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ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication
ATAD2 (ATPase family AAA domain-containing protein 2) is a chromatin regulator harboring an AAA+ ATPase domain and a bromodomain, previously proposed to function as an oncogenic transcription co-factor. Here we suggest that ATAD2 is also required for DNA replication. ATAD2 is co-expressed with genes...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342555/ https://www.ncbi.nlm.nih.gov/pubmed/27612420 http://dx.doi.org/10.18632/oncotarget.11855 |
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author | Koo, Seong Joo Fernández-Montalván, Amaury E. Badock, Volker Ott, Christopher J. Holton, Simon J. von Ahsen, Oliver Toedling, Joern Vittori, Sarah Bradner, James E. Gorjánácz, Mátyás |
author_facet | Koo, Seong Joo Fernández-Montalván, Amaury E. Badock, Volker Ott, Christopher J. Holton, Simon J. von Ahsen, Oliver Toedling, Joern Vittori, Sarah Bradner, James E. Gorjánácz, Mátyás |
author_sort | Koo, Seong Joo |
collection | PubMed |
description | ATAD2 (ATPase family AAA domain-containing protein 2) is a chromatin regulator harboring an AAA+ ATPase domain and a bromodomain, previously proposed to function as an oncogenic transcription co-factor. Here we suggest that ATAD2 is also required for DNA replication. ATAD2 is co-expressed with genes involved in DNA replication in various cancer types and predominantly expressed in S phase cells where it localized on nascent chromatin (replication sites). Our extensive biochemical and cellular analyses revealed that ATAD2 is recruited to replication sites through a direct interaction with di-acetylated histone H4 at K5 and K12, indicative of newly synthesized histones during replication-coupled chromatin reassembly. Similar to ATAD2-depletion, ectopic expression of ATAD2 mutants that are deficient in binding to these di-acetylation marks resulted in reduced DNA replication and impaired loading of PCNA onto chromatin, suggesting relevance of ATAD2 in DNA replication. Taken together, our data show a novel function of ATAD2 in cancer and for the first time identify a reader of newly synthesized histone di-acetylation-marks during replication. |
format | Online Article Text |
id | pubmed-5342555 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-53425552017-03-24 ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication Koo, Seong Joo Fernández-Montalván, Amaury E. Badock, Volker Ott, Christopher J. Holton, Simon J. von Ahsen, Oliver Toedling, Joern Vittori, Sarah Bradner, James E. Gorjánácz, Mátyás Oncotarget Research Paper ATAD2 (ATPase family AAA domain-containing protein 2) is a chromatin regulator harboring an AAA+ ATPase domain and a bromodomain, previously proposed to function as an oncogenic transcription co-factor. Here we suggest that ATAD2 is also required for DNA replication. ATAD2 is co-expressed with genes involved in DNA replication in various cancer types and predominantly expressed in S phase cells where it localized on nascent chromatin (replication sites). Our extensive biochemical and cellular analyses revealed that ATAD2 is recruited to replication sites through a direct interaction with di-acetylated histone H4 at K5 and K12, indicative of newly synthesized histones during replication-coupled chromatin reassembly. Similar to ATAD2-depletion, ectopic expression of ATAD2 mutants that are deficient in binding to these di-acetylation marks resulted in reduced DNA replication and impaired loading of PCNA onto chromatin, suggesting relevance of ATAD2 in DNA replication. Taken together, our data show a novel function of ATAD2 in cancer and for the first time identify a reader of newly synthesized histone di-acetylation-marks during replication. Impact Journals LLC 2016-09-06 /pmc/articles/PMC5342555/ /pubmed/27612420 http://dx.doi.org/10.18632/oncotarget.11855 Text en Copyright: © 2016 Koo et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Koo, Seong Joo Fernández-Montalván, Amaury E. Badock, Volker Ott, Christopher J. Holton, Simon J. von Ahsen, Oliver Toedling, Joern Vittori, Sarah Bradner, James E. Gorjánácz, Mátyás ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication |
title | ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication |
title_full | ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication |
title_fullStr | ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication |
title_full_unstemmed | ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication |
title_short | ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication |
title_sort | atad2 is an epigenetic reader of newly synthesized histone marks during dna replication |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5342555/ https://www.ncbi.nlm.nih.gov/pubmed/27612420 http://dx.doi.org/10.18632/oncotarget.11855 |
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