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dc.contributor.authorFaria, J. P.por
dc.contributor.authorOverbeek, R.por
dc.contributor.authorXia, F.por
dc.contributor.authorRocha, Miguelpor
dc.contributor.authorRocha, I.por
dc.contributor.authorHenry, C. S.por
dc.date.accessioned2015-01-15T12:00:27Z-
dc.date.available2015-01-15T12:00:27Z-
dc.date.issued2014-
dc.identifier.citationFaria, J. P.; Overbeek, R.; Xia, F.; Rocha, Miguel; Rocha, I.; Henry, C. S., Genome-scale bacterial transcriptional regulatory networks: reconstruction and integrated analysis with metabolic models. Briefings in Bioinformatics, 15(4), 592-611, 2014por
dc.identifier.issn1477-4054por
dc.identifier.urihttps://hdl.handle.net/1822/32872-
dc.description.abstractAdvances in sequencing technology are resulting in the rapid emergence of large numbers of complete genome sequences. High throughput annotation and metabolic modeling of these genomes is now a reality. The high throughput reconstruction and analysis of genome-scale transcriptional regulatory networks represents the next frontier in microbial bioinformatics. The fruition of this next frontier will depend upon the integration of numerous data sources relating to mechanisms, components, and behavior of the transcriptional regulatory machinery, as well as the integration of the regulatory machinery into genome-scale cellular models. Here we review existing repositories for different types of transcriptional regulatory data, including expression data, transcription factor data, and binding site locations, and we explore how these data are being used for the reconstruction of new regulatory networks. From template network based methods to de novo reverse engineering from expression data, we discuss how regulatory networks can be reconstructed and integrated with metabolic models to improve model predictions and performance. Finally, we explore the impact these integrated models can have in simulating phenotypes, optimizing the production of compounds of interest or paving the way to a whole-cell model.por
dc.description.sponsorshipJ.P.F. acknowledges funding from [SFRH/BD/70824/2010] of the FCT (Portuguese Foundation for Science and Technology) PhD program. The work was supported in part by the ERDF—European Regional Development Fund through the COMPETE Programme (operational programme for competitiveness), National Funds through the FCT within projects [FCOMP-01-0124-FEDER015079] (ToMEGIM—Computational Tools for Metabolic Engineering using Genome-scale Integrated Models) and FCOMP-01-0124-FEDER009707 (HeliSysBio—molecular Systems Biology in Helicobacter pylori), the U.S. Department of Energy under contract [DE-ACO2-06CH11357] and the National Science Foundation under [0850546].por
dc.language.isoengpor
dc.publisherOxford University Presspor
dc.relationinfo:eu-repo/grantAgreement/FCT/SFRH/SFRH%2FBD%2F70824%2F2010/PT-
dc.relation0850546-
dc.rightsopenAccesspor
dc.subjectgenome-scale metabolic (GSM) modelpor
dc.subjecttranscriptional regulatory network (TRN)por
dc.subjectde novo reverse engineeringpor
dc.subjectintegrated metabolic and regulatory modelspor
dc.titleGenome-scale bacterial transcriptional regulatory networks: reconstruction and integrated analysis with metabolic modelspor
dc.typearticle-
dc.peerreviewedyespor
dc.commentsCEB14179por
sdum.publicationstatuspublishedpor
oaire.citationStartPage592por
oaire.citationEndPage611por
oaire.citationIssue4por
oaire.citationConferencePlaceUnited Kingdom-
oaire.citationTitleBriefings in Bioinformaticspor
oaire.citationVolume15por
dc.date.updated2015-01-15T10:10:31Z-
dc.identifier.eissn1467-5463-
dc.identifier.doi10.1093/bib/bbs071por
dc.identifier.pmid23422247por
dc.subject.wosScience & Technologypor
sdum.journalBriefings in Bioinformaticspor
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CEB - Publicações em Revistas/Séries Internacionais / Publications in International Journals/Series

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