DRAP1

From Wikipedia, the free encyclopedia


DR1-associated protein 1 (negative cofactor 2 alpha)
PDB rendering based on 1jfi.
Available structures: 1jfi
Identifiers
Symbol(s) DRAP1; NC2-alpha
External IDs OMIM: 602289 MGI1913806 HomoloGene4703
RNA expression pattern

More reference expression data

Orthologs
Human Mouse
Entrez 10589 66556
Ensembl ENSG00000175550 ENSMUSG00000024914
Uniprot Q14919 Q4FJW2
Refseq NM_006442 (mRNA)
NP_006433 (protein)
XM_976049 (mRNA)
XP_981143 (protein)
Location Chr 11: 65.44 - 65.45 Mb Chr 19: 5.42 - 5.42 Mb
Pubmed search [1] [2]

DR1-associated protein 1 (negative cofactor 2 alpha), also known as DRAP1, is a human gene.[1]

Transcriptional repression is a general mechanism for regulating transcriptional initiation in organisms ranging from yeast to humans. Accurate initiation of transcription from eukaryotic protein-encoding genes requires the assembly of a large multiprotein complex consisting of RNA polymerase II and general transcription factors such as TFIIA, TFIIB, and TFIID. DR1 is a repressor that interacts with the TATA-binding protein (TBP) of TFIID and prevents the formation of an active transcription complex by precluding the entry of TFIIA and/or TFIIB into the preinitiation complex. The protein encoded by this gene is a corepressor of transcription that interacts with DR1 to enhance DR1-mediated repression. The interaction between this corepressor and DR1 is required for corepressor function and appears to stabilize the TBP-DR1-DNA complex.[1]

[edit] References

[edit] Further reading

  • Mermelstein F, Yeung K, Cao J, et al. (1996). "Requirement of a corepressor for Dr1-mediated repression of transcription.". Genes Dev. 10 (8): 1033–48. PMID 8608938. 
  • Goppelt A, Stelzer G, Lottspeich F, Meisterernst M (1996). "A mechanism for repression of class II gene transcription through specific binding of NC2 to TBP-promoter complexes via heterodimeric histone fold domains.". EMBO J. 15 (12): 3105–16. PMID 8670811. 
  • Yeung K, Kim S, Reinberg D (1997). "Functional dissection of a human Dr1-DRAP1 repressor complex.". Mol. Cell. Biol. 17 (1): 36–45. PMID 8972183. 
  • Ikeda K, Halle JP, Stelzer G, et al. (1998). "Involvement of negative cofactor NC2 in active repression by zinc finger-homeodomain transcription factor AREB6.". Mol. Cell. Biol. 18 (1): 10–8. PMID 9418848. 
  • Castaño E, Gross P, Wang Z, et al. (2000). "The C-terminal domain-phosphorylated IIO form of RNA polymerase II is associated with the transcription repressor NC2 (Dr1/DRAP1) and is required for transcription activation in human nuclear extracts.". Proc. Natl. Acad. Sci. U.S.A. 97 (13): 7184–9. doi:10.1073/pnas.140202297. PMID 10852970. 
  • Kamada K, Shu F, Chen H, et al. (2001). "Crystal structure of negative cofactor 2 recognizing the TBP-DNA transcription complex.". Cell 106 (1): 71–81. PMID 11461703. 
  • Iratni R, Yan YT, Chen C, et al. (2003). "Inhibition of excess nodal signaling during mouse gastrulation by the transcriptional corepressor DRAP1.". Science 298 (5600): 1996–9. doi:10.1126/science.1073405. PMID 12471260. 
  • Denko N, Wernke-Dollries K, Johnson AB, et al. (2003). "Hypoxia actively represses transcription by inducing negative cofactor 2 (Dr1/DrAP1) and blocking preinitiation complex assembly.". J. Biol. Chem. 278 (8): 5744–9. doi:10.1074/jbc.M212534200. PMID 12477712. 
  • 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. 
  • Leonard D, Ajuh P, Lamond AI, Legerski RJ (2003). "hLodestar/HuF2 interacts with CDC5L and is involved in pre-mRNA splicing.". Biochem. Biophys. Res. Commun. 308 (4): 793–801. PMID 12927788. 
  • Gerhard DS, Wagner L, Feingold EA, et al. (2004). "The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).". Genome Res. 14 (10B): 2121–7. doi:10.1101/gr.2596504. PMID 15489334. 
  • Klejman MP, Pereira LA, van Zeeburg HJ, et al. (2004). "NC2alpha interacts with BTAF1 and stimulates its ATP-dependent association with TATA-binding protein.". Mol. Cell. Biol. 24 (22): 10072–82. doi:10.1128/MCB.24.22.10072-10082.2004. PMID 15509807. 
  • Lewis BA, Sims RJ, Lane WS, Reinberg D (2005). "Functional characterization of core promoter elements: DPE-specific transcription requires the protein kinase CK2 and the PC4 coactivator.". Mol. Cell 18 (4): 471–81. doi:10.1016/j.molcel.2005.04.005. PMID 15893730. 
  • Stelzl U, Worm U, Lalowski M, et al. (2005). "A human protein-protein interaction network: a resource for annotating the proteome.". Cell 122 (6): 957–68. doi:10.1016/j.cell.2005.08.029. PMID 16169070. 
  • Rual JF, Venkatesan K, Hao T, et al. (2005). "Towards a proteome-scale map of the human protein-protein interaction network.". Nature 437 (7062): 1173–8. doi:10.1038/nature04209. PMID 16189514. 
  • Assmann EM, Alborghetti MR, Camargo ME, Kobarg J (2006). "FEZ1 dimerization and interaction with transcription regulatory proteins involves its coiled-coil region.". J. Biol. Chem. 281 (15): 9869–81. doi:10.1074/jbc.M513280200. PMID 16484223. 
  • Lim J, Hao T, Shaw C, et al. (2006). "A protein-protein interaction network for human inherited ataxias and disorders of Purkinje cell degeneration.". Cell 125 (4): 801–14. doi:10.1016/j.cell.2006.03.032. PMID 16713569. 
  • Albert TK, Grote K, Boeing S, et al. (2007). "Global distribution of negative cofactor 2 subunit-alpha on human promoters.". Proc. Natl. Acad. Sci. U.S.A. 104 (24): 10000–5. doi:10.1073/pnas.0703490104. PMID 17548813.