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Mutations in the essential genes SUP45 and SUP35, encoding yeast translation termination factors eRF1 and eRF3, respectively, lead to a wide range of phenotypes and affect various cell processes. In this work, we show that nonsense and missense mutations in the SUP45, but not the SUP35, gene abolish diploid pseudohyphal and haploid invasive growth. Missense mutations that change phosphorylation sites of Sup45 protein do not affect the ability of yeast strains to form pseudohyphae. Deletion of the C-terminal part of eRF1 did not lead to impairment of filamentation. We show a correlation between the filamentation defect and the budding pattern in sup45 strains. Inhibition of translation with specific antibiotics causes a significant reduction in pseudohyphal growth in the wild-type strain, suggesting a strong correlation between translation and the ability for filamentous growth. Partial restoration of pseudohyphal growth by addition of exogenous cAMP assumes that sup45 mutants are defective in the cAMP-dependent pathway that control filament formation.
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http://dx.doi.org/10.1093/femsyr/fov033 | DOI Listing |
ACS Infect Dis
July 2025
Molecular Mycology Laboratory, Molecular Biology and Genetics Unit, Jawaharlal Nehru Centre for Advanced Scientific Research, Jakkur, Bengaluru 560064, India.
is an opportunistic pathogen associated with healthy humans. It is the major causative agent for superficial and invasive candidiasis in immunocompromised individuals globally. Lack of awareness toward fungal infections, poor disease management, and increasing drug resistance have contributed to the burden of -associated diseases.
View Article and Find Full Text PDFProc Natl Acad Sci U S A
June 2025
The Novo Nordisk Foundation Center for Biosustainability, Technical University of Denmark, Kgs. Lyngby DK-2800, Denmark.
The challenge of accurately predicting which genetic alternations lead to the desired phenotype necessitates high-throughput metabolic engineering approaches where numerous hypotheses can be tested simultaneously. We describe the CRISPR-Cas9-based method TUNE that enables high-throughput tuning of gene expression in the common industrial yeast . The method is based on replacing the promoters of the target genes with native promoters of varying strengths or removing the promoters entirely.
View Article and Find Full Text PDFFEMS Yeast Res
January 2025
Department of Biological Chemistry, The Institute of Life Science, The Hebrew University of Jerusalem, Jerusalem 91904, Israel.
Most laboratory strains of the yeast Saccharomyces cerevisiae are incapable of invading agar, to form large colonies (mats), and to develop filament-like structures (pseudohyphae). A prominent strain that manifests these morphologies is ∑1278b. While induced transcription of the FLO11 gene is critical for executing invasive growth, mat formation, and pseudohyphal growth, downregulation of the 'general stress response' also seems to be required.
View Article and Find Full Text PDFJ Dent
June 2025
Clinic of General, Special Care and Geriatric Dentistry, Center for Dental Medicine, University of Zurich, Zurich, Switzerland; Honorary Professor, Center of Excellence in Precision Medicine and Digital Health, Center of Excellance in Genomics and Precision Dentistry, Geriatric Dentistry and Special
Objective: This study assessed the biofilm formation of C. albicans on milled and 3D-printed denture resin surfaces and compared it to a control group of conventional heat-polymerized polymethylmethacrylate (PMMA) resin group.
Methods: Three groups of denture resin samples (n = 27) were fabricated: milled (Ivotion, Ivoclar Vivadent), 3D-printed (Saremco Print Denturetec), and heat-polymerized PMMA controls.
Mycobiology
February 2025
Department of Wellness Bio Industry, Gangneung-Wonju National University, Gangneung, Republic of Korea.
The ability of to switch among yeast, hyphal, and pseudohyphal forms underlies its adaptability and pathogenicity. While cAMP-dependent signaling has long been considered central to hyphal growth, recent multi-omics studies show that cAMP-independent mechanisms also drive morphological changes. Basal PKA activity, cyclin-dependent kinases (e.
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