The DOI matches its Crossref record; 39 of the 39 references it cites were found in a registry or an index.
Pan-viral specificity of IFN-induced genes reveals new roles for cGAS in innate immunity
Open accessAbstract
The type I interferon (IFN) response protects cells from viral infection by inducing hundreds of interferon-stimulated genes (ISGs), some of which encode direct antiviral effectors. Recent screening studies have begun to catalogue ISGs with antiviral activity against several RNA and DNA viruses. However, antiviral ISG specificity across multiple distinct classes of viruses remains largely unexplored. Here we used an ectopic expression assay to screen a library of more than 350 human ISGs for effects on 14 viruses representing 7 families and 11 genera. We show that 47 genes inhibit one or more viruses, and 25 genes enhance virus infectivity. Comparative analysis reveals that the screened ISGs target positive-sense single-stranded RNA viruses more effectively than negative-sense single-stranded RNA viruses. Gene clustering highlights the cytosolic DNA sensor cyclic GMP-AMP synthase (cGAS, also known as MB21D1) as a gene whose expression also broadly inhibits several RNA viruses. In vitro, lentiviral delivery of enzymatically active cGAS triggers a STING-dependent, IRF3-mediated antiviral program that functions independently of canonical IFN/STAT1 signalling. In vivo, genetic ablation of murine cGAS reveals its requirement in the antiviral response to two DNA viruses, and an unappreciated contribution to the innate control of an RNA virus. These studies uncover new paradigms for the preferential specificity of IFN-mediated antiviral pathways spanning several virus families.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
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?
In the citing paper
“For example, RNA viruses can activate the cGAS-STING pathway despite the specificity of cGAS for cytoplasmic DNA over RNA (Gao et al., 2013b; Schoggins et al., 2014).”
From Cytoplasmic DNA: sources, sensing, and role in aging and disease (2021) · cites this paper as Schoggins et al., 2014
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Cyclic GMP-AMP Synthase Is a Cytosolic DNA Sensor That Activates the Type I Interferon Pathway
Sun, L., Wu, J., Du, F., Chen, X., & Chen, Z. J. (2013) · Science · doi:10.1126/science.1232458 · Cited by 4,996
STRING v9.1: protein-protein interaction networks, with increased coverage and integration
Franceschini, A., Szklarczyk, D., Frankild, S., Kuhn, M., Simonovic, M., Roth, A., Lin, J., Minguez, P., Bork, P., von Mering, C., et al. (2012) · Nucleic Acids Research · doi:10.1093/nar/gks1094 · Cited by 4,398
Cyclic GMP-AMP Is an Endogenous Second Messenger in Innate Immune Signaling by Cytosolic DNA
Wu, J., Sun, L., Chen, X., Du, F., Shi, H., Chen, C., & Chen, Z. J. (2012) · Science · doi:10.1126/science.1229963 · Cited by 2,628
A diverse range of gene products are effectors of the type I interferon antiviral response
Schoggins, J. W., Wilson, S. J., Panis, M., Murphy, M. Y., Jones, C. T., Bieniasz, P. D., & Rice, C. M. (2011) · Nature · doi:10.1038/nature09907 · Cited by 2,412
Self-citationDer, S. D., Zhou, A., Williams, B. R. G., & Silverman, R. H. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.26.15623 · Cited by 1,840
Interferon-stimulated genes and their antiviral effector functions
Schoggins, J. W., & Rice, C. M. (2011) · Current Opinion in Virology · doi:10.1016/j.coviro.2011.10.008 · Cited by 1,342
Self-citationGao, P., Ascano, M., Wu, Y., Barchet, W., Gaffney, B. L., Zillinger, T., Serganov, A. A., Liu, Y., Jones, R. A., Hartmann, G., et al. (2013) · Cell · doi:10.1016/j.cell.2013.04.046 · Cited by 1,101
Pivotal Roles of cGAS-cGAMP Signaling in Antiviral Defense and Immune Adjuvant Effects
Li, X.-D., Wu, J., Gao, D., Wang, H., Sun, L., & Chen, Z. J. (2013) · Science · doi:10.1126/science.1244040 · Cited by 1,097
Cyclic GMP-AMP Synthase Is an Innate Immune Sensor of HIV and Other Retroviruses
Gao, D., Wu, J., Wu, Y.-T., Du, F., Aroh, C., Yan, N., Sun, L., & Chen, Z. J. (2013) · Science · doi:10.1126/science.1240933 · Cited by 1,032
Structural mechanism of cytosolic DNA sensing by cGAS
Çivril, F., Deimling, T., Mann, C. C. D. O., Ablasser, A., Moldt, M., Witte, G., Hornung, V., & Hopfner, K. (2013) · Nature · doi:10.1038/nature12305 · Cited by 916
Flagged first, then by citations
Cited by
Sorted by citations
Items 701–800 of 885
Role of Interferon Regulatory Factor 1 in acute and chronic virus infections
Rahlf, C. R., & Tarakanova, V. L. (2024) · Virology · doi:10.1016/j.virol.2024.110386 · Cited by 7
Innate Immune Sensing of Parapoxvirus Orf Virus and Viral Immune Evasion
AlDaif, B. A., & Fleming, S. B. (2025) · Viruses · doi:10.3390/v17040587 · Cited by 10
FAF1 downregulation by Toxoplasma gondii enables host IRF3 mobilization and promotes parasite growth
Gao, F., Quan, J., Choi, I., Lee, Y., Jang, S., Yuk, J., Lee, Y., & Cha, G. (2021) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.16889 · Cited by 7
B Cell Intrinsic STING Signaling Is Not Required for Autoreactive Germinal Center Participation
Green, K., Wittenborn, T. R., Hagert, C., Terczyńska‐Dyla, E., van Campen, N., Jensen, L., Reinert, L. S., Hartmann, R., Paludan, S. R., & Degn, S. E. (2021) · Frontiers in Immunology · doi:10.3389/fimmu.2021.782558 · Cited by 8
Perumal, N., White, B. E., Sánchez-Valdéz, F. J., & Tarleton, R. L. (2023) · The Journal of Immunology · doi:10.4049/jimmunol.2300373 · Cited by 7
Suen, W. W., Imoda, M., Thomas, A. W., Nasir, N. N. B. M., Tearnsing, N., Wang, W., & Bielefeldt‐Ohmann, H. (2019) · Pathogens · doi:10.3390/pathogens8040195 · Cited by 7
Szemere, Z. K., & Murphy, E. A. (2024) · Antiviral Research · doi:10.1016/j.antiviral.2024.105989 · Cited by 6
CD81 is a receptor for equine arteritis virus (family: Arteriviridae )
Maloney, S. M., Shaw, T. M., Nennig, K., Larsen, M. S., Shah, A. P., Kumar, A., Marcotrigiano, J., Grove, J., Snijder, E. J., Kirchdoerfer, R. N., et al. (2025) · mBio · doi:10.1128/mbio.00623-25 · Cited by 6
Self-citationMammalian innate antiviral defenses: beyond interferon
Rex, E. A., Shaffer, J., Deng, D. M., & Gammon, D. B. (2025) · Journal of Virology · doi:10.1128/jvi.01707-24 · Cited by 7
Dengue Fever in a One Health Perspective - Latest Research and Recent Advances
Sperança, M. A. (2023) · Infectious diseases · doi:10.5772/intechopen.104140 · Cited by 6
Low-dose radiation promotes high-fat diet-induced atherosclerosis by activating cGAS signal pathway
Liu, X., Huang, X., Luo, J., Gao, S.-N., Bai, C., Xie, D., Gao, S., Guan, H., Huang, R., & Zhou, P. (2024) · Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease · doi:10.1016/j.bbadis.2024.167443 · Cited by 6
DNA PAMPs as Molecular Tools for the cGAS-STING Signaling Pathways
Zheng, C., & Zhang, L. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-4108-8_13 · Cited by 6
Enteroviral 3C protease cleaves N4BP1 to impair the host inflammatory response
Zhang, D., Xie, Y., Cao, J., Huang, L., & Fan, W. (2024) · Journal of Virology · doi:10.1128/jvi.01758-24 · Cited by 6
Boys, I. N., Mar, K. B., & Schoggins, J. W. (2021) · PLoS Genetics · doi:10.1371/journal.pgen.1009578 · Cited by 6
Self-citationJohansen, E. R., Schmalzriedt, D. L., Avila, D., Sylvester, P. A., Rahlf, C. R., Bobek, J. M., Sahoo, D., Dittel, B. N., & Tarakanova, V. L. (2024) · mBio · doi:10.1128/mbio.01598-24 · Cited by 6
Contributions of Ubiquitin and Ubiquitination to Flaviviral Antagonism of Type I IFN
Hay-McCullough, E., & Morrison, J. M. (2021) · Viruses · doi:10.3390/v13050763 · Cited by 6
Innate Immune Priming by cGAS as a Preparatory Countermeasure Against RNA Virus InfectionPreprint
Parker, M. T., Gopinath, S., Perez, C. E., Linehan, M. M., Crawford, J. M., Iwasaki, A., & Lindenbach, B. D. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/434027 · Cited by 6
Cardiomyocyte β-arrestins mediate inflammation and cGAS-STING activation in CVB3 viral myocarditis
Lucero, E. Y., Jiang, H., D’Anniballe, V. M., Pakharukova, N., Galtes, D., Bassford, D. K., Jyothidasan, A., Knowlton, K. U., Gunn, M. D., Lefkowitz, R. J., et al. (2026) · American Journal of Physiology-Heart and Circulatory Physiology · doi:10.1152/ajpheart.00589.2025 · Cited by 5
The Chicken cGAS–STING Pathway Exerts Interferon-Independent Antiviral Function via Cell Apoptosis
Jiang, S., Lv, M., Zhang, D., Cao, Q., Xia, N., Luo, J., Zheng, W., Chen, N., Meurens, F., & Zhu, J. (2023) · Animals · doi:10.3390/ani13162573 · Cited by 5
Pharmacological potential of cyclic nucleotide signaling in immunity
Ednacot, E. M. Q., Nabhani, A., Dinh, D. M., & Morehouse, B. R. (2024) · Pharmacology & Therapeutics · doi:10.1016/j.pharmthera.2024.108653 · Cited by 5
Shan, Y., Pang, H., Tang, Y., Yang, N., Wang, R., Yang, F., & Qin, B. (2025) · Virology Journal · doi:10.1186/s12985-025-02689-8 · Cited by 5
Xu, Z., Jiang, Z., Feng, K., Zhang, H., Shi, C., Dèng, F., Wáng, H., & Ning, Y. (2025) · Nature Communications · doi:10.1038/s41467-025-63295-4 · Cited by 5
Pattern Recognition Receptors in Autoinflammation
Saavedra, V., Moghaddas, F., Latz, E., & Masters, S. L. (2019) · Springer eBooks · doi:10.1007/978-3-319-98605-0_4 · Cited by 5
Behari, J., Yadav, K., Khare, P. S., Kumar, B., & Kushwaha, A. K. (2024) · Virology · doi:10.1016/j.virol.2024.110267 · Cited by 5
Cyclic Dinucleotides in the Scope of the Mammalian Immune System
Mankan, A. K., Müller, M., Witte, G., & Hornung, V. (2016) · Handbook of experimental pharmacology · doi:10.1007/164_2016_5002 · Cited by 5
Innate immunity and alpha/gammaherpesviruses: first impressions last a lifetime
Jondle, C. N., & Tarakanova, V. L. (2020) · Current Opinion in Virology · doi:10.1016/j.coviro.2020.07.002 · Cited by 5
Dressel, N., Natusch, L., Munz, C. M., Ramon, S. C., Morcos, M. N. F., Loff, A., Hiller, B., Haase, C., Schulze, L., Müller, P., et al. (2023) · Cancer Research · doi:10.1158/0008-5472.can-22-3860 · Cited by 5
Viral pathogenesis: Dengue virus takes on cGAS
van Gent, M., & Gack, M. U. (2017) · Nature Microbiology · doi:10.1038/nmicrobiol.2017.50 · Cited by 5
Alcorn, J. F., & Sarkar, S. N. (2014) · Expert Review of Respiratory Medicine · doi:10.1586/17476348.2015.994608 · Cited by 5
Cruz-Rivera, P. C. D. L., Eitson, J. L., & Schoggins, J. W. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.05.02.592239 · Cited by 5
Self-citationSTAT1 and herpesviruses: Making lemonade from lemons
Johansen, E. R., & Tarakanova, V. L. (2024) · Virology · doi:10.1016/j.virol.2024.110364 · Cited by 4
Wang, W., Cathcart, B., Nguyen, Q. D., Lao, L. Q., Bryans, A., Coleman, S. E., Rouhi, L., Gurha, P., & Marian, A. J. (2025) · JCI Insight · doi:10.1172/jci.insight.192283 · Cited by 4
Ma, W., Chu, S., Ma, Y., Wang, S., & Ma, X. (2025) · Current Neuropharmacology · doi:10.2174/011570159x386374250623095520 · Cited by 4
Human cytomegalovirus long non-coding RNA counteracts nuclear cGAS to facilitate immune evasion
Lee, S., Kim, S., Kim, H., Lee, D., Jeong, D., Kim, H., Park, J., Park, K., Hur, J., Kim, S., et al. (2025) · Nature Microbiology · doi:10.1038/s41564-025-02078-5 · Cited by 4
T cell-intrinsic cGAS-CTCF regulation maintains regulatory T cell development and function
Li, H. P., Zhang, Y., Gao, S., & Yin, H. (2025) · Cell Reports · doi:10.1016/j.celrep.2025.116302 · Cited by 5
Context-dependent actions of STING pathway in colitis and associated colon cancer
Qu, J., Cai, Y., Li, F., Li, Y., & Liu, R. (2025) · Genes & Diseases · doi:10.1016/j.gendis.2025.101855 · Cited by 4
IRE1α translational suppression potentiates STING-dependent chemoresistance in pancreatic cancer
Luo, Y., Sun, M., Chang, L., He, Z., Zhou, X., Yuan, Y., Sun, H., Luo, S., Huang, J., Wu, H., et al. (2025) · Cell Death and Disease · doi:10.1038/s41419-025-07999-x · Cited by 4
The Role of cGAS – STING Pathway in Chronic Liver Diseases: Mechanisms and Therapeutic Perspectives
Yang, Z., Guo, G., Li, J., & Sun, C. (2025) · The FASEB Journal · doi:10.1096/fj.202501996r · Cited by 4
STING agonists as antiviral agents
Nelson, T. S., & Ma, Z. (2025) · FEBS Letters · doi:10.1002/1873-3468.70251 · Cited by 6
Krey, K., Risso-Ballester, J., Hamad, S., Maidl, S., Bilekova, S., Emslander, Q., Verin, M., Mundigl, S., Cernat, A., Piras, A., et al. (2026) · Nature Communications · doi:10.1038/s41467-026-72732-x · Cited by 4
Molecular mechanisms regulating cGAS/STING activation in health and disease
Cho, M.-G., Lee, R., Johnson, J., & Gupta, G. P. (2026) · Journal of Clinical Investigation · doi:10.1172/jci204548 · Cited by 4
cGAS-mediated type I IFN signaling contributes to disease progression in drug-refractory epilepsy
Huang, Y., Fan, L., Wong, M. Y., Lei, Z., Krishnamachary, B., Zhu, D., Cadiz, M. P., Nagiri, R. K., Ye, P., Norman, K., et al. (2026) · Nature Neuroscience · doi:10.1038/s41593-026-02384-z · Cited by 4
IFI207, a young and fast-evolving protein, controls retroviral replication via the STING pathway
Moran, E. A., Salas-Briceno, K., Zhao, W., Enya, T., Aguilera, A. N., Acosta, I., Alonzo, F., Kiani, D., Behnsen, J., Alvarez, C., et al. (2024) · mBio · doi:10.1128/mbio.01209-24 · Cited by 4
The role of post-translational modifications of cGAS in γδ T cells
Liu, Y., Huang, Y., Wei, H., Liang, X., & Luo, J. (2024) · Molecular Immunology · doi:10.1016/j.molimm.2024.10.002 · Cited by 4
Di, C., Jiang, Y., Li, L., Shi, M., Zhu, Y., Zhang, J., Song, Y., Su, X., & Qu, J. (2023) · Stem Cells · doi:10.1093/stmcls/sxad016 · Cited by 4
Virulence Determinants of New World Alphaviruses and Broad-Acting Therapeutic Strategies
Wu, J. (2015) · Future Virology · doi:10.2217/fvl.15.8 · Cited by 4
Kazmierski, J., Elsner, C., Döhner, K., Xu, S., Ducroux, A., Pott, F., Jansen, J., Thorball, C. W., Zeymer, O., Zhou, X., et al. (2022) · The Journal of Immunology · doi:10.4049/jimmunol.2100685 · Cited by 5
Schwanke, H., Magalhães, V. G., Schmelz, S., Wyler, E., Hennig, T., Günther, T., Grundhoff, A. T., Dölken, L., Landthaler, M., van Ham, M., et al. (2023) · Journal of Virology · doi:10.1128/jvi.00400-23 · Cited by 4
Mitochondria and Antiviral Immunity
Thomas, S., & Gale, M. (2016) · Springer eBooks · doi:10.1007/978-1-4939-3612-0_10 · Cited by 4
Schoggins, J. W. (2015) · Science · doi:10.1126/science.aad0942 · Cited by 4
Self-citationThe toll (like receptor 3) to the pathogenesis of herpes simplex encephalitis
Steiner, I., & Tyler, K. L. (2014) · Neurology · doi:10.1212/wnl.0000000000001011 · Cited by 4
Lai, W., Xia, J., Fei, S., Zhou, M., Huang, Y., Luo, W., Kong, Y., Swevers, L., Sun, J., & Feng, M. (2025) · Insect Biochemistry and Molecular Biology · doi:10.1016/j.ibmb.2025.104352 · Cited by 3
Context-Specific Diversity of Antimicrobial Functions of Interferon-Stimulated Genes
Harioudh, M. K., & Sarkar, S. N. (2025) · Viruses · doi:10.3390/v17121635 · Cited by 3
Innate immune sensing of alphavirus chikungunya: balancing antiviral defense and pathogenesis
da Silva, J. S. D. F., Ferreira, C. V., dos Santos, L. M. S., de Andrade‐Neto, V. F., Guedes, P. M. D. M., Yaochite, J. N. U., França, R. F. D. O., Brito, R. M. D. M., & Nascimento, M. S. L. (2026) · Frontiers in Immunology · doi:10.3389/fimmu.2026.1810208 · Cited by 3
Cladophorol-A is an inhibitor of cyclic GMP-AMP synthase
Kissai, M., Chin, E. N., Martínez‐Peña, F., Sulpizio, A., Stout, E. P., Usui, I., Barmare, F., Sanchez, B. B., Esquenazi, E., Stanfield, R. L., et al. (2024) · Bioorganic & Medicinal Chemistry Letters · doi:10.1016/j.bmcl.2024.130007 · Cited by 3
Herpes simplex virus-1 targets the 2′-3'cGAMP importer SLC19A1 as an antiviral countermeasure
Szemere, Z. K., Ijezie, E. C., & Murphy, E. A. (2024) · Virology · doi:10.1016/j.virol.2024.110320 · Cited by 3
RNA binding as an emerging regulatory dimension in the type I IFN response
Iselin, L., Demyanenko, Y., Palmalux, N., Buh, A. E., Ruscica, V., Brown, J. B., Raut, N., Kamel, W., Peter Simmonds, K., Mohammed, S., et al. (2026) · Cell Reports · doi:10.1016/j.celrep.2026.117174 · Cited by 3
Keeping your armour intact: How HIV‐1 evades detection by the innate immune system
Maelfait, J., Seiradake, E., & Rehwinkel, J. (2014) · BioEssays · doi:10.1002/bies.201400019 · Cited by 3
The Evasion of Antiviral Innate Immunity by Chicken DNA Viruses
Gao, L., Zheng, S. J., & Wang, Y. (2021) · Frontiers in Microbiology · doi:10.3389/fmicb.2021.771292 · Cited by 3
DeMarino, C., Nath, A., Zhuang, Z., & Doucet-O’Hare, T. T. (2023) · Extracellular Vesicles and Circulating Nucleic Acids · doi:10.20517/evcna.2023.45 · Cited by 3
Martin, G. R., Arcila, C. S., Hallihan, L. J., Scheidl-Yee, T., & Jirik, F. R. (2023) · Journal of Leukocyte Biology · doi:10.1093/jleuko/qiac019 · Cited by 3
Hertzog, P. J., Bourke, N. M., de Weerd, N. A., & Mangan, N. E. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-374279-7.10007-4 · Cited by 3
Human interferon stimulated genes target ancient features of animal and bacterial viral replicationPreprint
Fernandez, S. G., Hutchinson, J. E., Tan, J. M., Yamaguchi, S., Roffler, A. A., Schmidt, A. G., & Kranzusch, P. J. (2026) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.64898/2026.06.11.731453 · Cited by 3
Jayakumar, P., Jiang, T., Huang, H., & Deng, M. (2025) · Frontiers in Pharmacology · doi:10.3389/fphar.2025.1576151 · Cited by 2
Wei, Q., Zhao, K., Wu, Y., Wu, W., & Hao, N. (2025) · Clinical and Translational Medicine · doi:10.1002/ctm2.70531 · Cited by 2
Interferons Inhibit Ebola Virus Infection of Human Keratinocytes
Elliff, J. M., Ert, H. A. V., Sevcik, K. M., Djurkovic, M. A., Rudd, D., Gourronc, F. A., Klingelhutz, A. J., Shtanko, O., & Maury, W. J. (2025) · Viruses · doi:10.3390/v17121577 · Cited by 2
cGAS-STING dependent type I IFN reduces Leptospira interrogans renal colonization in mice
Gupta, S., Matsunaga, J., Ratitong, B., Manion, A., Ismaeel, S., Valadares, D. G., West, A. P., Kerur, N., Stehlik, C., Dorfleutner, A., et al. (2026) · PLoS Pathogens · doi:10.1371/journal.ppat.1013250 · Cited by 2
Li, H., Zhang, Y., Wang, J., Zhang, Q., Sun, H., & Wei, F. (2026) · Advanced Science · doi:10.1002/advs.202511012 · Cited by 2
Collet, B., & Boudinot, P. (2026) · Biomedical Journal · doi:10.1016/j.bj.2026.100987 · Cited by 2
Emerging roles of the cGAS/STING pathway in cardiovascular diseases
Saitoh, W., Higashikuni, Y., Bavuu, O., Sata, M., & Fukuda, D. (2026) · Journal of Clinical Investigation · doi:10.1172/jci204551 · Cited by 2
de Souza, M. P. M., Freitas, B. C. G., Holanda, G. M., Diniz, J. A. P., & Cruz, A. C. R. (2022) · Anais da Academia Brasileira de Ciências · doi:10.1590/0001-3765202220211189 · Cited by 2
Role of CIV NS1 Protein in Innate Immunity and Viral Replication
Fu, C., Zhu, W., Cao, N., Liu, W., Lu, Z., Wong, Z., Guan, K., Hu, C., Han, B., Zeng, S., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241210056 · Cited by 2
Bankers, L., Miller, C. M., Liu, G., Thongkittidilok, C., Morrison, J. H., & Poeschla, E. M. (2020) · The Journal of Immunology · doi:10.4049/jimmunol.1901421 · Cited by 2
Nonstructural protein VP2 of chicken anemia virus triggers IFN-β expression via host cGAS
Liu, X., Wang, Y., Song, T., Zheng, Y., Zhang, X., Li, J., Li, L., Augusto, G. S., & Sun, F. (2023) · Veterinary Microbiology · doi:10.1016/j.vetmic.2023.109842 · Cited by 2
Liang, X., Liu, H., Hu, H., Zhou, J., Abedini, A., Navarro, A., Kloetzer, K. A., & Suszták, K. (2024) · Journal of the American Society of Nephrology · doi:10.1681/asn.2024gp2qh30g · Cited by 2
Franz, K. M., & Kagan, J. C. (2014) · Immunology and Cell Biology · doi:10.1038/icb.2013.108 · Cited by 2
Verrier, E. R., Gack, M. U., Baumert, T. F., Schoggins, J. W., MacDuff, D. A., Imanaka, N., Gainey, M. D., Shrestha, B., & Eitson, J. L. (2014) · Hepatology · doi:10.1002/hep.27187 · Cited by 2
Self-citationCaddy, S., Wang, M., Krishnamurthy, P., Uttenthal, B. J., Chandra, A., Crawley, C. R., & James, L. C. (2018) · Innate Immunity · doi:10.1177/1753425918757898 · Cited by 2
Virology: Poxins Soothe the STING
Decout, A. C., & Ablasser, A. (2019) · Current Biology · doi:10.1016/j.cub.2019.03.031 · Cited by 2
Yakass, M. B., Franco, D., & Quaye, O. (2020) · Viruses · doi:10.3390/v12080802 · Cited by 2
Role of the dimerization domain of black carp STING during the antiviral innate immunity
Yan, J., Qiao, G., Chang, H., Wu, H., Liu, M., Tu, J., Zhang, Y., & Feng, H. (2023) · Reproduction and Breeding · doi:10.1016/j.repbre.2023.05.002 · Cited by 2
Bystander neuronal progenitors in forebrain organoids promote protective antiviral responses
Negatu, S. G., Vazquez, C., Bannerman, C., Amses, K. R., Ming, G., & Jurado, K. A. (2025) · Journal of Neuroinflammation · doi:10.1186/s12974-025-03381-y · Cited by 2
Innate Immunity in Viral Encephalitis
Reiss, C. S. (2016) · Springer eBooks · doi:10.1007/978-3-319-33189-8_8 · Cited by 3
MafF is an antiviral host factor that suppresses transcription from Hepatitis B Virus core promoterPreprint
Ibrahim, M. K., Abdelhafez, T. H., Takeuchi, J. S., Wakae, K., Sugiyama, M., Tsuge, M., Ito, M., Watashi, K., El‐Kassas, M., Kato, T., et al. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.07.29.227793 · Cited by 2
Species-specific Deamidation of cGAS Facilitates Herpes Simplex Virus Lytic ReplicationPreprint
Zhang, J., Zhao, J., Li, J., Xu, S., He, S., Zeng, Y., Xie, L., Xie, N., Liu, T., Lee, K., et al. (2018) · SSRN Electronic Journal · doi:10.2139/ssrn.3188495 · Cited by 2
LY6E protects mice from pathogenic effects of murine coronavirus and SARS-CoV-2Preprint
Mar, K. B., Dyke, M. C. C. V., Lopez, A. H., Eitson, J. L., Fan, W., Hanners, N. W., Evers, B. M., Shelton, J. M., & Schoggins, J. W. (2023) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2023.01.25.525551 · Cited by 2
Self-citationDowaidar, M. (2021) · doi:10.31219/osf.io/2ez7a · Cited by 2
New insight into the enhanced effect of pegylated interferon-α
Abe, H., Hayes, N. C., & Chayama, K. (2014) · Hepatology · doi:10.1002/hep.27269 · Cited by 1
In Vitro Cleavage Assay to Characterize DENV NS2B3 Antagonism of cGAS
Bhattacharya, M., Bhowmik, D., & Yin, Q. (2024) · Methods in molecular biology · doi:10.1007/978-1-0716-4108-8_16 · Cited by 1
Weigang, S., Serrero, M. C., Bogdanow, B., Hüsers, F., Lückel, J., Bauerfeind, R., Liu, F., Kochs, G., & Sodeik, B. (2026) · PLoS Pathogens · doi:10.1371/journal.ppat.1014370 · Cited by 1
Zou, J., Jian, J., Ge, D., Zhou, B., & Zhang, J. (2025) · Journal of Biochemical and Molecular Toxicology · doi:10.1002/jbt.70586 · Cited by 1
Wu, M.-H., Lee, S.-T., Chang, T.-H., Chao, W.-S., Lin, N.-K., & Lin, S.-L. (2025) · International Journal of Molecular Sciences · doi:10.3390/ijms27010389 · Cited by 1
Equine arteritis virus Nsp10 promotes MAVS proteasomal degradation via E3 ligases Smurf1/MARCH5
Zhou, B., Chen, K., Liang, H., 戚亭, Guo, X., Wen, Y., Du, C., & Wang, X. (2026) · Journal of Virology · doi:10.1128/jvi.02061-25 · Cited by 1
Innate Immune and Inflammatory Responses to Dengue Virus Infection
Hubner, L. J., Ascenção, F. R., & Mansur, D. S. (2025) · Current topics in microbiology and immunology · doi:10.1007/82_2025_291 · Cited by 1
The Pathogenic Role of the DNA Double-Stranded Breaks in Hereditary Cardiomyopathies
Marian, A. J. (2025) · Heart Failure Clinics · doi:10.1016/j.hfc.2025.08.006 · Cited by 1
Matos, A. D. O., Neto, J. R. D. C., Franco, F. C., Dietz, J. D. C., Dantas, P. H. D. S., Felice, A. G., Luchs, A., de Oliveira, M. A. P., da Silva, A. C. G., Soares, S. D. C., et al. (2025) · Pathogens · doi:10.3390/pathogens14101029 · Cited by 1
Does fever drive the evolution of antiviral genes?
Langlois, R. A. (2025) · The Journal of Experimental Medicine · doi:10.1084/jem.20251747 · Cited by 1
Zeng, L., Li, Y., Liu, J., Liu, C., Gao, N., He, J., & Zhang, Y. (2026) · Molecular Genetics and Genomics · doi:10.1007/s00438-025-02341-8 · Cited by 1
Wu, M., Wang, P., Wang, R., Zhan, M., Wang, J., Cai, H., Zha, L., Zhou, N., Luo, Q., Chen, L., et al. (2026) · PLoS neglected tropical diseases · doi:10.1371/journal.pntd.0014035 · Cited by 1
Liu, X., Xu, M., Wang, H., Wang, H., Wang, H., Fang, W., Li, M., Huang, J., Chen, F. C., Wang, H., et al. (2026) · Cell Communication and Signaling · doi:10.1186/s12964-026-02989-8 · Cited by 1
Metadata
- Authors
- Schoggins, J. W., MacDuff, D. A., Imanaka, N., Gainey, M. D., Shrestha, B., Eitson, J. L., Mar, K. B., Richardson, R. B., Ratushny, A. V., Litvak, V., Dabelic, R., Manicassamy, B., Aitchison, J. D., Aderem, A., Elliott, R. M., García-Sastre, A., Racaniello, V., Snijder, E. J., Yokoyama, W. M., Diamond, M. S., Virgin, H. W., & Rice, C. M.
- Affiliations
- MRC University of Glasgow Centre for Virus Research (GB)
- Washington University in St. Louis (US)
- Rockefeller University (US)
- Howard Hughes Medical Institute (US)
- The University of Texas Southwestern Medical Center (US)
- Center for Infectious Disease Research (US)
- Columbia University (US)
- University of Chicago (US)
- University of St Andrews (GB)
- Leiden University Medical Center (NL)
- Corresponding author
- Schoggins, John W.
- Rice, Charles M.
- ORCID
- Venue
- Nature
- Published
- 2013-11-27
- Volume
- 505
- Issue
- 7485
- Pages
- 691-695
- ISSN
- 0028-0836 (ISSN-L)
- 1476-4687
- PMC
- PMC4077721
- OpenAlex
- W2058277625
- Cited by
- 896
- References
- 39
- Citations by year
- 2026: 41 · 2025: 49 · 2024: 51 · 2023: 80 · 2022: 76 · 2021: 79 · 2020: 92 · 2019: 74 · 2018: 82 · 2017: 58 · 2016: 74 · 2015: 87 · 2014: 52
- FWCI
- 39.24
- Type
- journal article
- Language
- en
- Update notices
- erratum (2015-07-08)
- Open access
- green
- www.ncbi.nlm.nih.gov
- Licence
- Locations
- Nature (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Data Archiving and Networked Services (DANS) (submittedVersion)
- RePEc: Research Papers in Economics (submittedVersion)
- Leiden Repository (Leiden University) (submittedVersion)
- Funders
- Howard Hughes Medical Institute
- U.S. Department of Veterans Affairs (HHSN272200900041CU19)
- Wellcome Trust (099220)
- National Institutes of Health (5t32ai005284-45)
- National Institute of General Medical Sciences (U54GM103511, GM103511, GM 076547, P50GM076547)
- National Institute of Allergy and Infectious Diseases (T32-AI005284, AI 057160, AI091707, U01AI095611, HHSN266200700010C, AI057158, R01AI091707, AI104972, U19AI083025, R01AI032972, AI095611, U54AI057160, R01AI025032, R00AI095320, AI083025, U54AI057158, R01AI102597, R01AI104972, HHSN272200900041C)
- National Institute of Diabetes and Digestive and Kidney Diseases (K01DK095031, DK095031)
- National Institute of Arthritis and Musculoskeletal and Skin Diseases (T32AR007279)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Health Sciences › Medicine › Epidemiology › Virology and Viral Diseases
- Keywords
- cGAS, interferon-stimulated genes, antiviral innate immunity, positive-sense single-stranded RNA viruses, negative-sense RNA viruses, DNA viruses, STING, IRF3, type I interferon
- MeSH terms
- STING Protein, Cyclic Guanosine Monophosphate-Adenosine Monophosphate Synthase, Animals, DNA Viruses, Flow Cytometry, Immunity, Innate, Interferons, Membrane Proteins, Nucleotidyltransferases, RNA Viruses, Substrate Specificity, Viruses, Gene Library, Cluster Analysis, Mice, Knockout, STAT1 Transcription Factor, Interferon Regulatory Factor-3, Mice
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