4.4 Article

RefZ Facilitates the Switch from Medial to Polar Division during Spore Formation in Bacillus subtilis

Journal

JOURNAL OF BACTERIOLOGY
Volume 194, Issue 17, Pages 4608-4618

Publisher

AMER SOC MICROBIOLOGY
DOI: 10.1128/JB.00378-12

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Funding

  1. National Institutes of Health [GM086466]
  2. Giovanni Armenise-Harvard Foundation
  3. Hellman Family Faculty Fund
  4. Fundacao de Amparo a Pesquisa do Estado de Sao Paulo (FAPESP) [08/58821-1]
  5. Conselho Nacional de Desenvolvimento Cientifico e Tecnologico (CNPq) [478019/2009-2]
  6. David Rockefeller Center for Latin American Studies faculty grants program

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During sporulation, Bacillus subtilis redeploys the division protein FtsZ from midcell to the cell poles, ultimately generating an asymmetric septum. Here, we describe a sporulation-induced protein, RefZ, that facilitates the switch from a medial to a polar FtsZ ring placement. The artificial expression of RefZ during vegetative growth converts FtsZ rings into FtsZ spirals, arcs, and foci, leading to filamentation and lysis. Mutations in FtsZ specifically suppress RefZ-dependent division inhibition, suggesting that RefZ may target FtsZ. During sporulation, cells lacking RefZ are delayed in polar FtsZ ring formation, spending more time in the medial and transition stages of FtsZ ring assembly. A RefZ-green fluorescent protein (GFP) fusion localizes in weak polar foci at the onset of sporulation and as a brighter midcell focus at the time of polar division. RefZ has a TetR DNA binding motif, and point mutations in the putative recognition helix disrupt focus formation and abrogate cell division inhibition. Finally, chromatin immunoprecipitation assays identified sites of RefZ enrichment in the origin region and near the terminus. Collectively, these data support a model in which RefZ helps promote the switch from medial to polar division and is guided by the organization of the chromosome. Models in which RefZ acts as an activator of FtsZ ring assembly near the cell poles or as an inhibitor of the transient medial ring at midcell are discussed.

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