CTD-dependent and -independent mechanisms govern co-transcriptional capping of Pol II transcripts

Nat Commun. 2018 Aug 23;9(1):3392. doi: 10.1038/s41467-018-05923-w.

Abstract

Co-transcriptional capping of RNA polymerase II (Pol II) transcripts by capping enzyme proceeds orders of magnitude more efficiently than capping of free RNA. Previous studies brought to light a role for the phosphorylated Pol II carboxyl-terminal domain (CTD) in activation of co-transcriptional capping; however, CTD phosphorylation alone could not account for the observed magnitude of activation. Here, we exploit a defined Pol II transcription system that supports both CTD phosphorylation and robust activation of capping to dissect the mechanism of co-transcriptional capping. Taken together, our findings identify a CTD-independent, but Pol II-mediated, mechanism that functions in parallel with CTD-dependent processes to ensure optimal capping, and they support a "tethering" model for the mechanism of activation.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Base Sequence
  • Cyclin-Dependent Kinase-Activating Kinase
  • Cyclin-Dependent Kinases / metabolism
  • Humans
  • Models, Biological
  • Phosphorylation
  • Protein Domains
  • RNA Caps / metabolism
  • RNA Polymerase II / chemistry*
  • RNA Polymerase II / metabolism*
  • RNA, Messenger / genetics
  • RNA, Messenger / metabolism
  • Species Specificity
  • Structure-Activity Relationship
  • Transcription Factor TFIIH / metabolism
  • Transcription, Genetic*

Substances

  • RNA Caps
  • RNA, Messenger
  • Transcription Factor TFIIH
  • Cyclin-Dependent Kinases
  • RNA Polymerase II
  • Cyclin-Dependent Kinase-Activating Kinase