Elongation/Termination Factor Exchange Mediated by PP1 Phosphatase Orchestrates Transcription Termination

Cell Rep. 2018 Oct 2;25(1):259-269.e5. doi: 10.1016/j.celrep.2018.09.007.


Termination of RNA polymerase II (Pol II) transcription is a key step that is important for 3' end formation of functional mRNA, mRNA release, and Pol II recycling. Even so, the underlying termination mechanism is not yet understood. Here, we demonstrate that the conserved and essential termination factor Seb1 is found on Pol II near the end of the RNA exit channel and the Rpb4/7 stalk. Furthermore, the Seb1 interaction surface with Pol II largely overlaps with that of the elongation factor Spt5. Notably, Seb1 co-transcriptional recruitment is dependent on Spt5 dephosphorylation by the conserved PP1 phosphatase Dis2, which also dephosphorylates threonine 4 within the Pol II heptad repeated C-terminal domain. We propose that Dis2 orchestrates the transition from elongation to termination phase during the transcription cycle by mediating elongation to termination factor exchange and dephosphorylation of Pol II C-terminal domain.

Keywords: C-terminal domain; CID; CTD; CTD interacting domain; CTD phosphorylation; PP1 phosphatase; RNA polymerase II; Spt5; transcription termination.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Peptide Elongation Factors / genetics*
  • RNA Polymerase II / metabolism*
  • Schizosaccharomyces / metabolism*
  • Schizosaccharomyces pombe Proteins / metabolism*
  • Transcription Factors / genetics*
  • Transcription Termination, Genetic / physiology*
  • Transcription, Genetic / genetics*


  • Peptide Elongation Factors
  • Schizosaccharomyces pombe Proteins
  • Transcription Factors
  • RNA Polymerase II