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 401–500 of 885
Inhibition of type I interferon induction and signalling by mosquito-borne flaviviruses
Cumberworth, S. L., Clark, J. J., Kohl, A., & Donald, C. L. (2017) · Cellular Microbiology · doi:10.1111/cmi.12737 · Cited by 38
IFITM3 Restricts Human Metapneumovirus Infection
McMichael, T. M., Zhang, Y., Kenney, A. D., Zhang, L., Zani, A., Lu, M., Chemudupati, M., Lǐ, J., & Yount, J. S. (2018) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiy361 · Cited by 38
The Role of Mitochondrial DNA in the Development of Ischemia Reperfusion Injury
Hu, Q., Zhou, Q., Wu, J., Wu, X., & Ren, J. (2018) · Shock · doi:10.1097/shk.0000000000001190 · Cited by 39
Han, F., Guo, H., Wang, L., Zhang, Y., Sun, L., Dai, C., & Wu, X. (2020) · Experimental Eye Research · doi:10.1016/j.exer.2020.108366 · Cited by 38
Irudayam, J. I., Contreras, D. A., Spurka, L., Subramanian, A., Allen, J. R., Ren, S., Kanagavel, V., Nguyen, Q., Ramaiah, A., Ramamoorthy, K., et al. (2015) · Stem Cell Research · doi:10.1016/j.scr.2015.08.003 · Cited by 37
Reshaping of the Dendritic Cell Chromatin Landscape and Interferon Pathways during HIV Infection
Johnson, J. S., Lucas, S. Y., Amon, L. M., Skelton, S., Nazitto, R., Carbonetti, S., Sather, D. N., Littman, D. R., & Aderem, A. A. (2018) · Cell Host & Microbe · doi:10.1016/j.chom.2018.01.012 · Cited by 42
Self-citationLi, Q., Liu, C., Yue, R., El-Ashram, S. A., Wang, J., He, X., Zhao, D., Zhou, X., & Xu, L. (2019) · International Journal of Molecular Sciences · doi:10.3390/ijms20040895 · Cited by 37
Dynamic rewiring of the human interactome by interferon signaling
Kerr, C. H., Skinnider, M. A., Madero, A. M., Andrews, D. D. T., Stacey, R. G., Chan, Q. W. T., Stoynov, N., Jan, E., & Foster, L. J. (2020) · Genome biology · doi:10.1186/s13059-020-02050-y · Cited by 38
Type I interferon remodels lysosome function and modifies intestinal epithelial defense
Zhang, H., Zoued, A., Liu, X., Sit, B., & Waldor, M. K. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2010723117 · Cited by 37
Das, U. N. (2022) · European Journal of Clinical Nutrition · doi:10.1038/s41430-022-01173-8 · Cited by 37
Zheng, Q., Wang, D., Lin, R., Lv, Q., & Wang, W. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.1013322 · Cited by 38
Molecular cloning and functional characterization of porcine cyclic GMP–AMP synthase
Wang, J., Chu, B., Du, L., Han, Y.-Q., Zhang, X., Fan, S., Wang, Y., & Yang, G. (2015) · Molecular Immunology · doi:10.1016/j.molimm.2015.02.002 · Cited by 37
Cytomegalovirus immune evasion of myeloid lineage cells
Brinkmann, M. M., Dağ, F., Hengel, H., Messerle, M., Kalinke, U., & Čičin‐Šain, L. (2015) · Medical Microbiology and Immunology · doi:10.1007/s00430-015-0403-4 · Cited by 38
Zhao, P., Liu, S., Zhong, Z., Jiang, T., Weng, R., Xie, M., Yang, S., & Xia, X. (2018) · Scientific Reports · doi:10.1038/s41598-018-30359-z · Cited by 36
The Emerging Role of RNA Modifications in the Regulation of Antiviral Innate Immunity
Tong, J., Zhang, W., Chen, Y., Yuan, Q., Qin, N.-N., & Qu, G. (2022) · Frontiers in Microbiology · doi:10.3389/fmicb.2022.845625 · Cited by 37
Breaking barriers: The cGAS‐STING pathway as a novel frontier in cancer immunotherapy
Yan, Y., Tan, X., Song, B., Yi, M., Chu, Q., & Wu, K. (2025) · 癌症:英文版 · doi:10.1002/cac2.70067 · Cited by 35
Lemos, H. D. P., Huang, L., McGaha, T. L., & Mellor, A. L. (2014) · European Journal of Immunology · doi:10.1002/eji.201344407 · Cited by 37
Fourati, S., Ribeiro, S. P., Lopes, F. B. T. P., Talla, A., Lefebvre, F., Cameron, M. J., Kaewkungwal, J., Pitisuttithum, P., Nitayaphan, S., Rerks‐Ngarm, S., et al. (2019) · Nature Communications · doi:10.1038/s41467-019-08854-2 · Cited by 37
Analysis of Stop-Gain and Frameshift Variants in Human Innate Immunity Genes
Rausell, A., Mohammadi, P., McLaren, P. J., Bartha, I., Xénarios, I., Fellay, J., & Telenti, A. (2014) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1003757 · Cited by 37
Humanized Mice in Dengue Research: A Comparison with Other Mouse Models
Coronel-Ruiz, C., Gutiérrez-Barbosa, H., Medina-Moreno, S., Velandia-Romero, M. L., Chua, J. V., Castellanos, J. E., & Zapata, J. C. (2020) · Vaccines · doi:10.3390/vaccines8010039 · Cited by 35
Flaviviridae Nonstructural Proteins: The Role in Molecular Mechanisms of Triggering Inflammation
Latanova, A. A., Starodubova, E. S., & Карпов, В. Л. (2022) · Viruses · doi:10.3390/v14081808 · Cited by 36
Calvert, J. K., Helbig, K. J., Dimasi, D. P., Cockshell, M. P., Beard, M. R., Pitson, S. M., Bonder, C. S., & Carr, J. M. (2015) · Journal of Interferon & Cytokine Research · doi:10.1089/jir.2014.0195 · Cited by 35
Mosquito-borne flaviviruses and type I interferon: catch me if you can!
Zoladek, J., & Nisole, S. (2023) · Frontiers in Microbiology · doi:10.3389/fmicb.2023.1257024 · Cited by 34
Early host defense against virus infections
Paludan, S. R., Pradeu, T., Pichlmair, A., Wray, K. B., Mikkelsen, J. G., Olagnier, D. P., & Mogensen, T. H. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.115070 · Cited by 38
Wang, B., Lam, T. H., Soh, M. K., Ye, Z., Chen, J., & Ren, E. C. (2018) · Frontiers in Immunology · doi:10.3389/fimmu.2018.01193 · Cited by 34
Modulation of the innate immune response by human cytomegalovirus
Biolatti, M., Gugliesi, F., Dell’Oste, V., & Landolfo, S. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.06.025 · Cited by 40
Filament-like Assemblies of Intracellular Nucleic Acid Sensors: Commonalities and Differences
Cadena, C., & Hur, S. (2019) · Molecular Cell · doi:10.1016/j.molcel.2019.09.023 · Cited by 34
DNA-Sensing Antiviral Innate Immunity in Poxvirus Infection
Lu, Y., & Zhang, L. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.01637 · Cited by 34
Yu, Y., Yang, W., Bilotta, A. J., Yu, Y., Zhao, X., Zhou, Z., Yao, S., Xu, J., Zhou, J., Dann, S. M., et al. (2020) · The FASEB Journal · doi:10.1096/fj.202001524r · Cited by 34
Goubau, D., van der Veen, A. G., Chakravarty, P., Lin, R., Rogers, N. C., Rehwinkel, J., Deddouche, S., Rosewell, I. R., Hiscott, J. B., & Sousa, C. R. E. (2015) · European Journal of Immunology · doi:10.1002/eji.201545794 · Cited by 34
Interferon-stimulated genes: new platforms and computational approaches
Green, R. R., Ireton, R. C., & Gale, M. (2018) · Mammalian Genome · doi:10.1007/s00335-018-9755-6 · Cited by 37
Weiss, E., Rautou, P., Fasseu, M., Giabicani, M., de Chambrun, M. P., Wan, J., Minsart, C., Gustot, T., Couvineau, A., Maiwall, R., et al. (2016) · Journal of Hepatology · doi:10.1016/j.jhep.2016.12.008 · Cited by 34
Tao, R. N., Fang, L., Bai, D., Ke, W., Zhou, Y., Wang, D., & Xiao, S. (2018) · The Journal of Immunology · doi:10.4049/jimmunol.1701773 · Cited by 33
Function and Modulation of Type I Interferons during Respiratory Syncytial Virus Infection
Stephens, L. M., & Varga, S. M. (2020) · Vaccines · doi:10.3390/vaccines8020177 · Cited by 33
Mboko, W. P., Olteanu, H., Ray, A., Xin, G., Darrah, E. J., Kumar, S. N., Kulinski, J. M., Cui, W., Dittel, B. N., Gauld, S. B., et al. (2015) · Journal of Virology · doi:10.1128/jvi.02774-15 · Cited by 33
Tumour viruses and innate immunity
Hopcraft, S. E., & Damania, B. (2017) · Philosophical Transactions of the Royal Society B Biological Sciences · doi:10.1098/rstb.2016.0267 · Cited by 33
Massa, C., Wang, Y., Marr, N., & Seliger, B. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms24076736 · Cited by 32
Regulation of cGAS Activity and Downstream Signaling
Joshi, B., Joshi, J. C., & Mehta, D. (2022) · Cells · doi:10.3390/cells11182812 · Cited by 33
Innate immune recognition against SARS-CoV-2
Yamada, T., & Takaoka, A. (2023) · Inflammation and Regeneration · doi:10.1186/s41232-023-00259-5 · Cited by 33
Tuipulotu, D. E., Feng, S., Pandey, A., Zhao, A., Ngo, C., Mathur, A., Lee, J., Shen, C. X., Fox, D., Xue, Y., et al. (2023) · The EMBO Journal · doi:10.15252/embj.2022112558 · Cited by 32
McDonald, J. U., Kaforou, M., Clare, S., Hale, C., Ivanova, M., Huntley, D. M., Dorner, M., Wright, V., Levin, M., Martinón‐Torres, F., et al. (2016) · mSystems · doi:10.1128/msystems.00051-16 · Cited by 32
Mboko, W. P., Rekow, M. M., Ledwith, M. P., Lange, P. T., Schmitz, K. E., Anderson, S., & Tarakanova, V. L. (2016) · Journal of Virology · doi:10.1128/jvi.01444-16 · Cited by 34
Vertical transmission of hepatitis E virus in pregnant rhesus macaques
Yu, W., Hao, X., Li, Y., Yang, C., Li, Y., He, Z., & Huang, F. (2020) · Scientific Reports · doi:10.1038/s41598-020-74461-7 · Cited by 32
Wang, Y., Liu, Y., Zhang, J., Peng, Q., Wang, X., Xiao, X., & Shi, K. (2024) · Acta Biomaterialia · doi:10.1016/j.actbio.2024.01.008 · Cited by 31
Yang, H. M., Winkler, W., & Wu, X. (2021) · Journal of Virology · doi:10.1128/jvi.00283-21 · Cited by 31
Anwar, S., Islam, K. U., Azmi, M. I., & Iqbal, J. (2021) · Archives of Virology · doi:10.1007/s00705-021-05211-x · Cited by 31
Hanners, N. W., Mar, K. B., Boys, I. N., Eitson, J. L., Cruz-Rivera, P. C. D. L., Richardson, R. B., Fan, W., Wight‐Carter, M., & Schoggins, J. W. (2021) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2111266118 · Cited by 32
Self-citationPerelman, S. S., Abrams, M. E., Eitson, J. L., Chen, D., Jimenez, A., Mettlen, M., Schoggins, J. W., & Alto, N. M. (2016) · PLoS Pathogens · doi:10.1371/journal.ppat.1006102 · Cited by 32
Self-citationTLR7 Agonists Display Potent Antiviral Effects against Norovirus Infection via Innate Stimulation
Tuipulotu, D. E., Netzler, N. E., Lun, J. H., Mackenzie, J. M., & White, P. A. (2018) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.02417-17 · Cited by 31
Leist, S. R., & Baric, R. S. (2018) · Trends in Genetics · doi:10.1016/j.tig.2018.07.005 · Cited by 31
Gong, L.-K., Yang, X., Yang, J., Wu, S., Chen, Y., Zhang, J., Wang, Z., Chen, L., Xing, C., & Liu, T. (2022) · Frontiers in Pharmacology · doi:10.3389/fphar.2022.1020670 · Cited by 32
Chicken DNA Sensing cGAS-STING Signal Pathway Mediates Broad Spectrum Antiviral Functions
Li, S., Yang, J., Zhu, Y., Ji, X., Wang, K., Jiang, S., Luo, J., Wang, H., Zheng, W., Chen, N., et al. (2020) · Vaccines · doi:10.3390/vaccines8030369 · Cited by 30
Absence of cGAS-mediated type I IFN responses in HIV-1–infected T cells
Elsner, C., Ponnurangam, A., Kazmierski, J., Zillinger, T., Jansen, J., Tödt, D., Döhner, K., Xu, S., Ducroux, A., Kriedemann, N., et al. (2020) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2002481117 · Cited by 32
A Variety of Nucleic Acid Species Are Sensed by cGAS, Implications for Its Diverse Functions
Wang, D., Zhao, H., Shen, Y., & Chen, Q. (2022) · Frontiers in Immunology · doi:10.3389/fimmu.2022.826880 · Cited by 34
Ku proteins promote DNA binding and condensation of cyclic GMP-AMP synthase
Tao, X., Song, J., Song, Y., Zhang, Y., Yang, J., Zhang, P., Zhang, D., Chen, D., & Sun, Q. (2022) · Cell Reports · doi:10.1016/j.celrep.2022.111310 · Cited by 31
Type I IFN – A blunt spear in fighting HIV-1 infection
Acchioni, C., Marsili, G., Perrotti, E., Remoli, A. L., Sgarbanti, M., & Battistini, A. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.10.004 · Cited by 33
Oudshoorn, D., van der Hoeven, B., Limpens, R. W. A. L., Beugeling, C., Snijder, E. J., Bárcena, M., & Kikkert, M. (2016) · mBio · doi:10.1128/mbio.01991-16 · Cited by 30
Self-citationInterferon inhibits a model RNA virus via a limited set of inducible effector genes
McDougal, M. B., Maria, A. M. D., Ohlson, M. B., Kumar, A., Xing, C., & Schoggins, J. W. (2023) · EMBO Reports · doi:10.15252/embr.202356901 · Cited by 30
Self-citationActivation and Evasion of Innate Immunity by Gammaherpesviruses
Lange, P. T., White, M. C., & Damania, B. (2021) · Journal of Molecular Biology · doi:10.1016/j.jmb.2021.167214 · Cited by 31
Links between recognition and degradation of cytoplasmic viral RNA in innate immune response
Oshiumi, H., Mifsud, E. J., & Daito, T. (2015) · Reviews in Medical Virology · doi:10.1002/rmv.1865 · Cited by 29
Bussey, K. A., Lau, U., Schumann, S., Gallo, A., Osbelt, L., Stempel, M., Arnold, C. M., Wissing, J. B., Gad, H. H., Hartmann, R., et al. (2018) · PLoS Pathogens · doi:10.1371/journal.ppat.1006937 · Cited by 30
Delicate regulation of the cGAS–MITA-mediated innate immune response
Luo, W., & Shu, H. (2018) · Cellular and Molecular Immunology · doi:10.1038/cmi.2016.51 · Cited by 29
Li, Y., Fang, L., Zhou, Y., Tao, R. N., Wang, D., & Xiao, S. (2018) · Journal of Virology · doi:10.1128/jvi.00600-18 · Cited by 29
Korneenko, T. V., Pestov, N. B., Nevzorov, I. A., Daks, A. A., Николаевич, Т. К., Солопова, О. Н., & Barlev, N. A. (2023) · Pharmaceuticals · doi:10.3390/ph16121675 · Cited by 29
Huang, X., Xu, Y., Lin, Q., Guo, W., Zhao, D., Wang, C., Wang, L., Zhou, H., Jiang, Y., Cui, W., et al. (2019) · Virulence · doi:10.1080/21505594.2019.1707957 · Cited by 28
A Critical Role for STING Signaling in Limiting Pathogenesis of Chikungunya Virus
Geng, T., Lin, T., Yang, D., Harrison, A. G., Vella, A. T., Fikrig, E., & Wang, P. (2020) · The Journal of Infectious Diseases · doi:10.1093/infdis/jiaa694 · Cited by 28
Pott, F., Postmus, D., Brown, R. J. P., Wyler, E., Neumann, E., Landthaler, M., & Goffinet, C. (2021) · Emerging Microbes & Infections · doi:10.1080/22221751.2021.2000891 · Cited by 32
Regulation of cGAS/STING signaling and corresponding immune escape strategies of viruses
Ge, Z., & Ding, S. (2022) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2022.954581 · Cited by 28
Zhao, J., Vijay, R., Zhao, J., Gale, M., Diamond, M., & Perlman, S. M. (2016) · Journal of Virology · doi:10.1128/jvi.00707-16 · Cited by 28
Self-citationThe RAB2B-GARIL5 Complex Promotes Cytosolic DNA-Induced Innate Immune Responses
Takahama, M., Fukuda, M., Ohbayashi, N., Kozaki, T., Misawa, T., Okamoto, T., Matsuura, Y., Akira, S., & Saitoh, T. (2017) · Cell Reports · doi:10.1016/j.celrep.2017.08.085 · Cited by 29
Wang, B., Zhang, Y., Niu, H., Zhao, X., Chen, G., Zhao, Q., Ma, G., Du, S., & Zeng, Z. (2023) · International Journal of Radiation Oncology*Biology*Physics · doi:10.1016/j.ijrobp.2023.10.041 · Cited by 27
ILC3s sense gut microbiota through STING to initiate immune tolerance
Zhou, W., Zhou, J., Ahmed, A., Kim, M. J., Guo, C., & Sonnenberg, G. F. (2025) · Immunity · doi:10.1016/j.immuni.2025.05.016 · Cited by 27
Endosomal Toll-Like Receptors 7 and 9 Cooperate in Detection of Murine Gammaherpesvirus 68 Infection
Bussey, K. A., Murthy, S., Reimer, E., Chan, B., Hatesuer, B., Schughart, K., Glaunsinger, B. A., Adler, H., & Brinkmann, M. M. (2018) · Journal of Virology · doi:10.1128/jvi.01173-18 · Cited by 27
The Innate Immune cGAS-STING-Pathway in Cardiovascular Diseases – A Mini Review
Rech, L., & Rainer, P. P. (2021) · Frontiers in Cardiovascular Medicine · doi:10.3389/fcvm.2021.715903 · Cited by 27
Second messenger 2′3′-cyclic GMP–AMP (2′3′-cGAMP): Synthesis, transmission, and degradation
Su, M., Zheng, J., Gan, L., Zhao, Y., Fu, Y., & Chen, Q. (2022) · Biochemical Pharmacology · doi:10.1016/j.bcp.2022.114934 · Cited by 28
Zebrafish MARCH8 downregulates fish IFN response by targeting MITA and TBK1 for protein degradation
Zhao, X., Dan, C., Gong, X.-Y., Li, Y., Qu, Z.-L., Sun, H.-Y., An, L., Guo, W., Gui, J., & Zhang, Y.-B. (2022) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2022.104485 · Cited by 27
Emerging complexity and new roles for the RIG-I-like receptors in innate antiviral immunity
Errett, J. S., & Gale, M. (2015) · Virologica Sinica · doi:10.1007/s12250-015-3604-5 · Cited by 27
Sorouri, M., Chang, T., Jesudhasan, P. R. R., Pinkham, C., Elde, N. C., & Hancks, D. C. (2020) · PLoS Biology · doi:10.1371/journal.pbio.3001045 · Cited by 27
cGAS-STING at the crossroads in cancer therapy
Wang, R., Hussain, A., Guo, Q., & Ma, M. (2023) · Critical Reviews in Oncology/Hematology · doi:10.1016/j.critrevonc.2023.104194 · Cited by 27
Conservation of antiviral systems across domains of life reveals immune genes in humans
Cury, J., Haudiquet, M., Trejo, V. H., Mordret, E., Hanouna, A., Rotival, M., Tesson, F., Bonhomme, D., Ofir, G., Quintana‐Murci, L., et al. (2024) · Cell Host & Microbe · doi:10.1016/j.chom.2024.08.002 · Cited by 30
Han, Z., Rao, J. Y., Xie, Z., Wang, C., Xu, B., Qian, S., Wang, Y., Zhu, J., Yang, B., Xu, F., et al. (2020) · American Journal of Respiratory and Critical Care Medicine · doi:10.1164/rccm.201908-1567oc · Cited by 26
Mitochondrial DNA on Tumor-Associated Macrophages Polarization and Immunity
Guo, Y., Tsai, H., Zhang, L., & Zhu, H. (2022) · Cancers · doi:10.3390/cancers14061452 · Cited by 26
Yang, N., Wang, Y., Liu, S., Tariq, S. B., Luna, J. M., Mazo, G., Tan, A. Y., Zhang, T., Wang, J., Yan, W., et al. (2023) · The Journal of Experimental Medicine · doi:10.1084/jem.20221166 · Cited by 26
Self-citationThe African swine fever virus I10L protein inhibits the NF- κ B signaling pathway by targeting IKK β
Chen, X., Li, L., Yang, Z.-Y., Li, M., Fan, S., Shi, L.-F., Ren, Z.-Y., Cao, X.-J., Zhang, Y., Han, S., et al. (2023) · Journal of Virology · doi:10.1128/jvi.00569-23 · Cited by 26
Single Amino Acid Change in STING Leads to Constitutive Active Signaling
Tang, E., & Wang, C.-Y. (2015) · PLoS ONE · doi:10.1371/journal.pone.0120090 · Cited by 26
Antiviral Protection via RdRP-Mediated Stable Activation of Innate Immunity
Painter, M. M., Morrison, J. H., Zoecklein, L. J., Rinkoski, T. A., Watzlawik, J. O., Papke, L. M., Warrington, A. E., Bieber, A. J., Matchett, W. E., Turkowski, K. L., et al. (2015) · PLoS Pathogens · doi:10.1371/journal.ppat.1005311 · Cited by 26
A time-resolved molecular map of the macrophage response to VSV infection
Kandasamy, R. K., Vladimer, G. I., Snijder, B., Müller, A. C., Rebsamen, M., Bigenzahn, J. W., Moskovskich, A., Sabler, M., Stefanovic, A., Scorzoni, S., et al. (2016) · npj Systems Biology and Applications · doi:10.1038/npjsba.2016.27 · Cited by 27
Wang, J., Ba, G., Han, Y.-Q., Ming, S., Wang, M.-D., Fu, P.-F., Zhao, Q., Zhang, S., Wu, Y., Yang, G., et al. (2020) · International Journal of Biological Macromolecules · doi:10.1016/j.ijbiomac.2020.01.015 · Cited by 26
Recent strategies and progress in identifying host factors involved in virus replication
König, R., & Stertz, S. (2015) · Current Opinion in Microbiology · doi:10.1016/j.mib.2015.06.001 · Cited by 29
The cGAS‒STING pathway in colorectal cancer: bridging innate immunity and therapeutic strategies
Li, W., Dong, G.-H., Bi, Y., Han, Y.-Y., Sun, L., Wang, T., Lin, Z., & Ren, X.-S. (2025) · Journal of Experimental & Clinical Cancer Research · doi:10.1186/s13046-025-03544-y · Cited by 27
Macrophage scavenger receptor 1 controls Chikungunya virus infection through autophagy in mice
Yang, L., Geng, T., Yang, G., Ma, J., Wang, L., Ketkar, H., Yang, D., Lin, T., Hwang, J., Zhu, S., et al. (2020) · Communications Biology · doi:10.1038/s42003-020-01285-6 · Cited by 26
Yu, P., Miao, Z., Li, Y., Bansal, R., Peppelenbosch, M. P., & Pan, Q. (2021) · Gut Microbes · doi:10.1080/19490976.2021.1959839 · Cited by 25
Yang, N., Luna, J. M., Dai, P., Wang, Y., Rice, C. M., & Deng, L. (2022) · Nature Communications · doi:10.1038/s41467-022-29308-2 · Cited by 25
Self-citationCellular glycan modification by B3GAT1 broadly restricts influenza virus infection
Trimarco, J. D., Nelson, S. L., Chaparian, R. R., Wells, A. I., Murray, N. B., Azadi, P., Coyne, C. B., & Heaton, N. S. (2022) · Nature Communications · doi:10.1038/s41467-022-34111-0 · Cited by 25
Yan, Y., Wu, L., Yuan, Y., Wang, H., Yin, H., Li, M., Chai, L., Liang, R., Liu, Y., Zhao, D., et al. (2023) · PLoS Pathogens · doi:10.1371/journal.ppat.1011641 · Cited by 25
The poxvirus F17 protein counteracts mitochondrially orchestrated antiviral responses
Meade, N., Toreev, H. K., Chakrabarty, R. P., Hesser, C. R., Park, C., Chandel, N. S., & Walsh, D. (2023) · Nature Communications · doi:10.1038/s41467-023-43635-y · Cited by 25
Intracellular sensing of viral DNA by the innate immune system
Mansur, D. S., Smith, G. L., & Ferguson, B. J. (2014) · Microbes and Infection · doi:10.1016/j.micinf.2014.09.010 · Cited by 25
Döring, M., Lessin, I., Frenz, T., Spanier, J., Keßler, A., Tegtmeyer, P.-K., Dağ, F., Thiel, N., Trilling, M., Lienenklaus, S., et al. (2014) · Journal of Virology · doi:10.1128/jvi.00216-14 · Cited by 25
Cytomegaloviruses and Macrophages—Friends and Foes From Early on?
Baasch, S., Ruzsics, Z., & Henneke, P. (2020) · Frontiers in Immunology · doi:10.3389/fimmu.2020.00793 · Cited by 27
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., et al. (2015) · Nature · doi:10.1038/nature14555 · Cited by 25
Self-citation
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