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Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells

REV1-deficient chicken DT40 cells are compromised in replicating G quadruplex (G4)-forming DNA. This results in localised, stochastic loss of parental chromatin marks and changes in gene expression. We previously proposed that this epigenetic instability arises from G4-induced replication fork stall...

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Autores principales: Schiavone, Davide, Guilbaud, Guillaume, Murat, Pierre, Papadopoulou, Charikleia, Sarkies, Peter, Prioleau, Marie-Noëlle, Balasubramanian, Shankar, Sale, Julian E
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BlackWell Publishing Ltd 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282387/
https://www.ncbi.nlm.nih.gov/pubmed/25190518
http://dx.doi.org/10.15252/embj.201488398
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author Schiavone, Davide
Guilbaud, Guillaume
Murat, Pierre
Papadopoulou, Charikleia
Sarkies, Peter
Prioleau, Marie-Noëlle
Balasubramanian, Shankar
Sale, Julian E
author_facet Schiavone, Davide
Guilbaud, Guillaume
Murat, Pierre
Papadopoulou, Charikleia
Sarkies, Peter
Prioleau, Marie-Noëlle
Balasubramanian, Shankar
Sale, Julian E
author_sort Schiavone, Davide
collection PubMed
description REV1-deficient chicken DT40 cells are compromised in replicating G quadruplex (G4)-forming DNA. This results in localised, stochastic loss of parental chromatin marks and changes in gene expression. We previously proposed that this epigenetic instability arises from G4-induced replication fork stalls disrupting the accurate propagation of chromatin structure through replication. Here, we test this model by showing that a single G4 motif is responsible for the epigenetic instability of the BU-1 locus in REV1-deficient cells, despite its location 3.5 kb from the transcription start site (TSS). The effect of the G4 is dependent on it residing on the leading strand template, but is independent of its in vitro thermal stability. Moving the motif to more than 4 kb from the TSS stabilises expression of the gene. However, loss of histone modifications (H3K4me3 and H3K9/14ac) around the transcription start site correlates with the position of the G4 motif, expression being lost only when the promoter is affected. This supports the idea that processive replication is required to maintain the histone modification pattern and full transcription of this model locus.
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spelling pubmed-42823872015-01-15 Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells Schiavone, Davide Guilbaud, Guillaume Murat, Pierre Papadopoulou, Charikleia Sarkies, Peter Prioleau, Marie-Noëlle Balasubramanian, Shankar Sale, Julian E EMBO J Articles REV1-deficient chicken DT40 cells are compromised in replicating G quadruplex (G4)-forming DNA. This results in localised, stochastic loss of parental chromatin marks and changes in gene expression. We previously proposed that this epigenetic instability arises from G4-induced replication fork stalls disrupting the accurate propagation of chromatin structure through replication. Here, we test this model by showing that a single G4 motif is responsible for the epigenetic instability of the BU-1 locus in REV1-deficient cells, despite its location 3.5 kb from the transcription start site (TSS). The effect of the G4 is dependent on it residing on the leading strand template, but is independent of its in vitro thermal stability. Moving the motif to more than 4 kb from the TSS stabilises expression of the gene. However, loss of histone modifications (H3K4me3 and H3K9/14ac) around the transcription start site correlates with the position of the G4 motif, expression being lost only when the promoter is affected. This supports the idea that processive replication is required to maintain the histone modification pattern and full transcription of this model locus. BlackWell Publishing Ltd 2014-11-03 2014-09-04 /pmc/articles/PMC4282387/ /pubmed/25190518 http://dx.doi.org/10.15252/embj.201488398 Text en © 2014 MRC Laboratory of Molecular Biology. Published under the terms of the CC BY 4.0 license http://creativecommons.org/licenses/by/4.0/ This is an open access article under the terms of the Creative Commons Attribution 4.0 License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Articles
Schiavone, Davide
Guilbaud, Guillaume
Murat, Pierre
Papadopoulou, Charikleia
Sarkies, Peter
Prioleau, Marie-Noëlle
Balasubramanian, Shankar
Sale, Julian E
Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells
title Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells
title_full Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells
title_fullStr Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells
title_full_unstemmed Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells
title_short Determinants of G quadruplex-induced epigenetic instability in REV1-deficient cells
title_sort determinants of g quadruplex-induced epigenetic instability in rev1-deficient cells
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4282387/
https://www.ncbi.nlm.nih.gov/pubmed/25190518
http://dx.doi.org/10.15252/embj.201488398
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