Please use this identifier to cite or link to this item: https://biore.bio.bg.ac.rs/handle/123456789/400
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dc.contributor.authorSevostyanova, Anastasiyaen_US
dc.contributor.authorĐorđević, Markoen_US
dc.contributor.authorKuznedelov, Konstantinen_US
dc.contributor.authorNaryshkina, Tatyanaen_US
dc.contributor.authorGelfand, Mikhail S.en_US
dc.contributor.authorSeverinov, Konstantinen_US
dc.contributor.authorMinakhin, Leoniden_US
dc.date.accessioned2019-07-01T20:59:52Z-
dc.date.available2019-07-01T20:59:52Z-
dc.date.issued2007-02-16-
dc.identifier.issn0022-2836-
dc.identifier.urihttps://biore.bio.bg.ac.rs/handle/123456789/400-
dc.description.abstractRegulation of gene expression of lytic bacteriophage φ{symbol}YS40 that infects the thermophilic bacterium Thermus thermophilus was investigated and three temporal classes of phage genes, early, middle, and late, were revealed. φ{symbol}YS40 does not encode a (RNAP) and must rely on host RNAP for transcription of its genes. Bioinformatic analysis using a model of Thermus promoters predicted 43 putative σA-dependent -10/-35 class phage promoters. A randomly chosen subset of those promoters was shown to be functional in vivo and in vitro and to belong to the early temporal class. Macroarray analysis, primer extension, and bioinformatic predictions identified 36 viral middle and late promoters. These promoters have a single common consensus element, which resembles host σA RNAP holoenzyme -10 promoter consensus element sequence. The mechanism responsible for the temporal control of the three classes of promoters remains unknown, since host σA RNAP holoenzyme purified from either infected or uninfected cells efficiently transcribed all φ{symbol}YS40 promoters in vitro. Interestingly, our data showed that during infection, there is a significant increase and decreaseof transcript amounts of host translation initiation factors IF2 and IF3, respectively. This finding, together with the fact that most middle and late φ{symbol}YS40 transcripts were found to be leaderless, suggests that the shift to late viral gene expression may also occur at the level of mRNA translation. © 2006 Elsevier Ltd. All rights reserved.en_US
dc.language.isoenen_US
dc.relation.ispartofJournal of Molecular Biologyen_US
dc.subjectbacteriophageen_US
dc.subjectbioinformatic promoter searchen_US
dc.subjectleaderless mRNAen_US
dc.subjectmacroarray analysisen_US
dc.subjectThermus thermophilusen_US
dc.titleTemporal Regulation of Viral Transcription during Development of Thermus thermophilus Bacteriophage φ{symbol}YS40en_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.jmb.2006.11.050-
dc.identifier.pmid17187825-
dc.identifier.scopus2-s2.0-33846374007-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/33846374007-
item.languageiso639-1en-
item.cerifentitytypePublications-
item.openairetypeArticle-
item.fulltextWith Fulltext-
item.grantfulltextrestricted-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptChair of General Physiology and Biophysics-
crisitem.author.orcid0000-0002-2903-3119-
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