Transcriptional regulation of the heavy subunit chain of γ-glutamylcysteine synthetase by ionizing radiation

被引:60
|
作者
Morales, A
Miranda, M
Sanchez-Reyes, A
Colell, A
Biete, A
Fernández-Checa, JC
机构
[1] Hosp Clin & Prov, CSIC UB, Inst Invest Biomed, Barcelona 08036, Spain
[2] Hosp Clin & Prov, Liver Unit, Barcelona 08036, Spain
[3] Univ Barcelona, Hosp Clin & Prov, Radiotherapy Unit, E-08036 Barcelona, Spain
来源
FEBS LETTERS | 1998年 / 427卷 / 01期
关键词
oxidative stress; gene regulation; glutathione; transcription factor; radiobiology; NF-kappa B; AP-1;
D O I
10.1016/S0014-5793(98)00381-0
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
Since glutathione (GSH) protects against oxidative stress, we determined the regulation of cellular GSH by ionizing radiation in human hepatoblastoma cells, HepG2, The levels of GSH increased in irradiated HepG2 due to a greater gamma-glutamylcysteine synthetase (gamma-GCS) activity, which was paralleled by gamma-GCS heavy subunit chain (gamma-GCS-HS) mRNA levels, Transcription of deletion constructs of the gamma-GCS-NS promoter cloned in a reporter vector was associated with activator protein-1 (AP-1), consistent with the DNA binding of AP-1 in nuclear extracts of irradiated HepG2, Hence, the transcriptional regulation of gamma-GCS by ionizing radiation emerges as an adaptive mechanism, which may be of significance to control the consequences of the oxidative stress induced by radiation. (C) 1998 Federation of European Biochemical Societies.
引用
收藏
页码:15 / 20
页数:6
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