IRBIS: a systematic search for conserved complementarity.

TitleIRBIS: a systematic search for conserved complementarity.
Publication TypeJournal Article
Year of Publication2014
AuthorsPervouchine DD
JournalRNA (New York, N.Y.)
Volume20
Pagination1519–1531
Date PublishedOct
ISSN1469-9001
Abstract

IRBIS is a computational pipeline for detecting conserved complementary regions in unaligned orthologous sequences. Unlike other methods, it follows the ``first-fold-then-align'' principle in which all possible combinations of complementary k-mers are searched for simultaneous conservation. The novel trimming procedure reduces the size of the search space and improves the performance to the point where large-scale analyses of intra- and intermolecular RNA-RNA interactions become possible. In this article, I provide a rigorous description of the method, benchmarking on simulated and real data, and a set of stringent predictions of intramolecular RNA structure in placental mammals, drosophilids, and nematodes. I discuss two particular cases of long-range RNA structures that are likely to have a causal effect on single- and multiple-exon skipping, one in the mammalian gene Dystonin and the other in the insect gene Ca-$\alpha$1D. In Dystonin, one of the two complementary boxes contains a binding site of Rbfox protein similar to one recently described in Enah gene. I also report that snoRNAs and long noncoding RNAs (lncRNAs) have a high capacity of base-pairing to introns of protein-coding genes, suggesting possible involvement of these transcripts in splicing regulation. I also find that conserved sequences that occur equally likely on both strands of DNA (e.g., transcription factor binding sites) contribute strongly to the false-discovery rate and, therefore, would confound every such analysis. IRBIS is an open-source software that is available at http://genome.crg.es/{\textasciitilde}dmitri/irbis/.

URLhttp://www.ncbi.nlm.nih.gov/pubmed/25142064
DOI10.1261/rna.045088.114