Gene induction pathways mediated by distinct IRFs during viral infection

被引:153
作者
Nakaya, T
Sato, M
Hata, N
Asagiri, M
Suemori, H
Noguchi, S
Tanaka, N
Taniguchi, T
机构
[1] Univ Tokyo, Grad Sch Med, Dept Immunol, Bunkyo Ku, Tokyo 1130033, Japan
[2] Univ Tokyo, Grad Sch Med, Fac Med, Bunkyo Ku, Tokyo 1130033, Japan
[3] Kanagawa Acad Sci & Technol, Bio Signal Pathway Project, Odawara, Kanagawa 2500862, Japan
[4] Meiji Milk Prod Co Ltd, Meiji Inst Hlth Sci, Odawara, Kanagawa 2500862, Japan
关键词
anti-viral response; cytokines; DRAF1; IFN-inducible genes; interferons; IRF-3; IRF-7; ISGF3; ISRE; transcriptional regulation;
D O I
10.1006/bbrc.2001.4913
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
During viral infection, interferon-alpha/beta (IFN-alpha/beta) and many IFN-inducible genes are induced to elicit antiviral responses of the host. Using cells with a gene disruption(s) for the IRF family of transcription factors, we provide evidence that these genes, containing similar IRF-binding cis-elements, are classified into distinct groups, based on the gene induction pathway(s), The IFN-beta gene induction is dependent on either IRF-3 or IRF-7, whereas induction of the IFN-alpha gene family is IRF-7-dependent. On the other hand, ISG15, ISG54 and IP-10 are induced by either IRF-3 or IFN stimulated gene factor 3 (ISGF3). We also show that another group of genes is totally dependent on ISGF3, Thus, during viral infection, a given gene responds either directly to a virus or virus-induced IFN-alpha/beta or both through distinct pathways, The differential utilization of these induction pathways for these genes during viral infection may reflect their distinct functional roles in the efficient antiviral response. (C) 2001 Academic Press.
引用
收藏
页码:1150 / 1156
页数:7
相关论文
共 50 条
[1]   Viral mechanisms of immune evasion [J].
Alcami, A ;
Koszinowski, UH .
IMMUNOLOGY TODAY, 2000, 21 (09) :447-455
[2]   Characterization of the interferon regulatory factor-7 and its potential role in the transcription activation of interferon A genes [J].
Au, WC ;
Moore, PA ;
LaFleur, DW ;
Tombal, B ;
Pitha, PM .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (44) :29210-29217
[3]   STRUCTURE OF 2 FORMS OF THE INTERFERON-INDUCED (2-'-5-') OLIGO-A SYNTHETASE OF HUMAN-CELLS BASED ON CDNAS AND GENE-SEQUENCES [J].
BENECH, P ;
MORY, Y ;
REVEL, M ;
CHEBATH, J .
EMBO JOURNAL, 1985, 4 (09) :2249-2256
[4]  
Bluyssen Hans A. R., 1996, Cytokine and Growth Factor Reviews, V7, P11, DOI 10.1016/1359-6101(96)00005-6
[5]   Synergism between multiple virus-induced factor-binding elements involved in the differential expression of interferon A genes [J].
Braganca, J ;
Genin, P ;
Bandu, MT ;
Darracq, N ;
Vignal, R ;
Casse, C ;
Doly, J ;
Civas, A .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (35) :22154-22162
[6]   ENHANCER-LIKE INTERFERON RESPONSIVE SEQUENCES OF THE HUMAN AND MURINE (2'-5') OLIGOADENYLATE SYNTHETASE GENE PROMOTERS [J].
COHEN, B ;
PERETZ, D ;
VAIMAN, D ;
BENECH, P ;
CHEBATH, J .
EMBO JOURNAL, 1988, 7 (05) :1411-1419
[7]   CHARACTERIZATION OF SPECIFIC DNA-BINDING FACTORS ACTIVATED BY DOUBLE-STRANDED-RNA AS POSITIVE REGULATORS OF INTERFERON ALPHA/BETA-STIMULATED GENES [J].
DALY, C ;
REICH, NC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1995, 270 (40) :23739-23746
[8]   JAK-STAT PATHWAYS AND TRANSCRIPTIONAL ACTIVATION IN RESPONSE TO IFNS AND OTHER EXTRACELLULAR SIGNALING PROTEINS [J].
DARNELL, JE ;
KERR, IM ;
STARK, GR .
SCIENCE, 1994, 264 (5164) :1415-1421
[9]   Immunoregulatory properties of ISG15, an interferon-induced cytokine [J].
DCunha, J ;
Knight, E ;
Haas, AL ;
Truitt, RL ;
Borden, EC .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1996, 93 (01) :211-215
[10]  
De Maeyer E., 1988, INTERFERONS OTHER RE