RFX5
RFX5 (Regulatory factor X5) هوَ بروتين يُشَفر بواسطة جين RFX5 في الإنسان.[1]
الوظيفة
المراجع
- "Entrez Gene: RFX5 regulatory factor X, 5 (influences HLA class II expression)". مؤرشف من الأصل في 2010-12-05.
قراءة متعمقة
- Reith W، Mach B (2001). "The bare lymphocyte syndrome and the regulation of MHC expression". Annual Review of Immunology. ج. 19: 331–73. DOI:10.1146/annurev.immunol.19.1.331. PMID:11244040.
- Steimle V، Durand B، Barras E، Zufferey M، Hadam MR، Mach B، Reith W (مايو 1995). "A novel DNA-binding regulatory factor is mutated in primary MHC class II deficiency (bare lymphocyte syndrome)". Genes & Development. ج. 9 ع. 9: 1021–32. DOI:10.1101/gad.9.9.1021. PMID:7744245.
- Maruyama K، Sugano S (يناير 1994). "Oligo-capping: a simple method to replace the cap structure of eukaryotic mRNAs with oligoribonucleotides". Gene. ج. 138 ع. 1–2: 171–4. DOI:10.1016/0378-1119(94)90802-8. PMID:8125298.
- Durand B، Sperisen P، Emery P، Barras E، Zufferey M، Mach B، Reith W (مارس 1997). "RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency". The EMBO Journal. ج. 16 ع. 5: 1045–55. DOI:10.1093/emboj/16.5.1045. PMC:1169704. PMID:9118943.
- Scholl T، Mahanta SK، Strominger JL (يونيو 1997). "Specific complex formation between the type II bare lymphocyte syndrome-associated transactivators CIITA and RFX5". Proceedings of the National Academy of Sciences of the United States of America. ج. 94 ع. 12: 6330–4. DOI:10.1073/pnas.94.12.6330. PMC:21049. PMID:9177217.
- Moreno CS، Rogers EM، Brown JA، Boss JM (يونيو 1997). "Regulatory factor X, a bare lymphocyte syndrome transcription factor, is a multimeric phosphoprotein complex". Journal of Immunology. ج. 158 ع. 12: 5841–8. PMID:9190936.
- Suzuki Y، Yoshitomo-Nakagawa K، Maruyama K، Suyama A، Sugano S (أكتوبر 1997). "Construction and characterization of a full length-enriched and a 5'-end-enriched cDNA library". Gene. ج. 200 ع. 1–2: 149–56. DOI:10.1016/S0378-1119(97)00411-3. PMID:9373149.
- Masternak K، Barras E، Zufferey M، Conrad B، Corthals G، Aebersold R، Sanchez JC، Hochstrasser DF، Mach B، Reith W (نوفمبر 1998). "A gene encoding a novel RFX-associated transactivator is mutated in the majority of MHC class II deficiency patients". Nature Genetics. ج. 20 ع. 3: 273–7. DOI:10.1038/3081. PMID:9806546.
- Nagarajan UM، Louis-Plence P، DeSandro A، Nilsen R، Bushey A، Boss JM (فبراير 1999). "RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency". Immunity. ج. 10 ع. 2: 153–62. DOI:10.1016/S1074-7613(00)80016-3. PMID:10072068.
- Peijnenburg A، Van Eggermond MC، Van den Berg R، Sanal O، Vossen JM، Van den Elsen PJ (أبريل 1999). "Molecular analysis of an MHC class II deficiency patient reveals a novel mutation in the RFX5 gene". Immunogenetics. ج. 49 ع. 4: 338–45. DOI:10.1007/s002510050501. PMID:10079298.
- Villard J، Peretti M، Masternak K، Barras E، Caretti G، Mantovani R، Reith W (مايو 2000). "A functionally essential domain of RFX5 mediates activation of major histocompatibility complex class II promoters by promoting cooperative binding between RFX and NF-Y". Molecular and Cellular Biology. ج. 20 ع. 10: 3364–76. DOI:10.1128/MCB.20.10.3364-3376.2000. PMC:85629. PMID:10779326.
- Nekrep N، Jabrane-Ferrat N، Peterlin BM (يونيو 2000). "Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex". Molecular and Cellular Biology. ج. 20 ع. 12: 4455–61. DOI:10.1128/MCB.20.12.4455-4461.2000. PMC:85813. PMID:10825209.
- Sengupta PK، Fargo J، Smith BD (يوليو 2002). "The RFX family interacts at the collagen (COL1A2) start site and represses transcription". The Journal of Biological Chemistry. ج. 277 ع. 28: 24926–37. DOI:10.1074/jbc.M111712200. PMID:11986307.
- Nekrep N، Jabrane-Ferrat N، Wolf HM، Eibl MM، Geyer M، Peterlin BM (نوفمبر 2002). "Mutation in a winged-helix DNA-binding motif causes atypical bare lymphocyte syndrome". Nature Immunology. ج. 3 ع. 11: 1075–81. DOI:10.1038/ni840. PMID:12368908.
- Xu Y، Wang L، Buttice G، Sengupta PK، Smith BD (ديسمبر 2003). "Interferon gamma repression of collagen (COL1A2) transcription is mediated by the RFX5 complex". The Journal of Biological Chemistry. ج. 278 ع. 49: 49134–44. DOI:10.1074/jbc.M309003200. PMID:12968017.
- Nagarajan UM، Long AB، Harreman MT، Corbett AH، Boss JM (يوليو 2004). "A hierarchy of nuclear localization signals governs the import of the regulatory factor X complex subunits and MHC class II expression". Journal of Immunology. ج. 173 ع. 1: 410–9. DOI:10.4049/jimmunol.173.1.410. PMID:15210800.
- Hjerrild M، Stensballe A، Rasmussen TE، Kofoed CB، Blom N، Sicheritz-Ponten T، Larsen MR، Brunak S، Jensen ON، Gammeltoft S (2004). "Identification of phosphorylation sites in protein kinase A substrates using artificial neural networks and mass spectrometry". Journal of Proteome Research. ج. 3 ع. 3: 426–33. DOI:10.1021/pr0341033. PMID:15253423.
- بوابة علم الأحياء الخلوي والجزيئي
- بوابة طب
- بوابة الكيمياء الحيوية
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