Regulation of the bacterial cell cycle by an integrated genetic circuit

Emanuele G. Biondi, Sarah J. Reisinger, Jeffrey M. Skerker, Muhammad Arif, Barrett S. Perchuk, Kathleen R. Ryan and Michael T. Laub ()
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Emanuele G. Biondi: Harvard University
Sarah J. Reisinger: University of California
Jeffrey M. Skerker: Harvard University
Muhammad Arif: Harvard University
Barrett S. Perchuk: Harvard University
Kathleen R. Ryan: University of California
Michael T. Laub: Harvard University

Nature, 2006, vol. 444, issue 7121, 899-904

Abstract: Abstract How bacteria regulate cell cycle progression at a molecular level is a fundamental but poorly understood problem. In Caulobacter crescentus, two-component signal transduction proteins are crucial for cell cycle regulation, but the connectivity of regulators involved has remained elusive and key factors are unidentified. Here we identify ChpT, an essential histidine phosphotransferase that controls the activity of CtrA, the master cell cycle regulator. We show that the essential histidine kinase CckA initiates two phosphorelays, each requiring ChpT, which lead to the phosphorylation and stabilization of CtrA. Downregulation of CckA activity therefore results in the dephosphorylation and degradation of CtrA, which in turn allow the initiation of DNA replication. Furthermore, we show that CtrA triggers its own destruction by promoting cell division and inducing synthesis of the essential regulator DivK, which feeds back to downregulate CckA immediately before S phase. Our results define a single integrated circuit whose components and connectivity can account for the cell cycle oscillations of CtrA in Caulobacter.

Date: 2006
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DOI: 10.1038/nature05321

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