4.5 Article

Identifying DNA methylation in a nanochannel

期刊

出版社

TAYLOR & FRANCIS LTD
DOI: 10.1080/14686996.2016.1223516

关键词

DNA methylation; single DNA molecule; nanochannel; DNA contraction

资金

  1. Cabinet Office, Government of Japan
  2. Japan Society for the Promotion of Science (JSPS) through the Funding Program for World-Leading Innovative R&D on Science and Technology (FIRST Program)
  3. ImPACT Program of the Council for Science, Technology and Innovation (Cabinet Office, Government of Japan)
  4. Nanotechnology Platform Program (Molecule and Material Synthesis) of the Ministry of Education, Culture, Sports, Science and Technology (MEXT), Japan
  5. JSPS [16H02091]
  6. MEXT [26107709]
  7. PRESTO, Japan Science and Technology Agency (JST)
  8. Grants-in-Aid for Scientific Research [16H01692, 26107709, 16H02091, 15K13288] Funding Source: KAKEN

向作者/读者索取更多资源

DNA methylation is a stable epigenetic modification, which is well known to be involved in gene expression regulation. In general, however, analyzing DNA methylation requires rather time consuming processes (24-96 h) via DNA replication and protein modification. Here we demonstrate a methodology to analyze DNA methylation at a single DNA molecule level without any protein modifications by measuring the contracted length and relaxation time of DNA within a nanochannel. Our methodology is based on the fact that methylation makes DNA molecules stiffer, resulting in a longer contracted length and a longer relaxation time (a slower contraction rate). The present methodology offers a promising way to identify DNA methylation without any protein modification at a single DNA molecule level within 2 h. [GRAPHICS] .

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