POTENTIAL INVOLVEMENT OF A CONSTITUTIVE HEAT-SHOCK ELEMENT-BINDING FACTOR IN THE REGULATION OF CHEMICAL STRESS-INDUCED HSP70 GENE-EXPRESSION

被引:19
作者
LIU, RY [1 ]
CORRY, PM [1 ]
LEE, YJ [1 ]
机构
[1] WILLIAM BEAUMONT HOSP, DEPT RADIAT ONCOL, RES LABS, ROYAL OAK, MI 48073 USA
关键词
CHEMICAL STRESS; HSP70; SYNTHESIS; GENE REGULATION; HEAT SHOCK FACTORS;
D O I
10.1007/BF00926737
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
It was reported that chemical stresses such as arsenite, cadmium or salicylate fail to induce synthesis of the inducible form of HSP70 (HSP70i). We report here that exposure of cells to higher doses of these chemical treatments induced significant synthesis of HSP70i in CHO cells as well as other cell lines. The synthesis of HSP70i is primarily regulated at the transcriptional level. Although all tested chemical treatments induced heat shock factor (HSF) binding to the heat shock element (HSE), HSP70i synthesis appears to be regulated by an alternative factor (CHEF) which constitutively binds to the HSE at 37 degrees C. The treatments, which dissociate the HSE-CHBF complex, induced significant HSP70i synthesis. The treatments, which failed to induce HSP70i synthesis, still activated HSF binding to HSE but the HSE-CHBF complex remained as that of untreated control cells.
引用
收藏
页码:27 / 34
页数:8
相关论文
共 41 条
[1]   KEY FEATURES OF HEAT-SHOCK REGULATORY ELEMENTS [J].
AMIN, J ;
ANANTHAN, J ;
VOELLMY, R .
MOLECULAR AND CELLULAR BIOLOGY, 1988, 8 (09) :3761-3769
[2]   ABNORMAL PROTEINS SERVE AS EUKARYOTIC STRESS SIGNALS AND TRIGGER THE ACTIVATION OF HEAT-SHOCK GENES [J].
ANANTHAN, J ;
GOLDBERG, AL ;
VOELLMY, R .
SCIENCE, 1986, 232 (4749) :522-524
[3]  
AUGER EA, 1992, HYPERTHERMIC ONCOLOG, V1, P99
[4]   HEAT-SHOCK GENE-REGULATION BY NASCENT POLYPEPTIDES AND DENATURED PROTEINS - HSP70 AS A POTENTIAL AUTOREGULATORY FACTOR [J].
BALER, R ;
WELCH, WJ ;
VOELLMY, R .
JOURNAL OF CELL BIOLOGY, 1992, 117 (06) :1151-1159
[5]  
BRUCE JL, 1993, CANCER RES, V53, P12
[6]   POSSIBLE ROLE OF LOCALIZED PROTEIN DENATURATION IN THE MECHANISM OF INDUCTION OF THERMOTOLERANCE BY HEAT, SODIUM-ARSENITE AND ETHANOL [J].
BURGMAN, PWJJ ;
KAMPINGA, HH ;
KONINGS, AWT .
INTERNATIONAL JOURNAL OF HYPERTHERMIA, 1993, 9 (01) :151-162
[7]   HEAT-SHOCK RESPONSE IS ASSOCIATED WITH ENHANCED POSTISCHEMIC VENTRICULAR RECOVERY [J].
CURRIE, RW ;
KARMAZYN, M ;
KLOC, M ;
MAILER, K .
CIRCULATION RESEARCH, 1988, 63 (03) :543-549
[8]  
DAILEY HA, 1984, J BIOL CHEM, V259, P2711
[9]   ACTIVATION OF THE HEAT-SHOCK TRANSCRIPTION FACTOR BY HYPOXIA IN NORMAL AND TUMOR-CELL LINES INVIVO AND INVITRO [J].
GIACCIA, AJ ;
AUGER, EA ;
KOONG, A ;
TERRIS, DJ ;
MINCHINTON, AI ;
HAHN, GM ;
BROWN, JM .
INTERNATIONAL JOURNAL OF RADIATION ONCOLOGY BIOLOGY PHYSICS, 1992, 23 (04) :891-897
[10]   PRODUCTION OF ABNORMAL PROTEINS IN ESCHERICHIA-COLI STIMULATES TRANSCRIPTION OF ION AND OTHER HEAT-SHOCK GENES [J].
GOFF, SA ;
GOLDBERG, AL .
CELL, 1985, 41 (02) :587-595