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Articles |
32, CCR2-V64I, and SDF1-G801A Related to Pathogenesis of AIDS
1
Laboratory of Genomic Diversity, National Cancer Institute-Frederick Cancer Research and Development Center, Frederick, MD 21702.
2
PE Applied Biosystems, 850 Lincoln Centre Dr., Foster
City, CA 94404.
a Author for correspondence. Fax 301-846-6468; e-mail waters{at}avpaxp1.ncifcrf.gov
Background: Variations within the human genome play important roles in human disease. To study variations related to susceptibility to AIDS, we have developed 5' nuclease assays that eliminate post-PCR molecular biology steps.
Methods: TaqMan assays based on the 5' nuclease activity of Taq
polymerase and fluorescent resonance energy transfer were developed to
score alleles at the biallelic loci
CCR5-+/
32,
CCR2-V64I and SDF1-G801A. For each assay,
72 samples were analyzed. Data collection and analysis were performed
on the Prism 7700 Sequence Detection System. For comparison with gel
electrophoresis methods, each locus was also scored on a subset of 24
samples, using restriction enzymes or single-strand conformational
polymorphism (SSCP).
Results: Clear allelic discrimination was obtained on each of the 72 samples for all three TaqMan assays. The TaqMan scores for the subset of 24 samples were concordant with the restriction enzyme and SSCP scores.
Conclusions: Because of its simplicity, speed, and potential for automation and miniaturization, TaqMan is an excellent candidate for investigation of genetic variation in clinical, research, and forensic settings.
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