Biology:HOXA4
From HandWiki
Homeobox A4, also known as HOXA4, is a protein which in humans is encoded by the HOXA4 gene.[1][2]
Function
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.[3] 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.[1]
See also
References
- ↑ 1.0 1.1 "Entrez Gene: HOXA4 homeobox A4". https://www.ncbi.nlm.nih.gov/gene?Db=gene&Cmd=ShowDetailView&TermToSearch=3201.
- ↑ "Nomenclature for human homeobox genes". Genomics 7 (3): 460. July 1990. doi:10.1016/0888-7543(90)90186-X. PMID 1973146.
- ↑ "Vertebrate homeobox gene nomenclature". Cell 71 (4): 551–553. November 1992. doi:10.1016/0092-8674(92)90588-4. PMID 1358459.
Further reading
- "Vertebrate homeobox gene nomenclature". Cell 71 (4): 551–553. November 1992. doi:10.1016/0092-8674(92)90588-4. PMID 1358459.
- "Alteration of homeobox gene expression by N-ras transformation of PA-1 human teratocarcinoma cells". Molecular and Cellular Biology 11 (7): 3573–3583. July 1991. doi:10.1128/mcb.11.7.3573. PMID 1675427.
- "Nomenclature for human homeobox genes". Genomics 7 (3): 460. July 1990. doi:10.1016/0888-7543(90)90186-X. PMID 1973146.
- "Expression of HOX homeogenes in human neuroblastoma cell culture lines". Differentiation; Research in Biological Diversity 45 (1): 61–69. October 1990. doi:10.1111/j.1432-0436.1990.tb00458.x. PMID 1981366.
- "Isolation, chromosomal localization, and nucleotide sequence of the human HOX 1.4 homeobox". Genomics 5 (2): 250–258. August 1989. doi:10.1016/0888-7543(89)90054-2. PMID 2571574.
- "Organization of human class I homeobox genes". Genome 31 (2): 745–756. 1990. doi:10.1139/g89-133. PMID 2576652.
- "Homeobox gene expression in human oocytes and preembryos". Molecular Reproduction and Development 41 (2): 127–132. June 1995. doi:10.1002/mrd.1080410202. PMID 7654365.
- "Fine mapping of human HOX gene clusters". Cytogenetics and Cell Genetics 73 (1–2): 114–115. 1996. doi:10.1159/000134320. PMID 8646877.
- "Expression of homebox-containing genes in human preimplantation development and in embryos with chromosomal aneuploidies". Journal of Assisted Reproduction and Genetics 13 (2): 177–181. February 1996. doi:10.1007/BF02072541. PMID 8688592.
- "Changing intestinal connective tissue interactions alters homeobox gene expression in epithelial cells". Journal of Cell Science 110 (11): 1317–1324. June 1997. doi:10.1242/jcs.110.11.1317. PMID 9202392.
- "HOX homeobox genes exhibit spatial and temporal changes in expression during human skin development". The Journal of Investigative Dermatology 110 (2): 110–115. February 1998. doi:10.1046/j.1523-1747.1998.00092.x. PMID 9457903.
- "Isolation of cDNA libraries from individual human preimplantation embryos". Molecular Human Reproduction 4 (6): 571–575. June 1998. doi:10.1093/molehr/4.6.571. PMID 9665340.
- "Toward a complete human genome sequence". Genome Research 8 (11): 1097–1108. November 1998. doi:10.1101/gr.8.11.1097. PMID 9847074.
- "Complete mutation analysis panel of the 39 human HOX genes". Teratology 65 (2): 50–62. February 2002. doi:10.1002/tera.10009. PMID 11857506.
- "Overexpression of translocation-associated fusion genes of FGFRI, MYC, NPMI, and DEK, but absence of the translocations in acute myeloid leukemia. A microarray analysis". Haematologica 87 (6): 569–577. June 2002. PMID 12031912.
- "[Increased expression of HOXA9 gene in Hirschsprung disease]". Gastroenterologie Clinique et Biologique 26 (12): 1110–1117. December 2002. PMID 12520199.
- "Promoter hypermethylation silences expression of the HoxA4 gene and correlates with IgVh mutational status in CLL". Leukemia 20 (7): 1326–1329. July 2006. doi:10.1038/sj.leu.2404254. PMID 16688227.
External links
- HOXA4+protein,+human at the US National Library of Medicine Medical Subject Headings (MeSH)
This article incorporates text from the United States National Library of Medicine, which is in the public domain.
