Journal
BRIEFINGS IN FUNCTIONAL GENOMICS
Volume 20, Issue 5, Pages 304-311Publisher
OXFORD UNIV PRESS
DOI: 10.1093/bfgp/elab035
Keywords
non-CpG methylation; DNA methyltransferases; mitochondrial DNA; cancer; DNA methylation
Funding
- Department of Science and Technology, Science and Engineering Board, India [EMR/2015/001319]
- Department of Science and Technology-INSPIRE fellowship, India [IF190144]
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Non-CpG methylation, a distinct epigenetic modification in DNA, plays a crucial role in gene regulation. Advances in technology have allowed for a better understanding of its genome-wide distribution, but its specific role in cancer development remains unclear. This review focuses on the mechanism of non-CpG methylation in embryos and tissues, particularly its relevance to cancer progression.
The methylation of cytosine residues that precede adenine/thymine or other cytosine nucleotides instead of guanine in DNA is known as non-CpG methylation. It is a pronounced epigenetic modification with a central role in gene regulation similar to CpG methylation. Due to technological limitations, the locus-specific role of non-CpG methylation was scarcely understood. At present, high-throughput analyses and improved enrichment methods can elucidate the role of genome-wide non-CpG methylation distributions. Although the functional basis of non-CpG methylation in regulating gene expression control is known, its role in cancer development is yet to be ascertained. This review sheds light on the possible mechanism of non-CpG methylation in embryos and developed tissues with a special focus on cancer development and progression. In particular, the maintenance and alteration of non-CpG methylation levels and the crucial factors that determine this level of non-CpG methylation and its functional role in cancer are discussed.
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