Nucleic Acids Research, Vol 26, Issue 24 5738-5740, Copyright © 1998 by Oxford University Press
K Khrapko, HA Coller, JS Hanekamp and WG Thilly
We have developed a rapid method for unambiguous identification and mutant
fraction determination of individual mutants in mixtures of DNA sequence
variants each differing by one or a few nucleotides. This method has
applications to such diverse areas as interpretation of mutational spectra,
screening of populations for polymorphisms and identification of species in
environmental mixtures. In our approach, a mixture of unknown sequences
labeled with a fluorescent dye is combined with a set of predetermined
sequences (standards) representing the variants to be assayed. Labeling the
standards with another dye allows the two sets of variants to be measured
independently. Using constant denaturing capillary electrophoresis, the
sequence variants are separated as individual peaks on the basis of
differential melting equilibria. The unknown sequence variants are
initially identified based on co-migration with particular standards. This
preliminary identification is verified by hybridization of the unknown
variants with the co-migrating standards within the capillary. We
demonstrate the use of capillary electrophoresis hybridization to dissect
complex mutational spectra of human cells in culture.
ARTICLES
Identification of point mutations in mixtures by capillary electrophoresis hybridization
Center for Environmental Health Sciences, Massachusetts Institute of Technology, Cambridge, MA 02139, USA. khrapko@wccf.mit.edu
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