Frequencies of VNTR and RFLP polymorphisms associated with factor VIII gene in Singapore
Journal Article
·
· American Journal of Human Genetics
OSTI ID:134654
- National Univ. of Singapore (Malaysia); and others
The allelic frequency of any polymorphism within a population determines its usefulness for genetic counselling. This is important in populations of non-Caucasian origin as RFLPs may significantly differ among ethnic groups. We report a study of five intragenic polymorphisms in factor VIII gene carried out in Singapore. The three PCR-based RFLP markers studied were Intron 18/Bcl I, Intron 19/Hind III and Intron 22/Xba I. In an analysis of 148 unrelated normal X chromosomes, the allele frequencies were found to be A1 = 0.18, A2 = 0.82 (Bcl I RFLP), A1 = 0.80, A2 = 0.20 (Hind III RFLP) and A1 = 0.58, and A2 = 0.42 (Xba I RFLP). The heterozygosity rates of 74 females analyzed separately were 31%, 32% and 84.2%, respectively. Linkage disequilibrium was also observed to some degree between Bcl I and Hind III polymorphism in our population. We have also analyzed a sequence polymorphism in Intron 7 using hybridization with radioactive-labelled {sup 32}P allele-specific oligonucleotide probes. This polymorphism was not very polymorphic in our population with only 2% of 117 individuals analyzed being informative. However, the use of a hypervariable dinucleotide repeat sequence (VNTR) in Intron 13 showed that 25 of our of 27 (93%) females were heterozygous. Allele frequencies ranged from 1 to 55 %. We conclude that a viable strategy for molecular analysis of Hemophilia A families in our population should include the use of Intron 18/Bcl I and Intron 22/Xba I RFLP markers and the Intron 13 VNTR marker.
- OSTI ID:
- 134654
- Report Number(s):
- CONF-941009--
- Journal Information:
- American Journal of Human Genetics, Journal Name: American Journal of Human Genetics Journal Issue: Suppl.3 Vol. 55; ISSN AJHGAG; ISSN 0002-9297
- Country of Publication:
- United States
- Language:
- English
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Related Subjects
55 BIOLOGY AND MEDICINE
BASIC STUDIES
BIOLOGICAL MARKERS
BLOOD COAGULATION FACTORS
DETECTION
DNA HYBRIDIZATION
DNA SEQUENCING
GENE MUTATIONS
GENES
GENETIC VARIABILITY
HEMIC DISEASES
HEMOPHILIA
HUMAN POPULATIONS
HUMAN X CHROMOSOME
INTRONS
MUTATION FREQUENCY
OLIGONUCLEOTIDES
POLYMERASE CHAIN REACTION
PROBES
RFLPS
SCREENING
SINGAPORE
STATISTICS
BASIC STUDIES
BIOLOGICAL MARKERS
BLOOD COAGULATION FACTORS
DETECTION
DNA HYBRIDIZATION
DNA SEQUENCING
GENE MUTATIONS
GENES
GENETIC VARIABILITY
HEMIC DISEASES
HEMOPHILIA
HUMAN POPULATIONS
HUMAN X CHROMOSOME
INTRONS
MUTATION FREQUENCY
OLIGONUCLEOTIDES
POLYMERASE CHAIN REACTION
PROBES
RFLPS
SCREENING
SINGAPORE
STATISTICS