UHRF1 recruits the histone acetyltransferase Tip60 and controls its expression and activity

被引:63
作者
Achour, Mayada
Fuhrmann, Guy
Alhosin, Mahmoud
Ronde, Philippe
Chataigneau, Thierry
Mousli, Marc [2 ]
Schini-Kerth, Valerie B.
Bronner, Christian [1 ]
机构
[1] Univ Strasbourg, Fac Pharm, CNRS UMR 7213, Lab Biophoton & Pharmacol, F-67401 Illkirch Graffenstaden, France
[2] Univ Strasbourg, Fac Med, Physiopathol & Med Translat EA4438, F-67000 Strasbourg, France
关键词
DNMT1; Epigenetic; Histone H2A; Tip60; UHRF1; DNA-DAMAGE RESPONSE; UBIQUITIN LIGASE ACTIVITY; CCAAT-BINDING-PROTEIN; II-ALPHA EXPRESSION; DOWN-REGULATION; SRA DOMAIN; G1/S TRANSITION; CANCER-CELLS; ICBP90; COMPLEX;
D O I
10.1016/j.bbrc.2009.09.131
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Tat-interactive protein, 60 kDa (Tip60) is a histone acetyltransferase with specificity toward lysine 5 of histone H2A (H2AK5) and plays Multiple roles in chromatin remodeling processes. Co-immunoprecipitation experiments performed on Jurkat cells, showed that Tip60 is present in the same macro-molecular complex as UHRF1 (Ubiquitin-like containing PHD and RING domain 1), DNMT1 (DNA methyltransferase 1), and HDAC1 (histone deacetylase 1). Furthermore, immunocytochemistry experiments confirmed that Tip60 co-localizes with the UHRF1/DNMT1 complex. Although down-regulation of UHRF1 by RNA interference enhanced Tip60 expression, a significant decrease of the level of acetylated H2AK5 was observed. Consistently, we have observed that down-regulation of Tip60 and DNMT1 by RNA interference, dramatically reduced the levels of acetylated H2AK5. Altogether, these results Suggest that Tip60 is a novel partner of the epigenetic integration platform interplayed by UHRF1, DNMT1 and HDAC1 involved in the epigenetic code replication. (C) 2009 Elsevier Inc. All rights reserved.
引用
收藏
页码:523 / 528
页数:6
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