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J Am Chem Soc. 2011 Jan 26;133(3):486-92. doi: 10.1021/ja107836t. Epub 2010 Dec 14.

Discrimination of methylcytosine from hydroxymethylcytosine in DNA molecules.

Author information

1
Department of Physics and Astronomy, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States. wanunu@sas.upenn.edu

Abstract

Modified DNA bases are widespread in biology. 5-Methylcytosine (mC) is a predominant epigenetic marker in higher eukaryotes involved in gene regulation, development, aging, cancer, and disease. Recently, 5-hydroxymethylcytosine (hmC) was identified in mammalian brain tissue and stem cells. However, most of the currently available assays cannot distinguish mC from hmC in DNA fragments. We investigate here the physical properties of DNA with modified cytosines, in efforts to develop a physical tool that distinguishes mC from hmC in DNA fragments. Molecular dynamics simulations reveal that polar cytosine modifications affect internal base pair dynamics, while experimental evidence suggest a correlation between the modified cytosine's polarity, DNA flexibility, and duplex stability. On the basis of these physical differences, solid-state nanopores can rapidly discriminate among DNA fragments with mC or hmC modification by sampling a few hundred molecules in the solution. Further, the relative proportion of hmC in the sample can be determined from the electronic signature of the intact DNA fragment.

PMID:
21155562
PMCID:
PMC3081508
DOI:
10.1021/ja107836t
[Indexed for MEDLINE]
Free PMC Article

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