IRF Family of Transcription Factors as Regulators of Host Defense
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.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
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).”
From Review: ICSBP/IRF-8: Its Regulatory Roles in the Development of Myeloid Cells (2002) · cites this paper as [3]
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)”
From Review: ICSBP/IRF-8: Its Regulatory Roles in the Development of Myeloid Cells (2002) · cites this paper as [3]
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)”
From Review: ICSBP/IRF-8: Its Regulatory Roles in the Development of Myeloid Cells (2002) · cites this paper as [3]
The citation lists haven’t been fetched yet
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
- Publisher
- Annual Reviews
- Published
- 2001-04
- Volume
- 19
- Issue
- 1
- Pages
- 623-655
- ISSN
- 0732-0582 (ISSN-L)
- 1545-3278
- OpenAlex
- W2108399976
- Semantic Scholar
- 7b28bc9022d936f0ee025e5b38219899ee534cbd
- 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
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review