed
description BACKGROUND: L1 retrotransposons have co-evolved with their mammalian hosts for the entire history of mammals and currently compose ~ 20% of a mammalian genome. B1 retrotransposons are dependent on L1 for retrotransposition and span the evolutionary history of rodents since their radiation. L1s were found to have lost their activity in a group of South American rodents, the Sigmodontinae, and B1 inactivation preceded the extinction of L1 in the same group. Consequently, a basal group of sigmodontines have active L1s but inactive B1s and a derived clade have both inactive L1s and B1s. It has been suggested that B1s became extinct during a long period of L1 quiescence and that L1s subsequently reemerged in the basal group. RESULTS: Here we investigate the evolutionary histories of L1 and B1 in the sigmodontine rodents and show that L1 activity continued until after the L1-extinct clade and the basal group diverged. After the split, L1 had a small burst of activity in the former group, followed by extinction. In the basal group, activity was initially low but was followed by a dramatic increase in L1 activity. We found the last wave of B1 retrotransposition was large and probably preceded the split between the two rodent clades. CONCLUSIONS: Given that L1s had been steadily retrotransposing during the time corresponding to B1 extinction and that the burst of B1 activity preceding B1 extinction was large, we conclude that B1 extinction was not a result of L1 quiescence. Rather, the burst of B1 activity may have contributed to L1 extinction both by competition with L1 and by putting strong selective pressure on the host to control retrotransposition. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13100-019-0164-5) contains supplementary material, which is available to authorized users.
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spelling pubmed-65300042019-05-28 Tracing the history of LINE and SINE extinction in sigmodontine rodents Yang, Lei Scott, LuAnn Wichman, Holly A. Mob DNA Research BACKGROUND: L1 retrotransposons have co-evolved with their mammalian hosts for the entire history of mammals and currently compose ~ 20% of a mammalian genome. B1 retrotransposons are dependent on L1 for retrotransposition and span the evolutionary history of rodents since their radiation. L1s were found to have lost their activity in a group of South American rodents, the Sigmodontinae, and B1 inactivation preceded the extinction of L1 in the same group. Consequently, a basal group of sigmodontines have active L1s but inactive B1s and a derived clade have both inactive L1s and B1s. It has been suggested that B1s became extinct during a long period of L1 quiescence and that L1s subsequently reemerged in the basal group. RESULTS: Here we investigate the evolutionary histories of L1 and B1 in the sigmodontine rodents and show that L1 activity continued until after the L1-extinct clade and the basal group diverged. After the split, L1 had a small burst of activity in the former group, followed by extinction. In the basal group, activity was initially low but was followed by a dramatic increase in L1 activity. We found the last wave of B1 retrotransposition was large and probably preceded the split between the two rodent clades. CONCLUSIONS: Given that L1s had been steadily retrotransposing during the time corresponding to B1 extinction and that the burst of B1 activity preceding B1 extinction was large, we conclude that B1 extinction was not a result of L1 quiescence. Rather, the burst of B1 activity may have contributed to L1 extinction both by competition with L1 and by putting strong selective pressure on the host to control retrotransposition. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13100-019-0164-5) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-21 /pmc/articles/PMC6530004/ /pubmed/31139266 http://dx.doi.org/10.1186/s13100-019-0164-5 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Yang, Lei
Scott, LuAnn
Wichman, Holly A.
Tracing the history of LINE and SINE extinction in sigmodontine rodents
title Tracing the history of LINE and SINE extinction in sigmodontine rodents
title_full Tracing the history of LINE and SINE extinction in sigmodontine rodents
title_fullStr Tracing the history of LINE and SINE extinction in sigmodontine rodents
title_full_unstemmed Tracing the history of LINE and SINE extinction in sigmodontine rodents
title_short Tracing the history of LINE and SINE extinction in sigmodontine rodents
title_sort tracing the history of line and sine extinction in sigmodontine rodents
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6530004/
https://www.ncbi.nlm.nih.gov/pubmed/31139266
http://dx.doi.org/10.1186/s13100-019-0164-5
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