Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions

RNA molecules play crucial roles in various biological processes. Their three-dimensional configurations determine the functions and, in turn, influences the interaction with other molecules. RNAs and their interaction structures, the so-called RNA–RNA interactions, can be abstracted in terms of sec...

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Main Author: Quadrini Michela
Format: Article
Language:English
Published: De Gruyter 2021-05-01
Series:Journal of Integrative Bioinformatics
Subjects:
Online Access:https://doi.org/10.1515/jib-2020-0039
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spelling doaj-3fb9ffa6830845baa83dcbaaf885cf6f2021-09-06T19:40:33ZengDe GruyterJournal of Integrative Bioinformatics1613-45162021-05-0118211112610.1515/jib-2020-0039Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactionsQuadrini Michela0University of Camerino, School of Science and Technology, via Madonna delle Carceri, Camerino, ItalyRNA molecules play crucial roles in various biological processes. Their three-dimensional configurations determine the functions and, in turn, influences the interaction with other molecules. RNAs and their interaction structures, the so-called RNA–RNA interactions, can be abstracted in terms of secondary structures, i.e., a list of the nucleotide bases paired by hydrogen bonding within its nucleotide sequence. Each secondary structure, in turn, can be abstracted into cores and shadows. Both are determined by collapsing nucleotides and arcs properly. We formalize all of these abstractions as arc diagrams, whose arcs determine loops. A secondary structure, represented by an arc diagram, is pseudoknot-free if its arc diagram does not present any crossing among arcs otherwise, it is said pseudoknotted. In this study, we face the problem of identifying a given structural pattern into secondary structures or the associated cores or shadow of both RNAs and RNA–RNA interactions, characterized by arbitrary pseudoknots. These abstractions are mapped into a matrix, whose elements represent the relations among loops. Therefore, we face the problem of taking advantage of matrices and submatrices. The algorithms, implemented in Python, work in polynomial time. We test our approach on a set of 16S ribosomal RNAs with inhibitors of Thermus thermophilus, and we quantify the structural effect of the inhibitors.https://doi.org/10.1515/jib-2020-0039coreloopsrelation matrixrelationsshapestructural pattern
collection DOAJ
language English
format Article
sources DOAJ
author Quadrini Michela
spellingShingle Quadrini Michela
Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions
Journal of Integrative Bioinformatics
core
loops
relation matrix
relations
shape
structural pattern
author_facet Quadrini Michela
author_sort Quadrini Michela
title Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions
title_short Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions
title_full Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions
title_fullStr Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions
title_full_unstemmed Structural relation matching: an algorithm to identify structural patterns into RNAs and their interactions
title_sort structural relation matching: an algorithm to identify structural patterns into rnas and their interactions
publisher De Gruyter
series Journal of Integrative Bioinformatics
issn 1613-4516
publishDate 2021-05-01
description RNA molecules play crucial roles in various biological processes. Their three-dimensional configurations determine the functions and, in turn, influences the interaction with other molecules. RNAs and their interaction structures, the so-called RNA–RNA interactions, can be abstracted in terms of secondary structures, i.e., a list of the nucleotide bases paired by hydrogen bonding within its nucleotide sequence. Each secondary structure, in turn, can be abstracted into cores and shadows. Both are determined by collapsing nucleotides and arcs properly. We formalize all of these abstractions as arc diagrams, whose arcs determine loops. A secondary structure, represented by an arc diagram, is pseudoknot-free if its arc diagram does not present any crossing among arcs otherwise, it is said pseudoknotted. In this study, we face the problem of identifying a given structural pattern into secondary structures or the associated cores or shadow of both RNAs and RNA–RNA interactions, characterized by arbitrary pseudoknots. These abstractions are mapped into a matrix, whose elements represent the relations among loops. Therefore, we face the problem of taking advantage of matrices and submatrices. The algorithms, implemented in Python, work in polynomial time. We test our approach on a set of 16S ribosomal RNAs with inhibitors of Thermus thermophilus, and we quantify the structural effect of the inhibitors.
topic core
loops
relation matrix
relations
shape
structural pattern
url https://doi.org/10.1515/jib-2020-0039
work_keys_str_mv AT quadrinimichela structuralrelationmatchinganalgorithmtoidentifystructuralpatternsintornasandtheirinteractions
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