Skip to main content
. 2021 Aug 9;6(9):1175–1187. doi: 10.1038/s41564-021-00949-1

Fig. 6. Spatiotemporal localization of CcrZ via FtsZ ensures proper timing of DNA replication in S. pneumoniae.

Fig. 6

a, Microscopy of the origin of replication (yellow), replication fork (cyan) and CcrZ (red) in live S. pneumoniae wild-type background cells. Scale bar, 1 µm. b, DnaN, oriC and CcrZ localizations grouped by cell area (µm2) in five equally sized groups. Analysed from snapshots of exponentially growing cells. c, Single-cell kymographs of DnaN, CcrZ and oriC localizations in a 2:30 minute interval time-lapse video. d, Tracked DnaN, oriC and CcrZ over time in a single cell. Top: overlay of fluorescence, cell outline and phase-contrast of the cell displayed in panel c. Bottom: fluorescence localization on the length axis of the same single cell over time. e, Model for spatiotemporal control of replication by CcrZ. In S. pneumoniae, CcrZ is brought to the middle of the cell where the DnaA-bound origin of replication is already positioned. CcrZ then stimulates DnaA to trigger DNA replication by an as yet unknown activity, possibly involving a phosphor-transfer event. Whereas the precise regulation and localization of CcrZ seems diverse between different organisms, CcrZ’s activity to stimulate DNA replication is conserved, at least in S. pneumoniae, S. aureus and B. subtilis.

Source data