23 research outputs found
A new dominant peroxiredoxin allele identified by whole-genome re-sequencing of random mutagenized yeast causes oxidant-resistance and premature aging
The
combination of functional genomics with next generation sequencing
facilitates new experimental strategies for addressing complex biological
phenomena. Here, we report the identification of a gain-of-function allele
of peroxiredoxin (thioredoxin peroxidase, Tsa1p) via whole-genome
re-sequencing of a dominantSaccharomyces cerevisiae mutant obtained
by chemical mutagenesis. Yeast strain K6001, a screening system for
lifespan phenotypes, was treated with ethyl methanesulfonate (EMS). We
isolated an oxidative stress-resistant mutant (B7) which transmitted this
phenotype in a background-independent, monogenic and dominant way. By
massive parallel pyrosequencing, we generated an 38.8 fold whole-genome
coverage of the strains, which differed in 12,482 positions from the
reference (S288c) genome. Via a subtraction strategy, we could narrow this
number to 13 total and 4 missense nucleotide variations that were specific for
the mutant. Via expression in wild type backgrounds, we show that one of
these mutations, exchanging a residue in the peroxiredoxin Tsa1p, was
responsible for the mutant phenotype causing background-independent
dominant oxidative stress-resistance. These effects were not provoked by
altered Tsa1p levels, nor could they be simulated by deletion,
haploinsufficiency or over-expression of the wild-type allele. Furthermore,
via both a mother-enrichment technique and a micromanipulation assay, we
found a robust premature aging phenotype of this oxidant-resistant strain.
Thus, TSA1-B7 encodes for a novel dominant form of peroxiredoxin,
and establishes a new connection between oxidative stress and aging. In
addition, this study shows that the re-sequencing of entire genomes is
becoming a promising alternative for the identification of functional
alleles in approaches of classic molecular genetics
Saccharomyces cerevisiae genes involved in survival of heat shock
The heat-shock response in cells, involving increased transcription of a specific set of genes in response to a sudden increase in temperature, is a highly conserved biological response occurring in all organisms. Despite considerable attention to the processes activated during heat shock, less is known about the role of genes in survival of a sudden temperature increase. Saccharomyces cerevisiae genes involved in the maintenance of heat-shock resistance in exponential and stationary phase were identified by screening the homozygous diploid deletants in nonessential genes and the heterozygous diploid mutants in essential genes for survival after a sudden shift in temperature from 30 to 50. More than a thousand genes were identified that led to altered sensitivity to heat shock, with little overlap between them and those previously identified to affect thermotolerance. There was also little overlap with genes that are activated or repressed during heat-shock, with only 5% of them regulated by the heat-shock transcription factor. The target of rapamycin and protein kinase A pathways, lipid metabolism, vacuolar H+-ATPase, vacuolar protein sorting, and mitochondrial genome maintenance/translation were critical to maintenance of resistance. Mutants affected in l-tryptophan metabolism were heat-shock resistant in both growth phases; those affected in cytoplasmic ribosome biogenesis and DNA double-strand break repair were resistant in stationary phase, and in mRNA catabolic processes in exponential phase. Mutations affecting mitochondrial genome maintenance were highly represented in sensitive mutants. The cell division transcription factor Swi6p and Hac1p involved in the unfolded protein response also play roles in maintenance of heat-shock resistance
Retinoic acid-loading of the major birch pollen allergen Bet v 1 may improve specific allergen immunotherapy: in silico, in vitro and in vivo data in BALB/c mice
Retinoic acid-loading of the major birch pollen allergen Bet v 1 may improve specific allergen immunotherapy: In silico, in vitro and in vivo data in BALB/c mice
5 Pág.This work was supported by the SFB F4606-B28 grant of the Austrian Science Fund FWF.Peer reviewe
Slow Growth and Increased Spontaneous Mutation Frequency in Respiratory Deficient afo1- Yeast Suppressed by a Dominant Mutation in ATP3
A yeast deletion mutation in the nuclear-encoded gene, AFO1, which codes for a mitochondrial ribosomal protein, led to slow growth on glucose, the inability to grow on glycerol or ethanol, and loss of mitochondrial DNA and respiration. We noticed that afo1- yeast readily obtains secondary mutations that suppress aspects of this phenotype, including its growth defect. We characterized and identified a dominant missense suppressor mutation in the ATP3 gene. Comparing isogenic slowly growing rho-zero and rapidly growing suppressed afo1- strains under carefully controlled fermentation conditions showed that energy charge was not significantly different between strains and was not causal for the observed growth properties. Surprisingly, in a wild-type background, the dominant suppressor allele of ATP3 still allowed respiratory growth but increased the petite frequency. Similarly, a slow-growing respiratory deficient afo1- strain displayed an about twofold increase in spontaneous frequency of point mutations (comparable to the rho-zero strain) while the suppressed strain showed mutation frequency comparable to the repiratory-competent WT strain. We conclude, that phenotypes that result from afo1- are mostly explained by rapidly emerging mutations that compensate for the slow growth that typically follows respiratory deficiency
Involvement of oxidative stress response genes in redox homeostasis, the level of reactive oxygen species, and ageing in Saccharomyces cerevisiae
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