Precise timing of transcription by c-di-GMP coordinates cell cycle and morphogenesis in Caulobacter.
Andreas KaczmarczykAntje M HempelChristoph von ArxRaphael BöhmBadri Nath DubeyJutta NesperTilman SchirmerSebastian HillerUrs JenalPublished in: Nature communications (2020)
Bacteria adapt their growth rate to their metabolic status and environmental conditions by modulating the length of their G1 period. Here we demonstrate that a gradual increase in the concentration of the second messenger c-di-GMP determines precise gene expression during G1/S transition in Caulobacter crescentus. We show that c-di-GMP stimulates the kinase ShkA by binding to its central pseudo-receiver domain, activates the TacA transcription factor, and initiates a G1/S-specific transcription program leading to cell morphogenesis and S-phase entry. Activation of the ShkA-dependent genetic program causes c-di-GMP to reach peak levels, which triggers S-phase entry and promotes proteolysis of ShkA and TacA. Thus, a gradual increase of c-di-GMP results in precise control of ShkA-TacA activity, enabling G1/S-specific gene expression that coordinates cell cycle and morphogenesis.
Keyphrases
- biofilm formation
- cell cycle
- gene expression
- pseudomonas aeruginosa
- transcription factor
- staphylococcus aureus
- candida albicans
- cell proliferation
- escherichia coli
- dna methylation
- quality improvement
- cystic fibrosis
- single cell
- risk assessment
- genome wide
- stem cells
- dna binding
- human health
- protein kinase
- tyrosine kinase
- climate change