Literature DB >> 1703297

Quantitation of ColE1-encoded replication elements.

M Brenner1, J Tomizawa.   

Abstract

Replication of the Escherichia coli plasmid ColE1 initiates from an RNA primer. This primer is formed by a ColE1 RNA II molecule that remains hybridized to its DNA template in the origin region after transcription. Continued hybridization is inhibited by prior binding to RNA II of another ColE1 transcript, RNA I; and this interaction is regulated by the plasmid-encoded Rom protein. To understand the quantitative aspects of regulation of ColE1 synthesis, we have measured the levels of RNA I, RNA II, and Rom protein in vivo, as well as the half-lives of the RNAs. The intracellular concentrations of RNA I, RNA II, and Rom protein were found to be about 1 microM, 7 nM, and 1 microM, respectively; and the RNAs had half-lives of about 2 min. A simple model derived from these results indicates that the plasmid copy number is little affected by the rate of RNA II synthesis but is strongly dependent on that of RNA I.

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Year:  1991        PMID: 1703297      PMCID: PMC50819          DOI: 10.1073/pnas.88.2.405

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  25 in total

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Journal:  Nucleic Acids Res       Date:  1989-06-12       Impact factor: 16.971

8.  Nucleotide sequence and gene organization of ColE1 DNA.

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Journal:  Proc Natl Acad Sci U S A       Date:  1983-06       Impact factor: 11.205

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Authors:  J Tomizawa; T Som
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  14 in total

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7.  Antisense RNA-mediated transcriptional attenuation occurs faster than stable antisense/target RNA pairing: an in vitro study of plasmid pIP501.

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8.  Growth-rate dependence reveals design principles of plasmid copy number control.

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