References
- Arch, R. H., Gedrich, R. W. and Thompson, C. B. (1998) Tumor necrosis factor receptor-associated factors (TRAFs) a family of adapter proteins that regulates life and death. Genes & Dev. 12, 2821-2830. https://doi.org/10.1101/gad.12.18.2821
- Baker, S. J. and Reddy, E. P. (1996) Transducers of life and death: TNF receptor superfamily and associated proteins. Oncogene 12, 1-9.
-
Baldwin, A. S. J. (1996) The NF-
$\kappa$ B and I$\kappa$ B proteins: New discoveries and insights. Ann. Rev. Immunol. 14, 649-681. https://doi.org/10.1146/annurev.immunol.14.1.649 -
Beg, A. A. and Baltimore D. (1996) An essential role for
$NF-{\kappa}B$ in preventing TNF-$\alpha$ -induced cell death. Science 274, 782-784. https://doi.org/10.1126/science.274.5288.782 - Cao, Z., Xiong, J., Takeuchi, M., Kurama, T. and Goeddel, D. V. (1996) TRAF6 is a signal transducers for interleukin-1. Nature 383, 443-446. https://doi.org/10.1038/383443a0
- Cheng, G. and Baltimore, D. (1996) TANK, a co-inducer with TRAF2 of TNF- and CD40L-mediated NF-activation. Genes & Dev. 10,963-973. https://doi.org/10.1101/gad.10.8.963
-
Force, W. R., Cheung, T. C. and Ware, C. F. (1997) Dominant
negative mutants of TRAF3 reveal an important role for the
coiled coil domains in cell death signaling by the Iymphotoxin-
$\beta$ receptor J. BioI. Chem. 272, 30835-30840. https://doi.org/10.1074/jbc.272.49.30835 -
Hsu, H., Xiong, J. and Goeddel, D. V. (1995) The TNF receptor
1-associated protein TRADD signals cell death and
$NF-{\kappa}B$ activation. Cell 81, 495-504. https://doi.org/10.1016/0092-8674(95)90070-5 - Hsu, H., Shu, H. B., Pan, M. G. and Goeddel, D. V. (1996) TRADD-TRAF2 and TRADD-FADD interactions define two distinct TNF receptor 1 signal transduction pathways. Cell 84, 299-308. https://doi.org/10.1016/S0092-8674(00)80984-8
- Ishida, T., Tojo, T., Aoki, T., Kobayashi, N., Ohishi.T., Watanabe, T., Yamamoto,T. and Inoue, J. I. (1996) TRAF5, a novel tumor necrosis factor receptor-associated factor family protein, mediates CD40 signaling. Proc. Natl. Acad. Sci. USA 93, 9437- 9442. https://doi.org/10.1073/pnas.93.18.9437
- Jang, H. D., Chung, Y. M., Baik, J. Y., Choi, Y. G., Park, I. S., Jung, Y. K. and Lee, S. Y. (2001) Caspase-cleaved TRAFI negatively regulates the antiapoptotic signals of TRAF2 during TNF-induced cell death. Biochem. Biophy. Res. Commun. 281, 499-505. https://doi.org/10.1006/bbrc.2001.4369
- Kaufman, D. and Choi, Y. (1999) Signaling by tumor necrosis factor receptors: pathways, paradigms and targets for therapeutic modulation. Intern. Rev. Immunol. 18, 405-427. https://doi.org/10.3109/08830189909088491
-
Kelliher, M. A., Grimm, S., Ishida, Y., Kuo, E, Stanger, B. Z. and
Leder, p. (1998) The death domain kinase RIP mediates the
TNF-induced
$NF-{\kappa}B$ signal. Immunity 8, 297-303. https://doi.org/10.1016/S1074-7613(00)80535-X - Khaled, A. R. and Dururn, S. K. (2001) From cytosol to mito chondria: the Bax translocation story. J. Biochem. Mol. BioI. 34, 391-394.
- Kim, H. H., Kim, H. M., Kwack, K., Kim, S. W. and Lee, Z. H. (2001) Osteoclast differentiation factor engages the PI3-kinase, p38 and ERK pathways for avian osteoclast differentiation. J. Biochem. Mol. BioI. 34,421-427.
-
Lee, S. Y., Lee, S. Y., Kandala, G., Liou, M., Liou, H. and Choi,
Y. (1996a) CD30/TNF receptor-associated factor interaction:
$NF-{\kappa}B$ activation and binding specificity. Proc. Natl. Acad. Sci. USA 93, 9699-9703. https://doi.org/10.1073/pnas.93.18.9699 - Lee, S. Y., Lee, S. Y. and Choi, Y. (1997a) TRAF-interacting protein (TRIP): A novel component of the TNFR-and CD30- TRAF signaling complexes that inhibits TRAF2-mediated NF-kB activation. J. Exp. Med. 185, 1275-1285. https://doi.org/10.1084/jem.185.7.1275
- Lee, S. Y., Reichlin, A., Santana, A., Sokol, K. A., Nussenzweig, M., and Choi Y. (1997b) TRAF2 is essential for JNK but not NF-kB activation and regulates lymphocyte proliferation and survival. Immunity 7, 703-713. https://doi.org/10.1016/S1074-7613(00)80390-8
-
Lee, S. Y., Kaufman, D. R., Mora, A. L., Santana, A, Boothby,
M. and Choi, Y. (1998) Stimulus-dependent synergism of the
antiapoptotic tumor necrosis factor receptor-
$\beta$ associating factor 2 (TRAF2) and nuclear factor kappa B pathways. J. Exp. Med. 188, 1381-1384. https://doi.org/10.1084/jem.188.7.1381 - Locksley, R. M., Killeen, N. and Lenardo, M. J. (2001) The TNF and TNF receptor superfamilies: integrating mammalian biology. Cell 104, 487-501. https://doi.org/10.1016/S0092-8674(01)00237-9
- Lomaga, M. A., Yeh, W. C., Sarosi, I., Duncan, G. S., Furlonger, C., Ho, A., Morony, S., Capparelli, C., Van, Gwyneth., Kaufman, S., Van der Heiden, A., Itie, A., Wakeham, A., Khoo, W., Sasaki, T., Cao, Z., Penninger, J. M., Paige, C. J., Lacey, D. L., Dunstan, C. R., Boyle, W. J., Goeddel, D. V. and Mak, T. W. (1999) TRAF6 deficiency results in osteopetrosis and defective interleukin-1, CD40, and LPS signaling. Genes & Dev. 13, 1015-1024. https://doi.org/10.1101/gad.13.8.1015
-
Malinin, N. L., Boldin, M. P., Kovalenko, A. V. and Wallach, D.
(1997) MAP3K-related kinase involved in
$NF-{\kappa}B$ induction by TNF, CD95 and IL-1. Nature 385, 540-544. https://doi.org/10.1038/385540a0 - Means, T. K., Golenbock, D. T. and Fenton, M. J. The biology of Toll-like receptors. Cyto. Growth Factor. 11, 219-232. https://doi.org/10.1016/S1359-6101(00)00006-X
-
Nakano, H., Oshima, H., Chung, W., Williams-Abbott, L., Ware,
C. F., Yagita, H. and Okumura, K. (1996) TRAF5, an activator of
$NF-{\kappa}B$ and putative signal transducer for the Iymphotoxin-$\beta$ receptor. J. BioI. Chem. 271, 14661-14664. https://doi.org/10.1074/jbc.271.25.14661 - Park, Y. C., Burkitt, V., Villa, A. R., Tong, L. and Wu, H. (1999) Structural basis for self-association and receptor recognition of human TRAF2. Nature 398, 533-538 https://doi.org/10.1038/19110
-
Reinhard, C., Shamoon, B., Shyamala, V. and Williams, L. T.
(1997) Tumor necrosis factor-
$\alpha$ induced activation of c-jun Ntenninal kinase is mediated by TRAF2. EMBO J. 16, 1080- 1092. https://doi.org/10.1093/emboj/16.5.1080 - Rothe, M., Wong, S. C., Henzel, W. J. and Goeddel, D. V. (1994) A novel family of putative signal transducers associated with the cytoplasmic domain of the 75kDa tumor necrosis factor receptor. Cell 78, 681-692. https://doi.org/10.1016/0092-8674(94)90532-0
- Rothe, M., Pan, M. G., Henzel, W. J., Ayres, T. M. and Goeddel, D. V. (1995) The TNFR2-TRAF signaling complex contains two novel proteins related to baculoviral inhibitor of apoptosis proteins. Cell 83, 1243-1252. https://doi.org/10.1016/0092-8674(95)90149-3
- Rothe, M., Xiong, J., Shu, H. B., Williamson, K., Goddard, A. and Goeddel, D. V. (1996) I-TRAF is a novel TRAF-interacting protein that regulates TRAP-mediated signal transduction. Proc. Natl. Acad. Sci. USA 93, 8241-8246. https://doi.org/10.1073/pnas.93.16.8241
- Saitoh, M., Nishitoh, H., Fujii, M., Takeda, K., Tobiume, K., Sawada, Y., Kawabata, M., Miyazono, K. and Ichijo, H. (1998) Mammalian thioredoxin is a direct inhibitor of apoptosis signal-regulating kinase (ASK) 1. EMBO J. 17.2596-2606. https://doi.org/10.1093/emboj/17.9.2596
-
Shinkura, R., Kitada, K., Matsuda, F, Tashiro, K., Ikuta, K.,
Suzuki, M., Kogishi, K., Serikawa, T. and Honjo, T. (1999)
Alymphoplasia is caused by a point mutation in the mouse
gene encoding
$NF-{\kappa}B$ inducing kinase. Nature Genet. 22, 74- 77. https://doi.org/10.1038/8780 - Song, H. Y., Regnier, C. H., Kirschning, C. J., Goeddel, D. V. and Rothe, M. (1997) Tumor necrosis factor (TNF) mediated kinsae cascades: Bifurcation of nuclear factor-B and c-jun N-tenninal kinase (JNK/JSAPK) pathways at TNF receptor-associated factor 2. Proc. Natl. Acad. Sci. USA 94, 9792-9796. https://doi.org/10.1073/pnas.94.18.9792
- Speiser, D. E., Lee. S. Y., Wong, B., Arron, J., Santana, A., Kong, Y. Y., Ohashi, P. S. and Choi, Y. (1997) A regulatory role for TRAFI in antigen-induced apoptosis of T cells. J. Exp. Med. 185, 1777-1783. https://doi.org/10.1084/jem.185.10.1777
- Tsao, D. H. H., McDonagh, T., Telliez J. B., Hsu, S., Malakian, K., Xu, G. Y. and Lin, L. L. (2000) Solution structure of NTRADD and characterization of the interaction of N-TRADD and C-TRAF2. a key step in the TNFR1 signaling pathway. Mol. Cell 5, 1051-1057. https://doi.org/10.1016/S1097-2765(00)80270-1
- Tsitsikov, E. N., Laouin, D., Dunn, I. F., Sannikova, T. Y., Davidson, L., Alt, F. W. and Geha, R. S. (2001) TRAFI is a negative regulator of TNF signaling: enhanced TNF signaling in TRAF1-deficient mice. Immunity 15, 647-657. https://doi.org/10.1016/S1074-7613(01)00207-2
-
Van Antwerp, D. J., Martin, S. J., Kafri, T., Green, D. R. and
Verma, I.M. (1996) Suppression of TNF-
$\alpha$ induced apoptosis by$NF-{\kappa}B$ . Science 274, 787-789. https://doi.org/10.1126/science.274.5288.787 - Wallach, D., Varfolomeev, E. E., Malinin, N. L., Goltsev, Y. V., Kovalenko, A. V. and Boldin, M. P (1999) Tumor necrosis factor receptor and Fas signaling mechanisms. Annu. Rev. Immunol. 17, 331-367. https://doi.org/10.1146/annurev.immunol.17.1.331
- Wajant, H., Henkler, F. and Scheurich, P. (2001) The TNF-receptor- associated factor family Scaffold molecules for cytokine receptors, kinases and their regulators. Cellular Signaling 13, 389-400. https://doi.org/10.1016/S0898-6568(01)00160-7
- Wang,C., Deng, L., Hong, M., Akkaraju, G. R., Inoue, J. H. and Chen, Z. J. (2001) TAKI is a ubiquitin-dependent kinase of MKK and IKK. Nature 412,346-351. https://doi.org/10.1038/35085597
- Wang, C. Y., Mayo, M. W. and Baldwin, A. S. (1996) TNF- and cancer therapy-induced apoptosis: Potentiation by inhibition of NF-B. Science 274, 784-787. https://doi.org/10.1126/science.274.5288.784
-
Wong, B. R., Josien, R., Lee, S. Y. Vologodskaia, M., Steinman,
R. M. and Choi, Y. (1998) The TRAF family of signal
transducers mediates NF-
$\kappa$ B activation by the TRANCE receptor. J. Bioi. Chern. 273, 28355-28359. https://doi.org/10.1074/jbc.273.43.28355 - Wong, B. R., Besser, D., Kim, N., Arron, J. R., Vologodskaia, M., Hanafusa, H. and Choi, Y. (1999) TRANCE, a TNF family member, activates Akt/PKB through a signaling complex involving TRAP6 and c-Src. Mol. Cell 4, 1041-1049. https://doi.org/10.1016/S1097-2765(00)80232-4
- Xu, Y., Cheng, G. and Baltimore, D. (1996) Targeted disruption of TRAF3 leads to postnatal lethality and defective T-dependent immune responses. Immunity 5, 407-415. https://doi.org/10.1016/S1074-7613(00)80497-5
- Ye. H., Park, Y.C., Kreishman, M., Kieff, E. and Wu, H. (1999) The structural basis for the recognition of diverse receptor sequences by TRAF2. Mol. Cell 4, 321-330. https://doi.org/10.1016/S1097-2765(00)80334-2
- Yeh, W. C., Shahinian, A., Speiser, D., Kraunus, J., Billia, F., Wakeham, A., de la Pompa, J. L., Ferrick, D., Hum, B., Iscove, N., Ohashi, P., Rothe, M., Goeddel, D. V. and Mak, T.W. (1997) Early lethality, functional NF-KB activation and increased sensitivity to TNF-induced cell death in TRAF2- deficient mice. Immunity 7, 715-725. https://doi.org/10.1016/S1074-7613(00)80391-X
Cited by
- The possible functions of duplicated ets (GGAA) motifs located near transcription start sites of various human genes vol.68, pp.12, 2011, https://doi.org/10.1007/s00018-011-0674-x
- Characterization and expression analysis of TNFR-associated factor 1 (TRAF1) in grass carp Ctenopharyngodon idella vol.121, pp.1-2, 2008, https://doi.org/10.1016/j.vetimm.2007.08.001
- TRAF6 Activation in Multiple Myeloma: A Potential Therapeutic Target vol.12, pp.3, 2012, https://doi.org/10.1016/j.clml.2012.01.006
- Anti-Ischemic Effect of Selectin Blocker Through Modulation of Tumor Necrosis Factor-α and Interleukin-10 vol.138, pp.2, 2007, https://doi.org/10.1016/j.jss.2006.04.012
- The Telomere/Telomerase System in Chronic Inflammatory Diseases. Cause or Effect? vol.7, pp.9, 2016, https://doi.org/10.3390/genes7090060
- Metabolic Regulation of T Lymphocytes vol.31, pp.1, 2013, https://doi.org/10.1146/annurev-immunol-032712-095956
- Tumor necrosis factor-α and lymphotoxin-α increase macrophage ABCA1 by gene expression and protein stabilization via different receptors vol.209, pp.2, 2010, https://doi.org/10.1016/j.atherosclerosis.2009.10.019
- Mechanisms of apoptosis in Crustacea: what conditions induce versus suppress cell death? vol.15, pp.3, 2010, https://doi.org/10.1007/s10495-009-0443-6
- Toll-Like Receptor Pathways in Autoimmune Diseases vol.50, pp.1, 2016, https://doi.org/10.1007/s12016-015-8473-z
- Sensitivity of TLR4- and -7-induced NFκB1 p105-TPL2-ERK pathway to TNF-receptor-associated-factor-6 revealed by RNAi in mouse macrophages vol.44, pp.15, 2007, https://doi.org/10.1016/j.molimm.2007.04.002
- Molecular genetics of type 1 diabetes mellitus: Achievements and future trends vol.42, pp.5, 2008, https://doi.org/10.1134/S0026893308050142
- Role of the tumor necrosis factor receptor-associated factor-type zinc finger domain containing protein 1 (TRAFD1) from the hard tick Haemaphysalis longicornis in immunity against bacterial infection vol.7, pp.1, 2016, https://doi.org/10.1016/j.ttbdis.2015.08.002
- Ryanodine Receptor Antagonism Protects the Ischemic Liver and Modulates TNF-α and IL-10 vol.140, pp.1, 2007, https://doi.org/10.1016/j.jss.2006.12.003
- TRAF4, at the Crossroad between Morphogenesis and Cancer vol.3, pp.4, 2011, https://doi.org/10.3390/cancers3022734
- Osteoclastic differentiation and function regulated by old and new pathways vol.7, pp.1-2, 2007, https://doi.org/10.1007/s11154-006-9010-4
- Sexual dimorphism in white and brown adipose tissue with obesity and inflammation vol.66, pp.1, 2014, https://doi.org/10.1016/j.yhbeh.2014.02.007
- Differential induction of MyD88- and TRIF-dependent pathways in equine monocytes by Toll-like receptor agonists vol.127, pp.1-2, 2009, https://doi.org/10.1016/j.vetimm.2008.09.028
- TNF receptor-associated factor 6 in advanced non-small cell lung cancer: clinical and prognostic implications vol.138, pp.11, 2012, https://doi.org/10.1007/s00432-012-1255-6
- Molecular Identification and Expression Analysis of Tumor Necrosis Factor Receptor-associated Factor 2 in Grass Carp Ctenopharyngodon idella vol.39, pp.11, 2007, https://doi.org/10.1111/j.1745-7270.2007.00355.x
- Expression of Tumor Necrosis Factor Receptor-associated Factor 6 in Lung Cancer Tissues vol.15, pp.24, 2015, https://doi.org/10.7314/APJCP.2014.15.24.10591
- Ubiquitylation as a Rheostat for TCR Signaling: From Targeted Approaches Toward Global Profiling vol.6, 2015, https://doi.org/10.3389/fimmu.2015.00618
- Targeted ablation of TRAF6 inhibits skeletal muscle wasting in mice vol.191, pp.7, 2010, https://doi.org/10.1083/jcb.201006098
- CD40/CD40L signaling and its implication in health and disease vol.35, pp.6, 2009, https://doi.org/10.1002/biof.62
- TRAF2 mediates JNK and STAT3 activation in response to IL-1β and IFNγ and facilitates apoptotic death of insulin-producing β-cells vol.420, 2016, https://doi.org/10.1016/j.mce.2015.11.021
- Diagnostic and Predictive Levels of Calcium-binding Protein A8 and Tumor Necrosis Factor Receptor-associated Factor 6 in Sepsis-associated Encephalopathy: A Prospective Observational Study vol.129, pp.14, 2016, https://doi.org/10.4103/0366-6999.185860
- Pleiotropic functions of EAPII/TTRAP/TDP2 vol.10, pp.19, 2011, https://doi.org/10.4161/cc.10.19.17763
- Litopenaeus vannamei tumor necrosis factor receptor-associated factor 6 (TRAF6) responds to Vibrio alginolyticus and white spot syndrome virus (WSSV) infection and activates antimicrobial peptide genes vol.35, pp.1, 2011, https://doi.org/10.1016/j.dci.2010.08.013
- Mouse transmembrane BAX inhibitor Motif 3 (Tmbim3) encodes a 38 kDa transmembrane protein expressed in the central nervous system vol.357, pp.1-2, 2011, https://doi.org/10.1007/s11010-011-0877-3
- Life or death by NFκB, Losartan promotes survival in dy2J/dy2J mouse of MDC1A vol.6, pp.3, 2015, https://doi.org/10.1038/cddis.2015.60
- Retroviral insertions in the VISION database identify molecular pathways in mouse lymphoid leukemia and lymphoma vol.18, pp.10, 2007, https://doi.org/10.1007/s00335-007-9060-2
- Relationship between TRAF6 and deterioration of HCC: an immunohistochemical and in vitro study vol.16, pp.1, 2016, https://doi.org/10.1186/s12935-016-0352-z
- Src mediates cytokine-stimulated gene expression in airway myocytes through ERK MAPK vol.9, pp.1, 2011, https://doi.org/10.1186/1478-811X-9-14
- Altered Expression of TNF-α Signaling Pathway Proteins in Systemic Lupus Erythematosus vol.37, pp.8, 2010, https://doi.org/10.3899/jrheum.091123
- NF-κB-Mediated Inflammation in the Pathogenesis of Intracranial Aneurysm and Subarachnoid Hemorrhage. Does Autophagy Play a Role? vol.19, pp.4, 2018, https://doi.org/10.3390/ijms19041245