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Nuclear IFI16 induction of IRF-3 signaling during herpesviral infection and degradation of IFI16 by the viral ICP0 protein
Open accessAbstract
Innate sensing of microbial components is well documented to occur at many cellular sites, including at the cell surface, in the cytosol, and in intracellular vesicles, but there is limited evidence of nuclear innate signaling. In this study we have defined the mechanisms of interferon regulatory factor-3 (IRF-3) signaling in primary human foreskin fibroblasts (HFF) infected with herpes simplex virus 1 (HSV-1) in the absence of viral gene expression. We found that the interferon inducible protein 16 (IFI16) DNA sensor, which is required for induction of IRF-3 signaling in these cells, is nuclear, and its localization does not change detectably upon HSV-1 d 109 infection and induction of IRF-3 signaling. Consistent with the IFI16 sensor being nuclear, conditions that block viral DNA release from incoming capsids inhibit IRF-3 signaling. An unknown factor must be exported from the nucleus to activate IRF-3 through cytoplasmic STING, which is required for IRF-3 activation and signaling. However, when the viral ICP0 protein is expressed in the nucleus, it causes the nuclear relocalization and degradation of IFI16, inhibiting IRF-3 signaling. Therefore, HSV-1 infection is sensed in HFF by nuclear IFI16 upon release of encapsidated viral DNA into the nucleus, and the viral nuclear ICP0 protein can inhibit the process by targeting IFI16 for degradation. Together these results define a pathway for nuclear innate sensing of HSV DNA by IFI16 in infected HFF and document a mechanism by which a virus can block this nuclear innate response.
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“For instance, the DNA sensor IFI16 is an effector of innate immune responses during viral infection, detecting viral DNA in both the nucleus and the cytoplasm (71–73, 136, 137).”
From The Impact of Mass Spectrometry–Based Proteomics on Fundamental Discoveries in Virology (2014) · cites this paper as [72]
Experimental — accuracy not yet measuredIn the citing paper
“the HSV-1 immediate-early transactivating protein ICP0 was determined to be the most abundant viral interaction with IFI16. Further functional analyses [18] provided additional support for the current model that during early stages of HSV-1 infection, ICP0 employs a virus immune evasion strategy mediated by protein associations to target IFI16 for proteasome-dependent degradation. This early assoc”
From Proteomic approaches to uncovering virus–host protein interactions during the progression of viral infection (2016) · cites this paper as [19]
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Cites
Approaching the asymptote? Evolution and revolution in immunology.Preprint
Janeway, C. (1989) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.1989.054.01.003 · Cited by 3,396
NF-κB: linking inflammation and immunity to cancer development and progression
Karin, M., & Greten, F. R. (2005) · Nature reviews. Immunology · doi:10.1038/nri1703 · Cited by 3,175
STING regulates intracellular DNA-mediated, type I interferon-dependent innate immunity
Ishikawa, H., Ma, Z., & Barber, G. N. (2009) · Nature · doi:10.1038/nature08476 · Cited by 2,759 · cited 1×
“STING, a cytoplasmic scaffolding protein, is essential for the IFN-β response to immunostimulatory DNA molecules and HSV-1 infection in mouse embryonic fibroblasts (33).”
BackgroundIKKε and TBK1 are essential components of the IRF3 signaling pathway
Fitzgerald, K. A., McWhirter, S. M., Faia, K. L., Rowe, D. C., Latz, E., Golenbock, D. T., Coyle, A. J., Liao, S.-M., & Maniatis, T. (2003) · Nature Immunology · doi:10.1038/ni921 · Cited by 2,680
5'-Triphosphate RNA Is the Ligand for RIG-I
Hornung, V., Ellegast, J., Kim, S., Brzózka, K., Jung, A., Kato, H., Poeck, H., Akira, S., Conzelmann, K.-K., Schlee, M., et al. (2006) · Science · doi:10.1126/science.1132505 · Cited by 2,474
Regulation of Adaptive Immunity by the Innate Immune System
Iwasaki, A., & Medzhitov, R. M. (2010) · Science · doi:10.1126/science.1183021 · Cited by 2,220
The roles of TLRs, RLRs and NLRs in pathogen recognition
Kawai, T., & Akira, S. (2009) · International Immunology · doi:10.1093/intimm/dxp017 · Cited by 1,725
DAI (DLM-1/ZBP1) is a cytosolic DNA sensor and an activator of innate immune response
Takaoka, A., Wang, Z., Choi, M. K., Yanai, H., Negishi, H., Ban, T., Lu, Y., Miyagishi, M., Kodama, T., Honda, K., et al. (2007) · Nature · doi:10.1038/nature06013 · Cited by 1,704
Kato, H., Takeuchi, O., Mikamo, E., Hirai, R., Kawai, T., Matsushita, K., Hiiragi, A., Dermody, T. S., Fujita, T., & Akira, S. (2008) · The Journal of Experimental Medicine · doi:10.1084/jem.20080091 · Cited by 1,649
IFI16 is an innate immune sensor for intracellular DNA
Unterholzner, L., Keating, S. E., Baran, M., Horan, K. A., Jensen, S. B., Sharma, S., Sirois, C. M., Jin, T., Latz, E., Xiao, T. S., et al. (2010) · Nature Immunology · doi:10.1038/ni.1932 · Cited by 1,643
Research works printed but not linked: 5
- 10.1038/ni.1932 · DOI · Paper page
- 10.1128/JVI.75.2.750-758.2001 · DOI
- 10.1128/JVI.78.16.8411-8420.2004 · DOI
- 10.1128/jvi.76.5.2180-2191.2002 · DOI
- 10.1016/j.chom.2011.04.008 · DOI · Paper page
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Cao, L., Ji, Y., Zeng, L., Liu, Q., Zhang, Z., Guo, S., Guo, X., Tong, Y., Zhao, X., Li, C., et al. (2019) · PLoS Pathogens · doi:10.1371/journal.ppat.1008079 · Cited by 31
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Landolfo, S., Andrea, M. D., Dell’Oste, V., & Gugliesi, F. (2016) · World Journal of Virology · doi:10.5501/wjv.v5.i3.87 · Cited by 32
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Matz, K. M., Guzman, R. M., & Goodman, A. G. (2018) · International review of cytology · doi:10.1016/bs.ircmb.2018.08.002 · Cited by 32
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Full, F., & Ensser, A. (2019) · Journal of Clinical Medicine · doi:10.3390/jcm8091408 · Cited by 31
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Brulois, K., & Jung, J. U. (2014) · Cytokine & Growth Factor Reviews · doi:10.1016/j.cytogfr.2014.06.001 · Cited by 30
Patra, U., & Müller, S. P. (2021) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2021.696234 · Cited by 31
Gu, H. (2016) · World Journal of Virology · doi:10.5501/wjv.v5.i1.1 · Cited by 29
Hensel, N., Raker, V., Förthmann, B., Detering, N. T., Kubinski, S., Buch, A., Katzilieris‐Petras, G., Spanier, J., Gudi, V., Wagenknecht, S., et al. (2019) · Journal of Neuroinflammation · doi:10.1186/s12974-019-1647-5 · Cited by 29
Nuclear innate sensors for nucleic acids in immunity and inflammation
Lin, H., & Cao, X. (2020) · Immunological Reviews · doi:10.1111/imr.12893 · Cited by 29
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Gu, H., Zheng, Y., & Roizman, B. (2013) · Journal of Virology · doi:10.1128/jvi.01487-13 · Cited by 29
Bryant-Hudson, K. M., Conrady, C. D., & Carr, D. J. J. (2013) · Progress in Retinal and Eye Research · doi:10.1016/j.preteyeres.2013.06.003 · Cited by 28
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Walsh, M. J., Stump, C. T., Kureshi, R., Lenehan, P. J., Ali, L. R., Dougan, M. L., Knipe, D. M., & Dougan, S. K. (2023) · Cell Reports · doi:10.1016/j.celrep.2023.112219 · Cited by 28
Self-citationIdentification and Further Development of Potent TBK1 Inhibitors
Richters, A., Basu, D., Engel, J., Ercanoglu, M. S., Balke‐Want, H., Tesch, R., Thomas, R. K., & Rauh, D. (2014) · ACS Chemical Biology · doi:10.1021/cb500908d · Cited by 29
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Greenan, E., Gallagher, S., Khalil, R., Murphy, C. C., & Gabhann, J. N. (2021) · Viruses · doi:10.3390/v13091856 · Cited by 27
Howard, T. R., Lum, K. K., Kennedy, M. A., & Cristea, I. M. (2022) · mSystems · doi:10.1128/msystems.00198-22 · Cited by 27
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D’Urbano, V., Crignis, E. D., & Re, M. C. (2018) · Current HIV Research · doi:10.2174/1570162x16666180817115830 · Cited by 31
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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
Duan, Y., Zeng, J., Fan, S., Liao, Y., Feng, M. H., Wang, L., Zhang, Y., & Li, Q. (2019) · Viruses · doi:10.3390/v11080756 · Cited by 25
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Reddi, T. S., Merkl, P., Lim, S., Letvin, N. L., & Knipe, D. M. (2021) · PLoS Pathogens · doi:10.1371/journal.ppat.1009281 · Cited by 25
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Aho, V., Mäntylä, E., Ekman, A. A., Hakanen, S., Mattola, S., Chen, J.-H., Weinhardt, V., Ruokolainen, V., Sodeik, B., Larabell, C. A., et al. (2019) · Viruses · doi:10.3390/v11100935 · Cited by 25
Taylor, T. J., Diaz, F., Colgrove, R. C., Bernard, K. A., DeLuca, N. A., Whelan, S. P. J., & Knipe, D. M. (2016) · Virology · doi:10.1016/j.virol.2016.06.006 · Cited by 24
Self-citationYu, F., Wang, S., Zhang, W., Tang, J., Wang, H., Li, Y., Zhang, X., Fei, Z., & Li, J. (2019) · Current Genetics · doi:10.1007/s00294-019-00989-5 · Cited by 24
Wichit, S., Hamel, R., Yainoy, S., Gumpangseth, N., Panich, S., Phuadraksa, T., Saetear, P., Monteil, A., Vargas, R. E. M., & Missé, D. (2019) · EXCLI journal · doi:10.17179/excli2019-1271 · Cited by 26
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Chen, Y., Bian, S., Zhang, J., Luan, Y., Yin, B., Dai, W., Wang, H., Chen, X., Dong, Y., Cai, Y., et al. (2024) · Cell Reports · doi:10.1016/j.celrep.2024.114756 · Cited by 23
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Taylor, K. E., Chew, M. V., Ashkar, A. A., & Mossman, K. L. (2014) · Journal of Virology · doi:10.1128/jvi.00944-14 · Cited by 22
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Ren, J., Antony, F., Rouse, B. T., & Suryawanshi, A. S. (2023) · Pathogens · doi:10.3390/pathogens12030437 · Cited by 25
Jamin, A. V., Thunuguntla, P., Wicklund, A., Jones, C., & Wiebe, M. S. (2014) · PLoS ONE · doi:10.1371/journal.pone.0100511 · Cited by 22
Sato, Y., Kato, A., Maruzuru, Y., Oyama, M., Kozuka‐Hata, H., Arii, J., & Kawaguchi, Y. (2016) · Journal of Virology · doi:10.1128/jvi.03043-15 · Cited by 22
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Sodroski, C. N., & Knipe, D. M. (2023) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2310996120 · Cited by 20
Self-citationLiu, S., Zhang, Y., Ren, J., & Li, J. (2015) · Inflammatory Bowel Diseases · doi:10.1097/mib.0000000000000299 · Cited by 19
DNA-PKcs is required for cGAS/STING-dependent viral DNA sensing in human cells
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Meyer, C., Kerns, A. R., Haberthur, K., Dewane, J., Walker, J. M., Gray, W. L., & Messaoudi, I. (2012) · Journal of Virology · doi:10.1128/jvi.02369-12 · Cited by 19
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Zhang, L., Huang, F., Liu, J., Xu, Y., Miao, Y., Yuan, Y., Chen, X., Zhang, H.-G., Wang, J., Zheng, H., et al. (2021) · Molecular Immunology · doi:10.1016/j.molimm.2021.03.027 · Cited by 17
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Lum, K. K., Reed, T. J., Yang, J., & Cristea, I. M. (2024) · Journal of Proteome Research · doi:10.1021/acs.jproteome.3c00826 · Cited by 18
Lutz, G., Jurak, I., Kim, E. T., Kim, J. Y., Hackenberg, M., Leader, A. M., Stoller, M. L., Fekete, D. M., Weitzman, M. D., Coen, D. M., et al. (2017) · Viruses · doi:10.3390/v9080210 · Cited by 17
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Metadata
- Authors
- Orzalli, M. H., DeLuca, N. A., & Knipe, D. M.
- Affiliations
- Harvard University (US)
- University of Pittsburgh (US)
- Corresponding author
- Knipe, David M.
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-10
- Volume
- 109
- Issue
- 44
- Pages
- E3008-17
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC3497734
- OpenAlex
- W2163362670
- Cited by
- 422
- References
- 65
- Citations by year
- 2026: 13 · 2025: 20 · 2024: 21 · 2023: 15 · 2022: 25 · 2021: 35 · 2020: 32 · 2019: 44 · 2018: 30 · 2017: 24 · 2016: 38 · 2015: 49 · 2014: 34 · 2013: 39 · 2012: 3
- FWCI
- 17.56
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Funders
- National Institutes of Health
- National Institute of Allergy and Infectious Diseases (R01AI099081, AI099081, R01AI044821, P01AI083215, AI83215)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › interferon and immune responses
- Health Sciences › Medicine › Infectious Diseases › Herpesvirus Infections and Treatments
- Life Sciences › Immunology and Microbiology › Immunology › Immune Response and Inflammation
- Keywords
- IFI16, herpes simplex virus type 1, ICP0, viral DNA sensing, STING, protein degradation
- MeSH terms
- Cells, Cultured, DNA, Viral, Flow Cytometry, Herpes Labialis, Humans, Nuclear Proteins, Phosphoproteins, Signal Transduction, Polymerase Chain Reaction, Immediate-Early Proteins, Herpesvirus 1, Human, Fluorescent Antibody Technique, Indirect, Ubiquitin-Protein Ligases, Interferon Regulatory Factor-3
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