Jia Cang-Zhi, Zhang Jia-Jia, Gu Wei-Zhen
Department of Mathematics, Dalian Maritime University, Dalian 116026, China.
Department of Mathematics, Dalian Maritime University, Dalian 116026, China.
Anal Biochem. 2016 Oct 1;510:72-75. doi: 10.1016/j.ab.2016.06.012. Epub 2016 Jun 20.
N6-methyladenosine (m(6)A) is present ubiquitously in the RNA of living organisms from Escherichia coli to humans. Nonetheless, the exact molecular mechanism of this modification remains unclear. The experimental identification of m(6)A modification is time-consuming and expensive; therefore, bioinformatics tools with high accuracy represent desirable alternatives for the large-scale, rapid identification of N6-methyladenosine sites. In this study, RNA-MethylPred, a new bioinformatics model, was developed by incorporating bi-profile Bayes, dinucleotide composition, and k nearest neighbor (KNN) scores for three feature extractions. RNA-MethylPred yielded a Matthew's correlation coefficient (MCC) of 0.53 in a jackknife test, which was 0.24 higher than that of iRNA-Methyl and 0.13 higher than that of pRNAm-PC. The obvious improvements demonstrated that RNA-MethylPred might be a powerful and complementary tool for further experimental investigation of N6-methyladenosine modification.
N6-甲基腺苷(m(6)A)广泛存在于从大肠杆菌到人类等生物体的RNA中。尽管如此,这种修饰的确切分子机制仍不清楚。m(6)A修饰的实验鉴定既耗时又昂贵;因此,具有高精度的生物信息学工具是大规模、快速鉴定N6-甲基腺苷位点的理想选择。在本研究中,通过结合双轮廓贝叶斯、二核苷酸组成和k近邻(KNN)得分进行三种特征提取,开发了一种新的生物信息学模型RNA-MethylPred。在留一法测试中,RNA-MethylPred的马修斯相关系数(MCC)为0.53,比iRNA-Methyl高0.24,比pRNAm-PC高0.13。这些明显的改进表明,RNA-MethylPred可能是进一步实验研究N6-甲基腺苷修饰的有力且互补的工具。