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Rapid evolution and conserved function of the piRNA pathway

Transposons are major genome constituents that can mobilize and trigger mutations, DNA breaks and chromosome rearrangements. Transposon silencing is particularly important in the germline, which is dedicated to transmission of the inherited genome. Piwi-interacting RNAs (piRNAs) guide a host defence...

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Detalles Bibliográficos
Autores principales: Parhad, Swapnil S., Theurkauf, William E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Royal Society 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367137/
https://www.ncbi.nlm.nih.gov/pubmed/30958115
http://dx.doi.org/10.1098/rsob.180181
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author Parhad, Swapnil S.
Theurkauf, William E.
author_facet Parhad, Swapnil S.
Theurkauf, William E.
author_sort Parhad, Swapnil S.
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description Transposons are major genome constituents that can mobilize and trigger mutations, DNA breaks and chromosome rearrangements. Transposon silencing is particularly important in the germline, which is dedicated to transmission of the inherited genome. Piwi-interacting RNAs (piRNAs) guide a host defence system that transcriptionally and post-transcriptionally silences transposons during germline development. While germline control of transposons by the piRNA pathway is conserved, many piRNA pathway genes are evolving rapidly under positive selection, and the piRNA biogenesis machinery shows remarkable phylogenetic diversity. Conservation of core function combined with rapid gene evolution is characteristic of a host–pathogen arms race, suggesting that transposons and the piRNA pathway are engaged in an evolutionary tug of war that is driving divergence of the biogenesis machinery. Recent studies suggest that this process may produce biochemical incompatibilities that contribute to reproductive isolation and species divergence.
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spelling pubmed-63671372019-02-22 Rapid evolution and conserved function of the piRNA pathway Parhad, Swapnil S. Theurkauf, William E. Open Biol Review Transposons are major genome constituents that can mobilize and trigger mutations, DNA breaks and chromosome rearrangements. Transposon silencing is particularly important in the germline, which is dedicated to transmission of the inherited genome. Piwi-interacting RNAs (piRNAs) guide a host defence system that transcriptionally and post-transcriptionally silences transposons during germline development. While germline control of transposons by the piRNA pathway is conserved, many piRNA pathway genes are evolving rapidly under positive selection, and the piRNA biogenesis machinery shows remarkable phylogenetic diversity. Conservation of core function combined with rapid gene evolution is characteristic of a host–pathogen arms race, suggesting that transposons and the piRNA pathway are engaged in an evolutionary tug of war that is driving divergence of the biogenesis machinery. Recent studies suggest that this process may produce biochemical incompatibilities that contribute to reproductive isolation and species divergence. The Royal Society 2018-12-26 /pmc/articles/PMC6367137/ /pubmed/30958115 http://dx.doi.org/10.1098/rsob.180181 Text en © 2019 The Authors. http://creativecommons.org/licenses/by/4.0/ Published by the Royal Society under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/, which permits unrestricted use, provided the original author and source are credited.
spellingShingle Review
Parhad, Swapnil S.
Theurkauf, William E.
Rapid evolution and conserved function of the piRNA pathway
title Rapid evolution and conserved function of the piRNA pathway
title_full Rapid evolution and conserved function of the piRNA pathway
title_fullStr Rapid evolution and conserved function of the piRNA pathway
title_full_unstemmed Rapid evolution and conserved function of the piRNA pathway
title_short Rapid evolution and conserved function of the piRNA pathway
title_sort rapid evolution and conserved function of the pirna pathway
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6367137/
https://www.ncbi.nlm.nih.gov/pubmed/30958115
http://dx.doi.org/10.1098/rsob.180181
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