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Open Access Articles- Top Results for CD27

CD27

Template:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/rowTemplate:Infobox3cols/row
Identifiers
SymbolsCD27 ; S152; S152. LPFS2; T14; TNFRSF7; Tp55
External IDsOMIM186711 MGI88326 HomoloGene74386 IUPHAR: 1876 GeneCards: CD27 Gene
RNA expression pattern
File:PBB GE CD27 206150 at tn.png
More reference expression data
Orthologs
SpeciesHumanMouse
Entrez93921940
EnsemblENSG00000139193ENSMUSG00000030336
UniProtP26842P41272
RefSeq (mRNA)NM_001242NM_001033126
RefSeq (protein)NP_001233NP_001028298
Location (UCSC)Chr 12:
6.55 – 6.56 Mb
Chr 6:
125.23 – 125.24 Mb
PubMed search[1][2]

CD27 is a member of the tumor necrosis factor receptor superfamily.

The protein encoded by this gene is a member of the TNF-receptor superfamily. This receptor is required for generation and long-term maintenance of T cell immunity. It binds to ligand CD70, and plays a key role in regulating B-cell activation and immunoglobulin synthesis. This receptor transduces signals that lead to the activation of NF-κB and MAPK8/JNK. Adaptor proteins TRAF2 and TRAF5 have been shown to mediate the signaling process of this receptor. CD27-binding protein (SIVA), a proapoptotic protein, can bind to this receptor and is thought to play an important role in the apoptosis induced by this receptor.[1]

Interactions

CD27 has been shown to interact with SIVA1,[2] TRAF2[3][4] and TRAF3.[3][4]

References

  1. ^ "Entrez Gene: CD27 CD27 molecule". 
  2. ^ Prasad, K V; Ao Z; Yoon Y; Wu M X; Rizk M; Jacquot S; Schlossman S F (Jun 1997). "CD27, a member of the tumor necrosis factor receptor family, induces apoptosis and binds to Siva, a proapoptotic protein". Proc. Natl. Acad. Sci. U.S.A. (UNITED STATES) 94 (12): 6346–51. ISSN 0027-8424. PMC 21052. PMID 9177220. doi:10.1073/pnas.94.12.6346. 
  3. ^ a b Yamamoto, H; Kishimoto T; Minamoto S (Nov 1998). "NF-kappaB activation in CD27 signaling: involvement of TNF receptor-associated factors in its signaling and identification of functional region of CD27". J. Immunol. (UNITED STATES) 161 (9): 4753–9. ISSN 0022-1767. PMID 9794406. 
  4. ^ a b Akiba, H; Nakano H, Nishinaka S, Shindo M, Kobata T, Atsuta M, Morimoto C, Ware C F, Malinin N L, Wallach D, Yagita H, Okumura K (May 1998). "CD27, a member of the tumor necrosis factor receptor superfamily, activates NF-kappaB and stress-activated protein kinase/c-Jun N-terminal kinase via TRAF2, TRAF5, and NF-kappaB-inducing kinase". J. Biol. Chem. (UNITED STATES) 273 (21): 13353–8. ISSN 0021-9258. PMID 9582383. doi:10.1074/jbc.273.21.13353. 

Further reading

  • Lens SM, de Jong R, Hintzen RQ et al. (1996). "CD27-CD70 interaction: unravelling its implication in normal and neoplastic B-cell growth.". Leuk. Lymphoma 18 (1–2): 51–9. PMID 8580829. doi:10.3109/10428199509064922. 
  • Agematsu K (2000). "Memory B cells and CD27". Histol. Histopathol. 15 (2): 573–6. PMID 10809378. 
  • van Baarle D, Kostense S, van Oers MH et al. (2003). "Failing immune control as a result of impaired CD8+ T-cell maturation: CD27 might provide a clue". Trends Immunol. 23 (12): 586–91. PMID 12464570. doi:10.1016/S1471-4906(02)02326-8. 
  • Dörner T, Lipsky PE (2005). "Correlation of circulating CD27high plasma cells and disease activity in systemic lupus erythematosus". Lupus 13 (5): 283–9. PMID 15230280. doi:10.1191/0961203304lu1014oa. 
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