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Evolutionary dynamics of transposable elements in bdelloid rotifers

Transposable elements (TEs) are selfish genomic parasites whose ability to spread autonomously is facilitated by sexual reproduction in their hosts. If hosts become obligately asexual, TE frequencies and dynamics are predicted to change dramatically, but the long-term outcome is unclear. Here, we te...

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Autores principales: Nowell, Reuben W, Wilson, Christopher G, Almeida, Pedro, Schiffer, Philipp H, Fontaneto, Diego, Becks, Lutz, Rodriguez, Fernando, Arkhipova, Irina R, Barraclough, Timothy G
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943196/
https://www.ncbi.nlm.nih.gov/pubmed/33543711
http://dx.doi.org/10.7554/eLife.63194
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author Nowell, Reuben W
Wilson, Christopher G
Almeida, Pedro
Schiffer, Philipp H
Fontaneto, Diego
Becks, Lutz
Rodriguez, Fernando
Arkhipova, Irina R
Barraclough, Timothy G
author_facet Nowell, Reuben W
Wilson, Christopher G
Almeida, Pedro
Schiffer, Philipp H
Fontaneto, Diego
Becks, Lutz
Rodriguez, Fernando
Arkhipova, Irina R
Barraclough, Timothy G
author_sort Nowell, Reuben W
collection PubMed
description Transposable elements (TEs) are selfish genomic parasites whose ability to spread autonomously is facilitated by sexual reproduction in their hosts. If hosts become obligately asexual, TE frequencies and dynamics are predicted to change dramatically, but the long-term outcome is unclear. Here, we test current theory using whole-genome sequence data from eight species of bdelloid rotifers, a class of invertebrates in which males are thus far unknown. Contrary to expectations, we find a variety of active TEs in bdelloid genomes, at an overall frequency within the range seen in sexual species. We find no evidence that TEs are spread by cryptic recombination or restrained by unusual DNA repair mechanisms. Instead, we find that that TE content evolves relatively slowly in bdelloids and that gene families involved in RNAi-mediated TE suppression have undergone significant expansion, which might mitigate the deleterious effects of active TEs and compensate for the consequences of long-term asexuality.
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spelling pubmed-79431962021-03-10 Evolutionary dynamics of transposable elements in bdelloid rotifers Nowell, Reuben W Wilson, Christopher G Almeida, Pedro Schiffer, Philipp H Fontaneto, Diego Becks, Lutz Rodriguez, Fernando Arkhipova, Irina R Barraclough, Timothy G eLife Evolutionary Biology Transposable elements (TEs) are selfish genomic parasites whose ability to spread autonomously is facilitated by sexual reproduction in their hosts. If hosts become obligately asexual, TE frequencies and dynamics are predicted to change dramatically, but the long-term outcome is unclear. Here, we test current theory using whole-genome sequence data from eight species of bdelloid rotifers, a class of invertebrates in which males are thus far unknown. Contrary to expectations, we find a variety of active TEs in bdelloid genomes, at an overall frequency within the range seen in sexual species. We find no evidence that TEs are spread by cryptic recombination or restrained by unusual DNA repair mechanisms. Instead, we find that that TE content evolves relatively slowly in bdelloids and that gene families involved in RNAi-mediated TE suppression have undergone significant expansion, which might mitigate the deleterious effects of active TEs and compensate for the consequences of long-term asexuality. eLife Sciences Publications, Ltd 2021-02-05 /pmc/articles/PMC7943196/ /pubmed/33543711 http://dx.doi.org/10.7554/eLife.63194 Text en © 2021, Nowell et al http://creativecommons.org/licenses/by/4.0/ http://creativecommons.org/licenses/by/4.0/This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Evolutionary Biology
Nowell, Reuben W
Wilson, Christopher G
Almeida, Pedro
Schiffer, Philipp H
Fontaneto, Diego
Becks, Lutz
Rodriguez, Fernando
Arkhipova, Irina R
Barraclough, Timothy G
Evolutionary dynamics of transposable elements in bdelloid rotifers
title Evolutionary dynamics of transposable elements in bdelloid rotifers
title_full Evolutionary dynamics of transposable elements in bdelloid rotifers
title_fullStr Evolutionary dynamics of transposable elements in bdelloid rotifers
title_full_unstemmed Evolutionary dynamics of transposable elements in bdelloid rotifers
title_short Evolutionary dynamics of transposable elements in bdelloid rotifers
title_sort evolutionary dynamics of transposable elements in bdelloid rotifers
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7943196/
https://www.ncbi.nlm.nih.gov/pubmed/33543711
http://dx.doi.org/10.7554/eLife.63194
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