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Hybridisation of N4-methylcytosine-containing amplicons on DNA microarrays

Paper ID Volume ID Publish Year Pages File Format Full-Text
23060 43415 2014 7 PDF Available
Title
Hybridisation of N4-methylcytosine-containing amplicons on DNA microarrays
Abstract

•PCR amplicons modified with N4-methylcitosine were evaluated on microarrays.•The modified amplicons mostly show higher fluorescence values than the normal ones.•The advantage of the modified version was especially high in a GC-rich amplicon.

5′-Cy5-labelled PCR amplicons containing the analogue base, N4-methylcytosine, instead of cytosines were compared in microarray hybridisation experiments with the corresponding amplicons containing the canonical set of bases, with respect to the intensity of the fluorescence signal obtained, and cross hybridisation to non-corresponding probes. In general, higher hybridisation temperatures resulted in reduced signal intensities, particularly in the case of the N4-methylcytosine containing amplicons. At the lower hybridisation temperatures tested (40 °C, 30 °C), these modified amplicons gave about equal or stronger fluorescence signal than the corresponding regular amplicons. With the two GC-richest amplicons tested, in one instance the N4-methylated target gave a dramatically higher signal intensity than the unmodified amplicon, interpreted as reflecting the reduced formation of hairpin structures in the target sequence, due to the lower thermodynamic stability of the G:N4-methylC base pair, making the target more accessible, while in the other case no hybridisation was observed with either version of the amplicon, probably due to interference from a G-tetrad structure. Both for the regular and the N4-methylated amplicons, no significant cross hybridisation was seen in these experiments.

Keywords
GC-rich DNA; Microarrays; PCR; N4-methylcytosine; dCTP analogue
First Page Preview
Hybridisation of N4-methylcytosine-containing amplicons on DNA microarrays
Publisher
Database: Elsevier - ScienceDirect
Journal: Journal of Biotechnology - Volume 189, 10 November 2014, Pages 143–149
Authors
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Subjects
Physical Sciences and Engineering Chemical Engineering Bioengineering