Sub-milliMorgan map of the proximal part of mouse Chromosome 17 including the hybrid sterility 1 gene
Language English Country United States Media print
Document type Journal Article, Research Support, U.S. Gov't, P.H.S.
Grant support
HD28395-02
NICHD NIH HHS - United States
PubMed
8835526
DOI
10.1007/s003359900029
Knihovny.cz E-resources
- MeSH
- DNA Primers MeSH
- Genetic Markers MeSH
- Genotype MeSH
- H-2 Antigens genetics MeSH
- Hybridization, Genetic MeSH
- Chromosome Mapping * MeSH
- Molecular Sequence Data MeSH
- Multigene Family MeSH
- Infertility, Male genetics MeSH
- Mice, Inbred C3H MeSH
- Mice, Inbred C57BL MeSH
- Mice MeSH
- Polymorphism, Restriction Fragment Length MeSH
- Polymorphism, Single-Stranded Conformational MeSH
- Recombination, Genetic MeSH
- Base Sequence MeSH
- Animals MeSH
- Check Tag
- Male MeSH
- Mice MeSH
- Female MeSH
- Animals MeSH
- Publication type
- Journal Article MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Names of Substances
- DNA Primers MeSH
- Genetic Markers MeSH
- H-2 Antigens MeSH
We have generated a high-resolution genetic map, 0.071 cM per backcross animal, of the 13 cM T-H2 region of the mouse Chromosome (Chr) 17. The map contains two phenotypic loci, T and Hst1, 12 RFLP markers, and 24 microsatellite loci. The Hst1 gene was mapped to a chromosomal interval contained within a single 580-kb YAC clone. The FFEH11 YAC is 0.44 cM long and carries, besides the Hst1 gene, five polymorphic DNA markers and recombination breakpoints of six backcross animals. Two candidate genes for Hst1 were identified based on their location and testicular expression. These are Tbp and D17Ph4e. The submilliMorgan map of the T-H2 region revealed significant clustering of (CA)n loci. The clustering, if shown to be a common feature in the mouse genome, may cause gaps in the physical map of the mouse genome.
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