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Semiautomated DNA Mutation Analysis Using a Robotic Workstation and Molecular Beacons
Author(s) -
Maarten L. Smit,
B. Giesendorf,
Jacqueline A. M. Vet,
Frans J.M. Trijbels,
Henk J. Blom
Publication year - 2001
Publication title -
clinical chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.705
H-Index - 218
eISSN - 1530-8561
pISSN - 0009-9147
DOI - 10.1093/clinchem/47.4.739
Subject(s) - molecular beacon , genotyping , dna extraction , biology , mutation , genomic dna , genotype , dna , allele , dna sequencer , genetics , microbiology and biotechnology , polymerase chain reaction , gene , dna sequencing , oligonucleotide
BACKGROUNDOur increasing knowledge of the genetic basis of inheritable diseases requires the development of automated reliable methods for high-throughput analyses.METHODSWe investigated the combination of semiautomated DNA extraction from blood using a robotic workstation, followed by automated mutation detection using highly specific fluorescent DNA probes, so-called molecular beacons, which can discriminate between alleles with as little as one single-base mutation. We designed two molecular beacons, one recognizing the wild-type allele and the other the mutant allele, to determine genotypes in a single reaction. To evaluate this procedure, we examined the C677T mutation in the methylenetetrahydrofolate reductase (MTHFR) gene, which is associated with an increased risk for cardiovascular disease and neural tube defects. DNA was isolated from 10 microL of fresh EDTA-blood samples by use of a robotic workstation. The DNA samples were analyzed using molecular beacons as well as conventional methods.RESULTSBoth methods were compared, and no differences were found between outcomes of genotyping.CONCLUSIONSThe described assay enables robust and automated extraction of DNA and analysis of up to 96 samples (10 microL of blood per sample) within 5 h. This is superior to conventional methods and makes it suitable for high-throughput analyses.

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