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Nucleic Acids Research, 1994, Vol. 22, No. 21 4527-4534
© 1994

METHODS

High-density multiplex detection of nucleic acid sequences: oligonucleotide ligation assay and sequence-coded separation

Paul D. Grossman*, Will Bloch, Eleanor Brinson, Conway C. Chang, Faye A. Eggerding, Steven Fung, David A. lovannisci, Sam Woo and Emily S. Winn-Deen

Applied Biosystems Division of the Perkin Elmer Corporation 850 Linclon Center Drive, Foster City, CA 94404, USA

*To whom correspondence should be addressed

Received March 31, 1994. Revised August 8, 1994. Accepted August 8, 1994.

We describe a non-isotopic, semi-automated method for large-scale multiplex analysis of nucleic acid sequences, using the cystic fibrosis transmembrane regulator (CFTR) gene as an example. Products of a multiplex oligonucleotide ligation assay (OLA) are resolved electrophoretically from one another and from unligated probes under denaturing conditions with fluorescence detection. One ligation probe for each OLA target carries a fluorescent tag, while the other probe carries an oligomeric non-nucleotide mobility modifier. Each OLA product has a unique electrophoretic mobility determined by the ligated oligonucleotides and the mobility-modifier oligomer arbitrarily assigned (coded) to its target. The mobility range for practical mobility modifiers is much wider than the accessible range from unmodified ligated oligonucleotides of practical length. Each mobility modifier is built from phosphoramidite monomers in a stepwise manner on its associated oligonucleotide using an automated synthesizer. The resulting mobility modifiers lower the probe-target duplex Tm by less than 3°C and retard probe-target annealing by less than 50%, with negligible effect on OLA yield and specificity. This method is especially useful for allelic discrimination in highly polymorphic genes such as CFTR


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