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Transcription is a major driving force for plastid genome instability in Arabidopsis
Though it is an essential process, transcription can be a source of genomic instability. For instance, it may generate RNA:DNA hybrids as the nascent transcript hybridizes with the complementary DNA template. These hybrids, called R-loops, act as a major cause of replication fork stalling and DNA br...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447228/ https://www.ncbi.nlm.nih.gov/pubmed/30943245 http://dx.doi.org/10.1371/journal.pone.0214552 |
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author | Pérez Di Giorgio, Juliana Andrea Lepage, Étienne Tremblay-Belzile, Samuel Truche, Sébastien Loubert-Hudon, Audrey Brisson, Normand |
author_facet | Pérez Di Giorgio, Juliana Andrea Lepage, Étienne Tremblay-Belzile, Samuel Truche, Sébastien Loubert-Hudon, Audrey Brisson, Normand |
author_sort | Pérez Di Giorgio, Juliana Andrea |
collection | PubMed |
description | Though it is an essential process, transcription can be a source of genomic instability. For instance, it may generate RNA:DNA hybrids as the nascent transcript hybridizes with the complementary DNA template. These hybrids, called R-loops, act as a major cause of replication fork stalling and DNA breaks. In this study, we show that lowering transcription and R-loop levels in plastids of Arabidopsis thaliana reduces DNA rearrangements and mitigates plastid genome instability phenotypes. This effect can be observed on a genome-wide scale, as the loss of the plastid sigma transcription factor SIG6 prevents DNA rearrangements by favoring conservative repair in the presence of ciprofloxacin-induced DNA damage or in the absence of plastid genome maintenance actors such as WHY1/WHY3, RECA1 and POLIB. Additionally, resolving R-loops by the expression of a plastid-targeted exogenous RNAse H1 produces similar results. We also show that highly-transcribed genes are more susceptible to DNA rearrangements, as increased transcription of the psbD operon by SIG5 correlates with more locus-specific rearrangements. The effect of transcription is not specific to Sigma factors, as decreased global transcription levels by mutation of heat-stress-induced factor HSP21, mutation of nuclear-encoded polymerase RPOTp, or treatment with transcription-inhibitor rifampicin all prevent the formation of plastid genome rearrangements, especially under induced DNA damage conditions. |
format | Online Article Text |
id | pubmed-6447228 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-64472282019-04-17 Transcription is a major driving force for plastid genome instability in Arabidopsis Pérez Di Giorgio, Juliana Andrea Lepage, Étienne Tremblay-Belzile, Samuel Truche, Sébastien Loubert-Hudon, Audrey Brisson, Normand PLoS One Research Article Though it is an essential process, transcription can be a source of genomic instability. For instance, it may generate RNA:DNA hybrids as the nascent transcript hybridizes with the complementary DNA template. These hybrids, called R-loops, act as a major cause of replication fork stalling and DNA breaks. In this study, we show that lowering transcription and R-loop levels in plastids of Arabidopsis thaliana reduces DNA rearrangements and mitigates plastid genome instability phenotypes. This effect can be observed on a genome-wide scale, as the loss of the plastid sigma transcription factor SIG6 prevents DNA rearrangements by favoring conservative repair in the presence of ciprofloxacin-induced DNA damage or in the absence of plastid genome maintenance actors such as WHY1/WHY3, RECA1 and POLIB. Additionally, resolving R-loops by the expression of a plastid-targeted exogenous RNAse H1 produces similar results. We also show that highly-transcribed genes are more susceptible to DNA rearrangements, as increased transcription of the psbD operon by SIG5 correlates with more locus-specific rearrangements. The effect of transcription is not specific to Sigma factors, as decreased global transcription levels by mutation of heat-stress-induced factor HSP21, mutation of nuclear-encoded polymerase RPOTp, or treatment with transcription-inhibitor rifampicin all prevent the formation of plastid genome rearrangements, especially under induced DNA damage conditions. Public Library of Science 2019-04-03 /pmc/articles/PMC6447228/ /pubmed/30943245 http://dx.doi.org/10.1371/journal.pone.0214552 Text en © 2019 Pérez Di Giorgio 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Pérez Di Giorgio, Juliana Andrea Lepage, Étienne Tremblay-Belzile, Samuel Truche, Sébastien Loubert-Hudon, Audrey Brisson, Normand Transcription is a major driving force for plastid genome instability in Arabidopsis |
title | Transcription is a major driving force for plastid genome instability in Arabidopsis |
title_full | Transcription is a major driving force for plastid genome instability in Arabidopsis |
title_fullStr | Transcription is a major driving force for plastid genome instability in Arabidopsis |
title_full_unstemmed | Transcription is a major driving force for plastid genome instability in Arabidopsis |
title_short | Transcription is a major driving force for plastid genome instability in Arabidopsis |
title_sort | transcription is a major driving force for plastid genome instability in arabidopsis |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6447228/ https://www.ncbi.nlm.nih.gov/pubmed/30943245 http://dx.doi.org/10.1371/journal.pone.0214552 |
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