Microarray-based STR genotyping using RecA-mediated ligation
Author(s) -
D.C. Herrmann,
Elisabeth Rose,
Ulrich Müller,
Robert E. Wagner
Publication year - 2010
Publication title -
nucleic acids research
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 9.008
H-Index - 537
eISSN - 1362-4954
pISSN - 0305-1048
DOI - 10.1093/nar/gkq657
Subject(s) - biology , amplicon , genotyping , ligation , oligonucleotide , genetics , str analysis , dna , computational biology , microbiology and biotechnology , microsatellite , str multiplex system , multiplex ligation dependent probe amplification , base pair , polymerase chain reaction , genotype , allele , gene , exon
We describe a novel assay capable of accurately determining the length of short tandem repeat (STR) alleles. STR genotyping is achieved utilizing RecA-mediated ligation (RML), which combines the high fidelity of RecA-mediated homology searching with allele-specific ligation. RecA catalyzes the pairing of synthetic oligonucleotides with one strand of a double-stranded DNA target, in this case a PCR amplicon. Ligation occurs only when two adjacent oligonucleotides are base paired to the STR region without any overlap or gap. RecA activity is required to overcome the inherent difficulty of annealing repeated sequences in register. This assay is capable of determining STR genotypes of human samples, is easily adapted to high throughput or automated systems and can have widespread utility in diagnostic and forensic applications.
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