DksA–DnaJ redox interactions provide a signal for the activation of bacterial RNA polymerase

Ju-Sim Kim, Lin Liu, Liam F. Fitzsimmons, Yang Wang, Matthew A. Crawford, Mauricio Mastrogiovanni, Madia Trujillo, James Karl A. Till, Rafael Radí, Shaodong Dai,

Proceedings of the National Academy of Sciences · 2018 · 47 citations · 37 references

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Abstract

Significance Transcription in Gram-negative bacteria is greatly influenced by the synergistic interactions of DksA and the nucleotide alarmone guanosine tetraphosphate. Our investigations reveal a unique, previously unknown layer of transcriptional regulation that depends on redox-based protein–protein interactions between DksA and the molecular chaperone DnaJ. Tripartite connections between DksA, DnaJ, and guanosine tetraphosphate afford a dynamic range of transcriptional responses to H 2 O 2 concentrations associated with redox signaling or oxidative stress. The redox-based gene regulation dependent on the combined actions of DksA, DnaJ, and guanosine tetraphosphate confers resistance of Salmonella to the antimicrobial activity of the NADPH phagocyte oxidase.

References

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