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Detection of sequence variation in parasite ribosomal DNA by electrophoresis in agarose gels supplemented with a DNA‐intercalating agent
Author(s) -
Zhu Xing Quan,
Chilton Neil B.,
Gasser Robin B.
Publication year - 1998
Publication title -
electrophoresis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.666
H-Index - 158
eISSN - 1522-2683
pISSN - 0173-0835
DOI - 10.1002/elps.1150190511
Subject(s) - amplicon , biology , agarose , agarose gel electrophoresis , dna , ribosomal dna , ribosomal rna , polymerase chain reaction , microbiology and biotechnology , repeated sequence , genomic dna , electrophoresis , gene , genetics , genome , phylogenetics
This study evaluated the use of a commercially available DNA intercalating agent (Resolver Gold™) in agarose gels for the direct detection of sequence variation in ribosomal DNA (rDNA). This agent binds preferentially to AT sequence motifs in DNA. Regions of nuclear rDNA, known to provide genetic markers for the identification of species of parasitic ascarid nematodes (order Ascaridida), were amplified by polymerase chain reaction (PCR) and subjected to electrophoresis in standard agarose gels versus gels supplemented with Resolver Gold. Individual taxa examined could not be distinguished reliably based on the size of their amplicons in standard agarose gels, whereas they could be readily delineated based on mobility using Resolver Gold‐supplemented gels. The latter was achieved because of differences (approximately 0.1–8.2%) in the AT content of the fragments among different taxa, which were associated with significant interspecific differences (approximately 11–39%) in the rDNA sequences employed. There was a tendency for fragments with higher AT content to migrate slower in supplemented agarose gels compared with those of lower AT content. The results indicate the usefulness of this electrophoretic approach to rapidly screen for sequence variability within or among PCR‐amplified rDNA fragments of similar sizes but differing AT contents. Although evaluated on rDNA of parasites, the approach has potential to be applied to a range of genes of different groups of infectious organisms.