Design And Application Of Noncontinuously Binding Probes Used For Haplotyping And Genotyping

BACKGROUND: Many methods for genotyping use melting temperature (Tm) of sequence-specific probes. Usually the probes hybridize to a continuous stretch of DNA that contains the variant(s). In contrast, hybridization of noncontinuous probes to a template can form bulges. This report generates guidelines for the design of noncontinuous probes.METHODS: We used software to predict hybridization structures and Tms from 10 noncontinuous probes and 54 different templates. Predicted Tins were compared to existing experimental data. The bulging template's sequences (omitted in the probe) ranged in size from I to 73 nucleotides. In 36 cases, we compared observed and predicted Delta Tms between alleles complementary to the probe and mismatched alleles. In addition, using software that predicts effects of bulges, we designed a probe and then tested it experimentally.RESULTS: The mean differences between predicted and observed Tins were 0.65 (2.51) degrees C with the Visual OMP software and 0.28 (1.67) degrees C with the MeltCalc software. Delta Tms were within a mean (SD) of 0.36 (1.23) degrees C (Visual OMP) and -0.01 (1.02) degrees C (MeltCalc) of observed values. An increase in the size of the template bulge resulted in a decrease in Tins. In 2 templates, the presence of a variant in the bulge influenced the experimental Tin of 2 noncontinuous probes, a result that was not predicted by the software programs.CONCLUSIONS: The use of software prediction should prove useful for the design of noncontinuous probes that can be used as tools for molecular haplotyping, multiplex genotyping, or masking sequence variants. (c) 2008 American Association for Clinical Chemistry.