School of Physics and Key Laboratory of Molecular Biophysics of the Ministry of Education, Huazhong University of Science and Technology, Wuhan 430074, China.
Molecules. 2021 Jul 22;26(15):4420. doi: 10.3390/molecules26154420.
RNA molecules participate in many important biological processes, and they need to fold into well-defined secondary and tertiary structures to realize their functions. Like the well-known protein folding problem, there is also an RNA folding problem. The folding problem includes two aspects: structure prediction and folding mechanism. Although the former has been widely studied, the latter is still not well understood. Here we present a deep reinforcement learning algorithms 2dRNA-Fold to study the fastest folding paths of RNA secondary structure. 2dRNA-Fold uses a neural network combined with Monte Carlo tree search to select residue pairing step by step according to a given RNA sequence until the final secondary structure is formed. We apply 2dRNA-Fold to several short RNA molecules and one longer RNA 1Y26 and find that their fastest folding paths show some interesting features. 2dRNA-Fold is further trained using a set of RNA molecules from the dataset bpRNA and is used to predict RNA secondary structure. Since in 2dRNA-Fold the scoring to determine next step is based on possible base pairings, the learned or predicted fastest folding path may not agree with the actual folding paths determined by free energy according to physical laws.
RNA 分子参与许多重要的生物过程,它们需要折叠成明确的二级和三级结构才能实现其功能。与著名的蛋白质折叠问题一样,也存在 RNA 折叠问题。折叠问题包括两个方面:结构预测和折叠机制。尽管前者已经得到广泛研究,但后者仍未得到很好的理解。在这里,我们提出了一种深度强化学习算法 2dRNA-Fold 来研究 RNA 二级结构的最快折叠路径。2dRNA-Fold 使用神经网络结合蒙特卡罗树搜索,根据给定的 RNA 序列逐步选择残基配对,直到形成最终的二级结构。我们将 2dRNA-Fold 应用于几个短的 RNA 分子和一个较长的 RNA 1Y26,并发现它们最快的折叠路径具有一些有趣的特征。2dRNA-Fold 使用来自数据集 bpRNA 的一组 RNA 分子进行进一步训练,并用于预测 RNA 二级结构。由于在 2dRNA-Fold 中,确定下一步的评分是基于可能的碱基配对,因此,根据物理定律,学习或预测的最快折叠路径可能与由自由能确定的实际折叠路径不一致。