CcrZ is a pneumococcal spatiotemporal cell cycle regulator that interacts with FtsZ and controls DNA replication by modulating the activity of DnaA
Author(s)
Gallay, Clement; Sanselicio, Stefano; Anderson, Mary E; Soh, Young Min; Liu, Xue; Stamsås, Gro A; Pelliciari, Simone; van Raaphorst, Renske; Dénéréaz, Julien; Kjos, Morten; Murray, Heath; Gruber, Stephan; Grossman, Alan D; Veening, Jan-Willem; ... Show more Show less
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<jats:title>Abstract</jats:title><jats:p>Most bacteria replicate and segregate their DNA concomitantly while growing, before cell division takes place. How bacteria synchronize these different cell cycle events to ensure faithful chromosome inheritance by daughter cells is poorly understood. Here, we identify Cell Cycle Regulator protein interacting with FtsZ (CcrZ) as a conserved and essential protein in pneumococci and related Firmicutes such as <jats:italic>Bacillus subtilis</jats:italic> and <jats:italic>Staphylococcus aureus</jats:italic>. CcrZ couples cell division with DNA replication by controlling the activity of the master initiator of DNA replication, DnaA. The absence of CcrZ causes mis-timed and reduced initiation of DNA replication, which subsequently results in aberrant cell division. We show that CcrZ from <jats:italic>Streptococcus pneumoniae</jats:italic> interacts directly with the cytoskeleton protein FtsZ, which places CcrZ in the middle of the newborn cell where the DnaA-bound origin is positioned. This work uncovers a mechanism for control of the bacterial cell cycle in which CcrZ controls DnaA activity to ensure that the chromosome is replicated at the right time during the cell cycle.</jats:p>
Date issued
2021Department
Massachusetts Institute of Technology. Department of BiologyJournal
Nature Microbiology
Publisher
Springer Science and Business Media LLC
Citation
Gallay, Clement, Sanselicio, Stefano, Anderson, Mary E, Soh, Young Min, Liu, Xue et al. 2021. "CcrZ is a pneumococcal spatiotemporal cell cycle regulator that interacts with FtsZ and controls DNA replication by modulating the activity of DnaA." Nature Microbiology, 6 (9).
Version: Final published version