Cited by 1,658interferon and immune responsesImmune Response and InflammationCytokine Signaling Pathways and Interactions

IRF Family of Transcription Factors as Regulators of Host Defense

Taniguchi, Tadatsugu, Ogasawara, Kouetsu, Takaoka, Akinori, Tanaka, Nobuyuki·2001·Annual Review of Immunology

Abstract

Interferon regulatory factors (IRFs) constitute a family of transcription factors that commonly possess a novel helix-turn-helix DNA-binding motif. Following the initial identification of two structurally related members, IRF-1 and IRF-2, seven additional members have now been reported. In addition, virally encoded IRFs, which may interfere with cellular IRFs, have also been identified. Thus far, intensive functional analyses have been done on IRF-1, revealing a remarkable functional diversity of this transcription factor in the regulation of cellular response in host defense. Indeed, IRF-1 selectively modulates different sets of genes, depending on the cell type and/or the nature of cellular stimuli, in order to evoke appropriate responses in each. More recently, much attention has also been focused on other IRF family members. Their functional roles, through interactions with their own or other members of the family of transcription factors, are becoming clearer in the regulation of host defense, such as innate and adaptive immune responses and oncogenesis.

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Crossref · 10.1146/annurev.immunol.19.1.623

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  • ICSBP/IRF-8 is an IFN-γ-inducible transcription factor of the IRF family that regulates transcription through multiple target DNA elements, including ISRE, EICE, and GAS.

    “Interferon (IFN) consensus sequence binding protein (ICSBP)/IFN regulatory factor (IRF)-8 is an IFN g -inducible transcription factor of the IRF family and regulates transcription through multiple target DNA elements, such as IFN-stimulated response element (ISRE), Ets/IRF composite element, and IFNg activation site (GAS).”
  • ICSBP has a conserved DNA-binding domain (DBD) at the N-terminal region and an IRF association domain (IAD) in the C-terminal region.

    “ICSBP has the DNAbinding domain (DBD) conserved in the IRF family at the Nterminal region and the IRF association domain (IAD) in the C-terminal region (Fig. 1). (2-5)”
  • ICSBP belongs to the IRF transcription factor family, which includes nine mammalian members and four virally encoded homologs.

    “It belongs to the family of IRF transcription factors, which includes nine mammalian members and four virally encoded homologs. (2,3)”

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References 194 · Cited by 1,658

Authors
Taniguchi, T., Ogasawara, K., Takaoka, A., & Tanaka, N.
Affiliations
The University of Tokyo (JP)
Venue
Annual Review of Immunology
Published
2001-04
Volume
19
Issue
1
Pages
623-655
ISSN
  • 0732-0582 (ISSN-L)
  • 1545-3278
OpenAlex
W2108399976
Cited by
1,658
References
194
Citations by year
2026: 45 · 2025: 57 · 2024: 60 · 2023: 47 · 2022: 64 · 2021: 62 · 2020: 56 · 2019: 51 · 2018: 45 · 2017: 64 · 2016: 55 · 2015: 56 · 2014: 75 · 2013: 62 · 2012: 49
FWCI
7.28
Type
journal article
Language
en
Open access
closed
Locations
  • Annual Review of Immunology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
  • Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
  • Health Sciences › Medicine › Oncology › Cytokine Signaling Pathways and Interactions
Keywords
interferon regulatory factors, IRF1, IRF2, transcription factors, helix-turn-helix DNA-binding motif, host defense, innate immunity, adaptive immunity, carcinogenesis, gene expression regulation
MeSH terms
Interferon Regulatory Factor-8, Interferon Regulatory Factor-4, Animals, Cell Cycle, DNA-Binding Proteins, Gene Expression Regulation, Histocompatibility Antigens, Humans, Immunity, Interferons, Killer Cells, Natural, Macrophage Activation, Neoplasms, Phosphoproteins, Protein-Tyrosine Kinases, Repressor Proteins, Structure-Activity Relationship, Transcription Factors, Transcription, Genetic, Virus Diseases, Signal Transduction, Autoimmunity, Lymphocyte Subsets, Helix-Turn-Helix Motifs, Interferon-Stimulated Gene Factor 3, Interferon-Stimulated Gene Factor 3, gamma Subunit, Interferon Regulatory Factors, Interferon Regulatory Factor-2, Interferon Regulatory Factor-3, Interferon Regulatory Factor-7, Interferon Regulatory Factor-1

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