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dc.contributor.authorGoh, Shan
dc.contributor.authorBoberek, Jaroslaw M
dc.contributor.authorNakashima, Nobutaka
dc.contributor.authorStach, Jem
dc.contributor.authorGood, Liam
dc.date.accessioned2018-09-12T15:20:13Z
dc.date.available2018-09-12T15:20:13Z
dc.date.issued2009-06-26
dc.identifier.citationGoh , S , Boberek , J M , Nakashima , N , Stach , J & Good , L 2009 , ' Concurrent growth rate and transcript analyses reveal essential gene stringency in Escherichia coli ' , PLoS ONE , vol. 4 , no. 6 , pp. e6061 . https://doi.org/10.1371/journal.pone.0006061
dc.identifier.issn1932-6203
dc.identifier.otherPubMedCentral: PMC2698124
dc.identifier.otherORCID: /0000-0002-9028-0303/work/62751705
dc.identifier.urihttp://hdl.handle.net/2299/20577
dc.description.abstractBACKGROUND: Genes essential for bacterial growth are of particular scientific interest. Many putative essential genes have been identified or predicted in several species, however, little is known about gene expression requirement stringency, which may be an important aspect of bacterial physiology and likely a determining factor in drug target development. METHODOLOGY/PRINCIPAL FINDINGS: Working from the premise that essential genes differ in absolute requirement for growth, we describe silencing of putative essential genes in E. coli to obtain a titration of declining growth rates and transcript levels by using antisense peptide nucleic acids (PNA) and expressed antisense RNA. The relationship between mRNA decline and growth rate decline reflects the degree of essentiality, or stringency, of an essential gene, which is here defined by the minimum transcript level for a 50% reduction in growth rate (MTL(50)). When applied to four growth essential genes, both RNA silencing methods resulted in MTL(50) values that reveal acpP as the most stringently required of the four genes examined, with ftsZ the next most stringently required. The established antibacterial targets murA and fabI were less stringently required. CONCLUSIONS: RNA silencing can reveal stringent requirements for gene expression with respect to growth. This method may be used to validate existing essential genes and to quantify drug target requirement.en
dc.format.extent1010680
dc.language.isoeng
dc.relation.ispartofPLoS ONE
dc.subjectBacterial Physiological Phenomena
dc.subjectCloning, Molecular
dc.subjectEscherichia coli
dc.subjectEscherichia coli Proteins
dc.subjectGene Expression Regulation, Bacterial
dc.subjectGenes, Bacterial
dc.subjectGenes, Essential
dc.subjectGenetic Complementation Test
dc.subjectGenome, Bacterial
dc.subjectMicroscopy, Fluorescence
dc.subjectModels, Biological
dc.subjectOligonucleotides, Antisense
dc.subjectOpen Reading Frames
dc.subjectPolymerase Chain Reaction
dc.subjectRNA Interference
dc.subjectJournal Article
dc.subjectResearch Support, Non-U.S. Gov't
dc.titleConcurrent growth rate and transcript analyses reveal essential gene stringency in Escherichia colien
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionExtracellular Vesicle Research Unit
dc.contributor.institutionBiosciences Research Group
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionCentre for Agriculture, Food and Environmental Management Research
dc.description.statusPeer reviewed
rioxxterms.versionofrecord10.1371/journal.pone.0006061
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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