Detection of DNA Methylation of G-Quadruplex and i-Motif-Forming Sequences by Measuring the Initial Elongation Efficiency of Polymerase Chain Reaction

Journal: Analytical Chemistry

Published: 2016-06-28

DOI: 10.1021/acs.analchem.6b00982

Affiliations: 4

Authors: 7

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Research Highlight

Finding the genetic off-switch behind tumour growth

© SEBASTIAN KAULITZKI/Science Photo Library/Getty

© SEBASTIAN KAULITZKI/Science Photo Library/Getty

Detecting DNA methylation, a process used by cells to fix genes in the ‘off’ position, through a repeated enzyme reaction could help in the diagnosis of cancer.

DNA methylation can silence tumour suppressing genes and clear a path for tumour growth. It is used as a biomarker for cancers, but methods for detecting DNA methylation are time consuming or use chemicals that damage the DNA. A team including researchers from the Tokyo University of Agriculture and Technology developed a technique that detected methylation by measuring how efficiently a controlled enzyme reaction, the polymerase chain reaction (PCR), could copy and elongate two methylated DNA sequences. They demonstrated that, in human-derived genomic DNA, the elongation efficiency of PCR decreased as DNA methylation of the sequences increased. The results suggest that DNA methylation was thwarting the enzyme’s DNA copying activity.

The team concludes that measuring the elongation efficiency of PCR can be used to detect DNA methylation, with potential application in cancer diagnosis.

Supported content

  1. Analytical Chemistry 88,7101–7107 (2016). doi: 10.1021/acs.analchem.6b00982
Institutions FC WFC
Graduate School / School of Bioscience and Biotechnology, Tokyo Tech, Japan 0.50 0.50
Department of Biotechnology and Life Science, TUAT, Japan 0.29 0.29
Graduate School of Science and Engineering, Saitama University, Japan 0.14 0.14
Umm Al-Qura University, Saudi Arabia 0.07 0.07

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