Direct detection and automated sequencing of individual alleles after electrophoretic strand separation: identification of a common nonsense mutation in exon 9 of the human lipoprotein lipase gene

Nucleic Acids Res. 1990 Sep 25;18(18):5407-11. doi: 10.1093/nar/18.18.5407.

Abstract

Large-scale screening by direct sequencing of DNA to detect molecular variants remains a laborious endeavor whose difficulty is compounded by heterozygosity. We show that mobility shifts of single-stranded DNA electrophoresed under nondenaturing conditions can be used not only to detect variants (Orita,M. et al., 1989, Genomics, 5, 874-879), but also to separate and sequence directly individual alleles. In this manner, we have identified a common variant of human lipoprotein lipase resulting from a nonsense mutation in exon 9 of the gene. Whether this variant is of functional significance remains to be determined.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Alleles
  • Amino Acid Sequence
  • Base Sequence
  • Electrophoresis
  • Exons*
  • Genes
  • Heterozygote
  • Humans
  • Hypertriglyceridemia / enzymology
  • Hypertriglyceridemia / genetics
  • Lipoprotein Lipase / genetics*
  • Lipoprotein Lipase / metabolism
  • Molecular Sequence Data
  • Mutation*
  • Polymerase Chain Reaction

Substances

  • Lipoprotein Lipase