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cAMP-independent signal pathways stimulate hyphal morphogenesis inCandida albicans
- Source :
- Molecular Microbiology. 103:764-779
- Publication Year :
- 2016
- Publisher :
- Wiley, 2016.
-
Abstract
- Summary The fungal pathogen Candida albicans can transition from budding to hyphal growth, which promotes biofilm formation and invasive growth into tissues. Stimulation of adenylyl cyclase to form cAMP induces hyphal morphogenesis. The failure of cells lacking adenylyl cyclase (cyr1Δ) to form hyphae has suggested that cAMP signaling is essential for hyphal growth. However, cyr1Δ mutants also grow slowly and have defects in morphogenesis, making it unclear whether hyphal inducers must stimulate cAMP, or if normal basal levels of cAMP are required to maintain cellular health needed for hyphal growth. Interestingly, supplementation of cyr1Δ cells with low levels of cAMP enabled them to form hyphae in response to the inducer N-acetylglucosamine (GlcNAc), suggesting that a basal level of cAMP is sufficient for stimulation. Furthermore, we isolated faster-growing cyr1Δ pseudorevertant strains that can be induced to form hyphae even though they lack cAMP. The pseudorevertant strains were not induced by CO2, consistent with reports that CO2 directly stimulates adenylyl cyclase. Mutational analysis showed that induction of hyphae in a pseudorevertant strain was independent of RAS1, but was dependent on the EFG1 transcription factor that acts downstream of protein kinase A. Thus, cAMP-independent signals contribute to the induction of hyphal responses.
- Subjects :
- 0301 basic medicine
Hyphal growth
Hypha
fungi
Mutant
Morphogenesis
Biology
biology.organism_classification
Microbiology
Cell biology
Adenylyl cyclase
03 medical and health sciences
chemistry.chemical_compound
030104 developmental biology
chemistry
Protein kinase A
Candida albicans
Molecular Biology
Transcription factor
Subjects
Details
- ISSN :
- 0950382X
- Volume :
- 103
- Database :
- OpenAIRE
- Journal :
- Molecular Microbiology
- Accession number :
- edsair.doi...........4fcd2c831994bb13a87edc42d02b95e0
- Full Text :
- https://doi.org/10.1111/mmi.13588