| Literature DB >> 30502955 |
Tea Kecman1, Dong-Hyuk Heo1, Lidia Vasiljeva2.
Abstract
The RNA polymerase II carboxyl-terminal domain (CTD) consists of tandem repeats of consensus sequence Tyr1-Ser2-Pro3-Thr4-Ser5-Pro6-Ser7. Dynamic posttranslational modifications of the CTD generate a CTD code crucial for the cotranscriptional recruitment of factors that control transcription, chromatin modification, and RNA processing. Analysis of CTD phosphorylation by ChIP (Chromatin ImmunoPrecipitation) coupled with high-throughput DNA sequencing (ChIP-seq) is a powerful tool to investigate the changes in CTD phosphorylation during the transcription cycle. In this chapter, we describe a ChIP-seq protocol to profile the different CTD phospho-marks in fission yeast. Using this protocol, we have found that Tyr1P, Ser2P, and Thr4P signals are highest at gene 3' ends, whereas Ser5P is enriched across the gene bodies.Entities:
Keywords: CTD phosphorylation; ChIP-seq; Chromatin immunoprecipitation; Fission yeast; RNA polymerase II
Mesh:
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Year: 2018 PMID: 30502955 DOI: 10.1016/bs.mie.2018.07.009
Source DB: PubMed Journal: Methods Enzymol ISSN: 0076-6879 Impact factor: 1.600