TORC1-dependent sumoylation of Rpc82 promotes RNA polymerase III assembly and activity

Proc Natl Acad Sci U S A. 2017 Jan 31;114(5):1039-1044. doi: 10.1073/pnas.1615093114. Epub 2017 Jan 17.

Abstract

Maintaining cellular homeostasis under changing nutrient conditions is essential for the growth and development of all organisms. The mechanisms that maintain homeostasis upon loss of nutrient supply are not well understood. By mapping the SUMO proteome in Saccharomyces cerevisiae, we discovered a specific set of differentially sumoylated proteins mainly involved in transcription. RNA polymerase III (RNAPIII) components, including Rpc53, Rpc82, and Ret1, are particularly prominent nutrient-dependent SUMO targets. Nitrogen starvation, as well as direct inhibition of the master nutrient response regulator target of rapamycin complex 1 (TORC1), results in rapid desumoylation of these proteins, which is reflected by loss of SUMO at tRNA genes. TORC1-dependent sumoylation of Rpc82 in particular is required for robust tRNA transcription. Mechanistically, sumoylation of Rpc82 is important for assembly of the RNAPIII holoenzyme and recruitment of Rpc82 to tRNA genes. In conclusion, our data show that TORC1-dependent sumoylation of Rpc82 bolsters the transcriptional capacity of RNAPIII under optimal growth conditions.

Keywords: RNA polymerase III; Sumo; TORC1; tRNA; transcription.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Amino Acid Substitution
  • Gene Expression Regulation, Fungal*
  • Gene Ontology
  • Nitrogen / metabolism
  • Protein Processing, Post-Translational*
  • Protein Subunits
  • RNA Polymerase III / metabolism*
  • RNA, Fungal / biosynthesis
  • RNA, Fungal / genetics
  • RNA, Transfer / biosynthesis
  • RNA, Transfer / genetics
  • Saccharomyces cerevisiae / drug effects
  • Saccharomyces cerevisiae / growth & development
  • Saccharomyces cerevisiae / metabolism*
  • Saccharomyces cerevisiae Proteins / drug effects
  • Saccharomyces cerevisiae Proteins / metabolism*
  • Sirolimus / pharmacology
  • Sumoylation
  • Transcription Factors / drug effects
  • Transcription Factors / metabolism*
  • Transcription, Genetic*
  • Ubiquitin-Conjugating Enzymes / genetics

Substances

  • Protein Subunits
  • RNA, Fungal
  • Saccharomyces cerevisiae Proteins
  • TORC1 protein complex, S cerevisiae
  • Transcription Factors
  • RNA, Transfer
  • Ubiquitin-Conjugating Enzymes
  • RNA Polymerase III
  • RPC82 protein, S cerevisiae
  • ubiquitin-conjugating enzyme UBC9
  • Nitrogen
  • Sirolimus