Abstract
The epigenetic DNA modification 5-hydroxymethylcytosine (5-hmC) is important for the regulation of gene expression during development and in tumorigenesis. 5-hmC can be selectively glycosylated by T4 β-glucosyltransferase (β-GT); introduction of an azide on the attached sugar provides a chemical handle for isolation or fluorescent tagging of 5-hmC residues by click chemistry. This approach has not been broadly adopted because of the challenging synthesis and limited commercial availability of the glycosylation substrate, 6-deoxy-6-azido-α-D-glucopyranoside. We report the enzyme-assisted synthesis of this precursor by the uridylyltransferase from Pasteurella multocida (PmGlmU). We were able to directly label 5-hmC in genomic DNA by an enzymatic cascade involving successive action of PmGlmU and β-GT. This is a facile and cost-effective one-pot chemoenzymatic methodology for 5-hmC analysis.
Original language | English |
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Pages (from-to) | 1857-1860 |
Number of pages | 4 |
Journal | ChemBioChem |
Volume | 16 |
Issue number | 13 |
DOIs | |
State | Published - 1 Sep 2015 |
Keywords
- DNA methylation
- chemoenzymatic synthesis
- fluorescent probes
- hydroxymethylcytosine
- single molecules
- sugar nucleotides
All Science Journal Classification (ASJC) codes
- Biochemistry
- Molecular Medicine
- Molecular Biology
- Organic Chemistry