Fabrication of duplex DNA microarrays incorporating methyl-5-cytosine

Lab Chip. 2012 Jan 21;12(2):376-80. doi: 10.1039/c1lc20698b. Epub 2011 Dec 5.

Abstract

We synthesized customized double-stranded DNA microarrays including methyl-5-cytosine at CpG dinucleotides and produced all 163,555 possible 8-mers (un-, hemi-, and di-methylated) to gain insight into how methylation affects transcription factor binding. An antibody to methyl-5-cytidine showed greater binding to the methylated DNA, demonstrating efficient incorporation of methyl-5-cytosine into the synthesized DNA. In contrast, binding of the transcription factor CREB was inhibited by CpG methylation. This platform represents a powerful new technology to evaluate the effect of DNA methylation on protein binding in any sequence context.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, N.I.H., Intramural
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, Non-P.H.S.

MeSH terms

  • 5-Methylcytosine / immunology
  • 5-Methylcytosine / metabolism*
  • Antibodies / immunology
  • CpG Islands
  • Cyclic AMP Response Element-Binding Protein / genetics
  • DNA / metabolism*
  • DNA Methylation
  • Electrophoretic Mobility Shift Assay / instrumentation
  • Oligonucleotide Array Sequence Analysis / instrumentation*

Substances

  • Antibodies
  • Cyclic AMP Response Element-Binding Protein
  • 5-Methylcytosine
  • DNA