BANP

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BTG3 associated nuclear protein
Identifiers
Symbol(s) BANP; DKFZp761H172; FLJ10177; FLJ20538; SMAR1; SMARBP1
External IDs MGI: 1889023 HomoloGene: 9635
Orthologs
Human Mouse
Entrez 54971 53325
Ensembl n/a ENSMUSG00000025316
Refseq NM_017869 (mRNA)
NP_060339 (protein)		 NM_016812 (mRNA)
NP_058092 (protein)
Location n/a Chr 8: 124.84 - 124.91 Mb
Pubmed search [1] [2]

BTG3 associated nuclear protein, also known as BANP, is a human gene.[1]

This gene encodes a protein that binds to matrix attachment regions. The protein functions as a tumor suppressor and cell cycle regulator. Alternate transcriptional splice variants, encoding different isoforms, have been characterized.[1]

[edit] References

  1. ^ a b Entrez Gene: BANP BTG3 associated nuclear protein.

[edit] Further reading

  • Hillier LD, Lennon G, Becker M, et al. (1997). "Generation and analysis of 280,000 human expressed sequence tags.". Genome Res. 6 (9): 807–28. PMID 8889549. 
  • Birot A, Duret L, Bartholin L, et al. (2000). "Identification and molecular analysis of BANP.". Gene 253 (2): 189–96. PMID 10940556. 
  • Chattopadhyay S, Kaul R, Charest A, et al. (2001). "SMAR1, a novel, alternatively spliced gene product, binds the Scaffold/Matrix-associated region at the T cell receptor beta locus.". Genomics 68 (1): 93–6. doi:10.1006/geno.2000.6279. PMID 10950932. 
  • 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. 
  • Kaul R, Mukherjee S, Ahmed F, et al. (2003). "Direct interaction with and activation of p53 by SMAR1 retards cell-cycle progression at G2/M phase and delays tumor growth in mice.". Int. J. Cancer 103 (5): 606–15. doi:10.1002/ijc.10881. PMID 12494467. 
  • Ota T, Suzuki Y, Nishikawa T, et al. (2004). "Complete sequencing and characterization of 21,243 full-length human cDNAs.". Nat. Genet. 36 (1): 40–5. doi:10.1038/ng1285. PMID 14702039. 
  • Brandenberger R, Wei H, Zhang S, et al. (2005). "Transcriptome characterization elucidates signaling networks that control human ES cell growth and differentiation.". Nat. Biotechnol. 22 (6): 707–16. doi:10.1038/nbt971. PMID 15146197. 
  • Kaul-Ghanekar R, Jalota A, Pavithra L, et al. (2004). "SMAR1 and Cux/CDP modulate chromatin and act as negative regulators of the TCRbeta enhancer (Ebeta).". Nucleic Acids Res. 32 (16): 4862–75. doi:10.1093/nar/gkh807. PMID 15371550. 
  • Kaul-Ghanekar R, Majumdar S, Jalota A, et al. (2005). "Abnormal V(D)J recombination of T cell receptor beta locus in SMAR1 transgenic mice.". J. Biol. Chem. 280 (10): 9450–9. doi:10.1074/jbc.M412206200. PMID 15623522. 
  • Jalota A, Singh K, Pavithra L, et al. (2005). "Tumor suppressor SMAR1 activates and stabilizes p53 through its arginine-serine-rich motif.". J. Biol. Chem. 280 (16): 16019–29. doi:10.1074/jbc.M413200200. PMID 15701641. 
  • Rampalli S, Pavithra L, Bhatt A, et al. (2005). "Tumor suppressor SMAR1 mediates cyclin D1 repression by recruitment of the SIN3/histone deacetylase 1 complex.". Mol. Cell. Biol. 25 (19): 8415–29. doi:10.1128/MCB.25.19.8415-8429.2005. PMID 16166625. 
  • 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. 
  • Kimura K, Wakamatsu A, Suzuki Y, et al. (2006). "Diversification of transcriptional modulation: large-scale identification and characterization of putative alternative promoters of human genes.". Genome Res. 16 (1): 55–65. doi:10.1101/gr.4039406. PMID 16344560. 
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