BACH2
From Wikipedia, the free encyclopedia
BTB and CNC homology 1, basic leucine zipper transcription factor 2
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Identifiers | ||||||||||||||
Symbol(s) | BACH2; | |||||||||||||
External IDs | OMIM: 605394 HomoloGene: 7240 | |||||||||||||
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RNA expression pattern | ||||||||||||||
Orthologs | ||||||||||||||
Human | Mouse | |||||||||||||
Entrez | 60468 | n/a | ||||||||||||
Ensembl | ENSG00000112182 | n/a | ||||||||||||
Uniprot | Q9BYV9 | n/a | ||||||||||||
Refseq | NM_021813 (mRNA) NP_068585 (protein) |
n/a (mRNA) n/a (protein) |
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Location | Chr 6: 90.69 - 91.06 Mb | n/a | ||||||||||||
Pubmed search | [1] | n/a |
BTB and CNC homology 1, basic leucine zipper transcription factor 2, also known as BACH2, is a human gene.[1]
[edit] References
[edit] 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: . 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: . 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: . 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: . 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: . 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: . 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: . 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: . 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: . PMID 17383980.
[edit] External links
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
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