The glucocorticoid attenuated response genes GARG-16, GARG-39, and GARG-49/IRG2 encode inducible proteins containing multiple tetratricopeptide repeat domains

被引:61
作者
Smith, JB
Herschman, HR
机构
[1] UNIV CALIF LOS ANGELES,SCH MED,DEPT BIOL CHEM,LOS ANGELES,CA 90095
[2] UNIV CALIF LOS ANGELES,SCH MED,DEPT PHARMACOL,LOS ANGELES,CA 90095
[3] UNIV CALIF LOS ANGELES,SCH MED,DEPT PEDIAT,DIV NEONATOL,LOS ANGELES,CA 90095
[4] UNIV CALIF LOS ANGELES,SCH MED,INST MOLEC BIOL,LOS ANGELES,CA 90095
[5] UNIV CALIF LOS ANGELES,SCH MED,LAB STRUCT BIOL & MOL MED,LOS ANGELES,CA 90095
关键词
tetratricopeptide; TPR domain; interferons; lipopolysaccharide;
D O I
10.1006/abbi.1996.0256
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
In a search for glucocorticoid attenuated response genes (GARGs) induced by Lipopolysaccharide (LPS) in murine Swiss 3T3 cells, we cloned 12 GARG cDNAs (J. B. Smith and ii. R. Herschman, 1995, J. Biol. Chem. 270, 16756-16765). Analysis of complete cDNA sequences indicates that three of these genes encode members of a highly conserved family of proteins containing multiple tetratricopeptide repeat (TPR) domains. GARG-16 is a homologue of the interferon-induced human IFI-56K gene. GARG-39 is a homologue of the interferon-induced human ISG-54K and hamster CL-54K genes. The predicted GARG-49/IRG2 protein is 60-75 amino acids shorter than other known members of this gene family, and its carboxyl-terminal half is relatively divergent. Homologues of GARG-49/IRG2 in other species have not been reported. The predicted GARG-16 and GARG-39 proteins, and their homologues, contain 10 TPR, domains. GARG-49/IRG2 shares the first 6 domains and part of the 7th, but lacks domains 8, 9, and 10. Message levels of GARG-16, GARG-39, and GARG-49/IRG2 are increased by LPS stimulation in Swiss 3T3 cells and in peritoneal macrophages. Unlike many primary response genes, these three genes are not induced by serum stimulation in Swiss 3T3 cells, All three are induced in the RAW 264.7 macrophage cell line by LPS, by interferons-alpha/beta, and by interferon-gamma, Despite these similarities, quantitative differences in their responses to different stimuli indicate that GARG-16, GARG-39, and GARG-49/IRG2 are regulated independently. We speculate that the proteins encoded by these LPS- and interferon-inducible genes may participate in multicomponent assemblies via their TPR domains. (C) 1996 Academic Press, Inc.
引用
收藏
页码:290 / 300
页数:11
相关论文
共 38 条
[1]   ISSUES IN SEARCHING MOLECULAR SEQUENCE DATABASES [J].
ALTSCHUL, SF ;
BOGUSKI, MS ;
GISH, W ;
WOOTTON, JC .
NATURE GENETICS, 1994, 6 (02) :119-129
[2]  
ALTSCHUL SF, 1990, J MOL BIOL, V215, P403, DOI 10.1006/jmbi.1990.9999
[3]  
Bainton DF., 1992, Inflammation: basic principles and clinical correlates, V2nd ed., P303
[4]  
BAIROCH A, 1994, NUCLEIC ACIDS RES, V22, P3583
[5]   THE INTERFERON-STIMULATED GENE 54 K PROMOTER CONTAINS 2 ADJACENT FUNCTIONAL INTERFERON-STIMULATED RESPONSE ELEMENTS OF DIFFERENT STRENGTH, WHICH ACT SYNERGISTICALLY FOR MAXIMAL INTERFERON-ALPHA INDUCIBILITY [J].
BLUYSSEN, HAR ;
VLIETSTRA, RJ ;
VANDERMADE, A ;
TRAPMAN, J .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1994, 220 (02) :395-402
[6]   STRUCTURE, CHROMOSOME LOCALIZATION, AND REGULATION OF EXPRESSION OF THE INTERFERON-REGULATED MOUSE IFI54/IFI56 GENE FAMILY [J].
BLUYSSEN, HAR ;
VLIETSTRA, RJ ;
FABER, PW ;
SMIT, EME ;
HAGEMEIJER, A ;
TRAPMAN, J .
GENOMICS, 1994, 24 (01) :137-148
[7]   THE TETRATRICOPEPTIDE REPEAT-DOMAIN OF THE PAS10 PROTEIN OF SACCHAROMYCES-CEREVISIAE IS ESSENTIAL FOR BINDING THE PEROXISOMAL TARGETING SIGNAL-SKL [J].
BROCARD, C ;
KRAGLER, F ;
SIMON, MM ;
SCHUSTER, T ;
HARTIG, A .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1994, 204 (03) :1016-1022
[8]   IDENTIFICATION OF A COMMON NUCLEOTIDE-SEQUENCE IN THE 3'-UNTRANSLATED REGION OF MESSENGER-RNA MOLECULES SPECIFYING INFLAMMATORY MEDIATORS [J].
CAPUT, D ;
BEUTLER, B ;
HARTOG, K ;
THAYER, R ;
BROWNSHIMER, S ;
CERAMI, A .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (06) :1670-1674
[9]   INTERFERON-INDUCED 56,000 MR PROTEIN AND ITS MESSENGER-RNA IN HUMAN-CELLS - MOLECULAR-CLONING AND PARTIAL SEQUENCE OF THE CDNA [J].
CHEBATH, J ;
MERLIN, G ;
METZ, R ;
BENECH, P ;
REVEL, M .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1213-1226
[10]  
CHEN PL, 1995, CELL GROWTH DIFFER, V6, P199