Wikipedia

TRAF1

TNF receptor-associated factor 1 is a protein that in humans is encoded by the TRAF1 gene.[5]

TRAF1
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesTRAF1, EBI6, MGC:10353, TNF receptor associated factor 1
External IDsOMIM: 601711; MGI: 101836; HomoloGene: 4138; GeneCards: TRAF1; OMA:TRAF1 - orthologs
Orthologs
SpeciesHumanMouse
Entrez

7185

22029

Ensembl

ENSG00000056558

ENSMUSG00000026875

UniProt

Q13077

P39428

RefSeq (mRNA)

NM_005658
NM_001190945
NM_001190947

NM_009421
NM_001326601

RefSeq (protein)

NP_001177874
NP_001177876
NP_005649

NP_001313530
NP_033447

Location (UCSC)Chr 9: 120.9 – 120.93 MbChr 2: 34.83 – 34.85 Mb
PubMed search[3][4]
Wikidata
View/Edit HumanView/Edit Mouse

Function

edit

The protein encoded by this gene is a member of the TNF receptor (TNFR) associated factor (TRAF) protein family. TRAF proteins associate with, and mediate the signal transduction from various receptors of the TNFR superfamily. This protein and TRAF2 form a heterodimeric complex, which is required for TNF-alpha-mediated activation of MAPK8/JNK and NF-kappaB. The protein complex formed by this protein and TRAF2 also interacts with IAP, and thus mediates the anti-apoptotic signals from TNF receptors. The expression of this protein can be induced by Epstein-Barr virus (EBV). EBV infection membrane protein 1 (LMP1) is found to interact with this and other TRAF proteins; this interaction is thought to link LMP1-mediated B lymphocyte transformation to the signal transduction from TNFR family receptors.[6] TRAF1 also functions as a negative regulator of inflammation by interfering with the linear ubiquitination of NEMO downstream of TLR signaling.[7] This explains why TRAF1 polymorphisms cause an increased risk for rheumatic diseases.[8]

Interactions

edit

References

edit
  1. 1 2 3 GRCh38: Ensembl release 89: ENSG00000056558 – Ensembl, May 2017
  2. 1 2 3 GRCm38: Ensembl release 89: ENSMUSG00000026875 – Ensembl, May 2017
  3. ↑ "Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  4. ↑ "Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
  5. ↑ Rothe M, Wong SC, Henzel WJ, Goeddel DV (September 1994). "A novel family of putative signal transducers associated with the cytoplasmic domain of the 75 kDa tumor necrosis factor receptor". Cell. 78 (4): 681–692. doi:10.1016/0092-8674(94)90532-0. PMID 8069916. S2CID 28055231.
  6. ↑ "Entrez Gene: TRAF1 TNF receptor-associated factor 1".
  7. 1 2 3 4 Abdul-Sater AA, Edilova MI, Clouthier DL, Mbanwi A, Kremmer E, Watts TH (November 2016). "The signaling adaptor TRAF1 negatively regulates Toll-like receptor signaling and this underlies its role in rheumatic disease". Nature Immunology. 18 (1): 26–35. doi:10.1038/ni.3618. PMID 27893701. S2CID 19487408.
  8. ↑ Plenge RM, Seielstad M, Padyukov L, Lee AT, Remmers EF, Ding B, et al. (September 2007). "TRAF1-C5 as a risk locus for rheumatoid arthritis--a genomewide study". The New England Journal of Medicine. 357 (12): 1199–1209. doi:10.1056/NEJMoa073491. PMC 2636867. PMID 17804836.
  9. 1 2 Roy N, Deveraux QL, Takahashi R, Salvesen GS, Reed JC (December 1997). "The c-IAP-1 and c-IAP-2 proteins are direct inhibitors of specific caspases". The EMBO Journal. 16 (23): 6914–6925. doi:10.1093/emboj/16.23.6914. PMC 1170295. PMID 9384571.
  10. 1 2 Li X, Yang Y, Ashwell JD (March 2002). "TNF-RII and c-IAP1 mediate ubiquitination and degradation of TRAF2". Nature. 416 (6878): 345–347. Bibcode:2002Natur.416..345L. doi:10.1038/416345a. PMID 11907583. S2CID 4325926.
  11. ↑ Shu HB, Takeuchi M, Goeddel DV (November 1996). "The tumor necrosis factor receptor 2 signal transducers TRAF2 and c-IAP1 are components of the tumor necrosis factor receptor 1 signaling complex". Proceedings of the National Academy of Sciences of the United States of America. 93 (24): 13973–13978. Bibcode:1996PNAS...9313973S. doi:10.1073/pnas.93.24.13973. PMC 19479. PMID 8943045.
  12. ↑ Shu HB, Halpin DR, Goeddel DV (June 1997). "Casper is a FADD- and caspase-related inducer of apoptosis". Immunity. 6 (6): 751–763. doi:10.1016/s1074-7613(00)80450-1. PMID 9208847.
  13. ↑ Kataoka T, Budd RC, Holler N, Thome M, Martinon F, Irmler M, et al. (June 2000). "The caspase-8 inhibitor FLIP promotes activation of NF-kappaB and Erk signaling pathways". Current Biology. 10 (11): 640–648. doi:10.1016/s0960-9822(00)00512-1. PMID 10837247. S2CID 14819939.
  14. ↑ Micheau O, Tschopp J (July 2003). "Induction of TNF receptor I-mediated apoptosis via two sequential signaling complexes". Cell. 114 (2): 181–190. doi:10.1016/s0092-8674(03)00521-x. PMID 12887920. S2CID 17145731.
  15. ↑ Leo E, Deveraux QL, Buchholtz C, Welsh K, Matsuzawa S, Stennicke HR, et al. (March 2001). "TRAF1 is a substrate of caspases activated during tumor necrosis factor receptor-alpha-induced apoptosis". The Journal of Biological Chemistry. 276 (11): 8087–8093. doi:10.1074/jbc.M009450200. PMID 11098060.
  16. ↑ Oukka M, Kim ST, Lugo G, Sun J, Wu LC, Glimcher LH (January 2002). "A mammalian homolog of Drosophila schnurri, KRC, regulates TNF receptor-driven responses and interacts with TRAF2". Molecular Cell. 9 (1): 121–131. doi:10.1016/s1097-2765(01)00434-8. PMID 11804591.
  17. ↑ Galibert L, Tometsko ME, Anderson DM, Cosman D, Dougall WC (December 1998). "The involvement of multiple tumor necrosis factor receptor (TNFR)-associated factors in the signaling mechanisms of receptor activator of NF-kappaB, a member of the TNFR superfamily". The Journal of Biological Chemistry. 273 (51): 34120–34127. doi:10.1074/jbc.273.51.34120. PMID 9852070.
  18. ↑ Kim HH, Lee DE, Shin JN, Lee YS, Jeon YM, Chung CH, et al. (January 1999). "Receptor activator of NF-kappaB recruits multiple TRAF family adaptors and activates c-Jun N-terminal kinase". FEBS Letters. 443 (3): 297–302. doi:10.1016/s0014-5793(98)01731-1. PMID 10025951. S2CID 46210019.
  19. ↑ Song HY, Rothe M, Goeddel DV (June 1996). "The tumor necrosis factor-inducible zinc finger protein A20 interacts with TRAF1/TRAF2 and inhibits NF-kappaB activation". Proceedings of the National Academy of Sciences of the United States of America. 93 (13): 6721–6725. Bibcode:1996PNAS...93.6721S. doi:10.1073/pnas.93.13.6721. PMC 39093. PMID 8692885.
  20. ↑ Heyninck K, Beyaert R (January 1999). "The cytokine-inducible zinc finger protein A20 inhibits IL-1-induced NF-kappaB activation at the level of TRAF6". FEBS Letters. 442 (2–3): 147–150. doi:10.1016/s0014-5793(98)01645-7. PMID 9928991. S2CID 19072203.
  21. ↑ Lee SY, Lee SY, Choi Y (April 1997). "TRAF-interacting protein (TRIP): a novel component of the tumor necrosis factor receptor (TNFR)- and CD30-TRAF signaling complexes that inhibits TRAF2-mediated NF-kappaB activation". The Journal of Experimental Medicine. 185 (7): 1275–1285. doi:10.1084/jem.185.7.1275. PMC 2196258. PMID 9104814.
  22. ↑ Bouwmeester T, Bauch A, Ruffner H, Angrand PO, Bergamini G, Croughton K, et al. (February 2004). "A physical and functional map of the human TNF-alpha/NF-kappa B signal transduction pathway". Nature Cell Biology. 6 (2): 97–105. doi:10.1038/ncb1086. PMID 14743216. S2CID 11683986.
  23. ↑ Takeuchi M, Rothe M, Goeddel DV (August 1996). "Anatomy of TRAF2. Distinct domains for nuclear factor-kappaB activation and association with tumor necrosis factor signaling proteins". The Journal of Biological Chemistry. 271 (33): 19935–19942. doi:10.1074/jbc.271.33.19935. PMID 8702708.

Further reading

edit
Retrieved from "https://en.wikipedia.org/w/index.php?title=TRAF1&oldid=1358130849"