Fission yeast 26S proteasome mutants are multi-drug resistant due to stabilization of the Pap1transcription factor.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

  • Mary Penney
  • Itaru Samejima
  • Caroline Wilkinson
  • Christopher McInerny
  • Søs Mathiassen
  • Mairi Wallace
  • Takashi Toda
  • Hartmann-Petersen, Rasmus
  • Colin Gordon
Here we report the result of a genetic screen for mutants resistant to the microtubule poison methyl benzimidazol-2-yl carbamate (MBC) that were also temperature sensitive for growth. In total the isolated mutants were distributed in ten complementation groups. Cloning experiments revealed that most of the mutants were in essential genes encoding various 26S proteasome subunits. We found that the proteasome mutants are multi-drug resistant due to stabilization of the stress-activated transcription factor Pap1. We show that the ubiquitylation and ultimately the degradation of Pap1 depend on the Rhp6/Ubc2 E2 ubiquitin conjugating enzyme and the Ubr1 E3 ubiquitin-protein ligase. Accordingly, mutants lacking Rhp6 or Ubr1 display drug-resistant phenotypes.
OriginalsprogEngelsk
TidsskriftP L o S One
Vol/bind7
Udgave nummer11
Antal sider8
ISSN1932-6203
DOI
StatusUdgivet - 2012

Bibliografisk note

Artikel ID: e50796

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