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Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction
Kink turns are widely occurring motifs in RNA, located in internal loops and associated with many biological functions including translation, regulation and splicing. The associated sequence pattern, a 3-nt bulge and G-A, A-G base-pairs, generates an angle of ∼50° along the helical axis due to A-min...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435971/ https://www.ncbi.nlm.nih.gov/pubmed/28158755 http://dx.doi.org/10.1093/nar/gkx045 |
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author | Bayrak, Cigdem Sevim Kim, Namhee Schlick, Tamar |
author_facet | Bayrak, Cigdem Sevim Kim, Namhee Schlick, Tamar |
author_sort | Bayrak, Cigdem Sevim |
collection | PubMed |
description | Kink turns are widely occurring motifs in RNA, located in internal loops and associated with many biological functions including translation, regulation and splicing. The associated sequence pattern, a 3-nt bulge and G-A, A-G base-pairs, generates an angle of ∼50° along the helical axis due to A-minor interactions. The conserved sequence and distinct secondary structures of kink-turns (k-turn) suggest computational folding rules to predict k-turn-like topologies from sequence. Here, we annotate observed k-turn motifs within a non-redundant RNA dataset based on sequence signatures and geometrical features, analyze bending and torsion angles, and determine distinct knowledge-based potentials with and without k-turn motifs. We apply these scoring potentials to our RAGTOP (RNA-As-Graph-Topologies) graph sampling protocol to construct and sample coarse-grained graph representations of RNAs from a given secondary structure. We present graph-sampling results for 35 RNAs, including 12 k-turn and 23 non k-turn internal loops, and compare the results to solved structures and to RAGTOP results without special k-turn potentials. Significant improvements are observed with the updated scoring potentials compared to the k-turn-free potentials. Because k-turns represent a classic example of sequence/structure motif, our study suggests that other such motifs with sequence signatures and unique geometrical features can similarly be utilized for RNA structure prediction and design. |
format | Online Article Text |
id | pubmed-5435971 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-54359712017-05-22 Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction Bayrak, Cigdem Sevim Kim, Namhee Schlick, Tamar Nucleic Acids Res RNA Kink turns are widely occurring motifs in RNA, located in internal loops and associated with many biological functions including translation, regulation and splicing. The associated sequence pattern, a 3-nt bulge and G-A, A-G base-pairs, generates an angle of ∼50° along the helical axis due to A-minor interactions. The conserved sequence and distinct secondary structures of kink-turns (k-turn) suggest computational folding rules to predict k-turn-like topologies from sequence. Here, we annotate observed k-turn motifs within a non-redundant RNA dataset based on sequence signatures and geometrical features, analyze bending and torsion angles, and determine distinct knowledge-based potentials with and without k-turn motifs. We apply these scoring potentials to our RAGTOP (RNA-As-Graph-Topologies) graph sampling protocol to construct and sample coarse-grained graph representations of RNAs from a given secondary structure. We present graph-sampling results for 35 RNAs, including 12 k-turn and 23 non k-turn internal loops, and compare the results to solved structures and to RAGTOP results without special k-turn potentials. Significant improvements are observed with the updated scoring potentials compared to the k-turn-free potentials. Because k-turns represent a classic example of sequence/structure motif, our study suggests that other such motifs with sequence signatures and unique geometrical features can similarly be utilized for RNA structure prediction and design. Oxford University Press 2017-05-19 2017-02-01 /pmc/articles/PMC5435971/ /pubmed/28158755 http://dx.doi.org/10.1093/nar/gkx045 Text en © The Author(s) 2017. Published by Oxford University Press on behalf of Nucleic Acids Research. http://creativecommons.org/licenses/by-nc/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com |
spellingShingle | RNA Bayrak, Cigdem Sevim Kim, Namhee Schlick, Tamar Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction |
title | Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction |
title_full | Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction |
title_fullStr | Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction |
title_full_unstemmed | Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction |
title_short | Using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for RNA structure prediction |
title_sort | using sequence signatures and kink-turn motifs in knowledge-based statistical potentials for rna structure prediction |
topic | RNA |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5435971/ https://www.ncbi.nlm.nih.gov/pubmed/28158755 http://dx.doi.org/10.1093/nar/gkx045 |
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