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Gibbs/MCMC Sampling for Multiple RNA Interaction with Sub-optimal Solutions

机译:Gibbs / MCMC采样与次优溶液的多重RNA相互作用

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The interaction of two RNA molecules involves a complex interplay between folding and binding that warranted the development of RNA-RNA interaction algorithms. However, these algorithms do not handle more than two RNAs. We note our recent successful formulation for the multiple (more than two) RNA interaction problem based on a combinatorial optimization called Pegs and Rubber Bands. Even then, however, the optimal solution obtained does not necessarily correspond to the actual biological structure. Moreover, a structure produced by interacting RNAs may not be unique to start with. Multiple solutions (thus sub-optimal ones) are needed. Here, a sampling approach that extends our previous formulation for multiple RNA interaction is developed. By clustering the sampled solutions, we are able to reveal representatives that correspond to realistic structures. Specifically, our results on the U2-U6 complex and its introns in the spliceosome of yeast, and the CopA-CopT complex in E. Coli are consistent with published biological structures.
机译:两个RNA分子的相互作用涉及折叠和结合之间的复杂相互作用,从而保证了RNA-RNA相互作用算法的发展。但是,这些算法不能处理两个以上的RNA。我们注意到我们最近成功地基于称为“钉子和橡皮筋”的组合优化解决了多个(两个以上)RNA相互作用问题。然而,即使如此,获得的最佳解决方案也不一定对应于实际的生物学结构。此外,由相互作用的RNA产生的结构可能并不是一开始就独有的。需要多个解决方案(因此是次优的)。在这里,开发了一种采样方法,该方法扩展了我们先前对多种RNA相互作用的描述。通过对抽样解决方案进行聚类,我们能够揭示与现实结构相对应的代表。具体而言,我们对酵母剪接体中的U2-U6复合物及其内含子以及大肠杆菌中的CopA-CopT复合物的研究结果与已发表的生物学结构一致。

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