Involvement of the TIP60 histone acetylase complex in DNA repair and apoptosis

被引:871
作者
Ikura, T
Ogryzko, VV
Grigoriev, M
Groisman, R
Wang, J
Horikoshi, M
Scully, R
Qin, J
Nakatani, Y [1 ]
机构
[1] Dana Farber Canc Inst, Boston, MA 02115 USA
[2] NIDDKD, NIH, Bethesda, MD 20892 USA
[3] NICHHD, NIH, Bethesda, MD 20892 USA
[4] Harvard Univ, Sch Med, Boston, MA 02115 USA
[5] Baylor Coll Med, Dept Biochem, Houston, TX 77030 USA
[6] Baylor Coll Med, Dept Cell Biol, Houston, TX 77030 USA
[7] Univ Tokyo, Inst Mol & Cellular Biosci, Tokyo 1130032, Japan
[8] Japan Sci & Technol Corp, Exploratory Res Adv Technol, Horikoshi Gene Selector Project, Tsukuba, Ibaraki 3002635, Japan
关键词
D O I
10.1016/S0092-8674(00)00051-9
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
It is well known that histone acetylases are important chromatin modifiers and that they play a central role in chromatin transcription. Here, we present evidence for novel roles of histone acetylases. The TIP60 histone acetylase purifies as a multimeric protein complex. Besides histone acetylase activity on chromatin, the TIP60 complex possesses ATPase, DNA helicase, and structural DNA binding activities. Ectopic expression of mutated TIP60 lacking histone acetylase activity results in cells with defective double-strand DNA break repair. Importantly, the resulting cells lose their apoptotic competence, suggesting a defect in the cells' ability to signal the existence of DNA damage to the apoptotic machinery. These results indicate that the histone acetylase TIP60-containing complex plays a role in DNA repair and apoptosis.
引用
收藏
页码:463 / 473
页数:11
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