Human membrane type-4 matrix metalloproteinase (MT4-MMP) is encoded by a novel major transcript:: isolation of complementary DNA clones for human and mouse mt4-mmp transcripts

被引:41
作者
Kajita, M
Kinoh, H
Ito, N
Takamura, A
Itoh, Y
Okada, A
Sato, H
Seiki, M
机构
[1] Univ Tokyo, Inst Med Sci, Dept Canc Cell Res, Minato Ku, Tokyo 1088639, Japan
[2] Kanazawa Univ, Canc Res Inst, Dept Mol Virol & Oncol, Kanazawa, Ishikawa 9200934, Japan
关键词
matrix metalloproteinase; membrane-type enzyme; MT4-MMP;
D O I
10.1016/S0014-5793(99)01065-0
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
Five distinct membrane-type matrix metalloproteinases (MT-MMP) have been reported by cDNA cloning, However, the mt4-mmp gene product (MMP-17) has not been identified yet in spite of the cDNA isolation [Puente ct al, (1996), Cancer Res. 56, 944-949]. In this study, we re-examined the transcripts for human mt4-mmp by 5' RACE and identified two types of transcripts. The minor one corresponded to the cDNA reported by Puente et al, and failed to express protein, and the other is the major transcript that has an extended open reading frame and expressed 67 and 71 kDa translation products. Thus, functional mt4-mmp has been identified for the first time. (C) 1999 Federation of European Biochemical Societies.
引用
收藏
页码:353 / 356
页数:4
相关论文
共 17 条
[1]   Intermolecular autolytic cleavage can contribute to the activation of progelatinase A by cell membranes [J].
Atkinson, SJ ;
Crabbe, T ;
Cowell, S ;
Ward, RV ;
Butler, MJ ;
Sato, H ;
Seiki, M ;
Reynolds, JJ ;
Murphy, G .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (51) :30479-30485
[2]   MATRIX METALLOPROTEINASES - A REVIEW [J].
BIRKEDALHANSEN, H ;
MOORE, WGI ;
BODDEN, MK ;
WINDSOR, LJ ;
BIRKEDALHANSEN, B ;
DECARLO, A ;
ENGLER, JA .
CRITICAL REVIEWS IN ORAL BIOLOGY & MEDICINE, 1993, 4 (02) :197-250
[3]   Simple modifications to increase specificity of the 5'RACE procedure [J].
Chen, Z .
TRENDS IN GENETICS, 1996, 12 (03) :87-88
[4]   Membrane-type matrix metalloproteinases 1 and 2 exhibit broad-spectrum proteolytic capacities comparable to many matrix metalloproteinases [J].
d'Ortho, MP ;
Will, H ;
Atkinson, S ;
Butler, G ;
Messent, A ;
Gavrilovic, J ;
Smith, B ;
Timpl, R ;
Zardi, L ;
Murphy, G .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1997, 250 (03) :751-757
[5]  
Llano E, 1999, CANCER RES, V59, P2570
[6]   Matrix metalloproteinases: structures, evolution, and diversification [J].
Massova, I ;
Kotra, LP ;
Fridman, R ;
Mobashery, S .
FASEB JOURNAL, 1998, 12 (12) :1075-1095
[7]   THE MATRIX-DEGRADING METALLOPROTEINASES [J].
MATRISIAN, LM .
BIOESSAYS, 1992, 14 (07) :455-463
[8]   Identification and characterization of the fifth membrane-type matrix metalloproteinase MT5-MMP [J].
Pei, DQ .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (13) :8925-8932
[9]  
Puente XS, 1996, CANCER RES, V56, P944
[10]   ANALYSIS OF ENZYMATICALLY AMPLIFIED BETA-GLOBIN AND HLA-DQ-ALPHA DNA WITH ALLELE-SPECIFIC OLIGONUCLEOTIDE PROBES [J].
SAIKI, RK ;
BUGAWAN, TL ;
HORN, GT ;
MULLIS, KB ;
ERLICH, HA .
NATURE, 1986, 324 (6093) :163-166