Abstract

BackgroundPausing of DNA polymerase can indicate the presence of a DNA structure that differs from the canonical double-helix. Here we detail a method to investigate how polymerase pausing in the Pacific Biosciences sequencer reads can be related to DNA sequences. The Pacific Biosciences sequencer uses optics to view a polymerase and its interaction with a single DNA molecule in real-time, offering a unique way to detect potential alternative DNA structures.ResultsWe have developed a new way to examine polymerase kinetics data and relate it to the DNA sequence by using a wavelet transform of read information from the sequencer. We use this method to examine how polymerase kinetics are related to nucleotide base composition. We then examine tandem repeat sequences known for their ability to form different DNA structures: (CGG)n and (CG)n repeats which can, respectively, form G-quadruplex DNA and Z-DNA. We find pausing around the (CGG)n repeat that may indicate the presence of G-quadruplexes in some of the sequencer reads. The (CG)n repeat does not appear to cause polymerase pausing, but its kinetics signature nevertheless suggests the possibility that alternative nucleotide conformations may sometimes be present.ConclusionWe discuss the implications of using our method to discover DNA sequences capable of forming alternative structures. The analyses presented here can be reproduced on any Pacific Biosciences kinetics data for any DNA pattern of interest using an R package that we have made publicly available.

Highlights

  • Pausing of DNA polymerase can indicate the presence of a DNA structure that differs from the canonical double-helix

  • Using the wavelet analysis we examine these kinetics at multiple scales, for both the smoothed coefficients and the detail coefficients

  • The nucleotide smooth wavelet coefficients can be understood as the density of each nucleotide (A, T, C and G) at the varying scales, and the detail wavelet coefficients are the changes in this density

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Summary

Introduction

Pausing of DNA polymerase can indicate the presence of a DNA structure that differs from the canonical double-helix. The biological significance of these structures remains disputed, but compelling evidence for the biological function of two of these structures exists: Z-DNA, which is associated. Some of these non-B-DNA structures can be problematic for polymerase-chain-reactions (PCR, [9]). The promoter of the fragile-X mental retardation gene, FMR1, contains a (CGG)n repeat that can interfere with polymerase activity [16,17,18]. Expansion of this repeat causes fragile-X disease [19].

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