Voss Björn, Giegerich Robert, Rehmsmeier Marc
Faculty of Technology, Bielefeld University, 33594 Bielefeld, Germany.
BMC Biol. 2006 Feb 15;4:5. doi: 10.1186/1741-7007-4-5.
Soon after the first algorithms for RNA folding became available, it was recognised that the prediction of only one energetically optimal structure is insufficient to achieve reliable results. An in-depth analysis of the folding space as a whole appeared necessary to deduce the structural properties of a given RNA molecule reliably. Folding space analysis comprises various methods such as suboptimal folding, computation of base pair probabilities, sampling procedures and abstract shape analysis. Common to many approaches is the idea of partitioning the folding space into classes of structures, for which certain properties can be derived.
In this paper we extend the approach of abstract shape analysis. We show how to compute the accumulated probabilities of all structures that share the same shape. While this implies a complete (non-heuristic) analysis of the folding space, the computational effort depends only on the size of the shape space, which is much smaller. This approach has been integrated into the tool RNA shapes, and we apply it to various RNAs.
Analyses of conformational switches show the existence of two shapes with probabilities approximately 2/3 vs. 1/3, whereas the analysis of a microRNA precursor reveals one shape with a probability near to 1.0. Furthermore, it is shown that a shape can outperform an energetically more favourable one by achieving a higher probability. From these results, and the fact that we use a complete and exact analysis of the folding space, we conclude that this approach opens up new and promising routes for investigating and understanding RNA secondary structure.
在首批RNA折叠算法问世后不久,人们就认识到仅预测一个能量最优结构不足以获得可靠结果。对整个折叠空间进行深入分析似乎是可靠推断给定RNA分子结构特性所必需的。折叠空间分析包括多种方法,如次优折叠、碱基对概率计算、采样程序和抽象形状分析。许多方法的共同之处在于将折叠空间划分为不同结构类别的想法,从中可以推导出某些特性。
在本文中,我们扩展了抽象形状分析方法。我们展示了如何计算具有相同形状的所有结构的累积概率。虽然这意味着对折叠空间进行完整(非启发式)分析,但计算量仅取决于形状空间的大小,而形状空间要小得多。这种方法已被整合到工具RNA shapes中,我们将其应用于各种RNA。
构象转换分析表明存在两种概率约为2/3对1/3的形状,而对一种微小RNA前体的分析揭示了一种概率接近1.0的形状。此外,研究表明一种形状可以通过获得更高的概率而优于能量上更有利的形状。基于这些结果,以及我们对折叠空间进行了完整且精确分析这一事实,我们得出结论,这种方法为研究和理解RNA二级结构开辟了新的、有前景的途径。