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      Dual Graph Partitioning Highlights a Small Group of Pseudoknot-Containing RNA Submotifs

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          Abstract

          RNA molecules are composed of modular architectural units that define their unique structural and functional properties. Characterization of these building blocks can help interpret RNA structure/function relationships. We present an RNA secondary structure motif and submotif library using dual graph representation and partitioning. Dual graphs represent RNA helices as vertices and loops as edges. Unlike tree graphs, dual graphs can represent RNA pseudoknots (intertwined base pairs). For a representative set of RNA structures, we construct dual graphs from their secondary structures, and apply our partitioning algorithm to identify non-separable subgraphs (or blocks) without breaking pseudoknots. We report 56 subgraph blocks up to nine vertices; among them, 22 are frequently occurring, 15 of which contain pseudoknots. We then catalog atomic fragments corresponding to the subgraph blocks to define a library of building blocks that can be used for RNA design, which we call RAG-3Dual, as we have done for tree graphs. As an application, we analyze the distribution of these subgraph blocks within ribosomal RNAs of various prokaryotic and eukaryotic species to identify common subgraphs and possible ancestry relationships. Other applications of dual graph partitioning and motif library can be envisioned for RNA structure analysis and design.

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            How RNA folds.

            We describe the RNA folding problem and contrast it with the much more difficult protein folding problem. RNA has four similar monomer units, whereas proteins have 20 very different residues. The folding of RNA is hierarchical in that secondary structure is much more stable than tertiary folding. In RNA the two levels of folding (secondary and tertiary) can be experimentally separated by the presence or absence of Mg2+. Secondary structure can be predicted successfully from experimental thermodynamic data on secondary structure elements: helices, loops, and bulges. Tertiary interactions can then be added without much distortion of the secondary structure. These observations suggest a folding algorithm to predict the structure of an RNA from its sequence. However, to solve the RNA folding problem one needs thermodynamic data on tertiary structure interactions, and identification and characterization of metal-ion binding sites. These data, together with force versus extension measurements on single RNA molecules, should provide the information necessary to test and refine the proposed algorithm. Copyright 1999 Academic Press.
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              Algorithm 447: efficient algorithms for graph manipulation

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                Author and article information

                Journal
                Genes (Basel)
                Genes (Basel)
                genes
                Genes
                MDPI
                2073-4425
                25 July 2018
                August 2018
                : 9
                : 8
                : 371
                Affiliations
                [1 ]Department of Chemistry, New York University, New York, NY 10003, USA; swati.jain@ 123456nyu.edu (S.J.); cigdem.sevim@ 123456gmail.com (C.S.B.)
                [2 ]Computer Science Department, College of Staten Island, City University of New York, Staten Island, New York, NY 10314, USA; Louis.Petingi@ 123456csi.cuny.edu
                [3 ]Courant Institute of Mathematical Sciences, New York University, New York, NY 10012, USA
                [4 ]NYU-East China Normal University Center for Computational Chemistry, New York University Shanghai, Shanghai 3663, China
                Author notes
                [* ]Correspondence: schlick@ 123456nyu.edu ; Tel.: +1-212-998-3116
                [†]

                Current address: Institute for Personalized Medicine, Icahn School of Medicine at Mount Sinai, New York, NY 10029, USA.

                Author information
                https://orcid.org/0000-0002-3883-5535
                Article
                genes-09-00371
                10.3390/genes9080371
                6115904
                30044451
                13bbc47e-d01d-48b4-abc6-8bf24dfc28a8
                © 2018 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( http://creativecommons.org/licenses/by/4.0/).

                History
                : 07 May 2018
                : 26 June 2018
                Categories
                Article

                rna graphs,dual graphs,graph partitioning,rna substructures and submotifs,pseudoknots,ribosomal rnas

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