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TRIM21 Ubiquitylates SQSTM1/p62 and Suppresses Protein Sequestration to Regulate Redox Homeostasis
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Summary TRIM21 is a RING finger domain-containing ubiquitin E3 ligase whose expression is elevated in autoimmune disease. While TRIM21 plays an important role in immune activation during pathogen infection, little is known about its inherent cellular function. Here we show that TRIM21 plays an essential role in redox regulation by directly interacting with SQSTM1/p62 and ubiquitylating p62 at lysine(K)7 via K63-linkage. As p62 oligomerizes and sequesters client proteins in inclusions, the TRIM21-mediated p62 ubiquitylation abrogates p62 oligomerization and sequestration of proteins including Keap1, a negative regulator of antioxidant response. TRIM21-deficient cells display an enhanced antioxidant response and reduced cell death in response to oxidative stress. Genetic ablation of TRIM21 in mice confers protection from oxidative damages caused by arsenic-induced liver insult and pressure overload heart injury. Therefore, TRIM21 plays an essential role in p62-regulated redox homeostasis and may be a viable target for treating pathological conditions resulting from oxidative damage.
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Cites
Repertoires of Autophagy in the Pathogenesis of Ocular Diseases
Li, Y.-J., Jiang, Q., Cao, G.-F., Yao, J., & Yan, B. (2015) · Cellular Physiology and Biochemistry · doi:10.1159/000373980 · Cited by 16,304
Cui, C., Cui, J., Jin, F., Cui, Y., Li, R., Jiang, X., Tian, Y., Wang, K., Jiang, P., & Gao, J. (2017) · Cellular Physiology and Biochemistry · doi:10.1159/000479571 · Cited by 5,203
Pankiv, S., Clausen, T. H., Lamark, T., Brech, A., Bruun, J.-A., Outzen, H., Øvervatn, A., Bjørkøy, G., & Johansen, T. (2007) · Journal of Biological Chemistry · doi:10.1074/jbc.m702824200 · Cited by 4,578 · cited 1×
“At the protein stability level, p62 is degraded along with the protein aggregates by autophagy (Pankiv et al., 2007) and is often served as an indicator for autophagy induction.”
Bjørkøy, G., Lamark, T., Brech, A., Outzen, H., Perander, M., Øvervatn, A., Stenmark, H., & Johansen, T. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200507002 · Cited by 3,276
Impairment of starvation-induced and constitutive autophagy in Atg7 -deficient mice
Komatsu, M., Waguri, S., Ueno, T., Iwata, J., Murata, S., Tanida, I., Ezaki, J., Mizushima, N., Ohsumi, Y., Uchiyama, Y., et al. (2005) · The Journal of Cell Biology · doi:10.1083/jcb.200412022 · Cited by 2,331
Komatsu, M., Kurokawa, H., Waguri, S., Taguchi, K., Kobayashi, A., Ichimura, Y., Sou, Y.-S., Ueno, I., Sakamoto, A., Tong, K. I., et al. (2010) · Nature Cell Biology · doi:10.1038/ncb2021 · Cited by 2,288
Oncogene-induced Nrf2 transcription promotes ROS detoxification and tumorigenesis
DeNicola, G. M., Karreth, F. A., Humpton, T. J., Gopinathan, A., Wei, C., Frese, K., Mangal, D., Yu, K. H., Yeo, C. J., Calhoun, E. S., et al. (2011) · Nature · doi:10.1038/nature10189 · Cited by 2,277
Kobayashi, A., Kang, M.-I., Okawa, H., Ohtsuji, M., Zenke, Y., Chiba, T., Igarashi, K., & Yamamoto, M. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.16.7130-7139.2004 · Cited by 2,224
Autophagy Suppresses Tumorigenesis through Elimination of p62
Mathew, R., Karp, C. M., Beaudoin, B., Vuong, N., Chen, G., Chen, H.-Y., Bray, K., Reddy, A., Bhanot, G., Gelinas, C., et al. (2009) · Cell · doi:10.1016/j.cell.2009.03.048 · Cited by 1,719
Jain, A., Lamark, T., Sjøttem, E., Bowitz Larsen, K., Atesoh Awuh, J., Øvervatn, A., McMahon, M., Hayes, J. D., & Johansen, T. (2010) · Journal of Biological Chemistry · doi:10.1074/jbc.m110.118976 · Cited by 1,472
Keap1 Is a Redox-Regulated Substrate Adaptor Protein for a Cul3-Dependent Ubiquitin Ligase Complex
Zhang, D. D., Lo, S.-C., Cross, J. V., Templeton, D. J., & Hannink, M. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.24.10941-10953.2004 · Cited by 1,254
Phosphorylation of p62 Activates the Keap1-Nrf2 Pathway during Selective Autophagy
Ichimura, Y., Waguri, S., Sou, Y.-S., Kageyama, S., Hasegawa, J., Ishimura, R., Saito, T., Yang, Y., Kouno, T., Fukutomi, T., et al. (2013) · Molecular Cell · doi:10.1016/j.molcel.2013.08.003 · Cited by 1,205
p62 at the crossroads of autophagy, apoptosis, and cancer
Moscat, J., & Diaz-Meco, M. T. (2009) · Cell · doi:10.1016/j.cell.2009.05.023 · Cited by 1,073
Self-citationAntioxidant and oncogene rescue of metabolic defects caused by loss of matrix attachment
Schafer, Z. T., Grassian, A. R., Song, L., Jiang, Z., Gerhart-Hines, Z., Irie, H. Y., Gao, S., Puigserver, P., & Brugge, J. S. (2009) · Nature · doi:10.1038/nature08268 · Cited by 1,031
Antioxidants Accelerate Lung Cancer Progression in Mice
Sayin, V. I., Ibrahim, M. X., Larsson, E., Nilsson, J. A., Lindahl, P., & Bergo, M. O. (2014) · Science Translational Medicine · doi:10.1126/scitranslmed.3007653 · Cited by 867
Lau, A., Wang, X.-J., Zhao, F., Villeneuve, N. F., Wu, T., Jiang, T., Sun, Z., White, E., & Zhang, D. D. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00248-10 · Cited by 849
p62/SQSTM 1 functions as a signaling hub and an autophagy adaptor
Katsuragi, Y., Ichimura, Y., & Komatsu, M. (2015) · The FEBS Journal · doi:10.1111/febs.13540 · Cited by 788
TRIM family proteins: retroviral restriction and antiviral defence
Nisole, S., Stoye, J. P., & Saïb, A. (2005) · Nature Reviews Microbiology · doi:10.1038/nrmicro1248 · Cited by 761
Seibenhener, M. L., Babu, J. R., Geetha, T., Wong, H. C., Krishna, N. R., & Wooten, M. W. (2004) · Molecular and Cellular Biology · doi:10.1128/mcb.24.18.8055-8068.2004 · Cited by 710
Matsumoto, G., Wada, K., Okuno, M., Kurosawa, M., & Nukina, N. (2011) · Molecular Cell · doi:10.1016/j.molcel.2011.07.039 · Cited by 701
Signaling Pathways in Reactive Oxygen Species–Induced Cardiomyocyte Apoptosis
von Harsdorf, R., Li, P.-F., & Dietz, R. (1999) · Circulation · doi:10.1161/01.cir.99.22.2934 · Cited by 571
Oxygen free radicals and congestive heart failure.
Belch, J. J., Bridges, A. B., Scott, N., & Chopra, M. (1991) · Heart · doi:10.1136/hrt.65.5.245 · Cited by 550
The Signaling Adaptor p62 Is an Important NF-κB Mediator in Tumorigenesis
Duran, A., Linares, J. F., Galvez, A. S., Wikenheiser, K., Flores, J. M., Diaz-Meco, M. T., & Moscat, J. (2008) · Cancer Cell · doi:10.1016/j.ccr.2008.02.001 · Cited by 541
Self-citationAntibodies mediate intracellular immunity through tripartite motif-containing 21 (TRIM21)
Mallery, D. L., McEwan, W. A., Bidgood, S. R., Towers, G. J., Johnson, C. M., & James, L. C. (2010) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1014074107 · Cited by 516
p62 targeting to the autophagosome formation site requires self-oligomerization but not LC3 binding
Itakura, E., & Mizushima, N. (2011) · Journal of Cell Biology · doi:10.1083/jcb.201009067 · Cited by 416
A 52-kD protein is a novel component of the SS-A/Ro antigenic particle.
Ben-Chetrit, E., Chan, E. K., Sullivan, K. F., & Tan, E. M. (1988) · The Journal of experimental medicine · doi:10.1084/jem.167.5.1560 · Cited by 404
Structural basis for PRYSPRY-mediated tripartite motif (TRIM) protein function
James, L. C., Keeble, A. H., Khan, Z., Rhodes, D. A., & Trowsdale, J. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0609174104 · Cited by 386 · cited 3×
“An important molecular feature of TRIM21 is its binding to immunoglobulin G (IgG) via its PRYSPRY domain (James et al., 2007), which plays an important role in innate immune activation during viral infection (Mallery et al., 2010; McEwan et al., 2013).”
Class III PI3K Vps34 plays an essential role in autophagy and in heart and liver function
Jaber, N., Dou, Z., Chen, J.-S., Catanzaro, J., Jiang, Y.-P., Ballou, L. M., Selinger, E., Ouyang, X., Lin, R. Z., Zhang, J., et al. (2012) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1112848109 · Cited by 385
Self-citationPuissant, A., Robert, G., Fenouille, N., Luciano, F., Cassuto, J.-P., Raynaud, S., & Auberger, P. (2010) · Cancer Research · doi:10.1158/0008-5472.can-09-3537 · Cited by 374
Intracellular antibody-bound pathogens stimulate immune signaling via the Fc receptor TRIM21
McEwan, W. A., Tam, J. C. H., Watkinson, R. E., Bidgood, S. R., Mallery, D. L., & James, L. C. (2013) · Nature Immunology · doi:10.1038/ni.2548 · Cited by 372
Lim, J., Lachenmayer, M. L., Wu, S., Liu, W., Kundu, M., Wang, R., Komatsu, M., Oh, Y. J., Zhao, Y., & Yue, Z. (2015) · PLOS Genetics · doi:10.1371/journal.pgen.1004987 · Cited by 329
Espinosa, A., Dardalhon, V., Brauner, S., Ambrosi, A., Higgs, R., Quintana, F. J., Sjöstrand, M., Eloranta, M.-L., Ní Gabhann, J., Winqvist, O., et al. (2009) · Journal of Experimental Medicine · doi:10.1084/jem.20090585 · Cited by 313
Arsenic induces oxidant stress and NF-KB activation in cultured aortic endothelial cells
Barchowsky, A., Dudek, E. J., Treadwell, M. D., & Wetterhahn, K. E. (1996) · Free Radical Biology and Medicine · doi:10.1016/0891-5849(96)00174-8 · Cited by 287
MOLECULAR ASPECTS OF ARSENIC STRESS
Nriagu, L. B. (2000) · Journal of Toxicology and Environmental Health, Part B · doi:10.1080/109374000436355 · Cited by 280
Chou, W.-C., Jie, C., Kenedy, A. A., Jones, R. J., Trush, M. A., & Dang, C. V. (2004) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0306687101 · Cited by 234
Wilson, M. I., Gill, D. J., Perisic, O., Quinn, M. T., & Williams, R. L. (2003) · Molecular Cell · doi:10.1016/s1097-2765(03)00246-6 · Cited by 231
Song, B., Gold, B., O'hUigin, C., Javanbakht, H., Li, X., Stremlau, M., Winkler, C., Dean, M., & Sodroski, J. (2005) · Journal of Virology · doi:10.1128/jvi.79.10.6111-6121.2005 · Cited by 199
Caspase-Independent Cell Death by Arsenic Trioxide in Human Cervical Cancer Cells
Kang, Y.-H., Yi, M.-J., Kim, M.-J., Park, M.-T., Bae, S., Kang, C.-M., Cho, C.-K., Park, I.-C., Park, M.-J., Rhee, C. H., et al. (2004) · Cancer Research · doi:10.1158/0008-5472.can-04-1830 · Cited by 183
Harder, B., Jiang, T., Wu, T., Tao, S., de la Vega, M. R., Tian, W., Chapman, E., & Zhang, D. D. (2015) · Biochemical Society Transactions · doi:10.1042/bst20150020 · Cited by 170
Ben‐Chetrit, E., Fox, R. I., & Tan, E. M. (1990) · Arthritis & Rheumatism · doi:10.1002/art.1780330307 · Cited by 162
Yoshimi, R., Chang, T.-H., Wang, H., Atsumi, T., Morse, H. C., & Ozato, K. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0804121 · Cited by 159
Self-citationDate, M., Morita, T., Yamashita, N., Nishida, K., Yamaguchi, O., Higuchi, Y., Hirotani, S., Matsumura, Y., Hori, M., Tada, M., et al. (2002) · Journal of the American College of Cardiology · doi:10.1016/s0735-1097(01)01826-5 · Cited by 147
P62 and the sequestosome, a novel mechanism for protein metabolism
Shin, J. (1998) · Archives of Pharmacal Research · doi:10.1007/bf02976748 · Cited by 146
Autoantigen Ro52 is an E3 ubiquitin ligase
Wada, K., & Kamitani, T. (2005) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2005.11.029 · Cited by 136
Arsenite Stimulates Poly(ADP-Ribosylation) by Generation of Nitric Oxide
Lynn, S., Shiung, J.-N., Gurr, J.-R., & Jan, K. Y. (1998) · Free Radical Biology and Medicine · doi:10.1016/s0891-5849(97)00279-7 · Cited by 127
Pan, J.-A., Ullman, E., Dou, Z., & Zong, W. (2011) · Molecular and Cellular Biology · doi:10.1128/mcb.05460-11 · Cited by 114
Self-citationKim, J. Y., & Ozato, K. (2009) · The Journal of Immunology · doi:10.4049/jimmunol.0802755 · Cited by 98
Self-citationLinares, J. F., Amanchy, R., Díaz-Meco, M. T., & Moscat, J. (2010) · Molecular and Cellular Biology · doi:10.1128/mcb.00620-10 · Cited by 90
Self-citationIshii, T., Yanagawa, T., Kawane, T., Yuki, K., Seita, J., Yoshida, H., & Bannai, S. (1996) · Biochemical and Biophysical Research Communications · doi:10.1006/bbrc.1996.1377 · Cited by 87
Ding, Q., Du, H., He, K., Zhang, Q., Tang, M., Dai, J., Lv, H., Wang, X., Xiang, G., & Yu, H. (2015) · Tumor Biology · doi:10.1007/s13277-015-3572-2 · Cited by 79
Vadlamudi, R. K., & Shin, J. (1998) · FEBS Letters · doi:10.1016/s0014-5793(98)01021-7 · Cited by 71
Brauner, S., Zhou, W., Backlin, C., Green, T., Folkersen, L., Ivanchenko, M., Löfström, B., Xu-Monette, Z. Y., Young, K. H., Pedersen, L. M., et al. (2015) · Journal of Internal Medicine · doi:10.1111/joim.12375 · Cited by 63
Phosphorylation of serine 349 of p62 in Alzheimer’s disease brain
Tanji, K., Miki, Y., Ozaki, T., Maruyama, A., Yoshida, H., Mimura, J., Matsumiya, T., Mori, F., Imaizumi, T., Itoh, K., et al. (2014) · Acta Neuropathologica Communications · doi:10.1186/2051-5960-2-50 · Cited by 59
A quantitative assay for mitochondrial fusion using Renilla luciferase complementation
Huang, H., Choi, S., & Frohman, M. A. (2010) · Mitochondrion · doi:10.1016/j.mito.2010.05.003 · Cited by 18
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Sies, H., Berndt, C., & Jones, D. P. (2017) · Annual Review of Biochemistry · doi:10.1146/annurev-biochem-061516-045037 · Cited by 3,520
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Vargas, J. N. S., Hamasaki, M., Kawabata, T., Youle, R. J., & Yoshimori, T. (2023) · Nature Reviews Molecular Cell Biology · doi:10.1038/s41580-022-00542-2 · Cited by 1,016
Ubiquitin ligases in oncogenic transformation and cancer therapy
Senft, D., Qi, J., & Ronai, Z. A. (2018) · Nature Reviews Cancer · doi:10.1038/nrc.2017.105 · Cited by 489
Crosstalk Between Mammalian Autophagy and the Ubiquitin-Proteasome System
Kocaturk, N. M., & Gozuacik, D. (2018) · Frontiers in Cell and Developmental Biology · doi:10.3389/fcell.2018.00128 · Cited by 419
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Qian, H., Chao, X., Williams, J., Fulte, S., Li, T., Yang, L., & Ding, W.-X. (2021) · Molecular Aspects of Medicine · doi:10.1016/j.mam.2021.100973 · Cited by 373
Self-citation
Metadata
- Authors
- Pan, J.-A., Sun, Y., Jiang, Y.-P., Bott, A. J., Jaber, N., Dou, Z., Yang, B., Chen, J.-S., Catanzaro, J. M., Du, C., Ding, W.-X., Diaz-Meco, M. T., Moscat, J., Ozato, K., Lin, R. Z., & Zong, W.-X.
- Venue
- Molecular Cell
- Publisher
- Elsevier BV
- Published
- 2016-03
- Volume
- 61
- Issue
- 5
- Pages
- 720-733
- ISSN
- 1097-2765 (ISSN-L)
- OpenAlex
- W2289400344
- Cited by
- 265
- References
- 54
- FWCI
- 9.48
- Type
- journal article
- Language
- en
- Open access
- bronze
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