Quantitation of mixed-base populations of HIV-1 variants by automated DNA sequencing with BODIPY dye-labeled primers

Biotechniques. 1998 Sep;25(3):446-7, 450-2, 454, passim.

Abstract

Direct DNA sequencing of human immunodeficiency virus type 1 (HIV-1) pol and env gene regions was characterized for accuracy and precision. Restricted maximum likelihood (REML) analysis of molecular clone reconstruction experiments using a primer-walking strategy showed that the BODIPY and BODIPY energy-transfer (BET) dye primers sets were significantly more accurate in quantitating heterogenous base mixtures than the fluorescein/rhodamine dye primers. Of the three sets examined, the BET dye primers were the most accurate. The improved accuracy correlated with the reduced emission band-widths of BODIPY and BET dye primers and the more uniform signal intensities of BET dye primers. However, comparing % coefficients of variation (CV) for the three dye primer sets, revealed that BODIPY dye primers gave better precision than both BET and fluorescein/rhodamine dye primer sets. Several sequence-dependent motifs were identified that showed specific nucleotide-biased incorporation and were determined to be the major variable component of the total %CV. Taken together, these results show that BODIPY and BET direct DNA sequencing can accurately and precisely characterize complex mixed-base populations.

MeSH terms

  • Boron Compounds / chemistry*
  • DNA Primers / chemistry
  • DNA Primers / genetics*
  • DNA, Viral / chemistry
  • DNA, Viral / genetics
  • DNA-Directed DNA Polymerase / metabolism
  • Genes, env / genetics
  • Genes, pol / genetics
  • Genetic Heterogeneity
  • Genetic Variation
  • Genome, Viral
  • HIV Envelope Protein gp120 / genetics
  • HIV-1 / chemistry
  • HIV-1 / genetics*
  • Humans
  • Reproducibility of Results
  • Sequence Analysis, DNA / methods*

Substances

  • 4,4-difluoro-4-bora-3a,4a-diaza-s-indacene
  • Boron Compounds
  • DNA Primers
  • DNA, Viral
  • HIV Envelope Protein gp120
  • DNA-Directed DNA Polymerase