STRUCTURE AND REGULATION OF THE HUMAN INTERFERON REGULATORY FACTOR-1 (IRF-1) AND IRF-2 GENES - IMPLICATIONS FOR A GENE NETWORK IN THE INTERFERON SYSTEM

被引:291
作者
HARADA, H [1 ]
TAKAHASHI, E [1 ]
ITOH, S [1 ]
HARADA, K [1 ]
HORI, TA [1 ]
TANIGUCHI, T [1 ]
机构
[1] NATL INST RADIOL SCI,INAGE KU,CHIBA 263,JAPAN
关键词
D O I
10.1128/MCB.14.2.1500
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
Interferon regulatory factor 1 (IRF-1) and IRF-2 are structurally similar DNA-binding factors which were originally identified as regulators of the type I interferon (IFN) system; the former functions as a transcriptional activator, and the latter represses IRF-1 function by competing for the same cis elements. More recent studies have revealed new roles of the two factors in the regulation of cell growth; IRF-1 and IRF-2 manifest antioncogenic and oncogenic activities, respectively. In this study, we determined the structures and chromosomal locations of the human IRF-1 and IRF-2 genes and further characterized the promoters of the respective genes. Comparison of exon-intron organization of the two genes revealed a common evolutionary structure, notably within the exons encoding the N-terminal portions of the two factors. We confirmed the chromosomal mapping of the human IRF-1 gene to 5q31.1 and newly assigned the IRF-2 gene to 4q35.1, using fluorescence in situ hybridization. The 5' regulatory regions of both genes contain highly GC-rich sequences and consensus binding sequences for several known transcription factors, including NF-kappa B. Interestingly, one IRF binding site was found within the IRF-2 promoter, and expression of the IRF-2 gene was affected by both transient and stable IRF-1 expression. In addition, one potential IFN-gamma-activated sequence was found within the IRF-1 promoter. Thus, these results may shed light on the complex gene network involved in regulation of the IFN system.
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页码:1500 / 1509
页数:10
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共 61 条
[1]  
ABDOLLAHI A, 1991, CELL GROWTH DIFFER, V2, P401
[2]   PSV00CAT - LOW BACKGROUND CAT PLASMID [J].
ARAKI, E ;
SHIMADA, F ;
SHICHIRI, M ;
MORI, M ;
EBINA, Y .
NUCLEIC ACIDS RESEARCH, 1988, 16 (04) :1627-1627
[3]  
BAEUERLE PA, 1991, BIOCHIM BIOPHYS ACTA, V1088, P171
[4]   BINDING OF A NUCLEAR FACTOR TO A REGULATORY SEQUENCE IN THE PROMOTER OF THE MOUSE H-2KB CLASS-I MAJOR HISTOCOMPATIBILITY GENE [J].
BALDWIN, AS ;
SHARP, PA .
MOLECULAR AND CELLULAR BIOLOGY, 1987, 7 (01) :305-313
[5]  
CHA Y, 1993, DNA CELL BIOL, V11, P605
[6]   REGULATION OF CELL-PROLIFERATION AND DIFFERENTIATION BY INTERFERONS [J].
CLEMENS, MJ ;
MCNURLAN, MA .
BIOCHEMICAL JOURNAL, 1985, 226 (02) :345-360
[7]  
DeMaeyer EM., 1988, INTERFERONS OTHER RE
[8]   ACCURATE TRANSCRIPTION INITIATION BY RNA POLYMERASE-II IN A SOLUBLE EXTRACT FROM ISOLATED MAMMALIAN NUCLEI [J].
DIGNAM, JD ;
LEBOVITZ, RM ;
ROEDER, RG .
NUCLEIC ACIDS RESEARCH, 1983, 11 (05) :1475-1489
[9]   AN INTERFERON GAMMA-REGULATED PROTEIN THAT BINDS THE INTERFERON-INDUCIBLE ENHANCER ELEMENT OF MAJOR HISTOCOMPATIBILITY COMPLEX CLASS-I GENES [J].
DRIGGERS, PH ;
ENNIST, DL ;
GLEASON, SL ;
MAK, WH ;
MARKS, MS ;
LEVI, BZ ;
FLANAGAN, JR ;
APPELLA, E ;
OZATO, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (10) :3743-3747
[10]   MECHANISMS OF TRANSCRIPTIONAL SYNERGISM BETWEEN DISTINCT VIRUS-INDUCIBLE ENHANCER ELEMENTS [J].
DU, W ;
THANOS, D ;
MANIATIS, T .
CELL, 1993, 74 (05) :887-898