BACH2

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BTB and CNC homology 1, basic leucine zipper transcription factor 2
Identifiers
Symbol(s) BACH2;
External IDs OMIM: 605394 Homologene7240
RNA expression pattern

PBB GE BACH2 221234 s at tn.png

More reference expression data

Orthologs
Human Mouse
Entrez 60468 na
Ensembl ENSG00000112182 na
Uniprot Q9BYV9 na
Refseq NM_021813 (mRNA)
NP_068585 (protein)
na (mRNA)
na (protein)
Location Chr 6: 90.69 - 91.06 Mb na
Pubmed search [1] na

BTB and CNC homology 1, basic leucine zipper transcription factor 2, also known as BACH2, is a human gene.[1]



References

Further reading

  • Oyake T, Itoh K, Motohashi H, et al. (1996). "Bach proteins belong to a novel family of BTB-basic leucine zipper transcription factors that interact with MafK and regulate transcription through the NF-E2 site.". Mol. Cell. Biol. 16 (11): 6083-95. PMID 8887638.
  • Kobayashi A, Yamagiwa H, Hoshino H, et al. (2000). "A combinatorial code for gene expression generated by transcription factor Bach2 and MAZR (MAZ-related factor) through the BTB/POZ domain.". Mol. Cell. Biol. 20 (5): 1733-46. PMID 10669750.
  • Hoshino H, Kobayashi A, Yoshida M, et al. (2000). "Oxidative stress abolishes leptomycin B-sensitive nuclear export of transcription repressor Bach2 that counteracts activation of Maf recognition element.". J. Biol. Chem. 275 (20): 15370-6. PMID 10809773.
  • Sasaki S, Ito E, Toki T, et al. (2000). "Cloning and expression of human B cell-specific transcription factor BACH2 mapped to chromosome 6q15.". Oncogene 19 (33): 3739-49. doi:10.1038/sj.onc.1203716. PMID 10949928.
  • Vieira SA, Deininger MW, Sorour A, et al. (2002). "Transcription factor BACH2 is transcriptionally regulated by the BCR/ABL oncogene.". Genes Chromosomes Cancer 32 (4): 353-63. PMID 11746976.
  • Muto A, Tashiro S, Tsuchiya H, et al. (2002). "Activation of Maf/AP-1 repressor Bach2 by oxidative stress promotes apoptosis and its interaction with promyelocytic leukemia nuclear bodies.". J. Biol. Chem. 277 (23): 20724-33. doi:10.1074/jbc.M112003200. PMID 11923289.
  • Kamio T, Toki T, Kanezaki R, et al. (2004). "B-cell-specific transcription factor BACH2 modifies the cytotoxic effects of anticancer drugs.". Blood 102 (9): 3317-22. doi:10.1182/blood-2002-12-3656. PMID 12829606.
  • Mungall AJ, Palmer SA, Sims SK, et al. (2003). "The DNA sequence and analysis of human chromosome 6.". Nature 425 (6960): 805-11. doi:10.1038/nature02055. PMID 14574404.
  • Takakuwa T, Luo WJ, Ham MF, et al. (2004). "Integration of Epstein-Barr virus into chromosome 6q15 of Burkitt lymphoma cell line (Raji) induces loss of BACH2 expression.". Am. J. Pathol. 164 (3): 967-74. PMID 14982850.
  • Tashiro S, Muto A, Tanimoto K, et al. (2004). "Repression of PML nuclear body-associated transcription by oxidative stress-activated Bach2.". Mol. Cell. Biol. 24 (8): 3473-84. PMID 15060166.
  • Motamed-Khorasani A, Jurisica I, Letarte M, et al. (2007). "Differentially androgen-modulated genes in ovarian epithelial cells from BRCA mutation carriers and control patients predict ovarian cancer survival and disease progression.". Oncogene 26 (2): 198-214. doi:10.1038/sj.onc.1209773. PMID 16832351.
  • Yoshida C, Yoshida F, Sears DE, et al. (2007). "Bcr-Abl signaling through the PI-3/S6 kinase pathway inhibits nuclear translocation of the transcription factor Bach2, which represses the antiapoptotic factor heme oxygenase-1.". Blood 109 (3): 1211-9. doi:10.1182/blood-2005-12-040972. PMID 17018862.
  • Ono A, Kono K, Ikebe D, et al. (2007). "Nuclear positioning of the BACH2 gene in BCR-ABL positive leukemic cells.". Genes Chromosomes Cancer 46 (1): 67-74. doi:10.1002/gcc.20390. PMID 17044046.
  • Ikeda T, Shibata J, Yoshimura K, et al. (2007). "Recurrent HIV-1 integration at the BACH2 locus in resting CD4+ T cell populations during effective highly active antiretroviral therapy.". J. Infect. Dis. 195 (5): 716-25. doi:10.1086/510915. PMID 17262715.
  • Hoshino H, Nishino TG, Tashiro S, et al. (2007). "Co-repressor SMRT and class II histone deacetylases promote Bach2 nuclear retention and formation of nuclear foci that are responsible for local transcriptional repression.". J. Biochem. 141 (5): 719-27. doi:10.1093/jb/mvm073. PMID 17383980.

External links


This article incorporates text from the United States National Library of Medicine, which is in the public domain.


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