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Published on: November 8, 2006
Modulators of MAPK pathway activity during filamentous growth in Saccharomyces cerevisiae
Atindra N Pujari1, Paul J Cullen1
1Department of Biological Sciences, University at Buffalo, Buffalo, NY 14260, USA.
Abstract:
Mitogen-activated protein kinase (MAPK) pathways control the response to intrinsic and extrinsic stimuli. In the budding yeast Saccharomyces cerevisiae, cells undergo filamentous growth, which is regulated by the fMAPK pathway. To better understand the regulation of the fMAPK pathway, a genetic screen was performed to identify spontaneous mutants with elevated activity of an fMAPK pathway-dependent growth reporter (ste4 FUS1-HIS3). In total, 159 mutants were isolated and analyzed by secondary screens for invasive growth by the plate-washing assay and filament formation by microscopy. Thirty-two mutants were selected for whole-genome sequencing, which identified new alleles in genes encoding known regulators of the fMAPK pathway. These included gain-of-function alleles in STE11, which encodes the MAPKKK, as well as loss-of-function alleles in KSS1, which encodes the MAP kinase, and loss-of-function alleles in RGA1, which encodes a GTPase-activating protein (GAP) for CDC42. New alleles in previously identified pathway modulators were also uncovered in ALY1, AIM44, RCK2, IRA2, REG1, and in genes that regulate protein folding (KAR2), glycosylation (MNN4), and turnover (BLM10). Mutations leading to C-terminal truncations in the transcription factor Ste12p were also uncovered that resulted in elevated reporter activity, identifying an inhibitory domain of the protein from residues 491 to 688. We also find that a diversity of filamentous growth phenotypes can result from combinatorial effects of multiple mutations and by loss of different regulators of the response. The alleles identified here expand the connections surrounding MAPK pathway regulation and reveal new features of proteins that function in the signaling cascade.
Insights
Researchers identified new gene mutations affecting the filamentous growth (fMAPK) pathway in yeast. These findings reveal novel regulators and inhibitory domains, expanding our understanding of MAPK pathway control.
Area of Science:
- Cell Biology
- Molecular Biology
- Genetics
Background:
- Mitogen-activated protein kinase (MAPK) pathways are crucial for cellular responses to various stimuli.
- In Saccharomyces cerevisiae, the filamentous growth (fMAPK) pathway governs cell morphology and invasive growth.
- Understanding the intricate regulation of the fMAPK pathway is essential for deciphering cellular signaling.
Purpose of the Study:
- To identify novel genetic regulators of the fMAPK pathway in yeast.
- To characterize spontaneous mutants exhibiting enhanced fMAPK pathway activity.
- To elucidate the molecular mechanisms underlying filamentous growth control.
Main Methods:
- A genetic screen was employed to isolate mutants with elevated fMAPK pathway activity using a reporter system (ste4 FUS1-HIS3).
- Secondary screens included plate-washing assays for invasive growth and microscopy for filament formation.
- Whole-genome sequencing was performed on selected mutants to identify causative mutations.
Main Results:
- 159 mutants were isolated, with 32 selected for sequencing, revealing new alleles in known fMAPK pathway genes like STE11, KSS1, and RGA1.
- Mutations were identified in genes involved in protein folding (KAR2), glycosylation (MNN4), and turnover (BLM10), expanding pathway connections.
- C-terminal truncations in the transcription factor Ste12p identified an inhibitory domain (residues 491-688), impacting reporter activity.
Conclusions:
- The identified alleles provide new insights into the complex regulation of the MAPK signaling cascade.
- Combinatorial mutations and loss of various regulators contribute to diverse filamentous growth phenotypes.
- This study expands the known network of proteins involved in MAPK pathway signaling and filamentous growth in yeast.
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