Issue 9, 2018

Can 5-methylcytosine analogues with extended alkyl side chains guide DNA methylation?

Abstract

5-Methylcytosine (MeC) is an endogenous modification of DNA that plays a crucial role in DNA–protein interactions, chromatin structure, epigenetic regulation, and DNA repair. MeC is produced via enzymatic methylation of the C-5 position of cytosine by DNA-methyltransferases (DNMT) which use S-adenosylmethionine (SAM) as a cofactor. Hemimethylated CG dinucleotides generated as a result of DNA replication are specifically recognized and methylated by maintenance DNA methyltransferase 1 (DNMT1). The accuracy of DNMT1-mediated methylation is essential for preserving tissue-specific DNA methylation and thus gene expression patterns. In the present study, we synthesized DNA duplexes containing MeC analogues with modified C-5 side chains and examined their ability to guide cytosine methylation by the human DNMT1 protein. We found that the ability of 5-alkylcytosines to direct cytosine methylation decreased with increased alkyl chain length and rigidity (methyl > ethyl > propyl ∼ vinyl). Molecular modeling studies indicated that this loss of activity may be caused by the distorted geometry of the DNA–protein complex in the presence of unnatural alkylcytosines.

Graphical abstract: Can 5-methylcytosine analogues with extended alkyl side chains guide DNA methylation?

Supplementary files

Article information

Article type
Communication
Submitted
02 Sept. 2017
Accepted
02 Janv. 2018
First published
02 Janv. 2018

Chem. Commun., 2018,54, 1061-1064

Can 5-methylcytosine analogues with extended alkyl side chains guide DNA methylation?

D. Kotandeniya, C. L. Seiler, J. Fernandez, S. S. Pujari, L. Curwick, K. Murphy, S. Wickramaratne, S. Yan, D. Murphy, Y. Y. Sham and N. Y. Tretyakova, Chem. Commun., 2018, 54, 1061 DOI: 10.1039/C7CC06867K

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