Evolutionary Conservation, Expansion and Diversification of Interferon stimulated genes (ISG) in Vertebrates: insights from fish
Abstract
Interferons (IFNs) are central regulators of innate antiviral immunity, acting through conserved signalling pathways to induce a diverse repertoire of interferon-stimulated genes (ISGs). IFNs have been identified across all lineages of jawed vertebrates, while related antiviral strategies in invertebrates rely on different systems. However, antiviral integrated pathways based on secreted factors analogous to IFN, and using homologous signalling modules, have been reported in Arthropods and Molluscs. This review examines the evolutionary origin, regulation, and functional diversification of ISGs, with an emphasis on fish research. Comparative analyses across vertebrates have revealed a conserved core set of ISGs inherited from the last common ancestor of fish and tetrapods, alongside extensive lineage-specific expansions driven by host-pathogen arms races. In teleost fish, whole-genome duplication events have further shaped ISG repertoires through differential paralog retention, loss, and neo/sub-functionalization. Beyond classical IFN-dependent induction, a subset of ISGs can be activated directly by viral infection, perhaps reflecting remnants of primordial cell-autonomous antiviral responses. Functional redundancy among ISGs underpins the robustness of the IFN system. Finally, the review highlights how recognition of self versus non-self RNA-exemplified by CpG-targeting mechanisms mediated by ZAP-has shaped both viral genomes and ISG sequence evolution. The IFN system as a highly integrated network whose comparative study across vertebrates offers critical insights into antiviral defence and host-virus co-evolution.
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BibTeX
@article{collet2026evolutionary,
title = {{Evolutionary Conservation, Expansion and Diversification of Interferon stimulated genes (ISG) in Vertebrates: insights from fish}},
author = {Bertrand Collet and Pierre Boudinot},
journal = {Biomedical journal},
year = {2026},
month = nov,
doi = {10.1016/j.bj.2026.100987},
url = {https://hal.science/hal-05851884v1},
note = {CC BY},
}
RIS
TY - JOUR
TI - Evolutionary Conservation, Expansion and Diversification of Interferon stimulated genes (ISG) in Vertebrates: insights from fish
AU - Bertrand Collet
AU - Pierre Boudinot
PY - 2026
DA - 2026/11/04
JO - Biomedical journal
DO - 10.1016/j.bj.2026.100987
UR - https://hal.science/hal-05851884v1
AB - Interferons (IFNs) are central regulators of innate antiviral immunity, acting through conserved signalling pathways to induce a diverse repertoire of interferon-stimulated genes (ISGs). IFNs have been identified across all lineages of jawed vertebrates, while related antiviral strategies in invertebrates rely on different systems. However, antiviral integrated pathways based on secreted factors analogous to IFN, and using homologous signalling modules, have been reported in Arthropods and Molluscs. This review examines the evolutionary origin, regulation, and functional diversification of ISGs, with an emphasis on fish research. Comparative analyses across vertebrates have revealed a conserved core set of ISGs inherited from the last common ancestor of fish and tetrapods, alongside extensive lineage-specific expansions driven by host-pathogen arms races. In teleost fish, whole-genome duplication events have further shaped ISG repertoires through differential paralog retention, loss, and neo/sub-functionalization. Beyond classical IFN-dependent induction, a subset of ISGs can be activated directly by viral infection, perhaps reflecting remnants of primordial cell-autonomous antiviral responses. Functional redundancy among ISGs underpins the robustness of the IFN system. Finally, the review highlights how recognition of self versus non-self RNA-exemplified by CpG-targeting mechanisms mediated by ZAP-has shaped both viral genomes and ISG sequence evolution. The IFN system as a highly integrated network whose comparative study across vertebrates offers critical insights into antiviral defence and host-virus co-evolution.
SN - 2319-4170
SN - 2320-2890
ER -