A Graph-Based Similarity Approach to Classify Recurrent Complex Motifs from Their Context in RNA Structures

Coline Gianfrotta, Vladimir Reinharz, D. Barth, A. Denise
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引用次数: 3

Abstract

This article proposes to use an RNA graph similarity metric, based on the MCES resolution problem, to compare the occurrences of specific complex motifs in RNA graphs, according to their context represented as subgraph. We rely on a new modeling by graphs of these contexts, at two different levels of granularity, and obtain a classification of these graphs, which is consistent with the RNA 3D structure. RNA many non-translational functions, as a ribozyme, riboswitch, or ribosome, require complex structures. Those are composed of a rigid skeleton, a set of canonical interactions called the secondary structure. Decades of experimental and theoretical work have produced precise thermodynamic parameters and efficient algorithms to predict, from sequence, the secondary structure of RNA molecules. On top of the skeleton, the nucleotides form an intricate network of interactions that are not captured by present thermodynamic models. This network has been shown to be composed of modular motifs, that are linked to function, and have been leveraged for better prediction and design. A peculiar subclass of complex structural motifs are those connecting RNA regions far away in the secondary structure. They are crucial to predict since they determine the global shape of the molecule, therefore important for the function. In this paper, we show by using our graph approach that the context is important for the formation of conserved complex structural motifs. We furthermore show that a natural classification of structural variants of the motifs emerges from their context. We explore the cases of three known motif families and we exhibit their experimentally emerging classification. 2012 ACM Subject Classification Applied computing → Molecular structural biology
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基于图的相似性方法对RNA结构中反复出现的复杂基序进行分类
本文建议使用基于MCES分辨率问题的RNA图相似性度量来比较RNA图中特定复杂基序的出现情况,根据它们的上下文表示为子图。我们在两个不同的粒度级别上,依靠这些上下文的图的新建模,并获得这些图的分类,这与RNA的3D结构是一致的。RNA的许多非翻译功能,如核酶、核开关或核糖体,需要复杂的结构。它们由一个刚性骨架组成,这是一组被称为二级结构的规范相互作用。几十年的实验和理论工作已经产生了精确的热力学参数和有效的算法,可以从序列中预测RNA分子的二级结构。在骨架的顶部,核苷酸形成了一个复杂的相互作用网络,这是目前热力学模型所无法捕捉到的。该网络已被证明是由模块基序组成的,这些基序与功能有关,并已被用于更好的预测和设计。复杂结构基序的一个特殊子类是那些在二级结构中连接RNA区域的基序。它们对预测至关重要,因为它们决定了分子的整体形状,因此对功能很重要。在本文中,我们用我们的图方法证明了上下文对于保守的复杂结构基元的形成是重要的。我们进一步表明,基序的结构变体的自然分类是从它们的语境中出现的。我们探讨了三个已知基序家族的情况下,我们展示了他们的实验新兴分类。2012 ACM学科分类:应用计算→分子结构生物学
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