Kecman Tea, Heo Dong-Hyuk, Vasiljeva Lidia
Department of Biochemistry, University of Oxford, Oxford, United Kingdom.
Department of Biochemistry, University of Oxford, Oxford, United Kingdom.
Methods Enzymol. 2018;612:489-504. doi: 10.1016/bs.mie.2018.07.009. Epub 2018 Aug 23.
The RNA polymerase II carboxyl-terminal domain (CTD) consists of tandem repeats of consensus sequence Tyr-Ser-Pro-Thr-Ser-Pro-Ser. 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.
RNA聚合酶II羧基末端结构域(CTD)由共有序列Tyr-Ser-Pro-Thr-Ser-Pro-Ser的串联重复序列组成。CTD的动态翻译后修饰产生了一个CTD编码,这对于控制转录、染色质修饰和RNA加工的因子的共转录募集至关重要。通过染色质免疫沉淀(ChIP)结合高通量DNA测序(ChIP-seq)分析CTD磷酸化是研究转录周期中CTD磷酸化变化的有力工具。在本章中,我们描述了一种用于分析裂殖酵母中不同CTD磷酸化标记的ChIP-seq方案。使用该方案,我们发现Tyr1P、Ser2P和Thr4P信号在基因3'端最高,而Ser5P在基因体内富集。