ATAD2 is an epigenetic reader of newly synthesized histone marks during DNA replication

被引:58
|
作者
Koo, Seong Joo [1 ]
Fernandez-Montalvan, Amaury E. [1 ]
Badock, Volker [1 ]
Ott, Christopher J. [2 ,3 ,4 ]
Holton, Simon J. [1 ]
von Ahsen, Oliver [1 ]
Toedling, Joern [1 ]
Vittori, Sarah [2 ,3 ]
Bradner, James E. [2 ,3 ,4 ,5 ]
Gorjanacz, Matyas [1 ]
机构
[1] Bayer Pharma AG, Drug Discovery, Berlin, Germany
[2] Broad Inst, Ctr Sci Therapeut, Cambridge, MA USA
[3] Dana Farber Canc Inst, Dept Med Oncol, Boston, MA 02115 USA
[4] Harvard Med Sch, Dept Med, Boston, MA USA
[5] Novartis Inst BioMed Res, Cambridge, MA USA
关键词
cancer; ATAD2; DNA replication; bromodomain; histone acetylation; POOR-PROGNOSIS; COREGULATOR ANCCA; CHROMATIN; ACETYLATION; BROMODOMAIN; MAINTENANCE; CANCER; REPAIR; H3; OVEREXPRESSION;
D O I
10.18632/oncotarget.11855
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
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 diacetylation-marks during replication.
引用
收藏
页码:70323 / 70335
页数:13
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