Abstract

SummaryPrecise cell division in coordination with DNA replication and segregation is of utmost importance for all organisms. The earliest stage of cell division is the assembly of a division protein FtsZ into a ring, known as the Z ring, at midcell. What still eludes us, however, is how bacteria precisely position the Z ring at midcell. Work in B. subtilis over the last two decades has identified a link between the early stages of DNA replication and cell division. A recent model proposed that the progression of the early stages of DNA replication leads to an increased ability for the Z ring to form at midcell. This model arose through studies examining Z ring position in mutants blocked at different steps of the early stages of DNA replication. Here, we show that this model is unlikely to be correct and the mutants previously studied generate nucleoids with different capacity for blocking midcell Z ring assembly. Importantly, our data suggest that two proteins of the widespread ParB family, Noc and Spo0J are required to prevent Z ring assembly over the bacterial nucleoid and help fine tune the assembly of the Z ring at midcell during the cell cycle.

Highlights

  • Proper division site selection is essential for bacterial cell propagation and survival

  • Work in B. subtilis over the last two decades has identified a link between the early stages of DNA replication and cell division

  • A recent model proposed that the progression of the early stages of DNA replication leads to an increased ability for the Z ring to form at midcell

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Summary

Introduction

Proper division site selection is essential for bacterial cell propagation and survival. In bacteria such as Escherichia coli and Bacillus subtilis, cell division is instigated by the polymerisation of the highly conserved tubulin-like protein, FtsZ, into a cytokinetic Z ring at the centre of the cell, between segregated chromosomes (Haeusser and Margolin, 2016; Hajduk et al, 2016). Noc is only essential when DNA replication or segregation is perturbed, to prevent guillotining of the chromosome by the division machinery (Wu and Errington, 2004; Bernhardt and de Boer, 2005)

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