Cargando…

Asexual reproduction reduces transposable element load in experimental yeast populations

Theory predicts that sexual reproduction can either facilitate or restrain transposable element (TE) accumulation by providing TEs with a means of spreading to all individuals in a population, versus facilitating TE load reduction via purifying selection. By quantifying genomic TE loads over time in...

Descripción completa

Detalles Bibliográficos
Autores principales: Bast, Jens, Jaron, Kamil S, Schuseil, Donovan, Roze, Denis, Schwander, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: eLife Sciences Publications, Ltd 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783261/
https://www.ncbi.nlm.nih.gov/pubmed/31486772
http://dx.doi.org/10.7554/eLife.48548
_version_ 1783457531317714944
author Bast, Jens
Jaron, Kamil S
Schuseil, Donovan
Roze, Denis
Schwander, Tanja
author_facet Bast, Jens
Jaron, Kamil S
Schuseil, Donovan
Roze, Denis
Schwander, Tanja
author_sort Bast, Jens
collection PubMed
description Theory predicts that sexual reproduction can either facilitate or restrain transposable element (TE) accumulation by providing TEs with a means of spreading to all individuals in a population, versus facilitating TE load reduction via purifying selection. By quantifying genomic TE loads over time in experimental sexual and asexual Saccharomyces cerevisiae populations, we provide direct evidence that TE loads decrease rapidly under asexual reproduction. We show, using simulations, that this reduction may occur via evolution of TE activity, most likely via increased excision rates. Thus, sex is a major driver of genomic TE loads and at the root of the success of TEs.
format Online
Article
Text
id pubmed-6783261
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher eLife Sciences Publications, Ltd
record_format MEDLINE/PubMed
spelling pubmed-67832612019-10-09 Asexual reproduction reduces transposable element load in experimental yeast populations Bast, Jens Jaron, Kamil S Schuseil, Donovan Roze, Denis Schwander, Tanja eLife Evolutionary Biology Theory predicts that sexual reproduction can either facilitate or restrain transposable element (TE) accumulation by providing TEs with a means of spreading to all individuals in a population, versus facilitating TE load reduction via purifying selection. By quantifying genomic TE loads over time in experimental sexual and asexual Saccharomyces cerevisiae populations, we provide direct evidence that TE loads decrease rapidly under asexual reproduction. We show, using simulations, that this reduction may occur via evolution of TE activity, most likely via increased excision rates. Thus, sex is a major driver of genomic TE loads and at the root of the success of TEs. eLife Sciences Publications, Ltd 2019-09-05 /pmc/articles/PMC6783261/ /pubmed/31486772 http://dx.doi.org/10.7554/eLife.48548 Text en © 2019, Bast 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
Bast, Jens
Jaron, Kamil S
Schuseil, Donovan
Roze, Denis
Schwander, Tanja
Asexual reproduction reduces transposable element load in experimental yeast populations
title Asexual reproduction reduces transposable element load in experimental yeast populations
title_full Asexual reproduction reduces transposable element load in experimental yeast populations
title_fullStr Asexual reproduction reduces transposable element load in experimental yeast populations
title_full_unstemmed Asexual reproduction reduces transposable element load in experimental yeast populations
title_short Asexual reproduction reduces transposable element load in experimental yeast populations
title_sort asexual reproduction reduces transposable element load in experimental yeast populations
topic Evolutionary Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6783261/
https://www.ncbi.nlm.nih.gov/pubmed/31486772
http://dx.doi.org/10.7554/eLife.48548
work_keys_str_mv AT bastjens asexualreproductionreducestransposableelementloadinexperimentalyeastpopulations
AT jaronkamils asexualreproductionreducestransposableelementloadinexperimentalyeastpopulations
AT schuseildonovan asexualreproductionreducestransposableelementloadinexperimentalyeastpopulations
AT rozedenis asexualreproductionreducestransposableelementloadinexperimentalyeastpopulations
AT schwandertanja asexualreproductionreducestransposableelementloadinexperimentalyeastpopulations