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Fabrication of duplex DNA microarrays incorporating methyl-5-cytosine.

Identifieur interne : 002255 ( Main/Exploration ); précédent : 002254; suivant : 002256

Fabrication of duplex DNA microarrays incorporating methyl-5-cytosine.

Auteurs : Christopher L. Warren [États-Unis] ; Jianfei Zhao ; Kimberly Glass ; Vikas Rishi ; Aseem Z. Ansari ; Charles Vinson

Source :

RBID : pubmed:22139143

Descripteurs français

English descriptors

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.

DOI: 10.1039/c1lc20698b
PubMed: 22139143


Affiliations:


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<term>CpG Islands</term>
<term>Cyclic AMP Response Element-Binding Protein (genetics)</term>
<term>DNA (metabolism)</term>
<term>DNA Methylation</term>
<term>Electrophoretic Mobility Shift Assay (instrumentation)</term>
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<term>5-Méthyl-cytosine (immunologie)</term>
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