Le S Y, Zuker M
Institute for Biological Sciences, National Research Council of Canada, Ottawa, Ontario.
J Mol Biol. 1990 Dec 5;216(3):729-41. doi: 10.1016/0022-2836(90)90395-3.
A total of 4051 suboptimal secondary structures are predicted by folding the 5' non-coding region of ten polioviruses, five human rhinoviruses and three coxsackieviruses using our new suboptimal folding algorithm for the prediction of both optimal and suboptimal RNA secondary structures. A comparative analysis of these RNA secondary structures reveals the conservation of common secondary structure that can be supported by phylogenetic data. The thermodynamic stability and statistical significance of these predicted, conserved helical elements are assessed and significant structure motifs in the 5' non-coding region are proposed. The possible roles of these structure motifs in the virus life cycle are discussed.
使用我们新的用于预测最佳和次优RNA二级结构的次优折叠算法,对十种脊髓灰质炎病毒、五种人鼻病毒和三种柯萨奇病毒的5'非编码区进行折叠,共预测出4051个次优二级结构。对这些RNA二级结构的比较分析揭示了可由系统发育数据支持的常见二级结构的保守性。评估了这些预测的保守螺旋元件的热力学稳定性和统计显著性,并提出了5'非编码区的重要结构基序。讨论了这些结构基序在病毒生命周期中的可能作用。