Fine-Tuning Enhancer Models to Predict Transcriptional Targets across Multiple Genomes. Export

@article{citeulike:1873090, abstract = {Networks of regulatory relations between transcription factors (TF) and their target genes (TG)- implemented through TF binding sites (TFBS)- are key features of biology. An idealized approach to solving such networks consists of starting from a consensus TFBS or a position weight matrix (PWM) to generate a high accuracy list of candidate TGs for biological validation. Developing and evaluating such approaches remains a formidable challenge in regulatory bioinformatics. We perform a benchmark study on 34 Drosophila TFs to assess existing TFBS and cis-regulatory module (CRM) detection methods, with a strong focus on the use of multiple genomes. Particularly, for CRM-modelling we investigate the addition of orthologous sites to a known PWM to construct phyloPWMs and we assess the added value of phylogenentic footprinting to predict contextual motifs around known TFBSs. For CRM-prediction, we compare motif conservation with network-level conservation approaches across multiple genomes. Choosing the optimal training and scoring strategies strongly enhances the performance of TG prediction for more than half of the tested TFs. Finally, we analyse a 35(th) TF, namely Eyeless, and find a significant overlap between predicted TGs and candidate TGs identified by microarray expression studies. In summary we identify several ways to optimize TF-specific TG predictions, some of which can be applied to all TFs, and others that can be applied only to particular TFs. The ability to model known TF-TG relations, together with the use of multiple genomes, results in a significant step forward in solving the architecture of gene regulatory networks.}, address = {Laboratory of Neurogenetics, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium.}, author = {Aerts, S. and van Helden, J. and Sand, O. and Hassan, B. A.}, citeulike-article-id = {1873090}, citeulike-linkout-0 = {http://dx.doi.org/10.1371/journal.pone.0001115}, citeulike-linkout-1 = {http://view.ncbi.nlm.nih.gov/pubmed/17973026}, citeulike-linkout-2 = {http://www.hubmed.org/display.cgi?uids=17973026}, doi = {10.1371/journal.pone.0001115}, issn = {1932-6203}, journal = {PLoS ONE}, keywords = {enhancer-prediction}, number = {11}, posted-at = {2008-02-06 09:51:48}, priority = {2}, title = {Fine-Tuning Enhancer Models to Predict Transcriptional Targets across Multiple Genomes.}, url = {http://dx.doi.org/10.1371/journal.pone.0001115}, volume = {2}, year = {2007} }

TY - JOUR ID - citeulike:1873090 L3 - citeulike-article-id:1873090 N2 - Networks of regulatory relations between transcription factors (TF) and their target genes (TG)- implemented through TF binding sites (TFBS)- are key features of biology. An idealized approach to solving such networks consists of starting from a consensus TFBS or a position weight matrix (PWM) to generate a high accuracy list of candidate TGs for biological validation. Developing and evaluating such approaches remains a formidable challenge in regulatory bioinformatics. We perform a benchmark study on 34 Drosophila TFs to assess existing TFBS and cis-regulatory module (CRM) detection methods, with a strong focus on the use of multiple genomes. Particularly, for CRM-modelling we investigate the addition of orthologous sites to a known PWM to construct phyloPWMs and we assess the added value of phylogenentic footprinting to predict contextual motifs around known TFBSs. For CRM-prediction, we compare motif conservation with network-level conservation approaches across multiple genomes. Choosing the optimal training and scoring strategies strongly enhances the performance of TG prediction for more than half of the tested TFs. Finally, we analyse a 35(th) TF, namely Eyeless, and find a significant overlap between predicted TGs and candidate TGs identified by microarray expression studies. In summary we identify several ways to optimize TF-specific TG predictions, some of which can be applied to all TFs, and others that can be applied only to particular TFs. The ability to model known TF-TG relations, together with the use of multiple genomes, results in a significant step forward in solving the architecture of gene regulatory networks. IS - 11 JF - PLoS ONE SN - 1932-6203 AD - Laboratory of Neurogenetics, Department of Molecular and Developmental Genetics, Vlaams Instituut voor Biotechnologie (VIB), Leuven, Belgium. TI - Fine-Tuning Enhancer Models to Predict Transcriptional Targets across Multiple Genomes. VL - 2 KW - enhancer-prediction AU - Aerts, S AU - van Helden, J AU - Sand, O AU - Hassan, BA PY - 2007/// UR - http://dx.doi.org/10.1371/journal.pone.0001115 ER -