Wang Jian, Mao Kangkun, Zhao Yunjie, Zeng Chen, Xiang Jianjin, Zhang Yi, Xiao Yi
Institute of Biophysics, School of Physics and Key Laboratory of Molecular Biophysics of the Ministry of Education, Huazhong University of Science and Technology, Wuhan 430074, Hubei, China.
Institute of Biophysics and Department of Physics, Central China Normal University, Wuhan 430079, China.
Nucleic Acids Res. 2017 Jun 20;45(11):6299-6309. doi: 10.1093/nar/gkx386.
Direct coupling analysis of nucleotide coevolution provides a novel approach to identify which nucleotides in an RNA molecule are likely in direct contact, and this information obtained from sequence only can be used to predict RNA 3D structures with much improved accuracy. Here we present an efficient method that incorporates this information into current RNA 3D structure prediction methods, specifically 3dRNA. Our method makes much more accurate RNA 3D structure prediction than the original 3dRNA as well as other existing prediction methods that used the direct coupling analysis. In particular our method demonstrates a significant improvement in predicting multi-branch junction conformations, a major bottleneck for RNA 3D structure prediction. We also show that our method can be used to optimize the predictions by other methods. These results indicate that optimization of RNA 3D structure prediction using evolutionary restraints of nucleotide-nucleotide interactions from direct coupling analysis offers an efficient way for accurate RNA tertiary structure predictions.
核苷酸协同进化的直接耦合分析提供了一种新方法,用于识别RNA分子中哪些核苷酸可能直接接触,仅从序列中获得的这些信息可用于以更高的准确性预测RNA三维结构。在此,我们提出一种有效的方法,将此信息纳入当前的RNA三维结构预测方法,特别是3dRNA。我们的方法比原始的3dRNA以及其他使用直接耦合分析的现有预测方法能更准确地预测RNA三维结构。特别是,我们的方法在预测多分支连接构象方面有显著改进,而这是RNA三维结构预测的一个主要瓶颈。我们还表明,我们的方法可用于优化其他方法的预测。这些结果表明,利用直接耦合分析中核苷酸-核苷酸相互作用的进化约束来优化RNA三维结构预测,为准确预测RNA三级结构提供了一种有效方法。