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« Previous Abstract"Transfer origins in the conjugative Enterococcus faecalis plasmids pAD1 and pAM373: identification of the pAD1 nic site, a specific relaxase and a possible TraG-like protein"    Next AbstractVomeronasal Receptors and Signal Transduction in the Vomeronasal Organ of Mammals »

J Bacteriol


Title:Replication of Enterococcus faecalis pheromone-responding plasmid pAD1: location of the minimal replicon and oriV site and RepA involvement in initiation of replication
Author(s):Francia MV; Fujimoto S; Tille P; Weaver KE; Clewell DB;
Address:"Department of Biologic and Materials Sciences, School of Dentistry, University of Michigan, Ann Arbor, MI 48109-1078, USA"
Journal Title:J Bacteriol
Year:2004
Volume:186
Issue:15
Page Number:5003 - 5016
DOI: 10.1128/JB.186.15.5003-5016.2004
ISSN/ISBN:0021-9193 (Print) 1098-5530 (Electronic) 0021-9193 (Linking)
Abstract:"The hemolysin-determining plasmid pAD1 is a member of a widely disseminated family of highly conjugative elements commonly present in clinical isolates of Enterococcus faecalis. The determinants repA, repB, and repC, as well as adjacent iteron sequences, are believed to play important roles in pAD1 replication and maintenance. The repA gene encodes an initiator protein, whereas repB and repC encode proteins related to stability and copy number. The present study focuses specifically on repA and identifies a replication origin (oriV) within a central region of the repA determinant. A small segment of repA carrying oriV was able to support replication in cis of a plasmid vector otherwise unable to replicate, if an intact RepA was supplied in trans. We demonstrate that under conditions in which RepA is expressed from an artificial promoter, a segment of DNA carrying only repA is sufficient for stable replication in E. faecalis. We also show that RepA binds specifically to oriV DNA at several sites containing inverted repeat sequences (i.e., IR-1) and nonspecifically to single-stranded DNA, and related genetic analyses confirm that these sequences play an important role in replication. Finally, we reveal a relationship between the internal structure of RepA and its ability to recognize oriV. An in-frame deletion within repA resulting in loss of 105 nucleotides, including at least part of oriV, did not eliminate the ability of the altered RepA protein to initiate replication using an intact origin provided in trans. The relationship of RepA to other known initiator proteins is also discussed"
Keywords:"Amino Acid Sequence Base Sequence *DNA Helicases *DNA Replication *DNA-Binding Proteins Enterococcus faecalis/drug effects/*genetics *Gene Expression Regulation, Bacterial Humans Molecular Sequence Data Mutation Pheromones/*pharmacology Plasmids/*genetics;"
Notes:"MedlineFrancia, Maria Victoria Fujimoto, Shuhei Tille, Patricia Weaver, Keith E Clewell, Don B eng R01 GM055544/GM/NIGMS NIH HHS/ GM33956/GM/NIGMS NIH HHS/ GM55544/GM/NIGMS NIH HHS/ Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, P.H.S. 2004/07/21 J Bacteriol. 2004 Aug; 186(15):5003-16. doi: 10.1128/JB.186.15.5003-5016.2004"

 
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