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Nucleic Acids Res. 2008 Oct;36(18):e119. doi: 10.1093/nar/gkn534. Epub 2008 Aug 20.

DNA methylation determination by liquid chromatography-tandem mass spectrometry using novel biosynthetic [U-15N]deoxycytidine and [U-15N]methyldeoxycytidine internal standards.

Author information

1
Biomedical Mass Spectrometry Laboratory, General Clinical Research Center and Food Science and Human Nutrition Department, University of Florida, Gainesville, FL, USA. epq@ufl.edu

Abstract

Methylation of the promoter CpG regions regulates gene transcription by inhibiting transcription factor binding. Deoxycytidine methylation may regulate cell differentiation, while aberrations in the process may be involved in cancer etiology and the development of birth defects (e.g. neural tube defects). Similarly, nutritional deficiency and certain nutragenomic interactions are associated with DNA hypomethylation. While LC-MS has been used previously to measure percentage genomic deoxycytidine methylation, a lack of a secure source of internal standards and the need for laborious and time-consuming DNA digestion protocols constitute distinct limitations. Here we report a simple and inexpensive protocol for the biosynthesis of internal standards from readily available precursors. Using these biosynthetic stable-isotopic [U-(15)N]-labeled internal standards, coupled with an improved DNA digestion protocol developed in our lab, we have developed a low-cost, high-throughput (>500 samples in 4 days) assay for measuring deoxycytidine methylation in genomic DNA. Inter- and intraassay variation for the assay (%RSD, n = 6) was <2.5%.

PMID:
18718928
PMCID:
PMC2566864
DOI:
10.1093/nar/gkn534
[Indexed for MEDLINE]
Free PMC Article

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