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Updated: Nov 18, 2025

A Method for Measuring RNA N6-methyladenosine Modifications in Cells and Tissues
Published on: December 5, 2016
m6AmPred: Identifying RNA N6, 2'-O-dimethyladenosine (m6Am) sites based on sequence-derived information
Jie Jiang1, Bowen Song2, Kunqi Chen3
1Department of Biological Sciences, Xi'an Jiaotong-Liverpool University, Suzhou, Jiangsu 215123, China; Institute of Systems, Molecular and Integrative Biology, University of Liverpool, L7 8TX Liverpool, United Kingdom.
Abstract:
N6,2'-O-dimethyladenosine (m6Am) is a reversible modification widely occurred on varied RNA molecules. The biological function of m6Am is yet to be known though recent studies have revealed its influences in cellular mRNA fate. Precise identification of m6Am sites on RNA is vital for the understanding of its biological functions. We present here m6AmPred, the first web server for in silico identification of m6Am sites from the primary sequences of RNA. Built upon the eXtreme Gradient Boosting with Dart algorithm (XgbDart) and EIIP-PseEIIP encoding scheme, m6AmPred achieved promising prediction performance with the AUCs greater than 0.954 when tested by 10-fold cross-validation and independent testing datasets. To critically test and validate the performance of m6AmPred, the experimentally verified m6Am sites from two data sources were cross-validated. The m6AmPred web server is freely accessible at: https://www.xjtlu.edu.cn/biologicalsciences/m6am, and it should make a useful tool for the researchers who are interested in N6,2'-O-dimethyladenosine RNA modification.
Insights
N6,2'-O-dimethyladenosine (m6Am) is an RNA modification. m6AmPred is the first web server to accurately predict m6Am sites using RNA sequences, aiding research into its functions.
Area of Science:
- Molecular Biology
- Bioinformatics
- RNA Modifications
Background:
- N6,2 '-O-dimethyladenosine (m6Am) is a prevalent, reversible RNA modification.
- The precise biological roles of m6Am remain largely unelucidated.
- Accurate identification of m6Am sites is crucial for understanding its functional significance.
Purpose of the Study:
- To develop the first computational tool for identifying m6Am sites in RNA sequences.
- To provide researchers with a reliable method for predicting m6Am modification sites.
- To facilitate the study of m6Am's influence on cellular mRNA fate.
Main Methods:
- Development of m6AmPred, a web server utilizing the eXtreme Gradient Boosting with Dart algorithm (XgbDart).
- Implementation of the EIIP-PseEIIP encoding scheme for RNA sequence representation.
- Rigorous validation using 10-fold cross-validation, independent testing, and cross-validation with experimentally verified m6Am sites.
Main Results:
- m6AmPred demonstrated high prediction accuracy, achieving Area Under the Curve (AUC) values exceeding 0.954.
- The tool was validated against independent datasets and experimental data, confirming its robust performance.
- The web server provides a user-friendly platform for in silico identification of m6Am sites.
Conclusions:
- m6AmPred is the first web server for predicting N6,2 '-O-dimethyladenosine RNA modification sites.
- The tool offers high accuracy and reliability, serving as a valuable resource for RNA biology research.
- m6AmPred will aid researchers in investigating the functional roles of m6Am in various RNA molecules.
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