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Heptad-Specific Phosphorylation of RNA Polymerase II CTD.
- Source :
-
Molecular cell [Mol Cell] 2016 Jan 21; Vol. 61 (2), pp. 305-14. - Publication Year :
- 2016
-
Abstract
- The carboxy-terminal domain (CTD) of RNA polymerase II (Pol II) consists of heptad repeats with the consensus motif Y1-S2-P3-T4-S5-P6-S7. Dynamic phosphorylation of the CTD coordinates Pol II progression through the transcription cycle. Here, we use genetic and mass spectrometric approaches to directly detect and map phosphosites along the entire CTD. We confirm phosphorylation of CTD residues Y1, S2, T4, S5, and S7 in mammalian and yeast cells. Although specific phosphorylation signatures dominate, adjacent CTD repeats can be differently phosphorylated, leading to a high variation of coexisting phosphosites in mono- and di-heptad CTD repeats. Inhibition of CDK9 kinase specifically reduces S2 phosphorylation levels within the CTD.<br /> (Copyright © 2016 Elsevier Inc. All rights reserved.)
- Subjects :
- Amino Acid Motifs
Amino Acid Sequence
Animals
Cell Line, Tumor
Cyclin-Dependent Kinase 9 antagonists & inhibitors
Cyclin-Dependent Kinase 9 metabolism
Humans
Mammals
Mass Spectrometry
Molecular Sequence Data
Peptide Library
Phosphorylation
RNA-Binding Proteins chemistry
RNA-Binding Proteins metabolism
Repetitive Sequences, Amino Acid
Reproducibility of Results
Saccharomyces cerevisiae metabolism
Saccharomyces cerevisiae Proteins chemistry
Saccharomyces cerevisiae Proteins metabolism
Structure-Activity Relationship
RNA Polymerase II chemistry
RNA Polymerase II metabolism
Subjects
Details
- Language :
- English
- ISSN :
- 1097-4164
- Volume :
- 61
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Molecular cell
- Publication Type :
- Academic Journal
- Accession number :
- 26799765
- Full Text :
- https://doi.org/10.1016/j.molcel.2015.12.003