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Modulation of Life and Death by the Tumor Necrosis Factor Receptor-Associated Factors (TRAFs)

  • Lee, Na-Kyung (Division of Molecular Life Sciences and Center for Cell Signaling Research, Ewha Womans University) ;
  • Lee, Soo-Young (Division of Molecular Life Sciences and Center for Cell Signaling Research, Ewha Womans University)
  • Published : 2002.01.31

Abstract

The TNF receptor-associated factor (TRAF) family is a group of adapter proteins that link a wide variety of cell surface receptors. Including the TNF and IL-1 receptor superfamily to diverse signaling cascades, which lead to the activation of NF-${\kappa}B$ and mitogen-activated protein kinases. In addition, TRAFs interact with a variety of proteins that regulate receptor-induced cell death or survival. Thus, TRAF-mediated signals may directly induce cell survival or interfere with the death receptor-induced apoptosis.

Keywords

References

  1. 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
  2. Baker, S. J. and Reddy, E. P. (1996) Transducers of life and death: TNF receptor superfamily and associated proteins. Oncogene 12, 1-9.
  3. 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
  4. 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
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. Khaled, A. R. and Dururn, S. K. (2001) From cytosol to mito chondria: the Bax translocation story. J. Biochem. Mol. BioI. 34, 391-394.
  15. 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.
  16. 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
  17. 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
  18. 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
  19. 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
  20. 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
  21. 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
  22. 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
  23. 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
  24. 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
  25. 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
  26. 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
  27. 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
  28. 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
  29. 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
  30. 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
  31. 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
  32. 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
  33. 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
  34. 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
  35. 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
  36. 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
  37. 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
  38. 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
  39. 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
  40. 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
  41. 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
  42. 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
  43. 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
  44. 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
  45. 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

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