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iRNA-m2G: Identifying N2-methylguanosine Sites Based on Sequence-Derived Information
被引:38
|作者:
Chen, Wei
[1
,2
]
Song, Xiaoming
[2
]
Lv, Hao
[3
]
Lin, Hao
[3
]
机构:
[1] Chengdu Univ Tradit Chinese Med, Innovat Inst Chinese Med & Pharm, Chengdu 611730, Sichuan, Peoples R China
[2] North China Univ Sci & Technol, Sch Life Sci, Ctr Genom & Computat Biol, Tangshan 063000, Peoples R China
[3] Univ Elect Sci & Technol China, Ctr Informat Biol, Sch Life Sci & Technol, Key Lab Neuroinformat,Minist Educ, Chengdu 610054, Sichuan, Peoples R China
来源:
关键词:
TRANSFER-RNA;
MODIFIED NUCLEOSIDES;
DATABASE;
D O I:
10.1016/j.omtn.2019.08.023
中图分类号:
R-3 [医学研究方法];
R3 [基础医学];
学科分类号:
1001 ;
摘要:
RNA N-2-methylguanosine (m2G) is one kind of posttranscriptional modification and plays crucial roles in the control and stabilization of tRNA. However, our knowledge about the biological functions of m2G is still limited. The key step of revealing its new function is to recognize the m2G sites in the transcriptome. Since there is no effective method for detecting m2G sites, it is desirable to develop new methods to identify m2G sites. In this study, a computational predictor called iRNA-m2G was proposed to identify m2G sites in eukaryotic transcriptomes. In iRNA-m2G, the RNA sequences were encoded by using nucleotide chemical property and accumulated nucleotide frequency. iRNA-m2G was not only validated by the rigorous jackknife test on the benchmark dataset but also examined by performing cross-species validations. In addition, iRNA-m2G was also tested on an independent dataset. It was found that the accuracies obtained by iRNA-m2G were all quite promising in these tests, indicating that the proposed method could become a powerful tool for identifying m2G sites. Finally, a user-friendly web server for iRNA-m2G is freely accessible at http://lin-group.cn/server/iRNA-m2G.php.
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页码:253 / 258
页数:6
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