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DNA repair synthesis and histone deposition partner during homologous recombination
Chromatin remodeling is critical for the regulation of the DNA damage response. We highlight findings from our recent study showing that the deposition of the histone variant H3.3 by the alpha-thalassemia mental retardation X-linked protein (ATRX) and the death domain associated protein (DAXX) chrom...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154852/ https://www.ncbi.nlm.nih.gov/pubmed/30263950 http://dx.doi.org/10.1080/23723556.2018.1511210 |
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author | Elbakry, Amira Juhász, Szilvia Mathes, Arthur Löbrich, Markus |
author_facet | Elbakry, Amira Juhász, Szilvia Mathes, Arthur Löbrich, Markus |
author_sort | Elbakry, Amira |
collection | PubMed |
description | Chromatin remodeling is critical for the regulation of the DNA damage response. We highlight findings from our recent study showing that the deposition of the histone variant H3.3 by the alpha-thalassemia mental retardation X-linked protein (ATRX) and the death domain associated protein (DAXX) chromatin remodeling complex regulates DNA repair synthesis during homologous recombination. |
format | Online Article Text |
id | pubmed-6154852 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-61548522019-09-05 DNA repair synthesis and histone deposition partner during homologous recombination Elbakry, Amira Juhász, Szilvia Mathes, Arthur Löbrich, Markus Mol Cell Oncol Author’s Views Chromatin remodeling is critical for the regulation of the DNA damage response. We highlight findings from our recent study showing that the deposition of the histone variant H3.3 by the alpha-thalassemia mental retardation X-linked protein (ATRX) and the death domain associated protein (DAXX) chromatin remodeling complex regulates DNA repair synthesis during homologous recombination. Taylor & Francis 2018-09-05 /pmc/articles/PMC6154852/ /pubmed/30263950 http://dx.doi.org/10.1080/23723556.2018.1511210 Text en © 2018 The Authors. Published with license by Taylor & Francis Group http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivatives License (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited, and is not altered, transformed, or built upon in any way. |
spellingShingle | Author’s Views Elbakry, Amira Juhász, Szilvia Mathes, Arthur Löbrich, Markus DNA repair synthesis and histone deposition partner during homologous recombination |
title | DNA repair synthesis and histone deposition partner during homologous recombination |
title_full | DNA repair synthesis and histone deposition partner during homologous recombination |
title_fullStr | DNA repair synthesis and histone deposition partner during homologous recombination |
title_full_unstemmed | DNA repair synthesis and histone deposition partner during homologous recombination |
title_short | DNA repair synthesis and histone deposition partner during homologous recombination |
title_sort | dna repair synthesis and histone deposition partner during homologous recombination |
topic | Author’s Views |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6154852/ https://www.ncbi.nlm.nih.gov/pubmed/30263950 http://dx.doi.org/10.1080/23723556.2018.1511210 |
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