CRISPRstrand: predicting repeat orientations to determine the crRNA-encoding strand at CRISPR loci.

Bioinformatics

Department of Computer Science, University of Freiburg, Georges-Köhler-Allee 106, 79110 Freiburg, Germany, Department of Biology, University of Copenhagen, Archaea Centre, Ole Maaloes Vej 5, DK2200 Copenhagen, Denmark and BIOSS Centre for Biological Signalling Studies, Cluster of Excellence, University of Freiburg, Germany Department of Computer Science, University of Freiburg, Georges-Köhler-Allee 106, 79110 Freiburg, Germany, Department of Biology, University of Copenhagen, Archaea Centre, Ole Maaloes Vej 5, DK2200 Copenhagen, Denmark and BIOSS Centre for Biological Signalling Studies, Cluster of Excellence, University of Freiburg, Germany.

Published: September 2014

Motivation: The discovery of CRISPR-Cas systems almost 20 years ago rapidly changed our perception of the bacterial and archaeal immune systems. CRISPR loci consist of several repetitive DNA sequences called repeats, inter-spaced by stretches of variable length sequences called spacers. This CRISPR array is transcribed and processed into multiple mature RNA species (crRNAs). A single crRNA is integrated into an interference complex, together with CRISPR-associated (Cas) proteins, to bind and degrade invading nucleic acids. Although existing bioinformatics tools can recognize CRISPR loci by their characteristic repeat-spacer architecture, they generally output CRISPR arrays of ambiguous orientation and thus do not determine the strand from which crRNAs are processed. Knowledge of the correct orientation is crucial for many tasks, including the classification of CRISPR conservation, the detection of leader regions, the identification of target sites (protospacers) on invading genetic elements and the characterization of protospacer-adjacent motifs.

Results: We present a fast and accurate tool to determine the crRNA-encoding strand at CRISPR loci by predicting the correct orientation of repeats based on an advanced machine learning approach. Both the repeat sequence and mutation information were encoded and processed by an efficient graph kernel to learn higher-order correlations. The model was trained and tested on curated data comprising >4500 CRISPRs and yielded a remarkable performance of 0.95 AUC ROC (area under the curve of the receiver operator characteristic). In addition, we show that accurate orientation information greatly improved detection of conserved repeat sequence families and structure motifs. We integrated CRISPRstrand predictions into our CRISPRmap web server of CRISPR conservation and updated the latter to version 2.0.

Availability: CRISPRmap and CRISPRstrand are available at http://rna.informatik.uni-freiburg.de/CRISPRmap.

Supplementary Information: Supplementary data are available at Bioinformatics online.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4147912PMC
http://dx.doi.org/10.1093/bioinformatics/btu459DOI Listing

Publication Analysis

Top Keywords

crispr loci
16
determine crrna-encoding
8
crrna-encoding strand
8
crispr
8
strand crispr
8
sequences called
8
correct orientation
8
crispr conservation
8
repeat sequence
8
crisprstrand predicting
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!