Cargando…
Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding
BACKGROUND: Retrotransposons play a central role in plant evolution and could be a powerful endogenous source of genetic and epigenetic variability for crop breeding. To ensure genome integrity several silencing mechanisms have evolved to repress retrotransposon mobility. Even though retrotransposon...
Autores principales: | , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501947/ https://www.ncbi.nlm.nih.gov/pubmed/28687080 http://dx.doi.org/10.1186/s13059-017-1265-4 |
_version_ | 1783248881964810240 |
---|---|
author | Thieme, Michael Lanciano, Sophie Balzergue, Sandrine Daccord, Nicolas Mirouze, Marie Bucher, Etienne |
author_facet | Thieme, Michael Lanciano, Sophie Balzergue, Sandrine Daccord, Nicolas Mirouze, Marie Bucher, Etienne |
author_sort | Thieme, Michael |
collection | PubMed |
description | BACKGROUND: Retrotransposons play a central role in plant evolution and could be a powerful endogenous source of genetic and epigenetic variability for crop breeding. To ensure genome integrity several silencing mechanisms have evolved to repress retrotransposon mobility. Even though retrotransposons fully depend on transcriptional activity of the host RNA polymerase II (Pol II) for their mobility, it was so far unclear whether Pol II is directly involved in repressing their activity. RESULTS: Here we show that plants defective in Pol II activity lose DNA methylation at repeat sequences and produce more extrachromosomal retrotransposon DNA upon stress in Arabidopsis and rice. We demonstrate that combined inhibition of both DNA methylation and Pol II activity leads to a strong stress-dependent mobilization of the heat responsive ONSEN retrotransposon in Arabidopsis seedlings. The progenies of these treated plants contain up to 75 new ONSEN insertions in their genome which are stably inherited over three generations of selfing. Repeated application of heat stress in progeny plants containing increased numbers of ONSEN copies does not result in increased activation of this transposon compared to control lines. Progenies with additional ONSEN copies show a broad panel of environment-dependent phenotypic diversity. CONCLUSIONS: We demonstrate that Pol II acts at the root of transposon silencing. This is important because it suggests that Pol II can regulate the speed of plant evolution by fine-tuning the amplitude of transposon mobility. Our findings show that it is now possible to study induced transposon bursts in plants and unlock their use to induce epigenetic and genetic diversity for crop breeding. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1265-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5501947 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-55019472017-07-10 Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding Thieme, Michael Lanciano, Sophie Balzergue, Sandrine Daccord, Nicolas Mirouze, Marie Bucher, Etienne Genome Biol Research BACKGROUND: Retrotransposons play a central role in plant evolution and could be a powerful endogenous source of genetic and epigenetic variability for crop breeding. To ensure genome integrity several silencing mechanisms have evolved to repress retrotransposon mobility. Even though retrotransposons fully depend on transcriptional activity of the host RNA polymerase II (Pol II) for their mobility, it was so far unclear whether Pol II is directly involved in repressing their activity. RESULTS: Here we show that plants defective in Pol II activity lose DNA methylation at repeat sequences and produce more extrachromosomal retrotransposon DNA upon stress in Arabidopsis and rice. We demonstrate that combined inhibition of both DNA methylation and Pol II activity leads to a strong stress-dependent mobilization of the heat responsive ONSEN retrotransposon in Arabidopsis seedlings. The progenies of these treated plants contain up to 75 new ONSEN insertions in their genome which are stably inherited over three generations of selfing. Repeated application of heat stress in progeny plants containing increased numbers of ONSEN copies does not result in increased activation of this transposon compared to control lines. Progenies with additional ONSEN copies show a broad panel of environment-dependent phenotypic diversity. CONCLUSIONS: We demonstrate that Pol II acts at the root of transposon silencing. This is important because it suggests that Pol II can regulate the speed of plant evolution by fine-tuning the amplitude of transposon mobility. Our findings show that it is now possible to study induced transposon bursts in plants and unlock their use to induce epigenetic and genetic diversity for crop breeding. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s13059-017-1265-4) contains supplementary material, which is available to authorized users. BioMed Central 2017-07-07 /pmc/articles/PMC5501947/ /pubmed/28687080 http://dx.doi.org/10.1186/s13059-017-1265-4 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Thieme, Michael Lanciano, Sophie Balzergue, Sandrine Daccord, Nicolas Mirouze, Marie Bucher, Etienne Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding |
title | Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding |
title_full | Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding |
title_fullStr | Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding |
title_full_unstemmed | Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding |
title_short | Inhibition of RNA polymerase II allows controlled mobilisation of retrotransposons for plant breeding |
title_sort | inhibition of rna polymerase ii allows controlled mobilisation of retrotransposons for plant breeding |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501947/ https://www.ncbi.nlm.nih.gov/pubmed/28687080 http://dx.doi.org/10.1186/s13059-017-1265-4 |
work_keys_str_mv | AT thiememichael inhibitionofrnapolymeraseiiallowscontrolledmobilisationofretrotransposonsforplantbreeding AT lancianosophie inhibitionofrnapolymeraseiiallowscontrolledmobilisationofretrotransposonsforplantbreeding AT balzerguesandrine inhibitionofrnapolymeraseiiallowscontrolledmobilisationofretrotransposonsforplantbreeding AT daccordnicolas inhibitionofrnapolymeraseiiallowscontrolledmobilisationofretrotransposonsforplantbreeding AT mirouzemarie inhibitionofrnapolymeraseiiallowscontrolledmobilisationofretrotransposonsforplantbreeding AT bucheretienne inhibitionofrnapolymeraseiiallowscontrolledmobilisationofretrotransposonsforplantbreeding |