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Published on: August 4, 2019
Wide-Ranging Effects of the Yeast Ptc1 Protein Phosphatase Acting Through the MAPK Kinase Mkk1
Laura Tatjer1, Almudena Sacristán-Reviriego2, Carlos Casado1
1Institut de Biotecnologia i Biomedicina and Departament de Bioquímica i Biologia Molecular, Universitat Autònoma de Barcelona, Bellaterra 08193, Barcelona, Spain.
Abstract:
The Saccharomyces cerevisiae type 2C protein phosphatase Ptc1 is required for a wide variety of cellular functions, although only a few cellular targets have been identified. A genetic screen in search of mutations in protein kinase-encoding genes able to suppress multiple phenotypic traits caused by the ptc1 deletion yielded a single gene, MKK1, coding for a MAPK kinase (MAPKK) known to activate the cell-wall integrity (CWI) Slt2 MAPK. In contrast, mutation of the MKK1 paralog, MKK2, had a less significant effect. Deletion of MKK1 abolished the increased phosphorylation of Slt2 induced by the absence of Ptc1 both under basal and CWI pathway stimulatory conditions. We demonstrate that Ptc1 acts at the level of the MAPKKs of the CWI pathway, but only the Mkk1 kinase activity is essential for ptc1 mutants to display high Slt2 activation. We also show that Ptc1 is able to dephosphorylate Mkk1 in vitro. Our results reveal the preeminent role of Mkk1 in signaling through the CWI pathway and strongly suggest that hyperactivation of Slt2 caused by upregulation of Mkk1 is at the basis of most of the phenotypic defects associated with lack of Ptc1 function.
Insights
The protein phosphatase Ptc1 regulates the cell-wall integrity pathway by dephosphorylating Mkk1, a key MAPK kinase. Loss of Ptc1 leads to Mkk1 hyperactivation, causing Slt2 MAPK hyperphosphorylation and cellular defects.
Area of Science:
- Cellular biology
- Molecular genetics
- Signal transduction
Background:
- Saccharomyces cerevisiae type 2C protein phosphatase Ptc1 is crucial for cellular functions, but its targets are not fully understood.
- The cell-wall integrity (CWI) pathway, involving Slt2 MAPK, is vital for yeast survival.
Purpose of the Study:
- To identify the cellular targets of Ptc1 and elucidate its role in regulating the CWI pathway.
- To understand the mechanism behind the phenotypic defects observed in ptc1 deletion mutants.
Main Methods:
- Genetic screening to identify suppressors of ptc1 deletion phenotypes.
- Analysis of Slt2 MAPK phosphorylation levels.
- In vitro dephosphorylation assays.
Main Results:
- A screen identified MKK1, encoding a MAPK kinase (MAPKK), as a suppressor of ptc1 deletion phenotypes.
- Deletion of MKK1 abolished Slt2 hyperphosphorylation in ptc1 mutants.
- Ptc1 directly dephosphorylates Mkk1 in vitro.
Conclusions:
- Ptc1 regulates the CWI pathway by dephosphorylating Mkk1.
- Mkk1 kinase activity is essential for Slt2 hyperactivation in ptc1 mutants.
- Hyperactivation of Mkk1 and subsequent Slt2 hyperphosphorylation underlie the phenotypic defects of ptc1 deletion mutants.
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