Machine Learning to Enhance Biophysical Models for Riboswitch Discovery.

IF 4.4 2区 生物学 Q1 CELL BIOLOGY
Rami Zakh, Alexander Churkin, Ahmed Elbanna, Sumit Mukherjee, Danny Barash
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引用次数: 0

Abstract

Riboswitches are RNA-based genetic control elements that provide a unique mechanism of gene regulation. They function without the participation of proteins and are believed to represent ancient regulatory systems on the evolutionary timescale. To expand the search for novel riboswitches of significant interest, such as eukaryotic riboswitches beyond the purine riboswitch class, the integration of machine learning into RNA design offers considerable potential to improve the effectiveness of traditional search methods. Many riboswitch aptamers that could be targeted in such searches are larger than purine riboswitch aptamers, making their design time-consuming (e.g., SAM, lysine, FMN, glycine, and cobalamin riboswitches). In an example problem unrelated to the discovery of novel riboswitches, namely challenges in the eteRNA game, it has been shown that a transformer encoder-decoder model is effective in solving difficult inverse RNA folding challenges. In the outlined approach, machine learning is used as a preprocessing step before RNA design, rather than relying on random inputs to the Monte Carlo method, and the RNA design step crucially depends on a biophysical model for the forward problem of RNA folding prediction. It is therefore suggested to optimize the training of the machine learning model and then utilize this approach for riboswitch discovery to make searches for riboswitches larger than purine aptamers more efficient and robust.

机器学习增强核糖开关发现的生物物理模型。
核糖开关是基于rna的遗传控制元件,提供了一种独特的基因调控机制。它们在没有蛋白质参与的情况下发挥作用,被认为代表了进化时间尺度上的古老调节系统。为了扩大对新型核糖开关的搜索,如真核核糖开关超越嘌呤核糖开关类,将机器学习集成到RNA设计中,为提高传统搜索方法的有效性提供了相当大的潜力。在这种搜索中,许多核糖开关适配体比嘌呤核糖开关适配体更大,使得它们的设计更耗时(例如,SAM、赖氨酸、FMN、甘氨酸和钴胺素核糖开关)。在一个与发现新的核糖开关无关的示例问题中,即eteRNA游戏中的挑战,已经证明变压器编码器-解码器模型在解决困难的逆转录RNA折叠挑战方面是有效的。在概述的方法中,机器学习被用作RNA设计之前的预处理步骤,而不是依赖于蒙特卡罗方法的随机输入,RNA设计步骤关键地依赖于RNA折叠预测前向问题的生物物理模型。因此,我们建议优化机器学习模型的训练,然后利用这种方法进行核糖开关的发现,使比嘌呤适配体更大的核糖开关的搜索更有效和稳健。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
14.80
自引率
4.10%
发文量
67
审稿时长
6-12 weeks
期刊介绍: WIREs RNA aims to provide comprehensive, up-to-date, and coherent coverage of this interesting and growing field, providing a framework for both RNA experts and interdisciplinary researchers to not only gain perspective in areas of RNA biology, but to generate new insights and applications as well. Major topics to be covered are: RNA Structure and Dynamics; RNA Evolution and Genomics; RNA-Based Catalysis; RNA Interactions with Proteins and Other Molecules; Translation; RNA Processing; RNA Export/Localization; RNA Turnover and Surveillance; Regulatory RNAs/RNAi/Riboswitches; RNA in Disease and Development; and RNA Methods.
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