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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...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2021
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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. |
format | Online Article Text |
id | pubmed-7943196 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
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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