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1.
Bioinformatics ; 25(22): 2913-20, 2009 Nov 15.
Article in English | MEDLINE | ID: mdl-19736253

ABSTRACT

MOTIVATION: In general, each cell signaling pathway involves many proteins, each with one or more specific roles. As they are essential components of cell activity, it is important to understand how these proteins work-and in particular, to determine which of the species' proteins participate in each role. Experimentally determining this mapping of proteins to roles is difficult and time consuming. Fortunately, many pathways are similar across species, so we may be able to use known pathway information of one species to understand the corresponding pathway of another. RESULTS: We present an automatic approach, Predict Signaling Pathway (PSP), which uses the signaling pathways in well-studied species to predict the roles of proteins in less-studied species. We use a machine learning approach to create a predictor that achieves a generalization F-measure of 78.2% when applied to 11 different pathways across 14 different species. We also show our approach is very effective in predicting the pathways that have not yet been experimentally studied completely. AVAILABILITY: The list of predicted proteins for all pathways over all considered species is available at http://www.cs.ualberta.ca/~bioinfo/signaling.


Subject(s)
Artificial Intelligence , Computational Biology/methods , Signal Transduction , Databases, Protein , Information Storage and Retrieval , Proteins/metabolism , Proteomics/methods
2.
Nucleic Acids Res ; 37(8): 2461-70, 2009 May.
Article in English | MEDLINE | ID: mdl-19255090

ABSTRACT

Recent advances in DNA-sequencing technology have made it possible to obtain large datasets of small RNA sequences. Here we demonstrate that not all non-perfectly matched small RNA sequences are simple technological sequencing errors, but many hold valuable biological information. Analysis of three small RNA datasets originating from Oryza sativa and Arabidopsis thaliana small RNA-sequencing projects demonstrates that many single nucleotide substitution errors overlap when aligning homologous non-identical small RNA sequences. Investigating the sites and identities of substitution errors reveal that many potentially originate as a result of post-transcriptional modifications or RNA editing. Modifications include N1-methyl modified purine nucleotides in tRNA, potential deamination or base substitutions in micro RNAs, 3' micro RNA uridine extensions and 5' micro RNA deletions. Additionally, further analysis of large sequencing datasets reveal that the combined effects of 5' deletions and 3' uridine extensions can alter the specificity by which micro RNAs associate with different Argonaute proteins. Hence, we demonstrate that not all sequencing errors in small RNA datasets are technical artifacts, but that these actually often reveal valuable biological insights to the sites of post-transcriptional RNA modifications.


Subject(s)
MicroRNAs/chemistry , RNA Processing, Post-Transcriptional , RNA, Transfer/chemistry , Sequence Analysis, RNA , Algorithms , Arabidopsis/genetics , Artifacts , Base Sequence , Genome, Plant , MicroRNAs/metabolism , Oryza/genetics , Poly U/analysis , RNA Editing , RNA, Transfer/metabolism , Sequence Alignment
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