AT-hook proteins stimulate induction of senescence markers triggered by 5-bromodeoxyuridine in mammalian cells

被引:20
|
作者
Satou, W
Suzuki, T
Noguchi, T
Ogino, H
Fujii, M
Ayusawa, D
机构
[1] Yokohama City Univ, Kihara Inst Biol Res, Yokohama, Kanagawa 2440813, Japan
[2] Yokohama City Univ, Grad Sch Integrated Sci, Yokohama, Kanagawa 2440813, Japan
关键词
cellular senescence; 5-bromodeoxyuridine; HMGI; AT-hook; heterochromatin;
D O I
10.1016/j.exger.2003.10.008
中图分类号
R592 [老年病学]; C [社会科学总论];
学科分类号
03 ; 0303 ; 100203 ;
摘要
5-Bromodeoxyuridine (BrdU) induces a phenomenon similar to cellular senescence in mammalian cells. To address an underlying molecular mechanism in this phenomenon, we assessed the role of AT-hook proteins that bind to the minor grooves of specific AT-rich sequences. We expressed DsRed-tagged HMGI, MATH2, and MATH20 proteins in HeLa cells in a doxycycline dependent manner. Modest expression of these proteins revealed no apparent effect on the cells although high levels of expression were toxic to the cells. In contrast, their modest expression in the presence of low concentrations of BrdU similarly and dose-dependently induced senescence markers examined, although the same concentrations of BrdU alone showed no obvious effect. In both cases, DsRed fluorescence was mainly observed as foci or intense dots on Hoechst 33342-staining regions. These distribution patterns were not changed by addition of BrdU. Since AT-hook domains can displace chromatin compacting proteins pre-bound on AT-rich sequences, these results suggest that chromatin unpacking is one of the factors stimulating expression of the senescence markers in human cells. (C) 2003 Elsevier Inc. All rights reserved.
引用
收藏
页码:173 / 179
页数:7
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