Related Experiment Video
Updated: Mar 5, 2026

08:56
A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues
Published on: December 5, 2016
11.4K
Transcriptome-Wide Mapping of N 1-Methyladenosine Methylome
Xiaoyu Li1, Jinying Peng1, Chengqi Yi2,3
1State Key Laboratory of Protein and Plant Gene Research, School of Life Sciences, and Peking-Tsinghua Center for Life Sciences, Peking University, Beijing, 100871, China.
Methods in Molecular Biology (Clifton, N.J.)
|March 29, 2017
Summary
N1-Methyladenosine (m1A) is a crucial RNA modification found in various RNA types. A new method, m1A-ID-Seq, enables transcriptome-wide mapping of m1A modifications in mammals.
Area of Science:
- Molecular Biology
- Epigenetics
- RNA Biology
Background:
- N1-Methyladenosine (m1A) is a significant RNA modification.
- m1A is commonly found in transfer RNA (tRNA) and ribosomal RNA (rRNA).
- Recent studies indicate m1A is also prevalent in mammalian messenger RNA (mRNA).
Purpose of the Study:
- To develop a high-throughput method for transcriptome-wide m1A mapping.
- To facilitate functional investigations of m1A modifications.
- To accurately identify m1A sites across the transcriptome.
Main Methods:
- Development of the m1A-ID-Seq technique.
- Utilizing m1A immunoprecipitation.
- Leveraging the reverse transcription stalling property of m1A.
Main Results:
- Successful implementation of m1A-ID-Seq for transcriptome-wide analysis.
- Generation of highly confident m1A peaks.
- Demonstration of the technique's utility in mapping m1A.
Conclusions:
- m1A-ID-Seq is an effective tool for high-throughput m1A mapping.
- This method is crucial for advancing the functional study of m1A modifications.
- The technique provides a reliable way to identify m1A sites across the transcriptome.

