The copper efflux regulator CueR is subject to ATP-dependent proteolysis in \(\textit {Escherichia coli}\)

  • The trace element copper serves as cofactor for many enzymes but is toxic at elevated concentrations. In bacteria, the intracellular copper level is maintained by copper efflux systems including the Cue system controlled by the transcription factor CueR. CueR, a member of the MerR family, forms homodimers, and binds monovalent copper ions with high affinity. It activates transcription of the copper tolerance genes \(\it copA\) and \(\it cueO\) via a conserved DNA-distortion mechanism. The mechanism how CueR-induced transcription is turned off is not fully understood. Here, we report that \(\textit {Escherichia coli}\) CueR is prone to proteolysis by the \(AAA^{+}\) proteases Lon, ClpXP, and ClpAP. Using a set of CueR variants, we show that CueR degradation is not altered by mutations affecting copper binding, dimerization or DNA binding of CueR, but requires an accessible C terminus. Except for a twofold stabilization shortly after a copper pulse, proteolysis of CueR is largely copper-independent. Our results suggest that ATP-dependent proteolysis contributes to copper homeostasis in \(\textit {E. coli}\) by turnover of CueR, probably to allow steady monitoring of changes of the intracellular copper level and shut-off of CueR-dependent transcription.

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Metadaten
Author:Lisa-Marie BittnerGND, Alexander KrausGND, Sina SchäkermannORCiDGND, Franz NarberhausORCiDGND
URN:urn:nbn:de:hbz:294-70376
DOI:https://doi.org/10.3389/fmolb.2017.00009
Parent Title (English):Frontiers in molecular biosciences
Publisher:Frontiers
Place of publication:Lausanne
Document Type:Article
Language:English
Date of Publication (online):2020/03/05
Date of first Publication:2017/02/28
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:AAA+ proteases; ClpAP; ClpXP; CueR; Lon; MerR family; copper homeostasis; proteolysis
Volume:4
First Page:9-1
Last Page:9-13
Institutes/Facilities:Lehrstuhl für Biologie der Mikroorganismen
Research Department Plasmas with Complex Interactions
Protein Research Department
Research Department Solvation Science
open_access (DINI-Set):open_access
faculties:Fakultät für Biologie und Biotechnologie
Licence (English):License LogoCreative Commons - CC BY 4.0 - Attribution 4.0 International