4.8 Article

ParB spreading on DNA requires cytidine triphosphate in vitro

Journal

ELIFE
Volume 9, Issue -, Pages -

Publisher

ELIFE SCIENCES PUBLICATIONS LTD
DOI: 10.7554/eLife.53515

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Funding

  1. Biotechnology and Biological Sciences Research Council [BB/P018165/1, BBS/E/J/000PR9791, BBS/E/J/000PR9778]
  2. Royal Society [UF140053, RG150448]
  3. BBSRC [BB/P018165/1, BBS/E/J/000C0683, BBS/E/J/000PR9791] Funding Source: UKRI

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In all living organisms, it is essential to transmit genetic information faithfully to the next generation. The SMC-ParAB-parS system is widely employed for chromosome segregation in bacteria. A DNA-binding protein ParB nucleates on parS sites and must associate with neighboring DNA, a process known as spreading, to enable efficient chromosome segregation. Despite its importance, how the initial few ParB molecules nucleating at parS sites recruit hundreds of further ParB to spread is not fully understood. Here, we reconstitute a parS-dependent ParB spreading event using purified proteins from Caulobacter crescentus and show that CTP is required for spreading. We further show that ParB spreading requires a closed DNA substrate, and a DNA-binding transcriptional regulator can act as a roadblock to attenuate spreading unidirectionally in vitro. Our biochemical reconstitutions recapitulate many observed in vivo properties of ParB and opens up avenues to investigate the interactions between ParB-parS with ParA and SMC.

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