References
- Gack, M.U., Shin, Y.C., Joo, C.H., Urano, T., Liang, C., Sun, L., Takeuchi, O., Akira, S., Chen, Z., Inoue, S., et al. (2007). TRIM25 RING-finger E3 ubiquitin ligase is essential for RIG-Imediated antiviral activity. Nature 446, 916-920. https://doi.org/10.1038/nature05732
- Gack, M.U., Albrecht, R.A., Urano, T., Inn, K.S., Huang, I.C., Carnero, E., Farzan, M., Inoue, S., Jung, J.U., and Garcia-Sastre, A. (2009). Influenza A virus NS1 targets the ubiquitin ligase TRIM25 to evade recognition by the host viral RNA sensor RIG-I. Cell Host Microbe 5, 439-449. https://doi.org/10.1016/j.chom.2009.04.006
- Goubau, D., Deddouche, S., and Reis, E.S.C. (2013). Cytosolic sensing of viruses. Immunity 38, 855-869. https://doi.org/10.1016/j.immuni.2013.05.007
- Inn, K.S., Gack, M.U., Tokunaga, F., Shi, M., Wong, L.Y., Iwai, K., and Jung, J.U. (2011a). Linear ubiquitin assembly complex negatively regulates RIG-I- and TRIM25-mediated type I interferon induction. Mol. Cell 41, 354-365. https://doi.org/10.1016/j.molcel.2010.12.029
- Inn, K.S., Lee, S.H., Rathbun, J.Y., Wong, L.Y., Toth, Z., Machida, K., Ou, J.H., and Jung, J.U. (2011b). Inhibition of RIG-I-mediated signaling by Kaposi's sarcoma-associated herpesvirus-encoded deubiquitinase ORF64. J. Virol. 85, 10899-10904. https://doi.org/10.1128/JVI.00690-11
- Jiang, X., Kinch, L.N., Brautigam, C.A., Chen, X., Du, F., Grishin, N.V., and Chen, Z.J. (2012). Ubiquitin-induced oligomerization of the RNA sensors RIG-I and MDA5 activates antiviral innate immune response. Immunity 36, 959-973. https://doi.org/10.1016/j.immuni.2012.03.022
- Kato, H., Takeuchi, O., Sato, S., Yoneyama, M., Yamamoto, M., Matsui, K., Uematsu, S., Jung, A., Kawai, T., Ishii, K.J., et al. (2006). Differential roles of MDA5 and RIG-I helicases in the recognition of RNA viruses. Nature 441, 101-105. https://doi.org/10.1038/nature04734
- Kato, H., Takeuchi, O., Mikamo-Satoh, E., Hirai, R., Kawai, T., Matsushita, K., Hiiragi, A., Dermody, T.S., Fujita, T., and Akira, S. (2008). Length-dependent recognition of double-stranded ribonucleic acids by retinoic acid-inducible gene-I and melanoma differentiation-associated gene 5. J. Exp. Med. 205, 1601-1610. https://doi.org/10.1084/jem.20080091
- Kawai, T., Takahashi, K., Sato, S., Coban, C., Kumar, H., Kato, H., Ishii, K.J., Takeuchi, O., and Akira, S. (2005). IPS-1, an adaptor triggering RIG-I- and Mda5-mediated type I interferon induction. Nat. Immunol. 6, 981-988. https://doi.org/10.1038/ni1243
- Loo, Y.M., Fornek, J., Crochet, N., Bajwa, G., Perwitasari, O., Martinez-Sobrido, L., Akira, S., Gill, M.A., Garcia-Sastre, A., Katze, M.G., et al. (2008). Distinct RIG-I and MDA5 signaling by RNA viruses in innate immunity. J. Virol. 82, 335-345. https://doi.org/10.1128/JVI.01080-07
- Meylan, E., Curran, J., Hofmann, K., Moradpour, D., Binder, M., Bartenschlager, R., and Tschopp, J. (2005). Cardif is an adaptor protein in the RIG-I antiviral pathway and is targeted by hepatitis C virus. Nature 437, 1167-1172. https://doi.org/10.1038/nature04193
- Nakhaei, P., Genin, P., Civas, A., and Hiscott, J. (2009). RIG-I-like receptors: sensing and responding to RNA virus infection. Semin. Immunol. 21, 215-222. https://doi.org/10.1016/j.smim.2009.05.001
- Pichlmair, A., Schulz, O., Tan, C.P., Rehwinkel, J., Kato, H., Takeuchi, O., Akira, S., Way, M., Schiavo, G., and Reis e Sousa, C. (2009). Activation of MDA5 requires higher-order RNA structures generated during virus infection. J. Virol. 83, 10761-10769. https://doi.org/10.1128/JVI.00770-09
- Ramos, H.J., and Gale, M., Jr. (2011). RIG-I like receptors and their signaling crosstalk in the regulation of antiviral immunity. Curr. Opin. Virol. 1, 167-176. https://doi.org/10.1016/j.coviro.2011.04.004
- Seth, R.B., Sun, L., Ea, C.K., and Chen, Z.J. (2005). Identification and characterization of MAVS, a mitochondrial antiviral signaling protein that activates NF-kappaB and IRF 3. Cell 122, 669-682. https://doi.org/10.1016/j.cell.2005.08.012
- Sumpter, R., Jr., Loo, Y.M., Foy, E., Li, K., Yoneyama, M., Fujita, T., Lemon, S.M., and Gale, M., Jr. (2005). Regulating intracellular antiviral defense and permissiveness to hepatitis C virus RNA replication through a cellular RNA helicase, RIG-I. J. Virol. 79, 2689-2699. https://doi.org/10.1128/JVI.79.5.2689-2699.2005
- Wies, E., Wang, M.K., Maharaj, N.P., Chen, K., Zhou, S., Finberg, R.W., and Gack, M.U. (2013). Dephosphorylation of the RNA sensors RIG-I and MDA5 by the phosphatase PP1 is essential for innate immune signaling. Immunity 38, 437-449. https://doi.org/10.1016/j.immuni.2012.11.018
- Wu, B., Peisley, A., Richards, C., Yao, H., Zeng, X., Lin, C., Chu, F., Walz, T., and Hur, S. (2013). Structural basis for dsRNA recognition, filament formation, and antiviral signal activation by MDA5. Cell 152, 276-289. https://doi.org/10.1016/j.cell.2012.11.048
- Xu, L.G., Wang, Y.Y., Han, K.J., Li, L.Y., Zhai, Z., and Shu, H.B. (2005). VISA is an adapter protein required for virus-triggered IFN-beta signaling. Mol. Cell 19, 727-740. https://doi.org/10.1016/j.molcel.2005.08.014
- Yoboua, F., Martel, A., Duval, A., Mukawera, E., and Grandvaux, N. (2010). Respiratory syncytial virus-mediated NF-kappa B p65 phosphorylation at serine 536 is dependent on RIG-I, TRAF6, and IKK beta. J. Virol. 84, 7267-7277. https://doi.org/10.1128/JVI.00142-10
- Yoneyama, M., Kikuchi, M., Natsukawa, T., Shinobu, N., Imaizumi, T., Miyagishi, M., Taira, K., Akira, S., and Fujita, T. (2004). The RNA helicase RIG-I has an essential function in double-stranded RNA-induced innate antiviral responses. Nat. Immunol. 5, 730-737. https://doi.org/10.1038/ni1087
- Yoshida, R., Takaesu, G., Yoshida, H., Okamoto, F., Yoshioka, T., Choi, Y., Akira, S., Kawai, T., Yoshimura, A., and Kobayashi, T. (2008). TRAF6 and MEKK1 play a pivotal role in the RIG-I-like helicase antiviral pathway. J. Biol. Chem. 283, 36211-36220. https://doi.org/10.1074/jbc.M806576200
- Zeng, W., Sun, L., Jiang, X., Chen, X., Hou, F., Adhikari, A., Xu, M., and Chen, Z.J. (2010). Reconstitution of the RIG-I pathway reveals a signaling role of unanchored polyubiquitin chains in innate immunity. Cell 141, 315-330. https://doi.org/10.1016/j.cell.2010.03.029
Cited by
- TRIM25 in the Regulation of the Antiviral Innate Immunity vol.8, 2017, https://doi.org/10.3389/fimmu.2017.01187
- Molecular cloning and functional analysis of tumor necrosis factor receptor-associated factor 6 (TRAF6) in Crossastrea gigas vol.68, 2017, https://doi.org/10.1016/j.fsi.2017.06.049
- De novo annotation of the immune-enriched transcriptome provides insights into immune system genes of Chinese sturgeon (Acipenser sinensis) vol.55, 2016, https://doi.org/10.1016/j.fsi.2016.06.051
- Ubiquitin in the activation and attenuation of innate antiviral immunity vol.213, pp.1, 2016, https://doi.org/10.1084/jem.20151531
- The Severe Acute Respiratory Syndrome Coronavirus Nucleocapsid Inhibits Type I Interferon Production by Interfering with TRIM25-Mediated RIG-I Ubiquitination vol.91, pp.8, 2017, https://doi.org/10.1128/JVI.02143-16
- Herpesvirus deconjugases inhibit the IFN response by promoting TRIM25 autoubiquitination and functional inactivation of the RIG-I signalosome vol.14, pp.1, 2018, https://doi.org/10.1371/journal.ppat.1006852
- TRIM25 enhances cell growth and cell survival by modulating p53 signals via interaction with G3BP2 in prostate cancer vol.37, pp.16, 2018, https://doi.org/10.1038/s41388-017-0095-x
- USP4 positively regulates RLR-induced NF-κB activation by targeting TRAF6 for K48-linked deubiquitination and inhibits enterovirus 71 replication vol.8, pp.1, 2018, https://doi.org/10.1038/s41598-018-31734-6
- Gene in Chinese Patients with Dyschromatosis Symmetrica Hereditaria vol.22, pp.2, 2018, https://doi.org/10.1089/gtmb.2017.0207
- OASL1 Traps Viral RNAs in Stress Granules to Promote Antiviral Responses vol.41, pp.3, 2015, https://doi.org/10.14348/molcells.2018.2293
- To TRIM the Immunity: From Innate to Adaptive Immunity vol.11, pp.None, 2015, https://doi.org/10.3389/fimmu.2020.02157
- TRIM25 Promotes TNF-α–Induced NF-κB Activation through Potentiating the K63-Linked Ubiquitination of TRAF2 vol.204, pp.6, 2015, https://doi.org/10.4049/jimmunol.1900482
- TRIM25 and its emerging RNA‐binding roles in antiviral defense vol.11, pp.4, 2015, https://doi.org/10.1002/wrna.1588
- TRIM25 regulates oxaliplatin resistance in colorectal cancer by promoting EZH2 stability vol.12, pp.5, 2015, https://doi.org/10.1038/s41419-021-03734-4
- Transcriptome analysis reveals new insight of duck Tembusu virus (DTMUV)-infected DF-1 cells vol.137, pp.None, 2021, https://doi.org/10.1016/j.rvsc.2021.04.028
- TRIM25 inhibits infectious bursal disease virus replication by targeting VP3 for ubiquitination and degradation vol.17, pp.9, 2015, https://doi.org/10.1371/journal.ppat.1009900