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dc.contributor.authorWang, Ting
dc.contributor.authorGifford, David K.
dc.contributor.authorStormo, Gary D.
dc.contributor.authorFraenkel, Ernest
dc.contributor.authorMacIsaac, Kenzie Daniel
dc.contributor.authorGordon, D. Benjamin
dc.date.accessioned2010-09-29T15:37:39Z
dc.date.available2010-09-29T15:37:39Z
dc.date.issued2006-03
dc.date.submitted2005-09
dc.identifier.issn1471-2105
dc.identifier.urihttp://hdl.handle.net/1721.1/58756
dc.description.abstractBackground: The regulatory map of a genome consists of the binding sites for proteins that determine the transcription of nearby genes. An initial regulatory map for S. cerevisiae was recently published using six motif discovery programs to analyze genome-wide chromatin immunoprecipitation data for 203 transcription factors. The programs were used to identify sequence motifs that were likely to correspond to the DNA-binding specificity of the immunoprecipitated proteins. We report improved versions of two conservation-based motif discovery algorithms, PhyloCon and Converge. Using these programs, we create a refined regulatory map for S. cerevisiae by reanalyzing the same chromatin immunoprecipitation data. Results: Applying the same conservative criteria that were applied in the original study, we find that PhyloCon and Converge each separately discover more known specificities than the combination of all six programs in the previous study. Combining the results of PhyloCon and Converge, we discover significant sequence motifs for 36 transcription factors that were previously missed. The new set of motifs identifies 636 more regulatory interactions than the previous one. The new network contains 28% more regulatory interactions among transcription factors, evidence of greater cross-talk between regulators. Conclusion: Combining two complementary computational strategies for conservation-based motif discovery improves the ability to identify the specificity of transcriptional regulators from genome-wide chromatin immunoprecipitation data. The increased sensitivity of these methods significantly expands the map of yeast regulatory sites without the need to alter any of the thresholds for statistical significance. The new map of regulatory sites reveals a more elaborate and complex view of the yeast genetic regulatory network than was observed previously.en_US
dc.description.sponsorshipPfizer Inc.en_US
dc.description.sponsorshipNational Institute of General Medical Sciences (U.S.) (NRSA award)en_US
dc.description.sponsorshipNational Institutes of Health (U.S) ( grant 1R01 HG002668-01 )en_US
dc.description.sponsorshipNational Institutes of Health (U.S) ( grant HG00249 )en_US
dc.description.sponsorshipNational Institutes of Health (U.S) ( training grant in genomic science 2T32HG00045 )en_US
dc.description.sponsorshipSociety of Kauffman Fellowsen_US
dc.publisherBioMed Central Ltden_US
dc.relation.isversionofhttp://dx.doi.org/10.1186/1471-2105-7-113en_US
dc.rightsCreative Commons Attributionen_US
dc.rights.urihttp://creativecommons.org/licenses/by/2.0en_US
dc.sourceBioMed Central Ltden_US
dc.titleAn improved map of conserved regulatory sites for Saccharomyces cerevisiaeen_US
dc.typeArticleen_US
dc.identifier.citationBMC Bioinformatics. 2006 Mar 07;7(1):113en_US
dc.contributor.departmentMassachusetts Institute of Technology. Computer Science and Artificial Intelligence Laboratoryen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Biological Engineeringen_US
dc.contributor.departmentMassachusetts Institute of Technology. Department of Electrical Engineering and Computer Scienceen_US
dc.contributor.departmentWhitehead Institute for Biomedical Researchen_US
dc.contributor.mitauthorMacIsaac, Kenzie Daniel
dc.contributor.mitauthorGordon, D. Benjamin
dc.contributor.mitauthorGifford, David K.
dc.contributor.mitauthorFraenkel, Ernest
dc.relation.journalBMC Bioinformaticsen_US
dc.eprint.versionFinal published versionen_US
dc.type.urihttp://purl.org/eprint/type/JournalArticleen_US
eprint.statushttp://purl.org/eprint/status/PeerRevieweden_US
dc.date.updated2010-09-03T16:23:08Z
dc.language.rfc3066en
dc.rights.holderMacIsaac et al.; licensee BioMed Central Ltd.
dspace.orderedauthorsMacIsaac, Kenzie D; Wang, Ting; Gordon, D Benjamin; Gifford, David K; Stormo, Gary D; Fraenkel, Ernesten
dc.identifier.orcidhttps://orcid.org/0000-0001-9249-8181
dc.identifier.orcidhttps://orcid.org/0000-0003-1709-4034
mit.licensePUBLISHER_CCen_US
mit.metadata.statusComplete


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