| Literature DB >> 31444763 |
Fedor Kouzine1, Damian Wojtowicz1, Arito Yamane1, Rafael Casellas1, Teresa M Przytycka1, David L Levens2.
Abstract
While DNA inside the cells is predominantly canonical right-handed double helix, guanine-rich DNAs have potential to fold into four-stranded structures that contain stacks of G-quartets (G4 DNA quadruplex). Genome sequencing has revealed G4 sequences tend to localize at the gene control regions, especially in the promoters of oncogenes. A growing body of evidence indicates that G4 DNA quadruplexes might have important regulatory roles in genome function, highlighting the need for techniques to detect genome-wide folding of DNA into this structure. Potassium permanganate in vivo treatment of cells results in oxidizing of nucleotides in single-stranded DNA regions that accompany G4 DNA quadruplexes formation, providing an excellent probe for the conformational state of DNA inside the living cells. Here, we describe a permanganate-based methodology to detect G4 DNA quadruplex, genome-wide. This methodology combined with high-throughput sequencing provides a snapshot of the DNA conformation over the whole genome in vivo.Entities:
Keywords: Chromatin; DNA quadruplex; G4 DNA; High-throughput genomics; Non-B DNA; Potassium permanganate
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Year: 2019 PMID: 31444763 PMCID: PMC7444663 DOI: 10.1007/978-1-4939-9666-7_23
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745