Evidence map›Paper›PMID 25188365›Full record

ArticlePLoS genetics2014

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

Ines Teichert, Eva Katharina Steffens, Nicole Schnaß, Benjamin Fränzel, Christoph Krisp, Dirk A Wolters, Ulrich Kück

Open access · goldAbstract read
In one paragraph

Article in PLoS genetics, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 35 papers.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed
3.4field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 69 citations in OpenAlex.

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  9. Journal of fungi (Basel, Switzerland) · 2022
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  11. A dialogue-like cell communication mechanism is conserved in filamentous ascomycete fungi and mediates interspecies interactions.Proceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  12. Genetic Networks That Govern Sexual Reproduction in the Pezizomycotina.Microbiology and molecular biology reviews : MMBR · 2021
    Review
  13. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Ines TeichertDepartment for General and Molecular Botany, Ruhr-University Bochum, Bochum, Germany.
Eva Katharina SteffensDepartment for General and Molecular Botany, Ruhr-University Bochum, Bochum, Germany.
Nicole SchnaßDepartment for General and Molecular Botany, Ruhr-University Bochum, Bochum, Germany.
Benjamin FränzelDepartment of Analytical Chemistry, Ruhr-University Bochum, Bochum, Germany.
Christoph KrispDepartment of Analytical Chemistry, Ruhr-University Bochum, Bochum, Germany.
Dirk A WoltersDepartment of Analytical Chemistry, Ruhr-University Bochum, Bochum, Germany.
Ulrich KückDepartment for General and Molecular Botany, Ruhr-University Bochum, Bochum, Germany.
Ruhr University Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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 Sordaria macrospora. Using a forward genetic approach, we found that sterile mutant pro30 has a mutated 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.

Indexed as

Cell WallFungal ProteinsMAP Kinase Kinase KinasesMAP Kinase Signaling SystemMitogen-Activated Protein Kinase KinasesMitogen-Activated Protein KinasesPhosphorylationProtein Kinase CSaccharomyces cerevisiaeSaccharomyces cerevisiae ProteinsSignal TransductionFungal ProteinsMAP Kinase Kinase KinasesMitogen-Activated Protein Kinase KinasesMitogen-Activated Protein KinasesProtein Kinase CSaccharomyces cerevisiae Proteins

Identifiers

PMID25188365
PMCPMC4154660
OpenAlexW2045032814

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.