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Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages
Small RNA pathways act at the front line of defence against transposable elements across the Eukaryota. In animals, Piwi interacting small RNAs (piRNAs) are a crucial arm of this defence. However, the evolutionary relationships among piRNAs and other small RNA pathways targeting transposable element...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323106/ https://www.ncbi.nlm.nih.gov/pubmed/25668728 http://dx.doi.org/10.1371/journal.pbio.1002061 |
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author | Sarkies, Peter Selkirk, Murray E. Jones, John T. Blok, Vivian Boothby, Thomas Goldstein, Bob Hanelt, Ben Ardila-Garcia, Alex Fast, Naomi M. Schiffer, Phillip M. Kraus, Christopher Taylor, Mark J. Koutsovoulos, Georgios Blaxter, Mark L. Miska, Eric A. |
author_facet | Sarkies, Peter Selkirk, Murray E. Jones, John T. Blok, Vivian Boothby, Thomas Goldstein, Bob Hanelt, Ben Ardila-Garcia, Alex Fast, Naomi M. Schiffer, Phillip M. Kraus, Christopher Taylor, Mark J. Koutsovoulos, Georgios Blaxter, Mark L. Miska, Eric A. |
author_sort | Sarkies, Peter |
collection | PubMed |
description | Small RNA pathways act at the front line of defence against transposable elements across the Eukaryota. In animals, Piwi interacting small RNAs (piRNAs) are a crucial arm of this defence. However, the evolutionary relationships among piRNAs and other small RNA pathways targeting transposable elements are poorly resolved. To address this question we sequenced small RNAs from multiple, diverse nematode species, producing the first phylum-wide analysis of how small RNA pathways evolve. Surprisingly, despite their prominence in Caenorhabditis elegans and closely related nematodes, piRNAs are absent in all other nematode lineages. We found that there are at least two evolutionarily distinct mechanisms that compensate for the absence of piRNAs, both involving RNA-dependent RNA polymerases (RdRPs). Whilst one pathway is unique to nematodes, the second involves Dicer-dependent RNA-directed DNA methylation, hitherto unknown in animals, and bears striking similarity to transposon-control mechanisms in fungi and plants. Our results highlight the rapid, context-dependent evolution of small RNA pathways and suggest piRNAs in animals may have replaced an ancient eukaryotic RNA-dependent RNA polymerase pathway to control transposable elements. |
format | Online Article Text |
id | pubmed-4323106 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-43231062015-02-18 Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages Sarkies, Peter Selkirk, Murray E. Jones, John T. Blok, Vivian Boothby, Thomas Goldstein, Bob Hanelt, Ben Ardila-Garcia, Alex Fast, Naomi M. Schiffer, Phillip M. Kraus, Christopher Taylor, Mark J. Koutsovoulos, Georgios Blaxter, Mark L. Miska, Eric A. PLoS Biol Research Article Small RNA pathways act at the front line of defence against transposable elements across the Eukaryota. In animals, Piwi interacting small RNAs (piRNAs) are a crucial arm of this defence. However, the evolutionary relationships among piRNAs and other small RNA pathways targeting transposable elements are poorly resolved. To address this question we sequenced small RNAs from multiple, diverse nematode species, producing the first phylum-wide analysis of how small RNA pathways evolve. Surprisingly, despite their prominence in Caenorhabditis elegans and closely related nematodes, piRNAs are absent in all other nematode lineages. We found that there are at least two evolutionarily distinct mechanisms that compensate for the absence of piRNAs, both involving RNA-dependent RNA polymerases (RdRPs). Whilst one pathway is unique to nematodes, the second involves Dicer-dependent RNA-directed DNA methylation, hitherto unknown in animals, and bears striking similarity to transposon-control mechanisms in fungi and plants. Our results highlight the rapid, context-dependent evolution of small RNA pathways and suggest piRNAs in animals may have replaced an ancient eukaryotic RNA-dependent RNA polymerase pathway to control transposable elements. Public Library of Science 2015-02-10 /pmc/articles/PMC4323106/ /pubmed/25668728 http://dx.doi.org/10.1371/journal.pbio.1002061 Text en © 2015 Sarkies et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Sarkies, Peter Selkirk, Murray E. Jones, John T. Blok, Vivian Boothby, Thomas Goldstein, Bob Hanelt, Ben Ardila-Garcia, Alex Fast, Naomi M. Schiffer, Phillip M. Kraus, Christopher Taylor, Mark J. Koutsovoulos, Georgios Blaxter, Mark L. Miska, Eric A. Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages |
title | Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages |
title_full | Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages |
title_fullStr | Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages |
title_full_unstemmed | Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages |
title_short | Ancient and Novel Small RNA Pathways Compensate for the Loss of piRNAs in Multiple Independent Nematode Lineages |
title_sort | ancient and novel small rna pathways compensate for the loss of pirnas in multiple independent nematode lineages |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4323106/ https://www.ncbi.nlm.nih.gov/pubmed/25668728 http://dx.doi.org/10.1371/journal.pbio.1002061 |
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