Rolling Circle

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S D Ehrlich - One of the best experts on this subject based on the ideXlab platform.

  • UvrD-dependent replication of Rolling-Circle plasmids in Escherichia coli
    Molecular Microbiology, 2000
    Co-Authors: Claude Bruand, S D Ehrlich
    Abstract:

    The Escherichia coli UvrD helicase (or helicase II) is known for its involvement in DNA repair. We report that UvrD is required for DNA replication of several different Rolling-Circle plasmids in E. coli, whereas its homologue, the Rep helicase, is not. Lack of UvrD helicase does not impair the first step of plasmid replication, nicking of the double-stranded origin by the plasmid initiator protein. However, replication proceeds no further without UvrD. Indeed, the nicked plasmid molecules accumulate to a high level in uvrD mutants. We conclude that UvrD is the replicative helicase of various Rolling-Circle plasmids. This is the first description of a direct implication of UvrD in DNA replication in vivo.

  • Inhibition of a naturally occurring Rolling-Circle replicon in derivatives of the theta-replicating plasmid pIP501
    Molecular Microbiology, 1998
    Co-Authors: Catherine Pujol, Frédéric Chédin, S D Ehrlich, Laurent Jannière
    Abstract:

    The mechanisms ensuring regulation of DNA replication in genomes containing multiple replicons are poorly understood. In this report, we addressed this question by analysing in Bacillus subtilis the replication of a derivative of the promiscuous plasmid pIP501 that carries a Rolling-Circle and a theta replicon. Genetic analyses revealed that the Rolling-Circle replicon is strongly inhibited in the derivative and that inhibition requires three elements involved in theta replication: the replication origin, the initiator RepR protein and strong transcription of the repR gene. Inhibition is, however, independent of DNA synthesis at the theta origin. We conclude that Rolling-Circle inhibition is caused by an inhibitory signal encoded by the theta replicon and propose that the signal is composed, at least, of the RepR protein bound to its cognate origin.

Laurent Jannière - One of the best experts on this subject based on the ideXlab platform.

  • Inhibition of a naturally occurring RollingCircle replicon in derivatives of the theta‐replicating plasmid pIP501
    Molecular Microbiology, 1998
    Co-Authors: Catherine Pujol, Frédéric Chédin, S. Dusko Ehrlich, Laurent Jannière
    Abstract:

    : The mechanisms ensuring regulation of DNA replication in genomes containing multiple replicons are poorly understood. In this report, we addressed this question by analysing in Bacillus subtilis the replication of a derivative of the promiscuous plasmid pIP501 that carries a Rolling-Circle and a theta replicon. Genetic analyses revealed that the Rolling-Circle replicon is strongly inhibited in the derivative and that inhibition requires three elements involved in theta replication: the replication origin, the initiator RepR protein and strong transcription of the repR gene. Inhibition is, however, independent of DNA synthesis at the theta origin. We conclude that Rolling-Circle inhibition is caused by an inhibitory signal encoded by the theta replicon and propose that the signal is composed, at least, of the RepR protein bound to its cognate origin.

  • Inhibition of a naturally occurring Rolling-Circle replicon in derivatives of the theta-replicating plasmid pIP501
    Molecular Microbiology, 1998
    Co-Authors: Catherine Pujol, Frédéric Chédin, S D Ehrlich, Laurent Jannière
    Abstract:

    The mechanisms ensuring regulation of DNA replication in genomes containing multiple replicons are poorly understood. In this report, we addressed this question by analysing in Bacillus subtilis the replication of a derivative of the promiscuous plasmid pIP501 that carries a Rolling-Circle and a theta replicon. Genetic analyses revealed that the Rolling-Circle replicon is strongly inhibited in the derivative and that inhibition requires three elements involved in theta replication: the replication origin, the initiator RepR protein and strong transcription of the repR gene. Inhibition is, however, independent of DNA synthesis at the theta origin. We conclude that Rolling-Circle inhibition is caused by an inhibitory signal encoded by the theta replicon and propose that the signal is composed, at least, of the RepR protein bound to its cognate origin.

Antoine M. Van Oijen - One of the best experts on this subject based on the ideXlab platform.

  • Design of DNA Rolling-Circle templates with controlled fork topology to study mechanisms of DNA replication
    Analytical Biochemistry, 2018
    Co-Authors: Enrico Monachino, Harshad Ghodke, Richard R. Spinks, Ben S. Hoatson, Slobodan Jergic, Zhi-qiang Xu, Nicholas E. Dixon, Antoine M. Van Oijen
    Abstract:

    Rolling-Circle DNA amplification is a powerful tool employed in biotechnology to produce large from small amounts of DNA. This mode of DNA replication proceeds via a DNA topology that resembles a replication fork, thus also providing experimental access to the molecular mechanisms of DNA replication. However, conventional templates do not allow controlled access to multiple fork topologies, which is an important factor in mechanistic studies. Here we present the design and production of a Rolling-Circle substrate with a tunable length of both the gap and the overhang, and we show its application to the bacterial DNA-replication reaction.

  • real time single molecule observation of Rolling Circle dna replication
    Nucleic Acids Research, 2009
    Co-Authors: Nathan A Tanner, Slobodan Jergic, Nicholas E. Dixon, Joseph J Loparo, Samir M Hamdan, Antoine M. Van Oijen
    Abstract:

    We present a simple technique for visualizing replication of individual DNA molecules in real time. By attaching a Rolling-Circle substrate to a TIRF microscope-mounted flow chamber, we are able to monitor the progression of single-DNA synthesis events and accurately measure rates and processivities of single T7 and Escherichia coli replisomes as they replicate DNA. This method allows for rapid and precise characterization of the kinetics of DNA synthesis and the effects of replication inhibitors.

Catherine Pujol - One of the best experts on this subject based on the ideXlab platform.

  • Inhibition of a naturally occurring RollingCircle replicon in derivatives of the theta‐replicating plasmid pIP501
    Molecular Microbiology, 1998
    Co-Authors: Catherine Pujol, Frédéric Chédin, S. Dusko Ehrlich, Laurent Jannière
    Abstract:

    : The mechanisms ensuring regulation of DNA replication in genomes containing multiple replicons are poorly understood. In this report, we addressed this question by analysing in Bacillus subtilis the replication of a derivative of the promiscuous plasmid pIP501 that carries a Rolling-Circle and a theta replicon. Genetic analyses revealed that the Rolling-Circle replicon is strongly inhibited in the derivative and that inhibition requires three elements involved in theta replication: the replication origin, the initiator RepR protein and strong transcription of the repR gene. Inhibition is, however, independent of DNA synthesis at the theta origin. We conclude that Rolling-Circle inhibition is caused by an inhibitory signal encoded by the theta replicon and propose that the signal is composed, at least, of the RepR protein bound to its cognate origin.

  • Inhibition of a naturally occurring Rolling-Circle replicon in derivatives of the theta-replicating plasmid pIP501
    Molecular Microbiology, 1998
    Co-Authors: Catherine Pujol, Frédéric Chédin, S D Ehrlich, Laurent Jannière
    Abstract:

    The mechanisms ensuring regulation of DNA replication in genomes containing multiple replicons are poorly understood. In this report, we addressed this question by analysing in Bacillus subtilis the replication of a derivative of the promiscuous plasmid pIP501 that carries a Rolling-Circle and a theta replicon. Genetic analyses revealed that the Rolling-Circle replicon is strongly inhibited in the derivative and that inhibition requires three elements involved in theta replication: the replication origin, the initiator RepR protein and strong transcription of the repR gene. Inhibition is, however, independent of DNA synthesis at the theta origin. We conclude that Rolling-Circle inhibition is caused by an inhibitory signal encoded by the theta replicon and propose that the signal is composed, at least, of the RepR protein bound to its cognate origin.

Mats Nilsson - One of the best experts on this subject based on the ideXlab platform.