Title | Genetic map of the fused locus on mouse chromosome 17. |
Publication Type | Journal Article |
Year of Publication | 1994 |
Authors | Rossi, JM, Chen, H, Tilghman, SM |
Journal | Genomics |
Volume | 23 |
Issue | 1 |
Pagination | 178-84 |
Date Published | 1994 Sep 1 |
Keywords | Animals, Base Sequence, Chromosome Mapping, Congenital Abnormalities, Crosses, Genetic, Female, Genetic Markers, Humans, Male, Mice, Mice, Inbred Strains, Mice, Mutant Strains, Molecular Sequence Data, Muridae, Polymerase Chain Reaction, Recombination, Genetic, Tail |
Abstract | Fused (Fu) is a dominant mutation in mice resulting in the asymmetry and fusion of tail vertebrae in heterozygotes. Fu/Fu homozygotes are often viable and can exhibit a duplication of the terminal tail vertebrae resulting in bifurcated tails. There are two more severe alleles at Fu, Kinky (FuKi) and Knobbly (FuKb), which die between 9 and 10 days of gestation as homozygotes, exhibiting a duplication of the embryonic axis, leading to incomplete or complete twinning. To define the precise map position of the FuKi mutation on mouse Chromosome 17, a 983-animal (FuKi tf x Mus spretus)F1 x +tf/+tf interspecific backcross was generated and scored for FuKi, another tightly linked visible marker tufted (tf), and five linked molecular loci, D17MIT18, D17Leh54, D17Aus57, Hba-ps4, and Pim1. The order and genetic distances between the markers were determined to be centromere-D17MIT18-5.79 cM-D17Leh54-0.85 cM-D17Pri6-0.12 cM-D17Pri7-0.12 cM-Hba-ps4-1.20 cM-D17Pri8-0.48 cM-tf-2.05 cM-Pim1. The FuKi gene could not be genetically separated from three molecular markers, D17Pri6, D17Pri7, and Hba-ps4. Yeast artificial chromosome clones that contain these tightly linked markers have been isolated to form a contig that contains FuKi. Recombination breakpoints generated through the interspecies backcross were mapped onto the contig and demonstrate that recombination in this region is not random. |
Alternate Journal | Genomics |