Department of Molecular Epigenetics, Helmholtz Center Munich and Center for Integrated Protein Science Munich (CIPSM), Marchioninistrasse 25, 81377 Munich, Germany.
Biomedical Center Munich, ZFP and Bioinformatic Unit, Großhaderner Strasse 9, 82152 Planegg-Martinsried, Germany.
Mol Cell. 2016 Jan 21;61(2):305-14. doi: 10.1016/j.molcel.2015.12.003.
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.
RNA 聚合酶 II(Pol II)的羧基末端结构域(CTD)由具有一致基序 Y1-S2-P3-T4-S5-P6-S7 的七肽重复组成。CTD 的动态磷酸化协调 Pol II 通过转录周期的进展。在这里,我们使用遗传和质谱方法直接检测和绘制整个 CTD 上的磷酸化位点。我们在哺乳动物和酵母细胞中证实了 CTD 残基 Y1、S2、T4、S5 和 S7 的磷酸化。尽管特定的磷酸化特征占主导地位,但相邻的 CTD 重复可以被不同地磷酸化,导致单七肽和二七肽 CTD 重复中共存的磷酸化位点高度多样化。CDK9 激酶的抑制特异性降低 CTD 内 S2 的磷酸化水平。