151. Mitochondrial ribosomal proteins involved in tellurite resistance in yeast Saccharomyces cerevisiae.
- Author
-
Pontieri P, Hartings H, Di Salvo M, Massardo DR, De Stefano M, Pizzolante G, Romano R, Troisi J, Del Giudice A, Alifano P, and Del Giudice L
- Subjects
- Gene Expression Profiling, Gene Expression Regulation, Fungal drug effects, Microscopy, Electron, Transmission, Mitochondria drug effects, Mitochondria metabolism, Mitochondria ultrastructure, Mitochondrial Proteins genetics, Mutation, Ribosomal Proteins genetics, Ribosomes metabolism, Saccharomyces cerevisiae drug effects, Saccharomyces cerevisiae genetics, Saccharomyces cerevisiae ultrastructure, Saccharomyces cerevisiae Proteins genetics, Mitochondrial Proteins metabolism, Ribosomal Proteins metabolism, Saccharomyces cerevisiae metabolism, Saccharomyces cerevisiae Proteins metabolism, Tellurium toxicity
- Abstract
A considerable body of evidence links together mitochondrial dysfunctions, toxic action of metalloid oxyanions, and system and neurodegenerative disorders. In this study we have used the model yeast Saccharomyces cerevisiae to investigate the genetic determinants associated with tellurite resistance/sensitivity. Nitrosoguanidine-induced K
2 TeO3 -resistant mutants were isolated, and one of these mutants, named Sc57-Te5 R , was characterized. Both random spore analysis and tetrad analysis and growth of heterozygous (TeS /Te5 R ) diploid from Sc57-Te5 R mutant revealed that nuclear and recessive mutation(s) was responsible for the resistance. To get insight into the mechanisms responsible for K2 TeO3 -resistance, RNA microarray analyses were performed with K2 TeO3 -treated and untreated Sc57-Te5 R cells. A total of 372 differentially expressed loci were identified corresponding to 6.37% of the S. cerevisiae transcriptome. Of these, 288 transcripts were up-regulated upon K2 TeO3 treatment. About half of up-regulated transcripts were associated with the following molecular functions: oxidoreductase activity, structural constituent of cell wall, transporter activity. Comparative whole-genome sequencing allowed us to identify nucleotide variants distinguishing Sc57-Te5 R from parental strain Sc57. We detected 15 CDS-inactivating mutations, and found that 3 of them affected genes coding mitochondrial ribosomal proteins (MRPL44 and NAM9) and mitochondrial ribosomal biogenesis (GEP3) pointing out to alteration of mitochondrial ribosome as main determinant of tellurite resistance. more...- Published
- 2018
- Full Text
- View/download PDF