The role of interferon regulatory factors in the interferon system and cell growth control

被引:120
作者
Harada, H
Taniguchi, T
Tanaka, N
机构
[1] Washington Univ, Sch Med, Dept Med, Div Med Oncol, St Louis, MO 63110 USA
[2] Washington Univ, Sch Med, Dept Pathol, Div Med Oncol, St Louis, MO 63110 USA
[3] Univ Tokyo, Fac Med, Dept Immunol, Bunkyo Ku, Tokyo 113, Japan
关键词
interferon regulatory factor; transcription; interferon response; cell growth control;
D O I
10.1016/S0300-9084(99)80017-0
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
Complex cellular responses are often coordinated by a genetic regulatory network in which a given transcription factor controls the expression of a diverse set of target genes. Interferon regulatory factor (IRF)-1 and IRF-2 have originally been identified as a transcriptional activator and repressor, respectively, of the interferon-beta (IFN-beta) as well as of IFN-inducible genes. However, these factors have since been shown to modulate not only the cellular response to IFNs, but also cell growth, susceptibility to transformation by oncogenes, induction of apoptosis, and development of the T cell immune response. Furthermore, the evidence suggests that deletion and/or inactivation of the IRF-1 gene may be a critical step in the development of some human hematopoietic neoplasms. Subsequently, these factors have been shown to constitute a family of transcription factors, termed the IRF-family. Recent studies indicate that other IRF family members also involve the regulation of the IFN system and cell transformation. The IRF-family may be examples of transcription factors which can selectively modulate several sets of genes depending on the cell type and/or nature of the cellular stimuli, so as to evoke host defense mechanisms against infection and oncogenesis. (C) Societe francaise de biochimie et biologie moleculaire/Elsevier, Paris.
引用
收藏
页码:641 / 650
页数:10
相关论文
共 72 条
[1]   IDENTIFICATION OF A MEMBER OF THE INTERFERON REGULATORY FACTOR FAMILY THAT BINDS TO THE INTERFERON-STIMULATED RESPONSE ELEMENT AND ACTIVATES EXPRESSION OF INTERFERON-INDUCED GENES [J].
AU, WC ;
MOORE, PA ;
LOWTHER, W ;
JUANG, YT ;
PITHA, PM .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (25) :11657-11661
[2]  
Beretta L, 1996, ONCOGENE, V12, P1593
[3]  
Bluyssen Hans A. R., 1996, Cytokine and Growth Factor Reviews, V7, P11, DOI 10.1016/1359-6101(96)00005-6
[4]   COMBINATORIAL ASSOCIATION AND ABUNDANCE OF COMPONENTS OF INTERFERON-STIMULATED GENE FACTOR-3 DICTATE THE SELECTIVITY OF INTERFERON RESPONSES [J].
BLUYSSEN, HAR ;
MUZAFFAR, R ;
VLIESTSTRA, RJ ;
VANDERMADE, ACJ ;
LEUNG, S ;
STARK, GR ;
KERR, IM ;
TRAPMAN, J ;
LEVY, DE .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1995, 92 (12) :5645-5649
[5]  
BOULTWOOD J, 1993, BLOOD, V82, P2611
[6]   MOLECULAR-INTERACTIONS BETWEEN INTERFERON CONSENSUS SEQUENCE BINDING-PROTEIN AND MEMBERS OF THE INTERFERON REGULATORY FACTOR FAMILY [J].
BOVOLENTA, C ;
DRIGGERS, PH ;
MARKS, MS ;
MEDIN, JA ;
POLITIS, AD ;
VOGEL, SN ;
LEVY, DE ;
SAKAGUCHI, K ;
APPELLA, E ;
COLIGAN, JE ;
OZATO, K .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1994, 91 (11) :5046-5050
[7]  
BRIKEN V, 1995, MOL CELL BIOL, V15, P975
[8]  
CLARKE AR, 1993, NATURE, V362, P852
[9]   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
[10]  
De Maeyer E., 1988, INTERFERONS OTHER RE