AoStuA, an APSES transcription factor, regulates the conidiation, trap formation, stress resistance and pathogenicity of the nematode-trapping fungus Arthrobotrys oligospora.
Meihua XieYunchuan WangLiyan TangLe YangDuanxu ZhouQing LiXuemei NiuKe-Qin ZhangJin-Kui YangPublished in: Environmental microbiology (2019)
The APSES protein family comprises a conserved class of fungus-specific transcriptional regulators. Some members have been identified in partial ascomycetes. In this study, the APSES protein StuA (AoStuA) of the nematode-trapping fungus Arthrobotrys oligospora was characterized. Compared with the wild-type (WT) strain, three ΔAoStuA mutants grew relatively slowly, displayed a 96% reduction in sporulation capacity and a delay in conidial germination. The reduced sporulation capacity correlated with transcriptional repression of several sporulation-related genes. The mutants were also more sensitive to chemical stressors than the WT strain. Importantly, the mutants were unable to produce mycelial traps for nematode predation. Moreover, peroxisomes and Woronin bodies were abundant in the WT cells but hardly found in the cells of those mutants. The lack of such organelles correlated with transcriptional repression of some genes involved in the biogenesis of peroxisomes and Woronin bodies. The transcript levels of several genes involved in the cAMP/PKA signalling pathway were also significantly reduced in the mutants versus the WT strain, implicating a regulatory role of AoStuA in the transcription of genes involved in the cAMP/PKA signalling pathway that regulates an array of cellular processes and events. In particular, AoStuA is indispensable for A. oligospora trap formation and virulence.
Keyphrases
- transcription factor
- wild type
- induced apoptosis
- cell cycle arrest
- dna binding
- gene expression
- binding protein
- escherichia coli
- bacillus subtilis
- biofilm formation
- pseudomonas aeruginosa
- genome wide identification
- endoplasmic reticulum stress
- oxidative stress
- protein protein
- high throughput
- small molecule
- cell death
- amino acid
- mass spectrometry
- cystic fibrosis
- cell proliferation
- rna seq
- protein kinase
- stress induced