Identification and chromosomal location of two human genes encoding enzymes potentially involved in proteolytic maturation of farnesylated proteins

被引:41
作者
Freije, JMP
Blay, P
Pendás, AM
Cadiñanos, J
Crespo, P
López-Otín, C [1 ]
机构
[1] Univ Oviedo, Fac Med, Dept Bioquim & Biol Mol, Oviedo 33006, Spain
[2] Univ Cantabria, Fac Med, Dept Bioquim & Biol Mol, E-39005 Santander, Spain
关键词
a-factor; Ras; metalloproteases; oncogenes; prenylation;
D O I
10.1006/geno.1999.5834
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
Two human cDNAs encoding proteins similar to yeast enzymes involved in proteolytic processing of farnesylated proteins like a-factor mating pheromone and Ras2p have been cloned from an ovary cDNA library. These proteins have been tentatively called Face-1 and Face-2 (farnesylated protein-converting enzymes 1 and 2), respectively, and are integral membrane proteins, belonging to distinct families of metalloproteinases. Northern blot analysis of poly(A)(+) RNAs isolated from a wide variety of human tissues demonstrated that both genes are expressed in all examined tissues, which suggests that these enzymes play housekeeping roles in normal processes. Fluorescence in situ hybridization experiments showed that the human FACE-1 gene maps to 1p34, whereas FACE-2 is located at 11q13, a region frequently amplified in human carcinomas and lymphomas. On the basis of these results, we suggest that inhibition of Face-1 and/or Face-2 could be part of strategies directed to block the functioning of prenylated proteins activated in oncogenic processes, including Ras proteins. (C) 1999 Academic Press.
引用
收藏
页码:270 / 280
页数:11
相关论文
共 34 条
[1]   ENDOPROTEOLYTIC PROCESSING OF A FARNESYLATED PEPTIDE INVITRO [J].
ASHBY, MN ;
KING, DS ;
RINE, J .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1992, 89 (10) :4613-4617
[2]   RAS GENES [J].
BARBACID, M .
ANNUAL REVIEW OF BIOCHEMISTRY, 1987, 56 :779-827
[3]   A farnesyltransferase inhibitor induces tumor regression in transgenic mice harboring multiple oncogenic mutations by mediating alterations in both cell cycle control and apoptosis [J].
Barrington, RE ;
Subler, MA ;
Rands, E ;
Omer, CA ;
Miller, PJ ;
Hundley, JE ;
Koester, SK ;
Troyer, DA ;
Bearss, DJ ;
Conner, MW ;
Gibbs, JB ;
Hamilton, K ;
Koblan, KS ;
Mosser, SD ;
O'Neill, TJ ;
Schaber, MD ;
Senderak, ET ;
Windle, JJ ;
Oliff, A ;
Kohl, NE .
MOLECULAR AND CELLULAR BIOLOGY, 1998, 18 (01) :85-92
[4]  
BOS JL, 1989, CANCER RES, V49, P4682
[5]   Modulation of Ras and a-factor function by carboxyl-terminal proteolysis [J].
Boyartchuk, VL ;
Ashby, MN ;
Rine, J .
SCIENCE, 1997, 275 (5307) :1796-1800
[6]   Solubilization, partial purification, and affinity labeling of the membrane-bound isoprenylated protein endoprotease [J].
Chen, YL ;
Ma, YT ;
Rando, RR .
BIOCHEMISTRY, 1996, 35 (10) :3227-3237
[8]   Mammalian prenylcysteine carboxyl methyltransferase is in the endoplasmic reticulum [J].
Dai, Q ;
Choy, E ;
Chiu, V ;
Romano, J ;
Slivka, SR ;
Steitz, SA ;
Michaelis, S ;
Philips, MR .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (24) :15030-15034
[9]   A COMPREHENSIVE SET OF SEQUENCE-ANALYSIS PROGRAMS FOR THE VAX [J].
DEVEREUX, J ;
HAEBERLI, P ;
SMITHIES, O .
NUCLEIC ACIDS RESEARCH, 1984, 12 (01) :387-395
[10]   A novel membrane-associated metalloprotease, Ste24p, is required for the first step of NH2-terminal processing of the yeast a-factor precursor [J].
FujimuraKamada, K ;
Nouvet, FJ ;
Michaelis, S .
JOURNAL OF CELL BIOLOGY, 1997, 136 (02) :271-285