Reconstitution of DNA Segregation Driven by Assembly of a Prokaryotic Actin Homolog
- 2 March 2007
- journal article
- other
- Published by American Association for the Advancement of Science (AAAS) in Science
- Vol. 315 (5816) , 1270-1274
- https://doi.org/10.1126/science.1138527
Abstract
Multiple unrelated polymer systems have evolved to partition DNA molecules between daughter cells at division. To better understand polymer-driven DNA segregation, we reconstituted the three-component segregation system of the R1 plasmid from purified components. We found that the ParR/ parC complex can construct a simple bipolar spindle by binding the ends of ParM filaments, inhibiting dynamic instability, and acting as a ratchet permitting incorporation of new monomers and riding on the elongating filament ends. Under steady-state conditions, the dynamic instability of unattached ParM filaments provides the energy required to drive DNA segregation.Keywords
This publication has 16 references indexed in Scilit:
- Actin homolog MreB and RNA polymerase interact and are both required for chromosome segregation in Escherichia coliGenes & Development, 2006
- MreB Actin-Mediated Segregation of a Specific Region of a Bacterial ChromosomeCell, 2005
- Dynamic Instability in a DNA-Segregating Prokaryotic Actin HomologScience, 2004
- Bacterial Mitosis: ParM of Plasmid R1 Moves Plasmid DNA by an Actin-like Insertional Polymerization MechanismMolecular Cell, 2003
- The Polymerization MotorTraffic, 2000
- Three-dimensional structural characterization of centrosomes from early Drosophila embryos.The Journal of cell biology, 1995
- Dynamic instability of microtubules as an efficient way to search in space.Proceedings of the National Academy of Sciences, 1994
- Partitioning of plasmid R1Journal of Molecular Biology, 1986
- Dynamic instability of microtubule growthNature, 1984
- Cell Motility by Labile Association of MoleculesThe Journal of general physiology, 1967