Profiling RNA Polymerase II Phosphorylation Genome-Wide in Fission Yeast

被引:3
|
作者
Kecman, Tea [1 ]
Heo, Dong-Hyuk [1 ]
Vasiljeva, Lidia [1 ]
机构
[1] Univ Oxford, Dept Biochem, Oxford, England
关键词
CTD; TRANSCRIPTION; ENZYMES; KINASE;
D O I
10.1016/bs.mie.2018.07.009
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
The RNA polymerase II carboxyl-terminal domain (CTD) consists of tandem repeats of consensus sequence Tyr(1)-Ser(2)-Pro(3)-Thr(4)-Ser(5)-Pro(6)-Ser(7). 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 0 ends, whereas Ser5P is enriched across the gene bodies.
引用
收藏
页码:489 / 504
页数:16
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