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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...

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Autores principales: Pérez Di Giorgio, Juliana Andrea, Lepage, Étienne, Tremblay-Belzile, Samuel, Truche, Sébastien, Loubert-Hudon, Audrey, Brisson, Normand
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
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.
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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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