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« Previous AbstractDiagnosis by Volatile Organic Compounds in Exhaled Breath in Exhaled Breath from Patients with Gastric and Colorectal Cancers    Next AbstractGenetic analysis of a region of the Enterococcus faecalis plasmid pCF10 involved in positive regulation of conjugative transfer functions »

Proc Natl Acad Sci U S A


Title:"Cis-acting, orientation-dependent, positive control system activates pheromone-inducible conjugation functions at distances greater than 10 kilobases upstream from its target in Enterococcus faecalis"
Author(s):Chung JW; Dunny GM;
Address:"Institute for Advanced Studies in Biological Process Technology, University of Minnesota, St. Paul 55108"
Journal Title:Proc Natl Acad Sci U S A
Year:1992
Volume:89
Issue:19
Page Number:9020 - 9024
DOI: 10.1073/pnas.89.19.9020
ISSN/ISBN:0027-8424 (Print) 1091-6490 (Electronic) 0027-8424 (Linking)
Abstract:"The prgB gene encodes the surface protein, Asc10, which mediates cell aggregation, resulting in high-frequency conjugative transfer of the pheromone-inducible tetracycline-resistance plasmid pCF10 in Enterococcus faecalis. Messenger RNA analysis by Northern blot hybridization and primer extension indicates that prgB transcription is pheromone-inducible and monocistronic. Previous transposon mutagenesis and sequencing analysis of a 12-kilobase (kb) region of pCF10 indicated that several genes including prgR and prgS are required to activate expression of prgB. The distance (3-4 kb) between these regulatory genes and prgB suggested that the activation might function in trans. To test this, a promoterless lacZ gene fusion to prgB was constructed and cloned without some or all of the regulatory genes. Several restriction fragments of the regulatory region were cloned in a higher copy-number plasmid, and numerous complementation studies were carried out in E. faecalis. Complementation in trans was not observed in any of these experiments. However, when the regulatory region and target genes were cloned in different sites of the same plasmid, separated by as much as 12 kb, activation of prgB was observed. Interestingly, this activation occurred only when the regions were cloned in the same relative orientation in which they exist on wild-type pCF10. These results suggest that one or more regulatory molecules may bind to an upstream cis-acting site and track along the DNA to reach a target site to activate prgB transcription"
Keywords:"Bacterial Proteins/*genetics Base Sequence Blotting, Northern Enterococcus faecalis/drug effects/*genetics *Genes, Bacterial Membrane Proteins/*genetics Molecular Sequence Data Pheromones/*pharmacology RNA, Bacterial/genetics/isolation & purification RNA, ;"
Notes:"MedlineChung, J W Dunny, G M eng AI19310/AI/NIAID NIH HHS/ Research Support, U.S. Gov't, P.H.S. 1992/10/01 Proc Natl Acad Sci U S A. 1992 Oct 1; 89(19):9020-4. doi: 10.1073/pnas.89.19.9020"

 
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