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CTD-dependent and -independent mechanisms govern co-transcriptional capping of Pol II transcripts.
- Source :
-
Nature communications [Nat Commun] 2018 Aug 23; Vol. 9 (1), pp. 3392. Date of Electronic Publication: 2018 Aug 23. - Publication Year :
- 2018
-
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.
- Subjects :
- Base Sequence
Cyclin-Dependent Kinases metabolism
Humans
Models, Biological
Phosphorylation
Protein Domains
RNA Caps metabolism
RNA, Messenger genetics
RNA, Messenger metabolism
Species Specificity
Structure-Activity Relationship
Transcription Factor TFIIH metabolism
Cyclin-Dependent Kinase-Activating Kinase
RNA Polymerase II chemistry
RNA Polymerase II metabolism
Transcription, Genetic
Subjects
Details
- Language :
- English
- ISSN :
- 2041-1723
- Volume :
- 9
- Issue :
- 1
- Database :
- MEDLINE
- Journal :
- Nature communications
- Publication Type :
- Academic Journal
- Accession number :
- 30139934
- Full Text :
- https://doi.org/10.1038/s41467-018-05923-w