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Topological constraints of RNA pseudoknotted and loop-kissing motifs: applications to three-dimensional structure prediction

机译:RNA假打结和环吻基序的拓扑约束:在三维结构预测中的应用

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摘要

An RNA global fold can be described at the level of helix orientations and relatively flexible loop conformations that connect the helices. The linkage between the helices plays an essential role in determining the structural topology, which restricts RNA local and global folds, especially for RNA tertiary structures involving cross-linked base pairs. We quantitatively analyze the topological constraints on RNA 3D conformational space, in particular, on the distribution of helix orientations, for pseudoknots and loop-loop kissing structures. The result shows that a viable conformational space is predominantly determined by the motif type, helix size, and loop size, indicating a strong topological coupling between helices and loops in RNA tertiary motifs. Moreover, the analysis indicates that (cross-linked) tertiary contacts can cause much stronger topological constraints on RNA global fold than non-cross-linked base pairs. Furthermore, based on the topological constraints encoded in the 2D structure and the 3D templates, we develop a 3D structure prediction approach. This approach can be further combined with structure probing methods to expand the capability of computational prediction for large RNA folds.
机译:可以在螺旋方向和连接螺旋的相对灵活的环构象的水平上描述RNA的整体折叠。螺旋之间的连接在确定结构拓扑中起着至关重要的作用,这限制了RNA的局部和整体折叠,尤其是对于涉及交联碱基对的RNA三级结构。我们定量分析了对RNA 3D构象空间的拓扑约束,特别是对于假结和环环接吻结构的螺旋方向分布。结果表明,一个可行的构象空间主要由基序类型,螺旋大小和环大小决定,表明RNA三次基序中的螺旋和环之间存在强大的拓扑耦合。此外,分析表明(未交联的)三级接触比未交联的碱基对可对RNA的整体折叠造成更强的拓扑约束。此外,基于2D结构和3D模板中编码的拓扑约束,我们开发了3D结构预测方法。此方法可以进一步与结构探测方法结合使用,以扩展大RNA折叠的计算预测能力。

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