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dc.contributor.authorGardella, Thomas James
dc.contributor.authorMoyle, Henry
dc.contributor.authorSusskind, Miriam M.
dc.date2022-08-11T08:08:57.000
dc.date.accessioned2022-08-23T16:13:47Z
dc.date.available2022-08-23T16:13:47Z
dc.date.issued1989-04-20
dc.date.submitted2008-09-10
dc.identifier.citationJ Mol Biol. 1989 Apr 20;206(4):579-90.
dc.identifier.issn0022-2836 (Print)
dc.identifier.pmid2661827
dc.identifier.urihttp://hdl.handle.net/20.500.14038/33708
dc.description.abstractA mutation is described that alters the promoter specificity of sigma 70, the primary sigma factor of Escherichia coli RNA polymerase. In strains carrying both the mutant and wild-type sigma gene (rpoD), the mutant sigma causes a large increase in the activity of mutant P22 ant promoters with A.T or C.G instead of the wild-type, consensus G.C base-pair at position -33, the third position of the consensus -35 hexamer 5'-TTGACA-3'. There is little or no effect on the activities of the wild-type and 23 other mutant ant promoters, including one with T.A at -33. The mutant sigma also activates E. coli lac promoters with A.T or C.G, but not T.A, at the corresponding position. The rpoD mutation (rpoD-RH588) changes a CGT codon to CAT. The corresponding change in sigma 70 is Arg588----His. This residue is in a region that is conserved among most sigma factors, a region that is also homologous with the helix-turn-helix motif of DNA-binding proteins. These results suggest that this region of sigma 70 is directly involved in recognition of the -35 hexamer.
dc.language.isoen_US
dc.relation<a href="http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?cmd=Retrieve&db=PubMed&list_uids=2661827&dopt=Abstract">Link to article in PubMed</a>
dc.relation.urlhttp://dx.doi.org/10.1016/0022-2836(89)90567-6
dc.subjectBase Sequence; Chromosome Deletion; DNA-Directed RNA Polymerases; Escherichia coli; Genes, Bacterial; Lac Operon; Molecular Sequence Data; Mutation; *Promoter Regions (Genetics); Sigma Factor; Transcription Factors
dc.subjectLife Sciences
dc.subjectMedicine and Health Sciences
dc.titleA mutant Escherichia coli sigma 70 subunit of RNA polymerase with altered promoter specificity
dc.typeJournal Article
dc.source.journaltitleJournal of molecular biology
dc.source.volume206
dc.source.issue4
dc.identifier.legacycoverpagehttps://escholarship.umassmed.edu/gsbs_sp/371
dc.identifier.contextkey625998
html.description.abstract<p>A mutation is described that alters the promoter specificity of sigma 70, the primary sigma factor of Escherichia coli RNA polymerase. In strains carrying both the mutant and wild-type sigma gene (rpoD), the mutant sigma causes a large increase in the activity of mutant P22 ant promoters with A.T or C.G instead of the wild-type, consensus G.C base-pair at position -33, the third position of the consensus -35 hexamer 5'-TTGACA-3'. There is little or no effect on the activities of the wild-type and 23 other mutant ant promoters, including one with T.A at -33. The mutant sigma also activates E. coli lac promoters with A.T or C.G, but not T.A, at the corresponding position. The rpoD mutation (rpoD-RH588) changes a CGT codon to CAT. The corresponding change in sigma 70 is Arg588----His. This residue is in a region that is conserved among most sigma factors, a region that is also homologous with the helix-turn-helix motif of DNA-binding proteins. These results suggest that this region of sigma 70 is directly involved in recognition of the -35 hexamer.</p>
dc.identifier.submissionpathgsbs_sp/371
dc.contributor.departmentDepartment of Molecular Genetics and Microbiology
dc.contributor.departmentGraduate School of Biomedical Sciences
dc.source.pages579-90


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