ABSENCE OF THE TYPE-I IFN SYSTEM IN EC CELLS - TRANSCRIPTIONAL ACTIVATOR (IRF-1) AND REPRESSOR (IRF-2) GENES ARE DEVELOPMENTALLY REGULATED

被引:361
作者
HARADA, H
WILLISON, K
SAKAKIBARA, J
MIYAMOTO, M
FUJITA, T
TANIGUCHI, T
机构
[1] Institute for Molecular, Cellular Biology Osaka University Suita-shi, Osaka
关键词
D O I
10.1016/0092-8674(90)90163-9
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
Interferons (IFNs) are a heterogeneous family of cytokines that exhibits multiple biological activities. Upon viral infection, expression of type I IFNs (i.e., IFN-α and IFN-β) is induced in a variety of differentiated cells but not in cells of embryonal origin. IRF-1 and IRF-2, which bind to the same cis-elements within the promoters of type I IFN and IFN-inducible MHC class I genes, were identified previously. Here we demonstrate that the expression of both IRF and IFN genes is developmentally regulated in mouse EC cells; these genes become functional only after cell differentiation. Furthermore, cDNA-directed IRF-1 produced in undifferentiated but not differentiated EC cells efficiently activates the transfected IFN-α and IFN-β and endogenous IFN-α genes, whereas IRF-2 represses the IRF-1 effects. These findings emphasize the dual function of the IRF-responsive cis-elements as positive and negative regulators, since they can be occupied by transcriptionally active or inactive IRF molecules. This type of regulatory mechanism might operate in other cytokine systems. © 1990.
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页码:303 / 312
页数:10
相关论文
共 54 条
[1]  
[Anonymous], 1986, MANIPULATING MOUSE E
[2]   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
[3]   INTERFERON SYNTHESIS IN THE EARLY POST-IMPLANTATION MOUSE EMBRYO [J].
BARLOW, DP ;
RANDLE, BJ ;
BURKE, DC .
DIFFERENTIATION, 1984, 27 (03) :229-235
[4]   APPEARANCE OF INTERFERON INDUCIBILITY AND SENSITIVITY DURING DIFFERENTIATION OF MURINE TERATOCARCINOMA CELLS INVITRO [J].
BURKE, DC ;
GRAHAM, CF ;
LEHMAN, JM .
CELL, 1978, 13 (02) :243-248
[5]  
CHOMCZYNSKI P, 1987, ANAL BIOCHEM, V162, P156, DOI 10.1016/0003-2697(87)90021-2
[6]   GENOMIC SEQUENCING [J].
CHURCH, GM ;
GILBERT, W .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA-BIOLOGICAL SCIENCES, 1984, 81 (07) :1991-1995
[7]   SEQUENCE REQUIREMENT FOR SPECIFIC INTERACTION OF AN ENHANCER BINDING-PROTEIN (EBP1) WITH DNA [J].
CLARK, L ;
HAY, RT .
NUCLEIC ACIDS RESEARCH, 1989, 17 (02) :499-516
[8]   REGULATION OF CELL-PROLIFERATION AND DIFFERENTIATION BY INTERFERONS [J].
CLEMENS, MJ ;
MCNURLAN, MA .
BIOCHEMICAL JOURNAL, 1985, 226 (02) :345-360
[9]   COOPERATIVE INTERACTION OF MULTIPLE DNA ELEMENTS IN THE HUMAN INTERFERON-BETA PROMOTER [J].
DINTER, H ;
HAUSER, H .
EUROPEAN JOURNAL OF BIOCHEMISTRY, 1987, 166 (01) :103-109
[10]   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