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Regulation of cell reversal frequency in Myxococcus xanthus requires the balanced activity of CheY-like domains in FrzE and FrzZ. | LitMetric

AI Article Synopsis

  • The Frz pathway in Myxococcus xanthus regulates how often the cells reverse direction, which is important for their movement during swarming and forming fruiting bodies.
  • Experiments showed that increased levels of FrzZ slightly raised the levels of its phosphorylation and cell reversals, while overexpressing its kinase, FrzE, completely halted FrzZ phosphorylation.
  • Fluorescence microscopy revealed different localizations for FrzZ and FrzE, suggesting that the response regulator domain of FrzE inhibits its own kinase activity but that FrzZ can positively regulate this interaction, highlighting a complex regulatory relationship within the Frz pathway.

Article Abstract

The Frz pathway of Myxococcus xanthus controls cell reversal frequency to support directional motility during swarming and fruiting body formation. Previously, we showed that phosphorylation of the response regulator FrzZ correlates with reversal frequencies, suggesting that this activity represents the output of the Frz pathway. Here, we tested the effect of different expression levels of FrzZ and its cognate kinase FrzE on M. xanthus motility. FrzZ overexpression caused a slight increase in phosphorylation and reversals. By contrast, FrzE overexpression abolished phosphorylation of FrzZ; this inhibition required the response regulator domain of FrzE. FrzZ phosphorylation was restored when both FrzE and FrzZ were overexpressed together. Our results show that the response regulator domain of FrzE is a negative regulator of FrzE kinase activity. This inhibition can be modulated by FrzZ, which acts as a positive regulator. Interestingly, fluorescence microscopy revealed that FrzZ and FrzE localize differently: FrzE colocalizes with the FrzCD receptor and the nucleoid, while FrzZ shows dispersed and polar localization. However, FrzZ binds tightly to the truncated variant FrzEΔ(CheY) . This indicates that the response regulator domain of FrzE is required for the interaction between FrzE and FrzZ to be transient, providing an unexpected regulatory output to the Frz pathway.

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Source
http://dx.doi.org/10.1111/mmi.13323DOI Listing

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