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

Research output: Contribution to journalJournal articleResearchpeer-review

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.

Original languageEnglish
JournalNature Communications
Volume9
Issue number1
Pages (from-to)3392
ISSN2041-1723
DOIs
Publication statusPublished - 23 Aug 2018
Externally publishedYes

    Research areas

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

ID: 262753257