Please use this identifier to cite or link to this item: https://doi.org/10.18632/oncotarget.13562
Title: Whole genome DNA methylation: Beyond genes silencing
Authors: Tirado-Magallanes, R 
Rebbani, K 
Lim, R 
Pradhan, S
Benoukraf, T 
Keywords: genomic DNA
transcription factor
binding affinity
cell population
chromatin
DNA methylation
gene expression
gene silencing
genome analysis
genome imprinting
human
protein binding
Review
RNA splicing
Issue Date: 2017
Citation: Tirado-Magallanes, R, Rebbani, K, Lim, R, Pradhan, S, Benoukraf, T (2017). Whole genome DNA methylation: Beyond genes silencing. Oncotarget 8 (3) : 5629-5637. ScholarBank@NUS Repository. https://doi.org/10.18632/oncotarget.13562
Abstract: The combination of DNA bisulfite treatment with high-throughput sequencing technologies has enabled investigation of genome-wide DNA methylation at near base pair level resolution, far beyond that of the kilobase-long canonical CpG islands that initially revealed the biological relevance of this covalent DNA modification. The latest high-resolution studies have revealed a role for very punctual DNA methylation in chromatin plasticity, gene regulation and splicing. Here, we aim to outline the major biological consequences of DNA methylation recently discovered. We also discuss the necessity of tuning DNA methylation resolution into an adequate scale to ease the integration of the methylome information with other chromatin features and transcription events such as gene expression, nucleosome positioning, transcription factors binding dynamic, gene splicing and genomic imprinting. Finally, our review sheds light on DNA methylation heterogeneity in cell population and the different approaches used for its assessment, including the contribution of single cell DNA analysis technology.
Source Title: Oncotarget
URI: https://scholarbank.nus.edu.sg/handle/10635/173809
ISSN: 19492553
DOI: 10.18632/oncotarget.13562
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