RFXAP

From Wikipedia, the free encyclopedia

Regulatory factor X-associated protein

Identifiers

External IDs

OMIM: 601861 MGI: 2180854 HomoloGene: 452

Gene ontology
Molecular Function:	• transcription factor activity • transcription coactivator activity
Cellular Component:	• nucleus
Biological Process:	• transcription from RNA polymerase II promoter

RNA expression pattern

More reference expression data

Orthologs

Human

Mouse

n/a

Refseq

NM_000538 (mRNA)
NP_000529 (protein)

NM_133231 (mRNA)
NP_573494 (protein)

Location

Chr 13: 36.29 - 36.3 Mb

Chr 3: 54.89 - 54.9 Mb

Pubmed search

[1]

[2]

Regulatory factor X-associated protein, also known as RFXAP, is a human gene.^[1]

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.^[1]

[edit] References

^ ^a ^b Entrez Gene: RFXAP regulatory factor X-associated protein.

[edit] Further reading

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. PMID 8290561.
Durand B, Sperisen P, Emery P, et al. (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. PMID 9118943.
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. 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. 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. 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. 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. 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. 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. doi:10.1073/pnas.242603899. 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. 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.