Voss Björn, Meyer Carsten, Giegerich Robert
International NRW Graduate School in Bioinformatics and Genome Research, Bielefeld, Germany.
Bioinformatics. 2004 Jul 10;20(10):1573-82. doi: 10.1093/bioinformatics/bth129. Epub 2004 Feb 12.
There are various cases where the biological function of an RNA molecule involves a reversible change of conformation. paRNAss is a software approach to the prediction of such structural switching in RNA. It is based on three hypotheses about the secondary structure space of a switching RNA molecule that can be evaluated by RNA folding and structure comparison. In the positive case, the predicted structural switching must be verified experimentally.
After reviewing the strategy used in paRNAss, we present recent improvements on the algorithmic level of the approach, and the results of an evaluation procedure, comprising 1500 RNA sequences. It could be shown that the paRNAss approach performs well on known examples for conformational switching in RNA. The overall number of positive predictions was small, whereas for human 3' UTRs, representing regulatory important regions, it was substantially higher than for arbitrary natural and random sequences.
paRNAss is available as a Web service at http://bibiserv.techfak.uni-bielefeld.de/parnass
Detailed information on the analyses summarized in Table 1 can be found at http://bibiserv.techfak.uni-bielefeld.de/parnass/examples.html
在多种情况下,RNA分子的生物学功能涉及构象的可逆变化。paRNAss是一种预测RNA中此类结构转换的软件方法。它基于关于可通过RNA折叠和结构比较进行评估的转换RNA分子二级结构空间的三个假设。在阳性情况下,预测的结构转换必须通过实验验证。
在回顾了paRNAss中使用的策略后,我们展示了该方法在算法层面的最新改进以及包含1500个RNA序列的评估程序的结果。结果表明,paRNAss方法在RNA构象转换的已知示例上表现良好。阳性预测的总数较少,而对于代表调控重要区域的人类3'UTR,其阳性预测数明显高于任意天然和随机序列。
paRNAss可作为网络服务在http://bibiserv.techfak.uni-bielefeld.de/parnass获取。
表1中总结的分析的详细信息可在http://bibiserv.techfak.uni-bielefeld.de/parnass/examples.html找到。