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Analysis of nutR: A region of phage lambda required for antitermination of transcription

dc.contributor.authorOlson, Eric R.en_US
dc.contributor.authorFlamm, Eric L.en_US
dc.contributor.authorFriedman, David I.en_US
dc.date.accessioned2006-04-07T17:46:38Z
dc.date.available2006-04-07T17:46:38Z
dc.date.issued1982-11en_US
dc.identifier.citationOlson, Eric R., Flamm, Eric L., Friedman, David I. (1982/11)."Analysis of nutR: A region of phage lambda required for antitermination of transcription." Cell 31(1): 61-70. <http://hdl.handle.net/2027.42/23813>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6WSN-4C8973V-1P/2/08d91fd6900ecd614d6db3091ac9022cen_US
dc.identifier.urihttps://hdl.handle.net/2027.42/23813
dc.identifier.urihttp://www.ncbi.nlm.nih.gov/sites/entrez?cmd=retrieve&db=pubmed&list_uids=6218883&dopt=citationen_US
dc.description.abstractThe N gene product of coliphage lambda acts with host factors (Nus) through sites (nut) to render subsequent downstream transcription resistant to a variety of termination signals. These sites, nutR and nutL, are downstream, respectively, from the early promoters PR and PL. Thus a complicated set of molecular interactions are likely to occur at the nut sites. We have selected mutations in the nutR region that reduce the effectiveness of pN in altering transcription initiating at the PR promoter. DNA sequence analysis of three independently selected mutations revealed, in each case, a deletion of a single base pair in the cro gene. Consideration of the effect of such mutations on the extension of translation of cro message into the adjacent downstream nut region led to the identification of a consensus sequence CGCTCT(T)TAA that appears to play a role in the recognition of a host factor, possibly the NusA protein.en_US
dc.format.extent1172519 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleAnalysis of nutR: A region of phage lambda required for antitermination of transcriptionen_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelMolecular, Cellular and Developmental Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.subject.hlbtoplevelHealth Sciencesen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Microbiology and Immunology The University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Microbiology and Immunology The University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.contributor.affiliationumDepartment of Microbiology and Immunology The University of Michigan Medical School, Ann Arbor, Michigan 48109, USAen_US
dc.identifier.pmid6218883en_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/23813/1/0000052.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0092-8674(82)90405-6en_US
dc.identifier.sourceCellen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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