4.7 Article

Z-DNA as a Tool for Nuclease-Free DNA Methyltransferase Assay

Journal

Publisher

MDPI
DOI: 10.3390/ijms222111990

Keywords

Z-DNA; DNA methylation; nuclease-free; single-molecule FRET; methylcytosine sensitive; natural DNA methyltransferase inhibitors

Funding

  1. National Research Foundation (NRF) of Korea [NRF-2019R1A2C1089808]
  2. Global Research and Development Center Program through the NRF [2018K1A4A3A01064272]
  3. Ministry of Science and ICT

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Methylcytosines in mammalian genomes play a crucial role in gene regulation and are implicated in various diseases, including cancer. A new optical technique has been developed to characterize the activity of DNA methyltransferases (DMT) and the effects of inhibitors, offering a more direct and sensitive approach without the need for amplification steps or methylation-sensitive nucleases. This method has shown promise in evaluating the inhibitory effects of natural bio-active compounds on DMT, providing a potential avenue for the development of DMT-related anticancer drugs.
Methylcytosines in mammalian genomes are the main epigenetic molecular codes that switch off the repertoire of genes in cell-type and cell-stage dependent manners. DNA methyltransferases (DMT) are dedicated to managing the status of cytosine methylation. DNA methylation is not only critical in normal development, but it is also implicated in cancers, degeneration, and senescence. Thus, the chemicals to control DMT have been suggested as anticancer drugs by reprogramming the gene expression profile in malignant cells. Here, we report a new optical technique to characterize the activity of DMT and the effect of inhibitors, utilizing the methylation-sensitive B-Z transition of DNA without bisulfite conversion, methylation-sensing proteins, and polymerase chain reaction amplification. With the high sensitivity of single-molecule FRET, this method detects the event of DNA methylation in a single DNA molecule and circumvents the need for amplification steps, permitting direct interpretation. This method also responds to hemi-methylated DNA. Dispensing with methylation-sensitive nucleases, this method preserves the molecular integrity and methylation state of target molecules. Sparing methylation-sensing nucleases and antibodies helps to avoid errors introduced by the antibody's incomplete specificity or variable activity of nucleases. With this new method, we demonstrated the inhibitory effect of several natural bio-active compounds on DMT. All taken together, our method offers quantitative assays for DMT and DMT-related anticancer drugs.

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