PRO40 is a Scaffold protein of the cell wall integrity pathway, linking the MAP kinase module to the upstream activator protein kinase C

  • Mitogen-activated protein kinase (MAPK) pathways are crucial signaling instruments in eukaryotes. Most ascomycetes possess three MAPK modules that are involved in key developmental processes like sexual propagation or pathogenesis. However, the regulation of these modules by adapters or scaffolds is largely unknown. Here, we studied the function of the cell wall integrity (CWI) MAPK module in the model fungus \(\textit {Sordaria macrospora}\). Using a forward genetic approach, we found that sterile mutant pro30 has a mutated \(\it mik1\) gene that encodes the MAPK kinase kinase (MAPKKK) of the proposed CWI pathway. We generated single deletion mutants lacking MAPKKK MIK1, MAPK kinase (MAPKK) MEK1, or MAPK MAK1 and found them all to be sterile, cell fusion-deficient and highly impaired in vegetative growth and cell wall stress response. By searching for MEK1 interaction partners via tandem affinity purification and mass spectrometry, we identified previously characterized developmental protein PRO40 as a MEK1 interaction partner. Although fungal PRO40 homologs have been implicated in diverse developmental processes, their molecular function is currently unknown. Extensive affinity purification, mass spectrometry, and yeast two-hybrid experiments showed that PRO40 is able to bind MIK1, MEK1, and the upstream activator protein kinase C (PKC1). We further found that the PRO40 N-terminal disordered region and the central region encompassing a WW interaction domain are sufficient to govern interaction with MEK1. Most importantly, time- and stress-dependent phosphorylation studies showed that PRO40 is required for MAK1 activity. The sum of our results implies that PRO40 is a scaffold protein for the CWI pathway, linking the MAPK module to the upstream activator PKC1. Our data provide important insights into the mechanistic role of a protein that has been implicated in sexual and asexual development, cell fusion, symbiosis, and pathogenicity in different fungal systems.

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Metadaten
Author:Ines TeichertORCiDGND, Eva Katharina SteffensGND, Nicole SchnaßGND, Benjamin FränzelGND, Christoph KrispGND, Dirk WoltersGND, Ulrich KückORCiDGND
URN:urn:nbn:de:hbz:294-57531
DOI:https://doi.org/10.1371/journal.pgen.1004582
Parent Title (English):PLoS Genetics
Document Type:Article
Language:English
Date of Publication (online):2018/06/26
Date of first Publication:2014/09/04
Publishing Institution:Ruhr-Universität Bochum, Universitätsbibliothek
Tag:Open Access Fonds
Volume:10
Issue:9
First Page:e1004582-1
Last Page:e1004582-17
Note:
Article Processing Charge funded by the Deutsche Forschungsgemeinschaft (DFG) and the Open Access Publication Fund of Ruhr-Universität Bochum.
Note:
PLoS ONE, Bd. 10.2014, H. 9, Artikelnummer e1004582
Institutes/Facilities:Lehrstuhl für Allgemeine und Molekulare Botanik
Dewey Decimal Classification:Naturwissenschaften und Mathematik / Biowissenschaften, Biologie, Biochemie
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