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Induction of protein aggregation and starvation response by tRNA modification defects.

Abstract
Posttranscriptional modifications of anticodon loops contribute to the decoding efficiency of tRNAs by supporting codon recognition and loop stability. Consistently, strong synthetic growth defects are observed in yeast strains simultaneously lacking distinct anticodon loop modifications. These phenotypes are accompanied by translational inefficiency of certain mRNAs and disturbed protein homeostasis resulting in accumulation of protein aggregates. Different combinations of anticodon loop modification defects were shown to affect distinct tRNAs but provoke common transcriptional changes that are reminiscent of the cellular response to nutrient starvation. Multiple mechanisms may be involved in mediating inadequate starvation response upon loss of critical tRNA modifications. Recent evidence suggests protein aggregate induction to represent one such trigger.
AuthorsRoland Klassen, Alexander Bruch, Raffael Schaffrath
JournalCurrent genetics (Curr Genet) Vol. 66 Issue 6 Pg. 1053-1057 (Dec 2020) ISSN: 1432-0983 [Electronic] United States
PMID32860511 (Publication Type: Journal Article, Review)
Chemical References
  • Anticodon
  • Codon
  • Protein Aggregates
  • Saccharomyces cerevisiae Proteins
  • RNA, Transfer
Topics
  • Anticodon (genetics)
  • Codon (genetics)
  • Nucleic Acid Conformation
  • Protein Aggregates (genetics)
  • Protein Biosynthesis (genetics)
  • RNA Processing, Post-Transcriptional (genetics)
  • RNA, Transfer (genetics)
  • Saccharomyces cerevisiae (genetics)
  • Saccharomyces cerevisiae Proteins (genetics)

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