A new Pax gene, Pax-9, maps to mouse chromosome 12
- PMID: 8358169
- DOI: 10.1007/BF00360584
A new Pax gene, Pax-9, maps to mouse chromosome 12
Abstract
Members of the Pax gene family have recently been shown to play important roles in mouse embryogenesis. Of eight so far characterized Pax genes, three have been associated with mouse developmental mutants. Here we report the cloning of a new Pax gene, Pax-9. Most of the DNA sequence encoding the highly conserved paired domain has been determined and compared with previously known paired domains. This comparison classifies Pax-9 as a member of the same subgroup as Pax-1/undulated. By analysis of the segregation of a Pax-9 restriction fragment length polymorphism and a large number of simple sequence length polymorphisms in an interspecific C57BL/6 x Mus musculus mollosinus backcross, Pax-9 was mapped close to the D12Nds1 locus on the proximal part of Chromosome (Chr) 12.
Similar articles
-
Chromosomal localization of seven PAX genes and cloning of a novel family member, PAX-9.Nat Genet. 1993 Apr;3(4):292-8. doi: 10.1038/ng0493-292. Nat Genet. 1993. PMID: 7981748
-
The molecular basis of the undulated/Pax-1 mutation.Cell. 1991 Sep 6;66(5):873-84. doi: 10.1016/0092-8674(91)90434-z. Cell. 1991. PMID: 1889089
-
Pax: a murine multigene family of paired box-containing genes.Genomics. 1991 Oct;11(2):424-34. doi: 10.1016/0888-7543(91)90151-4. Genomics. 1991. PMID: 1685142
-
Pax genes and organogenesis.Bioessays. 1997 Sep;19(9):755-65. doi: 10.1002/bies.950190905. Bioessays. 1997. PMID: 9297966 Review.
-
Pax genes and organogenesis: Pax9 meets tooth development.Eur J Oral Sci. 1998 Jan;106 Suppl 1:38-43. doi: 10.1111/j.1600-0722.1998.tb02151.x. Eur J Oral Sci. 1998. PMID: 9541201 Review.
Cited by
-
Targeted disruption of Pax1 defines its null phenotype and proves haploinsufficiency.Proc Natl Acad Sci U S A. 1998 Jul 21;95(15):8692-7. doi: 10.1073/pnas.95.15.8692. Proc Natl Acad Sci U S A. 1998. PMID: 9671740 Free PMC article.
-
Pax9-deficient mice lack pharyngeal pouch derivatives and teeth and exhibit craniofacial and limb abnormalities.Genes Dev. 1998 Sep 1;12(17):2735-47. doi: 10.1101/gad.12.17.2735. Genes Dev. 1998. PMID: 9732271 Free PMC article.
-
Embryology and bony malformations of the craniovertebral junction.Childs Nerv Syst. 2011 Apr;27(4):523-64. doi: 10.1007/s00381-010-1358-9. Epub 2010 Dec 31. Childs Nerv Syst. 2011. PMID: 21193993 Free PMC article. Review.
-
Molecular basis for skeletal variation: insights from developmental genetic studies in mice.Birth Defects Res B Dev Reprod Toxicol. 2007 Dec;80(6):425-50. doi: 10.1002/bdrb.20136. Birth Defects Res B Dev Reprod Toxicol. 2007. PMID: 18157899 Free PMC article. Review.
-
Pax-1, a regulator of sclerotome development is induced by notochord and floor plate signals in avian embryos.Anat Embryol (Berl). 1995 Apr;191(4):297-310. doi: 10.1007/BF00534682. Anat Embryol (Berl). 1995. PMID: 7645756
References
Publication types
MeSH terms
Substances
Associated data
- Actions
LinkOut - more resources
Other Literature Sources
Molecular Biology Databases