Concentration-dependent effects of endogenous S-nitrosoglutathione on gene regulation by specificity proteins Sp3 and Sp1

被引:42
作者
Zaman, K [1 ]
Palmer, LA [1 ]
Doctor, A [1 ]
Hunt, JF [1 ]
Gaston, B [1 ]
机构
[1] Univ Virginia, Sch Med, Dept Pediat, Div Pulm Med, Charlottesville, VA 22908 USA
关键词
cystic fibrosis; cystic fibrosis transmembrane conductance regulator; S-nitrosoglutathione; S-nitrosylation; specificity protein 1;
D O I
10.1042/BJ20031687
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
The activities of certain nuclear regulatory proteins are modified by high concentrations of S-nitrosothiols associated with nitrosative stress. In the present study, we have studied the effect of physiological (low muM) concentrations of the endogenous S-nitrosothiol, GSNO (S-nitrosoglutathione), on the activities of nuclear regulatory proteins Sp3 and Sp1 (specificity proteins 3 and 1). Low concentrations of GSNO increased Sp3 binding, as well as Sp3-dependent transcription of the cystic fibrosis transmembrane conductance regulatory gene, cftr. However, higher GSNO levels prevented Sp3 binding, augmented Sp1 binding and prevented both cftr transcription and CFTR (cystic fibrosis transmembrane conductance regulator) expression. We conclude that low concentrations of GSNO favour Sp3 binding to 'house-keeping' genes such as cftr, whereas nitrosative stress-associated GSNO concentrations shut off Sp3-dependent transcription, possibly to redirect cellular resources. Since low micromolar concentrations of GSNO also increase the maturation and activity of a clinically common CFTR mutant, whereas higher concentrations have the opposite effect, these observations may have implications for dosing of S-nitrosylating agents used in cystic fibrosis clinical trials.
引用
收藏
页码:67 / 74
页数:8
相关论文
共 48 条
[1]   S-nitrosoglutathione induces functional ΔF508-CFTR in airway epithelial cells [J].
Andersson, C ;
Gaston, B ;
Roomans, GM .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2002, 297 (03) :552-557
[2]   CHEMICAL MECHANISMS UNDERLYING THE VASODILATOR AND PLATELET ANTI-AGGREGATING PROPERTIES OF S-NITROSO-N-ACETYL-DL-PENICILLAMINE AND S-NITROSOGLUTATHIONE [J].
ASKEW, SC ;
BUTLER, AR ;
FLITNEY, FW ;
KEMP, GD ;
MEGSON, IL .
BIOORGANIC & MEDICINAL CHEMISTRY, 1995, 3 (01) :1-9
[3]   Nitric oxide inhibits lipopolysaccharide-induced apoptosis in pulmonary artery endothelial cells [J].
Ceneviva, GD ;
Tzeng, E ;
Hoyt, DG ;
Yee, E ;
Gallagher, A ;
Engelhardt, JF ;
Kim, YM ;
Billiar, TR ;
Watkins, SA ;
Pitt, BR .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1998, 275 (04) :L717-L728
[4]  
CHOU JL, 1991, J BIOL CHEM, V266, P24471
[5]   CYSTIC-FIBROSIS - MOLECULAR-BIOLOGY AND THERAPEUTIC IMPLICATIONS [J].
COLLINS, FS .
SCIENCE, 1992, 256 (5058) :774-779
[6]  
COVREY AJ, 1988, CELL CAMBRIDGE, V55, P887
[7]   PROCESSING OF MUTANT CYSTIC-FIBROSIS TRANSMEMBRANE CONDUCTANCE REGULATOR IS TEMPERATURE-SENSITIVE [J].
DENNING, GM ;
ANDERSON, MP ;
AMARA, JF ;
MARSHALL, J ;
SMITH, AE ;
WELSH, MJ .
NATURE, 1992, 358 (6389) :761-764
[8]   CHLORIDE CONDUCTANCE EXPRESSED BY DELTA-F508 AND OTHER MUTANT CFTRS IN XENOPUS OOCYTES [J].
DRUMM, ML ;
WILKINSON, DJ ;
SMIT, LS ;
WORRELL, RT ;
STRONG, TV ;
FRIZZELL, RA ;
DAWSON, DC ;
COLLINS, FS .
SCIENCE, 1991, 254 (5039) :1797-1799
[9]   Abnormal glutathione transport in cystic fibrosis airway epithelia [J].
Gao, L ;
Kim, KJ ;
Yankaskas, JR ;
Forman, HJ .
AMERICAN JOURNAL OF PHYSIOLOGY-LUNG CELLULAR AND MOLECULAR PHYSIOLOGY, 1999, 277 (01) :L113-L118
[10]  
GASTON B, 1994, J PHARMACOL EXP THER, V268, P978