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Gene expression profiling in the rmt1∆, rmt5∆, rmt1∆rmt5∆ and gis2∆ mutants of Cryptococcus neoformans.

ABSTRACT: This study aimed to investigate transcriptomic changes in Cryptococcus neoformans mutants. We report transcriptome wide remodeling in the rmt1∆, rmt5∆, rmt1∆rmt5∆ and gis2∆ mutants compared to wildtpe cells. We also report transcriptome remodeling following fluconazole treatment in wildtype and gis2∆ cells.

ORGANISM(S): Cryptococcus neoformans

PROVIDER: GSE193199 | GEO | 2026/04/11

REPOSITORIES: GEO

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Project description:The yeast Cryptococcus neoformans is an opportunistic human pathogen capable of surviving within various environmental conditions. The repertoire of antifungal agents effective in treating cryptococcal infection is limited, necessitating the identification of alternative treatment strategies. Nonsense-mediated decay (NMD) is an RNA decay mechanism that serves as a post-transcriptional regulator of gene expression. While the absence of NMD in C. neoformans sensitizes cells to the antifungal fluconazole, the mechanism underlying this sensitivity and role of NMD in C. neoformans biology remained unexplored. Using phenotypic analysis and RNA-sequencing analysis, we identify basal dysregulation of thermal- and nutrient-adaptive genes and demonstrate temperature- and/or nutrient-dependent phenotypic suppression of upf1Δ phenotypes, including fluconazole sensitivity and resistance to rapamycin. We determine rapamycin co-treatment also suppresses the upf1Δ fluconazole sensitivity, implicating dysregulation of Tor signaling in phenotypic outcomes when NMD is absent. We then investigate Tor-sensitive signaling in the upf1Δ mutant, finding inhibition of cell wall integrity (CWI) signaling and hyperactivation of the kinase Gcn2, both of which returned to wildtype-like levels by either rapamycin treatment, nutrient limitation, or constitutive thermal stress. These results indicated NMD is required for appropriate regulation of Tor signaling in unstressed conditions and suggested upf1Δ phenotypes are driven in part by Tor hyperactivation. A phenotypic screen of mutants lacking Tor regulators revealed that deletion of the Tor-suppressing IML1 gene recapitulates upf1Δ phenotypes and signaling defects, consistent with Tor hyperactivation. Taken together, our results suggest NMD participates in the regulation of Tor signaling in C. neoformans. Future work will investigate how specific targets of NMD impact Tor signaling and promote fluconazole sensitivity in C. neoformans.

Dataset Information

Gene expression profiling in the rmt1∆, rmt5∆, rmt1∆rmt5∆ and gis2∆ mutants of Cryptococcus neoformans.

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