RFXAP

RFXAP
Available structures
PDB	Ortholog search: PDBe RCSB
List of PDB id codes
	2KW3
Identifiers
Aliases	RFXAP, regulatory factor X associated protein
External IDs	OMIM: 601861 MGI: 2180854 HomoloGene: 452 GeneCards: RFXAP
Gene location (Human)
Chr.	Chromosome 13 (human)[1]
End	36,829,104 bp[1]
Gene location (Mouse)
Chr.	Chromosome 3 (mouse)[2]
End	54,807,791 bp[2]
RNA expression pattern
	; ;
	More reference expression data
Gene ontology
Molecular function	• GO:0001105 transcription coactivator activity; • GO:0001131, GO:0001151, GO:0001130, GO:0001204 DNA-binding transcription factor activity; • DNA binding;
Cellular component	• cell nucleus; • nuclear speck;
Biological process	• positive regulation of transcription, DNA-templated;
	Sources:Amigo / QuickGO
Orthologs
	5994
	170767
	ENSG00000133111
	ENSMUSG00000036615
	O00287
	Q8VCG9
	NM_000538
	NM_133231
	NP_000529
	NP_573494
	Wikidata
View/Edit Human	View/Edit Mouse

Regulatory factor X-associated protein is a protein that in humans is encoded by the RFXAP gene.[5][6]

Major histocompatibility (MHC) class II molecules are transmembrane proteins that have a central role in development and control of the immune system. The protein encoded by this gene, along with regulatory factor X-associated ankyrin-containing protein and regulatory factor-5, forms a complex that binds to the X box motif of certain MHC class II gene promoters and activates their transcription. Once bound to the promoter, this complex associates with the non-DNA-binding factor MHC class II transactivator, which controls the cell type specificity and inducibility of MHC class II gene expression. Mutations in this gene have been linked to bare lymphocyte syndrome type II, complementation group D. Transcript variants utilizing different polyA signals have been found for this gene.[6]

Interactions

RFXAP has been shown to interact with RFXANK.[7][8]

References

GRCh38: Ensembl release 89: ENSG00000133111 - Ensembl, May 2017
GRCm38: Ensembl release 89: ENSMUSG00000036615 - Ensembl, May 2017
"Human PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
"Mouse PubMed Reference:". National Center for Biotechnology Information, U.S. National Library of Medicine.
Durand B, Sperisen P, Emery P, Barras E, Zufferey M, Mach B, Reith W (April 1997). "RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency". EMBO J. 16 (5): 1045–55. doi:10.1093/emboj/16.5.1045. PMC 1169704. PMID 9118943.
"Entrez Gene: RFXAP regulatory factor X-associated protein".
Nekrep, N; Geyer M; Jabrane-Ferrat N; Peterlin B M (August 2001). "Analysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndrome". Mol. Cell. Biol. United States. 21 (16): 5566–76. doi:10.1128/MCB.21.16.5566-5576.2001. ISSN 0270-7306. PMC 87278. PMID 11463838.
Nekrep, N; Jabrane-Ferrat N; Peterlin B M (June 2000). "Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex". Mol. Cell. Biol. UNITED STATES. 20 (12): 4455–61. doi:10.1128/MCB.20.12.4455-4461.2000. ISSN 0270-7306. PMC 85813. PMID 10825209.

Mach B, Steimle V, Martinez-Soria E, Reith W (1996). "Regulation of MHC class II genes: lessons from a disease". Annu. Rev. Immunol. 14: 301–31. doi:10.1146/annurev.immunol.14.1.301. PMID 8717517.
Reith W, Mach B (2001). "The bare lymphocyte syndrome and the regulation of MHC expression". Annu. Rev. Immunol. 19: 331–73. doi:10.1146/annurev.immunol.19.1.331. PMID 11244040.
Reith W, Siegrist CA, Durand B, et al. (1994). "Function of major histocompatibility complex class II promoters requires cooperative binding between factors RFX and NF-Y". Proc. Natl. Acad. Sci. U.S.A. 91 (2): 554–8. Bibcode:1994PNAS...91..554R. doi:10.1073/pnas.91.2.554. PMC 42987. PMID 8290561.
Villard J, Lisowska-Grospierre B, van den Elsen P, et al. (1997). "Mutation of RFXAP, a regulator of MHC class II genes, in primary MHC class II deficiency". N. Engl. J. Med. 337 (11): 748–53. doi:10.1056/NEJM199709113371104. PMID 9287230.
Gobin SJ, Peijnenburg A, van Eggermond M, et al. (1998). "The RFX complex is crucial for the constitutive and CIITA-mediated transactivation of MHC class I and beta2-microglobulin genes". Immunity. 9 (4): 531–41. doi:10.1016/S1074-7613(00)80636-6. PMID 9806639.
Nagarajan UM, Louis-Plence P, DeSandro A, et al. (1999). "RFX-B is the gene responsible for the most common cause of the bare lymphocyte syndrome, an MHC class II immunodeficiency". Immunity. 10 (2): 153–62. doi:10.1016/S1074-7613(00)80016-3. PMID 10072068.
Nekrep N, Jabrane-Ferrat N, Peterlin BM (2000). "Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex". Mol. Cell. Biol. 20 (12): 4455–61. doi:10.1128/MCB.20.12.4455-4461.2000. PMC 85813. PMID 10825209.
Nekrep N, Geyer M, Jabrane-Ferrat N, Peterlin BM (2001). "Analysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndrome". Mol. Cell. Biol. 21 (16): 5566–76. doi:10.1128/MCB.21.16.5566-5576.2001. PMC 87278. PMID 11463838.
Kutsenko AS, Gizatullin RZ, Al-Amin AN, et al. (2002). "NotI flanking sequences: a tool for gene discovery and verification of the human genome". Nucleic Acids Res. 30 (14): 3163–70. doi:10.1093/nar/gkf428. PMC 135748. PMID 12136098.
Strausberg RL, Feingold EA, Grouse LH, et al. (2003). "Generation and initial analysis of more than 15,000 full-length human and mouse cDNA sequences". Proc. Natl. Acad. Sci. U.S.A. 99 (26): 16899–903. Bibcode:2002PNAS...9916899M. doi:10.1073/pnas.242603899. PMC 139241. PMID 12477932.
Nagarajan UM, Long AB, Harreman MT, et al. (2004). "A hierarchy of nuclear localization signals governs the import of the regulatory factor X complex subunits and MHC class II expression". J. Immunol. 173 (1): 410–9. doi:10.4049/jimmunol.173.1.410. PMID 15210800.
Mudhasani R, Fontes JD (2005). "Multiple interactions between BRG1 and MHC class II promoter binding proteins". Mol. Immunol. 42 (6): 673–82. doi:10.1016/j.molimm.2004.09.021. PMID 15781111.
Long AB, Ferguson AM, Majumder P, et al. (2006). "Conserved residues of the bare lymphocyte syndrome transcription factor RFXAP determine coordinate MHC class II expression". Mol. Immunol. 43 (5): 395–409. doi:10.1016/j.molimm.2005.03.008. PMID 16337482.

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[refGRCh38Ensembl-1] GRCh38: Ensembl release 89: ENSG00000133111 - Ensembl, May 2017

[refGRCm38Ensembl-2] GRCm38: Ensembl release 89: ENSMUSG00000036615 - 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.

[pmid9118943-5] Durand B, Sperisen P, Emery P, Barras E, Zufferey M, Mach B, Reith W (April 1997). "RFXAP, a novel subunit of the RFX DNA binding complex is mutated in MHC class II deficiency". EMBO J. 16 (5): 1045–55. doi:10.1093/emboj/16.5.1045. PMC 1169704. PMID 9118943.

[entrez-6] "Entrez Gene: RFXAP regulatory factor X-associated protein".

[pmid11463838-7] Nekrep, N; Geyer M; Jabrane-Ferrat N; Peterlin B M (August 2001). "Analysis of ankyrin repeats reveals how a single point mutation in RFXANK results in bare lymphocyte syndrome". Mol. Cell. Biol. United States. 21 (16): 5566–76. doi:10.1128/MCB.21.16.5566-5576.2001. ISSN 0270-7306. PMC 87278. PMID 11463838.

[pmid10825209-8] Nekrep, N; Jabrane-Ferrat N; Peterlin B M (June 2000). "Mutations in the bare lymphocyte syndrome define critical steps in the assembly of the regulatory factor X complex". Mol. Cell. Biol. UNITED STATES. 20 (12): 4455–61. doi:10.1128/MCB.20.12.4455-4461.2000. ISSN 0270-7306. PMC 85813. PMID 10825209.

RFXAP

Interactions

References

Further reading