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A peroxisomal glutathione transferase of Saccharomyces cerevisiae is functionally related to sulfur amino acid metabolism

Barreto, L. (författare)
Garcera, A. (författare)
Jansson, Kristina, 1969 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för cell- och molekylärbiologi,Department of Cell and Molecular Biology
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Sunnerhagen, Per, 1959 (författare)
Gothenburg University,Göteborgs universitet,Institutionen för cell- och molekylärbiologi,Department of Cell and Molecular Biology
Herrero, E. (författare)
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 (creator_code:org_t)
2006
2006
Engelska.
Ingår i: Eukaryot Cell. ; 5:10, s. 1748-59
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
Stäng  
  • Saccharomyces cerevisiae cells contain three omega-class glutathione transferases with glutaredoxin activity (Gto1, Gto2, and Gto3), in addition to two glutathione transferases (Gtt1 and Gtt2) not classifiable into standard classes. Gto1 is located at the peroxisomes, where it is targeted through a PTS1-type sequence, whereas Gto2 and Gto3 are in the cytosol. Among the GTO genes, GTO2 shows the strongest induction of expression by agents such as diamide, 1-chloro-2,4-dinitrobenzene, tert-butyl hydroperoxide or cadmium, in a manner that is dependent on transcriptional factors Yap1 and/or Msn2/4. Diamide and 1-chloro-2,4-dinitrobenzene (causing depletion of reduced glutathione) also induce expression of GTO1 over basal levels. Phenotypic analyses with single and multiple mutants in the S. cerevisiae glutathione transferase genes show that, in the absence of Gto1 and the two Gtt proteins, cells display increased sensitivity to cadmium. A gto1-null mutant also shows growth defects on oleic acid-based medium, which is indicative of abnormal peroxisomal functions, and altered expression of genes related to sulfur amino acid metabolism. As a consequence, growth of the gto1 mutant is delayed in growth medium without lysine, serine, or threonine, and the mutant cells have low levels of reduced glutathione. The role of Gto1 at the S. cerevisiae peroxisomes could be related to the redox regulation of the Str3 cystathionine beta-lyase protein. This protein is also located at the peroxisomes in S. cerevisiae, where it is involved in transulfuration of cysteine into homocysteine, and requires a conserved cysteine residue for its biological activity.

Ämnesord

NATURVETENSKAP  -- Biologi -- Biokemi och molekylärbiologi (hsv//swe)
NATURAL SCIENCES  -- Biological Sciences -- Biochemistry and Molecular Biology (hsv//eng)

Nyckelord

Amino Acid Sequence
Amino Acids
Sulfur/biosynthesis/*metabolism
Cytosol/enzymology
Down-Regulation/drug effects
Gene Expression
Gene Expression Regulation
Enzymologic/drug effects/genetics
Gene Expression Regulation
Fungal/drug effects/genetics
Genes
Fungal/genetics
Glucose/pharmacology
Glutathione/metabolism
Glutathione Transferase/chemistry/genetics/*metabolism
Molecular Sequence Data
Mutant Proteins/metabolism
Mutation/genetics
Oleic Acid/pharmacology
Oxidants/pharmacology
Peroxisomes/*enzymology
Phenotype
RNA
Messenger/genetics/metabolism
development
Sequence Alignment
Up-Regulation/drug effects

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Av författaren/redakt...
Barreto, L.
Garcera, A.
Jansson, Kristin ...
Sunnerhagen, Per ...
Herrero, E.
Om ämnet
NATURVETENSKAP
NATURVETENSKAP
och Biologi
och Biokemi och mole ...
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Göteborgs universitet

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