Transcriptional analysis of the response of Neurospora crassa to phytosphingosine reveals links to mitochondrial function
| Autor: | Chaoguang Tian, N. Louise Glass, Ana Castro, Takao Kasuga, Arnaldo Videira, Catarina L. Lemos |
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| Rok vydání: | 2009 |
| Předmět: |
inorganic chemicals
Programmed cell death Transcription Genetic Genes Fungal Mutant Apoptosis Mitochondrion Microbiology Drug Administration Schedule Neurospora crassa fluids and secretions Sphingosine Gene Expression Regulation Fungal Gene expression Gene Electron Transport Complex I biology Gene Expression Profiling Crassa Hydrogen Peroxide equipment and supplies Oxidants biology.organism_classification Mitochondria Gene expression profiling Genes Mitochondrial Biochemistry Genes and Genomes bacteria |
| Zdroj: | Microbiology. 155:3134-3141 |
| ISSN: | 1465-2080 1350-0872 |
| DOI: | 10.1099/mic.0.029710-0 |
| Popis: | Treatment ofNeurospora crassacells with phytosphingosine (PHS) induces programmed cell death (PCD) by an unknown mechanism. To determine the relationship between PHS treatment and PCD, we determined changes in global gene expression levels inN. crassaduring a time-course of PHS treatment. Most genes having differential expression levels compared to untreated samples showed an increase in relative expression level upon PHS exposure. However, genes encoding mitochondrial proteins were highly enriched among ∼100 genes that showed a relative decrease in expression levels after PHS treatment, suggesting that repression of these genes might be related to the death-inducing effects of PHS. Since mutants in respiratory chain complex I are more resistant to both PHS and hydrogen peroxide (H2O2) than the wild-type strain, possibly related to the production of reactive oxygen species, we also compared gene expression profiles of a complex I mutant (nuo14) and wild-type in response to H2O2. Genes with higher expression levels in the mutant, in the presence of H2O2, are also significantly enriched in genes encoding mitochondrial proteins. These data suggest that complex I mutants cope better with drug-induced decrease in expression of genes encoding mitochondrial proteins and may explain their increased resistance to both PHS and H2O2. As a way of identifying new components required for PHS-induced death, we analysed the PHS sensitivity of 24 strains carrying deletions in genes that showed a significant alteration in expression pattern when the wild-type was exposed to the sphingolipid. Two additional mutants showing increased resistance to PHS were identified and both encode predicted mitochondrial proteins, further supporting the role of the mitochondria in PHS-induced PCD. |
| Databáze: | OpenAIRE |
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