Development of genomic resources in the domestic cat is key to application of this species as a model for heritable and infectious disease, and for comparative genome analysis. Previous versions of the cat gene map, based on somatic cell hybrid analysis, revealed considerable conservation of synteny with the human genome. However, these maps provided no knowledge of gene order and genome rearrangement between the two species, information which is critical to applying the comparative candidate approach to positional cloning in gene poor model systems. Radiation hybrid (RH) mapping has emerged as the most powerful tool for constructing moderate- to high-density gene maps in vertebrates by obviating the need to identify interspecific polymorphisms. A domestic cat radiation hybrid panel has been developed and serves as the backbone for feline gene mapping, while also serving to cross-reference microsatellite positions on the current domestic cat-Asian leopard cat interspecies linkage map. We have currently generated a 600-locus map integrating 425 coding loci (expressed sequence tags, genes, and comparative anchor tagged sequences [CATS] markers) with 175 microsatellites selected from the current linkage map. The observed 100 conserved homologous gene segments between cat and human agree well with theoretical expectations (using the methods of Nadeau & Taylor), suggesting we have accurate cross-reference to the majority of the human genome. By comparison to the genetic map, the 600-marker RH map has a mean density of 5 cM/26 cR5000 now useful for comparative candidate positional clone analysis of the over 200 described feline hereditary phenotypes. Current efforts focus on increasing the microsatellite coverage at least five-fold, and developing new CATS to fill regions in the cat genome with sparse gene representation. The latter approach will allow further cross-reference to most mammalian species for use in diverse studies of genetics and genome evolution. - radiation hybrid mapping, comparative mapping, - Neither Human Subjects nor Human Tissues

Agency
National Institute of Health (NIH)
Institute
National Cancer Institute (NCI)
Type
Intramural Research (Z01)
Project #
1Z01BC010265-03
Application #
6289334
Study Section
Special Emphasis Panel (LGD)
Project Start
Project End
Budget Start
Budget End
Support Year
3
Fiscal Year
1999
Total Cost
Indirect Cost
Name
National Cancer Institute Division of Basic Sciences
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Murphy, William J; Pevzner, Pavel A; O'Brien, Stephen J (2004) Mammalian phylogenomics comes of age. Trends Genet 20:631-9
Murphy, William J; Bourque, Guillaume; Tesler, Glenn et al. (2003) Reconstructing the genomic architecture of mammalian ancestors using multispecies comparative maps. Hum Genomics 1:30-40
Teeling, Emma C; Madsen, Ole; Murphy, William J et al. (2003) Nuclear gene sequences confirm an ancient link between New Zealand's short-tailed bat and South American noctilionoid bats. Mol Phylogenet Evol 28:308-19
Springer, Mark S; Murphy, William J; Eizirik, Eduardo et al. (2003) Placental mammal diversification and the Cretaceous-Tertiary boundary. Proc Natl Acad Sci U S A 100:1056-61
Murphy, William J; Fronicke, Lutz; O'Brien, Stephen J et al. (2003) The origin of human chromosome 1 and its homologs in placental mammals. Genome Res 13:1880-8
O'Brien, Stephen J; Murphy, William J (2003) Genomics. A dog's breakfast? Science 301:1854-5
Kuznetsov, S B; Matveeva, N M; Murphy, W J et al. (2003) Mapping of 53 loci in American mink (Mustela vison). J Hered 94:386-91