Genetic mapping of the whirler mutation
pmid: 10337627
Genetic mapping of the whirler mutation
The whirler (wi) mutation on mouse Chromosome (Chr) 4 results in an autosomal recessive neuroepithelial deafness and vestibular dysfunction exhibited as a characteristic shaker-waltzer behavior (deafness, circling, and head-bobbing). We have constructed a genetic linkage map across the wi region in both an interspecific [(wi/wi x CAST/Ei)F1 x wi/wi] backcross (n = 817) and an intraspecific [(wi/wi x CBA/Ca)F1 x wi/wi)] backcross (n = 335). In the interspecific backcross, wi was found to be non-recombinant with Orm1, 0.12 cM distal of D4Mit87 and Ambp, and 0.12 cM proximal of CD301. In the intraspecific backcross, wi was found to be non-recombinant with Orm1 and D4Mit244, 0.3 cM distal of Mup1, and 0.6 cM proximal of Tnc. We also report a family from the interspecific backcross that shows evidence of multiple recombinations across the region of mouse Chr 4 around the wi locus. These rearrangements appear specific to both the region and the family.
- University of Nottingham United Kingdom
- MRC Institute of Hearing Research United Kingdom
- Nottingham Trent University United Kingdom
- Medical Research Council United Kingdom
Mice, Species Specificity, Mutation, Mice, Inbred CBA, Animals, Chromosome Mapping, Crosses, Genetic, Mice, Mutant Strains
Mice, Species Specificity, Mutation, Mice, Inbred CBA, Animals, Chromosome Mapping, Crosses, Genetic, Mice, Mutant Strains
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