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Informative priors based on transcription factor structural class improve de novo motif discovery

Item Type:Article
Title:Informative priors based on transcription factor structural class improve de novo motif discovery
Creators Name:Narlikar, L. and Gordan, R. and Ohler, U. and Hartemink, A.J.
Abstract:MOTIVATION: An important problem in molecular biology is to identify the locations at which a transcription factor (TF) binds to DNA, given a set of DNA sequences believed to be bound by that TF. In previous work, we showed that information in the DNA sequence of a binding site is sufficient to predict the structural class of the TF that binds it. In particular, this suggests that we can predict which locations in any DNA sequence are more likely to be bound by certain classes of TFs than others. Here, we argue that traditional methods for de novo motif finding can be significantly improved by adopting an informative prior probability that a TF binding site occurs at each sequence location. To demonstrate the utility of such an approach, we present priority, a powerful new de novo motif finding algorithm. RESULTS: Using data from TRANSFAC, we train three classifiers to recognize binding sites of basic leucine zipper, forkhead, and basic helix loop helix TFs. These classifiers are used to equip priority with three class-specific priors, in addition to a default prior to handle TFs of other classes. We apply priority and a number of popular motif finding programs to sets of yeast intergenic regions that are reported by ChIP-chip to be bound by particular TFs. priority identifies motifs the other methods fail to identify, and correctly predicts the structural class of the TF recognizing the identified binding sites.
Keywords:Algorithms, Amino Acid Motifs, Base Sequence, Binding Sites, Chemical Models, Computer Simulation, DNA, Genetic Models, Molecular Models, Molecular Sequence Data, Protein Binding, Sequence Alignment, Sequence Analysis, Transcription Factors
Source:Bioinformatics
ISSN:1367-4803
Publisher:Oxford University Press
Volume:22
Number:14
Page Range:e384-392
Date:15 July 2006
Official Publication:https://doi.org/10.1093/bioinformatics/btl251
PubMed:View item in PubMed

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