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Development and applications of next-generation epigenomics technologies
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- Ito Takashi
- Principal Investigator
- 九州大学
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- 梅山 大地
- Co-Investigator
- 国立研究開発法人理化学研究所
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- 荒木 啓充
- Co-Investigator
- 九州大学
About This Project
- Japan Grant Number
- JP17H06305 (JGN)
- Funding Program
- Grants-in-Aid for Scientific Research
- Funding Organization
- Japan Society for the Promotion of Science
Kakenhi Information
- Project/Area Number
- 17H06305
- Research Category
- Grant-in-Aid for Scientific Research on Innovative Areas (Research in a proposed research area)
- Allocation Type
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- Single-year Grants
- Review Section / Research Field
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- Biological Sciences
- Research Institution
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- Kyushu University
- Project Period (FY)
- 2017-06-30 〜 2022-03-31
- Project Status
- Completed
- Budget Amount*help
- 127,270,000 Yen (Direct Cost: 97,900,000 Yen Indirect Cost: 29,370,000 Yen)
Research Abstract
In this project, we aimed to develop highly-sensitive and/or multiplexed epigenome sequencing methods, which should be critical to accelerate trans-omic analyses. First, we developed a highly efficient method for single-stranded DNA ligation termed TACS ligation and introduced it to further improve the performance of PBAT, the most sensitive and reliable methylome sequencing method of our own. Second, we developed DMS-seq for in vivo genome-wide mapping of protein-DNA interactions and nucleosome centers, thus adding a unique method to the toolbox for epigenomics. Third, we applied TACS ligation to cell-free DNA analysis and revealed a novel class of short single-stranded DNA enriched with noncanonical DNA structure, or antisense of G-quadruplex structure. Fourth, we identified a novel DNA methyltransferase, which should lay a basis for a multiplexed epigenomics method to encode histone modification information to methylation of neighborhood DNA.
Keywords
Details 詳細情報について
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- CRID
- 1040000781959524224
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- Text Lang
- ja
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- Data Source
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- KAKEN