Sub-milliMorgan map of the proximal part of mouse Chromosome 17 including the hybrid sterility 1 gene
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu časopisecké články, Research Support, U.S. Gov't, P.H.S.
Grantová podpora
HD28395-02
NICHD NIH HHS - United States
PubMed
8835526
DOI
10.1007/s003359900029
Knihovny.cz E-zdroje
- MeSH
- DNA primery MeSH
- genetické markery MeSH
- genotyp MeSH
- H-2 antigeny genetika MeSH
- hybridizace genetická MeSH
- mapování chromozomů * MeSH
- molekulární sekvence - údaje MeSH
- multigenová rodina MeSH
- mužská infertilita genetika MeSH
- myši inbrední C3H MeSH
- myši inbrední C57BL MeSH
- myši MeSH
- polymorfismus délky restrikčních fragmentů MeSH
- polymorfismus konformace jednovláknové DNA MeSH
- rekombinace genetická MeSH
- sekvence nukleotidů MeSH
- zvířata MeSH
- Check Tag
- mužské pohlaví MeSH
- myši MeSH
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
- Názvy látek
- DNA primery MeSH
- genetické markery MeSH
- H-2 antigeny 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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