Abstract |
One thousand sixty-six progeny have been generated from a backcross segregating for the mouse deafness mutation, shaker-1 (sh-1). One thousand fifty-two mice were analyzed for a protein polymorphism segregating for the distal flanking marker, beta-globin (Hbb), and 13 recombinants between Hbb and sh-1 were identified. One thousand eight mice were analyzed for a restriction fragment length polymorphism segregating for the proximal flanking marker, tyrosinase (c), and 54 recombinants between c and sh-1 were identified, completing a panel of 67 recombinant mice from the backcross in the vicinity of the sh-1 mutation. This panel allows the identification of markers closely linked to the sh-1 mutation that may act as start points for a chromosomal walk to the gene. One such marker, the olfactory marker protein gene (Omp), is recombinant with sh-1 in only one mouse from the recombinant panel. Thus, the Omp gene lies 0.1 cM from sh-1, on average, a distance of 200 kb. Haplotype analysis indicates that Omp lies proximal to sh-1.
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Authors | K A Brown, M J Sutcliffe, K P Steel, S D Brown |
Journal | Genomics
(Genomics)
Vol. 13
Issue 1
Pg. 189-93
(May 1992)
ISSN: 0888-7543 [Print] United States |
PMID | 1349573
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
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Chemical References |
- Nerve Tissue Proteins
- Olfactory Marker Protein
- Omp protein, mouse
- Globins
- Monophenol Monooxygenase
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Topics |
- Animals
- Base Sequence
- Blotting, Southern
- Crosses, Genetic
- Deafness
(genetics)
- Female
- Genetic Linkage
(genetics)
- Globins
(genetics)
- Male
- Mice
- Mice, Inbred Strains
- Molecular Sequence Data
- Monophenol Monooxygenase
(genetics)
- Mutation
(genetics)
- Nerve Tissue Proteins
(genetics)
- Olfactory Marker Protein
- Polymerase Chain Reaction
- Polymorphism, Restriction Fragment Length
- Restriction Mapping
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