4.7 Article

ParB spreading requires DNA bridging

Journal

GENES & DEVELOPMENT
Volume 28, Issue 11, Pages 1228-1238

Publisher

COLD SPRING HARBOR LAB PRESS, PUBLICATIONS DEPT
DOI: 10.1101/gad.242206.114

Keywords

ParB; Spo0J; single-molecule fluorescence; bacterial chromosome segregation

Funding

  1. National Science Foundation CAREER [MCB-1148818]
  2. National Institute of Health [GM086466, GM073831]
  3. Human Frontier Science Program
  4. National Science Foundation Graduate Research Fellowship
  5. Molecular Biophysics Training Grant
  6. Harvard University, National Institutes of Health NIGMS [5T32 GM008313]
  7. Div Of Molecular and Cellular Bioscience
  8. Direct For Biological Sciences [1148818] Funding Source: National Science Foundation

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The parABS system is a widely employed mechanism for plasmid partitioning and chromosome segregation in bacteria. ParB binds to parS sites on plasmids and chromosomes and associates with broad regions of adjacent DNA, a phenomenon known as spreading. Although essential for ParB function, the mechanism of spreading remains poorly understood. Using single-molecule approaches, we discovered that Bacillus subtilis ParB (Spo0J) is able to trap DNA loops. Point mutants in Spo0J that disrupt DNA bridging are defective in spreading and recruitment of structural maintenance of chromosomes (SMC) condensin complexes in vivo. DNA bridging helps to explain how a limited number of Spo0J molecules per parS site (similar to 20) can spread over many kilobases and suggests a mechanism by which ParB proteins could facilitate the loading of SMC complexes. We show that DNA bridging is a property of diverse ParB homologs, suggesting broad evolutionary conservation.

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