Intracellular mobility of plasmid DNA is limited by the ParA family of partitioning systems

Summary The highly conserved ParA family of partitioning systems is responsible for positioning DNA and protein complexes in bacteria. In Escherichia coli, plasmids that rely upon these systems are positioned at mid‐cell and are repositioned at the quarter‐cell positions after replication. How they...

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Veröffentlicht in:Molecular microbiology 2008-03, Vol.67 (5), p.935-946
Hauptverfasser: Derman, Alan I., Lim‐Fong, Grace, Pogliano, Joe
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creator Derman, Alan I.
Lim‐Fong, Grace
Pogliano, Joe
description Summary The highly conserved ParA family of partitioning systems is responsible for positioning DNA and protein complexes in bacteria. In Escherichia coli, plasmids that rely upon these systems are positioned at mid‐cell and are repositioned at the quarter‐cell positions after replication. How they remain fixed at these positions throughout the cell cycle is unknown. We use fluorescence recovery after photobleaching and time‐lapse microscopy to measure plasmid mobility in living E. coli cells. We find that a minimalized version of plasmid RK2 that lacks its Par system is highly mobile, that the intact RK2 plasmid is relatively immobile, and that the addition of a Par system to the minimalized RK2 plasmid limits its mobility to that of the intact RK2. Mobility is thus the default state, and Par systems are required not only to position plasmids, but also to hold them at these positions. The intervention of Par systems is required continuously throughout the cell cycle to restrict plasmid movement that would, if unrestricted, subvert the segregation process. Our results reveal an important function for Par systems in plasmid DNA segregation that is likely to be conserved in bacteria.
doi_str_mv 10.1111/j.1365-2958.2007.06066.x
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In Escherichia coli, plasmids that rely upon these systems are positioned at mid‐cell and are repositioned at the quarter‐cell positions after replication. How they remain fixed at these positions throughout the cell cycle is unknown. We use fluorescence recovery after photobleaching and time‐lapse microscopy to measure plasmid mobility in living E. coli cells. We find that a minimalized version of plasmid RK2 that lacks its Par system is highly mobile, that the intact RK2 plasmid is relatively immobile, and that the addition of a Par system to the minimalized RK2 plasmid limits its mobility to that of the intact RK2. Mobility is thus the default state, and Par systems are required not only to position plasmids, but also to hold them at these positions. The intervention of Par systems is required continuously throughout the cell cycle to restrict plasmid movement that would, if unrestricted, subvert the segregation process. 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In Escherichia coli, plasmids that rely upon these systems are positioned at mid‐cell and are repositioned at the quarter‐cell positions after replication. How they remain fixed at these positions throughout the cell cycle is unknown. We use fluorescence recovery after photobleaching and time‐lapse microscopy to measure plasmid mobility in living E. coli cells. We find that a minimalized version of plasmid RK2 that lacks its Par system is highly mobile, that the intact RK2 plasmid is relatively immobile, and that the addition of a Par system to the minimalized RK2 plasmid limits its mobility to that of the intact RK2. Mobility is thus the default state, and Par systems are required not only to position plasmids, but also to hold them at these positions. The intervention of Par systems is required continuously throughout the cell cycle to restrict plasmid movement that would, if unrestricted, subvert the segregation process. Our results reveal an important function for Par systems in plasmid DNA segregation that is likely to be conserved in bacteria.</description><subject>Bacterial Proteins - genetics</subject><subject>Bacterial Proteins - metabolism</subject><subject>Bacteriology</subject><subject>Biological and medical sciences</subject><subject>Cell cycle</subject><subject>Cells</subject><subject>DNA Replication</subject><subject>E coli</subject><subject>Electroporation</subject><subject>Escherichia coli - cytology</subject><subject>Escherichia coli - genetics</subject><subject>Escherichia coli Proteins - genetics</subject><subject>Escherichia coli Proteins - metabolism</subject><subject>Fluorescence Recovery After Photobleaching</subject><subject>Fundamental and applied biological sciences. 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In Escherichia coli, plasmids that rely upon these systems are positioned at mid‐cell and are repositioned at the quarter‐cell positions after replication. How they remain fixed at these positions throughout the cell cycle is unknown. We use fluorescence recovery after photobleaching and time‐lapse microscopy to measure plasmid mobility in living E. coli cells. We find that a minimalized version of plasmid RK2 that lacks its Par system is highly mobile, that the intact RK2 plasmid is relatively immobile, and that the addition of a Par system to the minimalized RK2 plasmid limits its mobility to that of the intact RK2. Mobility is thus the default state, and Par systems are required not only to position plasmids, but also to hold them at these positions. The intervention of Par systems is required continuously throughout the cell cycle to restrict plasmid movement that would, if unrestricted, subvert the segregation process. 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subjects Bacterial Proteins - genetics
Bacterial Proteins - metabolism
Bacteriology
Biological and medical sciences
Cell cycle
Cells
DNA Replication
E coli
Electroporation
Escherichia coli - cytology
Escherichia coli - genetics
Escherichia coli Proteins - genetics
Escherichia coli Proteins - metabolism
Fluorescence Recovery After Photobleaching
Fundamental and applied biological sciences. Psychology
Growth, nutrition, cell differenciation
Intracellular Space - metabolism
Microbiology
Plasmids
Recombinant Fusion Proteins - genetics
Recombinant Fusion Proteins - metabolism
title Intracellular mobility of plasmid DNA is limited by the ParA family of partitioning systems
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