| Literature DB >> 26799765 |
Roland Schüller1, Ignasi Forné2, Tobias Straub2, Amelie Schreieck3, Yves Texier1, Nilay Shah1, Tim-Michael Decker1, Patrick Cramer4, Axel Imhof2, Dirk Eick5.
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.Entities:
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Year: 2016 PMID: 26799765 DOI: 10.1016/j.molcel.2015.12.003
Source DB: PubMed Journal: Mol Cell ISSN: 1097-2765 Impact factor: 17.970