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ATF2对TIP60的调控调节了ATM的激活。

Regulation of TIP60 by ATF2 modulates ATM activation.

作者信息

Bhoumik Anindita, Singha Netai, O'Connell Matthew J, Ronai Ze'ev A

机构信息

Signal Transduction Program, Burnham Institute for Medical Research, La Jolla, California 92037, USA.

出版信息

J Biol Chem. 2008 Jun 20;283(25):17605-14. doi: 10.1074/jbc.M802030200. Epub 2008 Apr 8.

Abstract

TIP60 (HTATIP) is a histone acetyltransferase (HAT) whose function is critical in regulating ataxia-telangiectasia mutated (ATM) activation, gene expression, and chromatin acetylation in DNA repair. Here we show that under non-stressed conditions, activating transcription factor-2 (ATF2) in cooperation with Cul3 ubiquitin ligase promotes degradation of TIP60, thereby attenuating its HAT activity. Inhibiting either ATF2 or Cul3 expression by small interfering RNA stabilizes the TIP60 protein. ATF2 association with TIP60 on chromatin is decreased following exposure to ionizing radiation (IR), resulting in enhanced TIP60 stability and activity. We also identified a panel of melanoma and prostate cancer cell lines whose ATF2 expression is inversely correlated with TIP60 levels and ATM activation after IR. Inhibition of ATF2 expression in these lines restored TIP60 protein levels and both basal and IR-induced levels of ATM activity. Our study provides novel insight into regulation of ATM activation by ATF2-dependent control of TIP60 stability and activity.

摘要

TIP60(HTATIP)是一种组蛋白乙酰转移酶(HAT),其功能在调节共济失调毛细血管扩张症突变基因(ATM)激活、基因表达以及DNA修复中的染色质乙酰化方面至关重要。在此我们表明,在非应激条件下,激活转录因子2(ATF2)与Cul3泛素连接酶协同作用促进TIP60的降解,从而减弱其HAT活性。通过小干扰RNA抑制ATF2或Cul3的表达可使TIP60蛋白稳定。暴露于电离辐射(IR)后,ATF2与染色质上TIP60的结合减少,导致TIP60稳定性和活性增强。我们还鉴定出一组黑色素瘤和前列腺癌细胞系,其ATF2表达与IR后TIP60水平及ATM激活呈负相关。在这些细胞系中抑制ATF2表达可恢复TIP60蛋白水平以及基础和IR诱导的ATM活性水平。我们的研究为ATF2依赖的TIP60稳定性和活性调控对ATM激活的影响提供了新的见解。

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