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H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing
DNA replication is a tightly regulated process that initiates from multiple replication origins and leads to the faithful transmission of the genetic material. For proper DNA replication, the chromatin surrounding origins needs to be remodeled. However, remarkably little is known on which epigenetic...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2015
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357704/ https://www.ncbi.nlm.nih.gov/pubmed/25712104 http://dx.doi.org/10.1093/nar/gkv090 |
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author | Rondinelli, Beatrice Schwerer, Hélène Antonini, Elena Gaviraghi, Marco Lupi, Alessio Frenquelli, Michela Cittaro, Davide Segalla, Simona Lemaitre, Jean-Marc Tonon, Giovanni |
author_facet | Rondinelli, Beatrice Schwerer, Hélène Antonini, Elena Gaviraghi, Marco Lupi, Alessio Frenquelli, Michela Cittaro, Davide Segalla, Simona Lemaitre, Jean-Marc Tonon, Giovanni |
author_sort | Rondinelli, Beatrice |
collection | PubMed |
description | DNA replication is a tightly regulated process that initiates from multiple replication origins and leads to the faithful transmission of the genetic material. For proper DNA replication, the chromatin surrounding origins needs to be remodeled. However, remarkably little is known on which epigenetic changes are required to allow the firing of replication origins. Here, we show that the histone demethylase KDM5C/JARID1C is required for proper DNA replication at early origins. JARID1C dictates the assembly of the pre-initiation complex, driving the binding to chromatin of the pre-initiation proteins CDC45 and PCNA, through the demethylation of the histone mark H3K4me3. Fork activation and histone H4 acetylation, additional early events involved in DNA replication, are not affected by JARID1C downregulation. All together, these data point to a prominent role for JARID1C in a specific phase of DNA replication in mammalian cells, through its demethylase activity on H3K4me3. |
format | Online Article Text |
id | pubmed-4357704 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-43577042015-03-20 H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing Rondinelli, Beatrice Schwerer, Hélène Antonini, Elena Gaviraghi, Marco Lupi, Alessio Frenquelli, Michela Cittaro, Davide Segalla, Simona Lemaitre, Jean-Marc Tonon, Giovanni Nucleic Acids Res Gene regulation, Chromatin and Epigenetics DNA replication is a tightly regulated process that initiates from multiple replication origins and leads to the faithful transmission of the genetic material. For proper DNA replication, the chromatin surrounding origins needs to be remodeled. However, remarkably little is known on which epigenetic changes are required to allow the firing of replication origins. Here, we show that the histone demethylase KDM5C/JARID1C is required for proper DNA replication at early origins. JARID1C dictates the assembly of the pre-initiation complex, driving the binding to chromatin of the pre-initiation proteins CDC45 and PCNA, through the demethylation of the histone mark H3K4me3. Fork activation and histone H4 acetylation, additional early events involved in DNA replication, are not affected by JARID1C downregulation. All together, these data point to a prominent role for JARID1C in a specific phase of DNA replication in mammalian cells, through its demethylase activity on H3K4me3. Oxford University Press 2015-03-11 2015-02-23 /pmc/articles/PMC4357704/ /pubmed/25712104 http://dx.doi.org/10.1093/nar/gkv090 Text en © The Author(s) 2015. Published by Oxford University Press on behalf of Nucleic Acids Research. 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 reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Gene regulation, Chromatin and Epigenetics Rondinelli, Beatrice Schwerer, Hélène Antonini, Elena Gaviraghi, Marco Lupi, Alessio Frenquelli, Michela Cittaro, Davide Segalla, Simona Lemaitre, Jean-Marc Tonon, Giovanni H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing |
title | H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing |
title_full | H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing |
title_fullStr | H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing |
title_full_unstemmed | H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing |
title_short | H3K4me3 demethylation by the histone demethylase KDM5C/JARID1C promotes DNA replication origin firing |
title_sort | h3k4me3 demethylation by the histone demethylase kdm5c/jarid1c promotes dna replication origin firing |
topic | Gene regulation, Chromatin and Epigenetics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4357704/ https://www.ncbi.nlm.nih.gov/pubmed/25712104 http://dx.doi.org/10.1093/nar/gkv090 |
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