Protein Degradation of RNA Polymerase II-Association Factor 1(PAF1) Is Controlled by CNOT4 and 26S Proteasome

PLoS One. 2015 May 1;10(5):e0125599. doi: 10.1371/journal.pone.0125599. eCollection 2015.

Abstract

The PAF complex (PAFc) participates in various steps of the transcriptional process, from initiation to termination, by interacting with and recruiting various proteins to the proper locus for each step. PAFc is an evolutionarily conserved, multi-protein complex comprising PAF1, CDC73, CTR9, LEO1, yRTF1 and, in humans, hSKI8. These components of PAFc work together, and their protein levels are closely interrelated. In the present study, we investigated the mechanism of PAF1 protein degradation. We found that PAF1 protein levels are negatively regulated by the expression of CNOT4, an ortholog of yNOT4 and a member of the CCR4-NOT complex. CNOT4 specifically controls PAF1 but not other components of PAFc at the protein level by regulating the polyubiquitination of PAF1 and its subsequent degradation by the 26S proteasome. The degradation of PAF1 was found to require nuclear localization, as no PAF1 degradation by CNOT4 and the 26S proteasome was observed with NLS (nucleus localization signal)-deficient PAF1 mutants. However, chromatin binding by PAF1 was not necessary for 26S proteasome- or CNOT4-mediated degradation. Our results suggest that CNOT4 controls the degradation of chromatin-unbound PAF1 via the 26S proteasome.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cell Nucleus / metabolism
  • Chromatin / metabolism
  • HEK293 Cells
  • Hep G2 Cells
  • Humans
  • Nuclear Proteins / metabolism*
  • Proteasome Endopeptidase Complex / metabolism*
  • Protein Binding
  • Protein Transport
  • Proteolysis*
  • RNA Polymerase II / metabolism*
  • Transcription Factors / metabolism*
  • Ubiquitination

Substances

  • CNOT4 protein, human
  • Chromatin
  • Nuclear Proteins
  • PAF1 protein, human
  • Transcription Factors
  • RNA Polymerase II
  • Proteasome Endopeptidase Complex
  • ATP dependent 26S protease

Grants and funding

This work was supported by the National Research Foundation of Korea (NRF; http://www.nrf.re.kr/) grant funded by the Korea government (MSIP) (NO.NRF-2012R1A2A2A01007525, NRF-2012R1A4 A1028200). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.