核糖核酸
核酸二级结构
蛋白质二级结构
核酸结构
计算生物学
点突变
遗传学
生物
生物信息学
碱基对
非编码RNA
突变
基因
生物化学
作者
Risa Karakida Kawaguchi,Hisanori Kiryu
出处
期刊:Methods in molecular biology
日期:2023-01-01
卷期号:: 107-120
标识
DOI:10.1007/978-1-0716-2768-6_7
摘要
A point mutation in coding RNA can cause not only an amino acid substitution but also a dynamic change of RNA secondary structure, leading to a dysfunctional RNA. Although in silico structure prediction has been used to detect structure-disrupting point mutations known as riboSNitches, exhaustive simulation of long RNAs is needed to detect a significant enrichment or depletion of riboSNitches in functional RNAs. Here, we have developed a novel algorithm Radiam (RNA secondary structure Analysis with Deletion, Insertion, And substitution Mutations) for a comprehensive riboSNitch analysis of long RNAs. Radiam is based on the ParasoR framework, which efficiently computes local RNA secondary structures for long RNAs. ParasoR can compute a variety of structure scores over globally consistent structures with maximal span constraints for the base pair distance. Using the reusable structure database made by ParasoR, Radiam performs an efficient recomputation of the secondary structures for mutated sequences. An exhaustive simulation of Radiam is expected to find reliable riboSNitch candidates on long RNAs by evaluating their statistical significance in terms of the change of local structure stability.
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