• Medientyp: E-Artikel
  • Titel: The peroxisomal transporter gene ANT1 is regulated by a deviant oleate response element (ORE): characterization of the signal for fatty acid induction
  • Beteiligte: ROTTENSTEINER, Hanspeter; PALMIERI, Luigi; HARTIG, Andreas; HAMILTON, Barbara; RUIS, Helmut; ERDMANN, Ralf; GURVITZ, Aner
  • Erschienen: Portland Press Ltd., 2002
  • Erschienen in: Biochemical Journal
  • Sprache: Englisch
  • DOI: 10.1042/bj20011495
  • ISSN: 0264-6021; 1470-8728
  • Schlagwörter: Cell Biology ; Molecular Biology ; Biochemistry
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  • Beschreibung: <jats:p>Saccharomyces cerevisiae ANT1/YPR128c encodes the peroxisomal adenine nucleotide transporter that provides ATP for intra-peroxisomal activation of medium-chain fatty acids. A lacZ reporter construct comprising the ANT1 promoter was shown to be comparatively more highly expressed in a wild-type strain grown on oleic acid, a long-chain fatty acid, than in pip2Δoaf1Δ mutant cells that are defective in fatty acid induction. The ANT1 promoter was demonstrated to contain a deviant oleate response element (ORE) that could bind the Pip2p-Oaf1p transcription factor and confer activation on a basal CYC1-lacZ reporter gene. Expression of Ant1p as well as other enzymes whose genes are known to be regulated by a canonical ORE was found to be increased in cells grown on lauric acid, a medium-chain fatty acid. We concluded that the signal for induction does not differentiate between long- and medium-chain fatty acids. This signal was independent of β-oxidation or the biogenesis of the peroxisomal compartment where this process occurs, since a pox1Δ strain blocked in the first and rate-limiting step of β-oxidation as well as various pex mutant cells devoid of intact peroxisomes produced sufficient amounts of Pip2p-Oaf1p for binding OREs in vitro and for expressing an ORE-driven reporter gene. The signal's durability was shown to be related to the concentration of fatty acids in the medium, since a pex6Δ strain expressed an ORE-driven reporter gene at high levels for a longer period than did isogenic wild-type cells. Generation of the signal was also independent of protein synthesis, as demonstrated by cycloheximide treatment.</jats:p>
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