RNA Secondary Structure Alteration Caused by Single Nucleotide Variants
- PMID: 36705901
- DOI: 10.1007/978-1-0716-2768-6_7
RNA Secondary Structure Alteration Caused by Single Nucleotide Variants
Abstract
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.
Keywords: Local structure; Maximal span constraint; Mutation; RNA secondary structure; SNP; riboSNitch.
© 2023. Springer Science+Business Media, LLC, part of Springer Nature.
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References
-
- Mathews DH, Disney MD, Childs JL, Schroeder SJ, Zuker M, Turner DH (2004) Incorporating chemical modification constraints into a dynamic programming algorithm for prediction of RNA secondary structure. Proc Natl Acad Sci U S A 101:7287–7292. https://doi.org/10.1073/pnas.0401799101 - DOI - PubMed - PMC
-
- Serganov A, Nudler E (2013) A decade of riboswitches. Cell 152:17–24. https://doi.org/10.1016/j.cell.2012.12.024 - DOI - PubMed - PMC
-
- Halvorsen M, Martin JS, Broadaway S, Laederach A (2010) Disease-associated mutations that alter the RNA structural ensemble. PLoS Genet 6:e1001074. https://doi.org/10.1371/journal.pgen.1001074 - DOI - PubMed - PMC
-
- Shatoff E, Bundschuh R (2020) Single nucleotide polymorphisms affect RNA-protein interactions at a distance through modulation of RNA secondary structures. PLoS Comput Biol 16:e1007852. https://doi.org/10.1371/journal.pcbi.1007852 - DOI - PubMed - PMC
-
- He F, Wei R, Zhou Z, Huang L, Wang Y, Tang J, Zou Y, Shi L, Gu X, Davis MJ, Su Z (2019) Integrative analysis of somatic mutations in non-coding regions altering RNA secondary structures in cancer genomes. Sci Rep 9:8205. https://doi.org/10.1038/s41598-019-44489-5 - DOI - PubMed - PMC
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