Literature DB >> 11743008

Origin pairing ('handcuffing') as a mode of negative control of P1 plasmid copy number.

K Park1, E Han, J Paulsson, D K Chattoraj.   

Abstract

In one family of bacterial plasmids, multiple initiator binding sites, called iterons, are used for initiation of plasmid replication as well as for the control of plasmid copy number. Iterons can also pair in vitro via the bound initiators. This pairing, called handcuffing, has been suggested to cause steric hindrance to initiation and thereby control the copy number. To test this hypothesis, we have compared copy numbers of isogenic miniP1 plasmid monomer and dimer. The dimer copy number was only one-quarter that of the monomer, suggesting that the higher local concentration of origins in the dimer facilitated their pairing. Physical evidence consistent with iteron-mediated pairing of origins preferentially in the dimer was obtained in vivo. Thus, origin handcuffing can be a mechanism to control P1 plasmid replication.

Mesh:

Year:  2001        PMID: 11743008      PMCID: PMC125786          DOI: 10.1093/emboj/20.24.7323

Source DB:  PubMed          Journal:  EMBO J        ISSN: 0261-4189            Impact factor:   11.598


  48 in total

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Authors:  B J Brewer; W L Fangman
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Authors:  S Sozhamannan; D K Chattoraj
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Authors:  T C Hodgman; H Griffiths; D K Summers
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  16 in total

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5.  Plasmid Characteristics Modulate the Propensity of Gene Exchange in Bacterial Vesicles.

Authors:  Frances Tran; James Q Boedicker
Journal:  J Bacteriol       Date:  2019-03-13       Impact factor: 3.490

6.  Evolutionary competitiveness of two natural variants of the IncQ-like plasmids, pRAS3.1 and pRAS3.2.

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7.  Cluster of DnaA boxes involved in regulation of Streptomyces chromosome replication: from in silico to in vivo studies.

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8.  Mechanism of origin activation by monomers of R6K-encoded pi protein.

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Review 9.  Replication and conjugative mobilization of broad host-range IncQ plasmids.

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10.  Molecular handcuffing of the relaxosome at the origin of conjugative transfer of the plasmid R1162.

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Journal:  Nucleic Acids Res       Date:  2003-08-15       Impact factor: 16.971

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