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Sarrazin-Gendron, R.

Publications and source records attributed to Sarrazin-Gendron, R..

2 recordsLinked to original sources

Finding recurrent RNA structural networks with fast maximal common subgraphs of edge-colored graphs

MotivationsRNA tertiary structure is crucial to its many non-coding molecular functions. RNA architecture is shaped by its secondary structure composed of stems, stacked canonical base pairs, enclosing loops. While stems are captured by free-energy models, loops composed of non-canonical base pairs are not. Nor are distant interactions linking together those secondary structure elements (SSEs). Databases of conserved 3D geometries (a.k.a. modules) not captured by energetic models are lever-aged for structure prediction and design, but the computational complexity has limited their study to local elements, loops, and recently to those covering pairs of SSEs. Systematically capturing recurrent patterns on a large scale is a main challenge in the study of RNA structures. ResultsIn this paper, we present an efficient algorithm to compute maximal isomorphisms in edge colored graphs. This framework is well suited to RNA structures and allows us to generalize previous approaches. In particular, we apply our techniques to find for the first time modules spanning more than 2 SSEs, while improving speed a hundredfold. We extract all recurrent base pair networks among all non-redundant RNA tertiary structures and identify a module connecting 36 different SSEs common to the 23S ribosome of E. Coli and Thermus thermophilus. We organize this information as a hierarchy of modules sharing similarities in their structure, which can serve as a basis for future research on the emergence of structural patterns. Availabilityhttp://csb.cs.mcgill.ca/carnaval2

bioinformatics↗

Stochastic Sampling of Structural Contexts Improves the Scalability and Accuracy of RNA 3D Modules Identification

RNA structures possess multiple levels of structural organization. Secondary structures are made of canonical (i.e. Watson-Crick and Wobble) helices, connected by loops whose local conformations are critical determinants of global 3D architectures. Such local 3D structures consist of conserved sets of non-canonical base pairs, called RNA modules. Their prediction from sequence data is thus a milestone toward 3D structure modelling. Unfortunately, the computational efficiency and scope of the current 3D module identification methods are too limited yet to benefit from all the knowledge accumulated in modules databases. Here, we introduce BayesPairing 2, a new sequence search algorithm leveraging secondary structure tree decomposition which allows to reduce the computational complexity and improve predictions on new sequences. We benchmarked our methods on 75 modules and 6380 RNA sequences, and report accuracies that are comparable to the state of the art, with considerable running time improvements. When identifying 200 modules on a single sequence, BayesPairing 2 is over 100 times faster than its previous version, opening new doors for genome-wide applications.

bioinformatics↗