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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...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BlackWell Publishing Ltd
2014
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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. |
format | Online Article Text |
id | pubmed-4282387 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BlackWell Publishing Ltd |
record_format | MEDLINE/PubMed |
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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