dna suspension arrays silencing discrete artifacts for high-sensitivity applicationsdna悬浮阵列沉默离散构件进行高灵敏度的应用程序.pdfVIP
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dna suspension arrays silencing discrete artifacts for high-sensitivity applicationsdna悬浮阵列沉默离散构件进行高灵敏度的应用程序
DNA Suspension Arrays: Silencing Discrete Artifacts for
High-Sensitivity Applications
1 1,2
Matthew S. Lalonde , Eric J. Arts *
1 Department of Biochemistry, Case Western Reserve University, Cleveland, Ohio, United States of America, 2 Division of Infectious Diseases, Department of Medicine,
Case Western Reserve University, Cleveland, Ohio, United States of America
Abstract
Detection of low frequency single nucleotide polymorphisms (SNPs) has important implications in early screening for tumorgenesis,
genetic disorders and pathogen drug resistance. Nucleic acid arrays are a powerful tool for genome-scale SNP analysis, but
detection of low-frequency SNPs in a mixed population on an array is problematic. We demonstrate a model assay for HIV-1 drug
resistance mutations, wherein ligase discrimination products are collected on a suspension array. In developing this system, we
discovered that signal from multiple polymorphisms was obscured by two discrete hybridization artifacts. Specifically: 1) tethering of
unligated probes on the template DNA elicited false signal and 2) unpredictable probe secondary structures impaired probe capture
and suppressed legitimate signal from the array. Two sets of oligonucleotides were used to disrupt these structures; one to displace
unligated reporter labels from the bead-bound species and another to occupy sequences which interfered with array hybridization.
This artifact silencing system resulted in a mean 21-fold increased sensitivity for 29 minority variants of 17 codons in our model assay
for mutations most commonly associated with HIV-1 drug resistance. Furthermore, since the artifacts we characterized are not
unique to our system, their specific inhibition might improve the quality of data from solid-state microarrays as well as from the
growing number
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