Integrating Diverse Datasets Improves Developmental Enhancer Prediction
Identifieur interne : 002706 ( Ncbi/Curation ); précédent : 002705; suivant : 002707Integrating Diverse Datasets Improves Developmental Enhancer Prediction
Auteurs : Genevieve D. Erwin [États-Unis] ; Nir Oksenberg [États-Unis] ; Rebecca M. Truty [États-Unis] ; Dennis Kostka [États-Unis] ; Karl K. Murphy [États-Unis] ; Nadav Ahituv [États-Unis] ; Katherine S. Pollard [États-Unis] ; John A. Capra [États-Unis]Source :
- PLoS Computational Biology [ 1553-734X ] ; 2014.
Descripteurs français
- KwdFr :
- MESH :
English descriptors
- KwdEn :
- MESH :
- chemical , genetics : Histones.
- genetics : Enhancer Elements, Genetic, Organ Specificity.
- methods : Genomics.
- Animals, Artificial Intelligence, Databases, Genetic, Genome-Wide Association Study, Humans, Mice, Mice, Transgenic, Models, Statistical.
Abstract
Gene-regulatory enhancers have been identified using various approaches, including evolutionary conservation, regulatory protein binding, chromatin modifications, and DNA sequence motifs. To integrate these different approaches, we developed EnhancerFinder, a two-step method for distinguishing developmental enhancers from the genomic background and then predicting their tissue specificity. EnhancerFinder uses a multiple kernel learning approach to integrate DNA sequence motifs, evolutionary patterns, and diverse functional genomics datasets from a variety of cell types. In contrast with prediction approaches that define enhancers based on histone marks or p300 sites from a single cell line, we trained EnhancerFinder on hundreds of experimentally verified human developmental enhancers from the VISTA Enhancer Browser. We comprehensively evaluated EnhancerFinder using cross validation and found that our integrative method improves the identification of enhancers over approaches that consider a single type of data, such as sequence motifs, evolutionary conservation, or the binding of enhancer-associated proteins. We find that VISTA enhancers active in embryonic heart are easier to identify than enhancers active in several other embryonic tissues, likely due to their uniquely high GC content. We applied EnhancerFinder to the entire human genome and predicted 84,301 developmental enhancers and their tissue specificity. These predictions provide specific functional annotations for large amounts of human non-coding DNA, and are significantly enriched near genes with annotated roles in their predicted tissues and lead SNPs from genome-wide association studies. We demonstrate the utility of EnhancerFinder predictions through
Url:
DOI: 10.1371/journal.pcbi.1003677
PubMed: 24967590
PubMed Central: 4072507
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PMC:4072507Le document en format XML
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<term>Artificial Intelligence</term>
<term>Databases, Genetic</term>
<term>Enhancer Elements, Genetic (genetics)</term>
<term>Genome-Wide Association Study</term>
<term>Genomics (methods)</term>
<term>Histones (genetics)</term>
<term>Humans</term>
<term>Mice</term>
<term>Mice, Transgenic</term>
<term>Models, Statistical</term>
<term>Organ Specificity (genetics)</term>
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<term>Bases de données génétiques</term>
<term>Génomique ()</term>
<term>Histone (génétique)</term>
<term>Humains</term>
<term>Intelligence artificielle</term>
<term>Modèles statistiques</term>
<term>Souris</term>
<term>Souris transgéniques</term>
<term>Spécificité d'organe (génétique)</term>
<term>Éléments activateurs (génétique) (génétique)</term>
<term>Étude d'association pangénomique</term>
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<keywords scheme="MESH" type="chemical" qualifier="genetics" xml:lang="en"><term>Histones</term>
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<term>Organ Specificity</term>
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<term>Spécificité d'organe</term>
<term>Éléments activateurs (génétique)</term>
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<term>Artificial Intelligence</term>
<term>Databases, Genetic</term>
<term>Genome-Wide Association Study</term>
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<term>Models, Statistical</term>
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<term>Bases de données génétiques</term>
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<term>Intelligence artificielle</term>
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<front><div type="abstract" xml:lang="en"><p>Gene-regulatory enhancers have been identified using various approaches, including evolutionary conservation, regulatory protein binding, chromatin modifications, and DNA sequence motifs. To integrate these different approaches, we developed EnhancerFinder, a two-step method for distinguishing developmental enhancers from the genomic background and then predicting their tissue specificity. EnhancerFinder uses a multiple kernel learning approach to integrate DNA sequence motifs, evolutionary patterns, and diverse functional genomics datasets from a variety of cell types. In contrast with prediction approaches that define enhancers based on histone marks or p300 sites from a single cell line, we trained EnhancerFinder on hundreds of experimentally verified human developmental enhancers from the VISTA Enhancer Browser. We comprehensively evaluated EnhancerFinder using cross validation and found that our integrative method improves the identification of enhancers over approaches that consider a single type of data, such as sequence motifs, evolutionary conservation, or the binding of enhancer-associated proteins. We find that VISTA enhancers active in embryonic heart are easier to identify than enhancers active in several other embryonic tissues, likely due to their uniquely high GC content. We applied EnhancerFinder to the entire human genome and predicted 84,301 developmental enhancers and their tissue specificity. These predictions provide specific functional annotations for large amounts of human non-coding DNA, and are significantly enriched near genes with annotated roles in their predicted tissues and lead SNPs from genome-wide association studies. We demonstrate the utility of EnhancerFinder predictions through <italic>in vivo</italic>
validation of novel embryonic gene regulatory enhancers from three developmental transcription factor loci. Our genome-wide developmental enhancer predictions are freely available as a UCSC Genome Browser track, which we hope will enable researchers to further investigate questions in developmental biology.</p>
</div>
</front>
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