Prokaryotic DNA segregation by an actin-like filament
Open Access
- 17 June 2002
- journal article
- research article
- Published by Springer Nature in The EMBO Journal
- Vol. 21 (12) , 3119-3127
- https://doi.org/10.1093/emboj/cdf320
Abstract
The mechanisms responsible for prokaryotic DNA segregation are largely unknown. The partitioning locus ( par ) encoded by the Escherichia coli plasmid R1 actively segregates its replicon to daughter cells. We show here that the ParM ATPase encoded by par forms dynamic actin‐like filaments with properties expected for a force‐generating protein. Filament formation depended on the other components encoded by par , ParR and the centromere‐like parC region to which ParR binds. Mutants defective in ParM ATPase exhibited hyperfilamentation and did not support plasmid partitioning. ParM polymerization was ATP dependent, and depolymerization of ParM filaments required nucleotide hydrolysis. Our in vivo and in vitro results indicate that ParM polymerization generates the force required for directional movement of plasmids to opposite cell poles and that the ParR– parC complex functions as a nucleation point for ParM polymerization. Hence, we provide evidence for a simple prokaryotic analogue of the eukaryotic mitotic spindle apparatus.Keywords
This publication has 44 references indexed in Scilit:
- Replication-Dependent Recruitment of the β-Subunit of DNA Polymerase III from Cytosolic Spaces to Replication Forks in Escherichia coliJournal of Bacteriology, 2002
- The extrusion-capture model for chromosome partitioning in bacteriaGenes & Development, 2001
- Escherichia coli contains a DNA replication compartment in the cell centerBiochimie, 1999
- An atomic model of crystalline actin tubes: combining electron microscopy with X-ray crystallographyJournal of Molecular Biology, 1998
- Partitioning of plasmid R1. The ParM protein exhibits ATPase activity and interacts with the centromere-like ParR-parC complexJournal of Molecular Biology, 1997
- Partitioning of plasmid R1 The parA operon is autoregulated by parR and its transcription is highly stimulated by a downstream activating elementJournal of Molecular Biology, 1994
- Partitioning of plasmid R1 Ten direct repeats flanking the parA promoter constitute a centromere-like partition site parC, that expresses incompatibilityJournal of Molecular Biology, 1994
- Partitioning of plasmid R1Journal of Molecular Biology, 1986
- Improved M13 phage cloning vectors and host strains: nucleotide sequences of the M13mpl8 and pUC19 vectorsGene, 1985
- Analysis of gene control signals by DNA fusion and cloning in Escherichia coliJournal of Molecular Biology, 1980