Transcriptional control of matrix metalloproteinases and the tissue inhibitors of matrix metalloproteinases

被引:287
作者
Borden, P
Heller, RA
机构
[1] SYNTEX INC,DISCOVERY RES,INST BIOCHEM & CELL BIOL,PALO ALTO,CA 94304
[2] STANFORD DNA SEQUENCE & TECHNOL CTR,PALO ALTO,CA 94305
来源
CRITICAL REVIEWS IN EUKARYOTIC GENE EXPRESSION | 1997年 / 7卷 / 1-2期
关键词
MMP-expression; MMP-promoters; MMP-gene structure; MMP-regulation;
D O I
10.1615/CritRevEukarGeneExpr.v7.i1-2.90
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Matrix metalloproteinases (MMPs) are enzymes with important roles in a Variety of normal physiological processes; these same enzymes are also operative in a range of pathologies. The proteins known as the tissue inhibitors of matrix metalloproteinases (TIMPs) act to limit the enzymatic function of the MMPs. MMPs and TIMPs can be divided into two groups with respect to gene expression: the majority exhibit inducible expression and a small number are produced constitutively or are expressed at very low levels and are not inducible. Among the agents that induce MMP and TIMP production are the inflammatory cytokines TNF alpha and IL1 beta. A marked cell type specificity is a hallmark of both MMP and TIMP gene expression (i.e., a limited number of cell types can be induced to make these proteins). An analysis of the control elements in the promoter regions of these proteins reveals a correlation between the presence of both AP-1 and Ets binding sites and inducible expression. The chromosomal locations of most of the MMPs and TIMPs have been verified; these data will provide the basis for investigations into possible correlations between mutations in these genes and disease states.
引用
收藏
页码:159 / 178
页数:20
相关论文
共 140 条
[1]  
Alexander CM, 1991, CELL BIOL EXTRACELLU, P255
[2]   THE ROLE OF JUN, FOS AND THE AP-1 COMPLEX IN CELL-PROLIFERATION AND TRANSFORMATION [J].
ANGEL, P ;
KARIN, M .
BIOCHIMICA ET BIOPHYSICA ACTA, 1991, 1072 (2-3) :129-157
[3]   INDUCTION OF METALLOTHIONEIN AND OTHER MESSENGER-RNA SPECIES BY CARCINOGENS AND TUMOR PROMOTERS IN PRIMARY HUMAN-SKIN FIBROBLASTS [J].
ANGEL, P ;
POTING, A ;
MALLICK, U ;
RAHMSDORF, HJ ;
SCHORPP, M ;
HERRLICH, P .
MOLECULAR AND CELLULAR BIOLOGY, 1986, 6 (05) :1760-1766
[4]   12-O-TETRADECANOYL-PHORBOL-13-ACETATE INDUCTION OF THE HUMAN COLLAGENASE GENE IS MEDIATED BY AN INDUCIBLE ENHANCER ELEMENT LOCATED IN THE 5'-FLANKING REGION [J].
ANGEL, P ;
BAUMANN, I ;
STEIN, B ;
DELIUS, H ;
RAHMSDORF, HJ ;
HERRLICH, P .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (06) :2256-2266
[5]   PHORBOL ESTER INDUCIBLE GENES CONTAIN A COMMON CIS ELEMENT RECOGNIZED BY A TPA-MODULATED TRANS-ACTING FACTOR [J].
ANGEL, P ;
IMAGAWA, M ;
CHIU, R ;
STEIN, B ;
IMBRA, RJ ;
RAHMSDORF, HJ ;
JONAT, C ;
HERRLICH, P ;
KARIN, M .
CELL, 1987, 49 (06) :729-739
[6]   STRUCTURE AND PROMOTER CHARACTERIZATION OF THE HUMAN STROMELYSIN-3 GENE [J].
ANGLARD, P ;
MELOT, T ;
GUERIN, E ;
THOMAS, G ;
BASSET, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (35) :20337-20344
[7]   CLONING OF THE CDNA-ENCODING HUMAN TISSUE INHIBITOR OF METALLOPROTEINASES-3 (TIMP-3) AND MAPPING OF THE TIMP3 GENE TO CHROMOSOME-22 [J].
APTE, SS ;
MATTEI, MG ;
OLSEN, BR .
GENOMICS, 1994, 19 (01) :86-90
[8]   A NOVEL METALLOPROTEINASE GENE SPECIFICALLY EXPRESSED IN STROMAL CELLS OF BREAST CARCINOMAS [J].
BASSET, P ;
BELLOCQ, JP ;
WOLF, C ;
STOLL, I ;
HUTIN, P ;
LIMACHER, JM ;
PODHAJCER, OL ;
CHENARD, MP ;
RIO, MC ;
CHAMBON, P .
NATURE, 1990, 348 (6303) :699-704
[9]  
BASSET P, 1994, CANCER-AM CANCER SOC, V74, P1045, DOI 10.1002/1097-0142(19940801)74:3+<1045::AID-CNCR2820741511>3.0.CO
[10]  
2-7