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VNTR and microsatellite polymorphisms within the subtelomeric region of 7q
- Publication Year :
- 1993
-
Abstract
- The molecular basis of a highly polymorphic RFLP marker, HTY146c3 (D7S591), within the subtelomeric region of human chromosome 7q was determined by restriction-fragment and DNA sequence analysis. Two polymorphic systems were found--a simple base-substitution polymorphism and a GC-rich VNTR element with a core structure of C3AG2C2. In addition, a compound-imperfect CA dinucleotide-repeat element was identified approximately 10-20 kb from the telomeric sequence repeat (T2AG3), demonstrating that microsatellites can extend essentially to the ends of human chromosomes. The microsatellite marker, sAVH-6 (D7S594), is highly polymorphic, with 10 alleles and an observed heterozygosity of 84% found with the CEPH (Centre d'Etude du Polymorphisme Humain) reference pedigree collection. In combination with the RFLPs, the informativeness of the markers contained within 240 kb at the telomere approaches 100%. A unique genetic and physical STS marker, sAVH-6, defines the endpoint of the long arm of human chromosome 7.
- Subjects :
- Genetic Markers
Male
Base Sequence
Genome, Human
Molecular Sequence Data
Chromosome Mapping
Sequence Analysis, DNA
DNA, Satellite
Telomere
Deoxyribonuclease HpaII
Pedigree
Blotting, Southern
Humans
Female
Crossing Over, Genetic
Chromosomes, Fungal
Deoxyribonucleases, Type II Site-Specific
Chromosomes, Human, Pair 7
Polymorphism, Restriction Fragment Length
Research Article
Gene Library
Repetitive Sequences, Nucleic Acid
Subjects
Details
- Language :
- English
- Database :
- OpenAIRE
- Accession number :
- edsair.pmid..........f0b20ea67b8edf5fd27ae065420b74c5