HOXA9

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Homeobox A9
PDB rendering based on 1puf.
Available structures
PDB Ortholog search: Template:Homologene2PDBe PDBe, Template:Homologene2uniprot RCSB
Identifiers
Symbols HOXA9 ; HOX1; ABD-B; HOX1.7; HOX1G; MGC1934
External IDs Template:OMIM5 Template:MGI HomoloGene7766
RNA expression pattern
More reference expression data
Orthologs
Template:GNF Ortholog box
Species Human Mouse
Entrez n/a n/a
Ensembl n/a n/a
UniProt n/a n/a
RefSeq (mRNA) n/a n/a
RefSeq (protein) n/a n/a
Location (UCSC) n/a n/a
PubMed search n/a n/a

Homeobox A9, also known as HOXA9, is a human gene.

In vertebrates, the genes encoding the class of transcription factors called homeobox genes are found in clusters named A, B, C, and D on four separate chromosomes. Expression of these proteins is spatially and temporally regulated during embryonic development. This gene is part of the A cluster on chromosome 7 and encodes a DNA-binding transcription factor which may regulate gene expression, morphogenesis, and differentiation. This gene is highly similar to the abdominal-B (Abd-B) gene of Drosophila. A specific translocation event which causes a fusion between this gene and the NUP98 gene has been associated with myeloid leukemogenesis.[1]

See also

References

  1. "Entrez Gene: HOXA9 homeobox A9".

Further reading

  • Scott MP (1992). "Vertebrate homeobox gene nomenclature". Cell. 71 (4): 551–3. PMID 1358459.
  • McAlpine PJ, Shows TB (1990). "Nomenclature for human homeobox genes". Genomics. 7 (3): 460. PMID 1973146.
  • Acampora D, D'Esposito M, Faiella A; et al. (1990). "The human HOX gene family". Nucleic Acids Res. 17 (24): 10385–402. PMID 2574852.
  • Nakamura T, Largaespada DA, Lee MP; et al. (1996). "Fusion of the nucleoporin gene NUP98 to HOXA9 by the chromosome translocation t(7;11)(p15;p15) in human myeloid leukaemia". Nat. Genet. 12 (2): 154–8. doi:10.1038/ng0296-154. PMID 8563753.
  • Borrow J, Shearman AM, Stanton VP; et al. (1996). "The t(7;11)(p15;p15) translocation in acute myeloid leukaemia fuses the genes for nucleoporin NUP98 and class I homeoprotein HOXA9". Nat. Genet. 12 (2): 159–67. doi:10.1038/ng0296-159. PMID 8563754.
  • Apiou F, Flagiello D, Cillo C; et al. (1996). "Fine mapping of human HOX gene clusters". Cytogenet. Cell Genet. 73 (1–2): 114–5. PMID 8646877.
  • Lawrence HJ, Helgason CD, Sauvageau G; et al. (1997). "Mice bearing a targeted interruption of the homeobox gene HOXA9 have defects in myeloid, erythroid, and lymphoid hematopoiesis". Blood. 89 (6): 1922–30. PMID 9058712.
  • Kim MH, Chang HH, Shin C; et al. (1998). "Genomic structure and sequence analysis of human HOXA-9". DNA Cell Biol. 17 (5): 407–14. PMID 9628584.
  • Izon DJ, Rozenfeld S, Fong ST; et al. (1998). "Loss of function of the homeobox gene Hoxa-9 perturbs early T-cell development and induces apoptosis in primitive thymocytes". Blood. 92 (2): 383–93. PMID 9657735.
  • Patel CV, Sharangpani R, Bandyopadhyay S, DiCorleto PE (1999). "Endothelial cells express a novel, tumor necrosis factor-alpha-regulated variant of HOXA9". J. Biol. Chem. 274 (3): 1415–22. PMID 9880515.
  • Shen WF, Rozenfeld S, Kwong A; et al. (1999). "HOXA9 forms triple complexes with PBX2 and MEIS1 in myeloid cells". Mol. Cell. Biol. 19 (4): 3051–61. PMID 10082572.
  • Shi X, Bai S, Li L, Cao X (2001). "Hoxa-9 represses transforming growth factor-beta-induced osteopontin gene transcription". J. Biol. Chem. 276 (1): 850–5. doi:10.1074/jbc.M005955200. PMID 11042172.
  • Hartley JL, Temple GF, Brasch MA (2001). "DNA cloning using in vitro site-specific recombination". Genome Res. 10 (11): 1788–95. PMID 11076863.
  • Schaefer LK, Wang S, Schaefer TS (2001). "Functional interaction of Jun and homeodomain proteins". J. Biol. Chem. 276 (46): 43074–82. doi:10.1074/jbc.M102552200. PMID 11551904.
  • Fujino T, Suzuki A, Ito Y; et al. (2002). "Single-translocation and double-chimeric transcripts: detection of NUP98-HOXA9 in myeloid leukemias with HOXA11 or HOXA13 breaks of the chromosomal translocation t(7;11)(p15;p15)". Blood. 99 (4): 1428–33. PMID 11830496.
  • Kosaki K, Kosaki R, Suzuki T; et al. (2002). "Complete mutation analysis panel of the 39 human HOX genes". Teratology. 65 (2): 50–62. doi:10.1002/tera.10009. PMID 11857506.
  • Calvo KR, Sykes DB, Pasillas MP, Kamps MP (2002). "Nup98-HoxA9 immortalizes myeloid progenitors, enforces expression of Hoxa9, Hoxa7 and Meis1, and alters cytokine-specific responses in a manner similar to that induced by retroviral co-expression of Hoxa9 and Meis1". Oncogene. 21 (27): 4247–56. doi:10.1038/sj.onc.1205516. PMID 12082612.
  • Taketani T, Taki T, Ono R; et al. (2002). "The chromosome translocation t(7;11)(p15;p15) in acute myeloid leukemia results in fusion of the NUP98 gene with a HOXA cluster gene, HOXA13, but not HOXA9". Genes Chromosomes Cancer. 34 (4): 437–43. doi:10.1002/gcc.10077. PMID 12112533.
  • Kawakami K, Miyanishi S, Nishii K; et al. (2002). "A case of acute myeloid leukemia with t(7;11)(p15;p15) mimicking myeloid crisis of chronic myelogenous leukemia". Int. J. Hematol. 76 (1): 80–3. PMID 12138901.
  • Mayotte N, Roy DC, Yao J; et al. (2003). "Oncogenic interaction between BCR-ABL and NUP98-HOXA9 demonstrated by the use of an in vitro purging culture system". Blood. 100 (12): 4177–84. doi:10.1182/blood-2002-04-1244. PMID 12393433.

External links

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

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