Elongation factor-specific capture of RNA polymerase II complexes

被引:1
|
作者
Gregersen, Lea H. [1 ]
Mitter, Richard [2 ]
Svejstrup, Jesper Q. [1 ,3 ]
机构
[1] Univ Copenhagen, Dept Cellular & Mol Med, Blegdamsvej 3B, DK-2200 Copenhagen, Denmark
[2] Francis Crick Inst, Bioinformat & Biostat, 1 Midland Rd, London NW1 1AT, England
[3] Francis Crick Inst, Mech Transcript Lab, 1 Midland Rd, London NW1 1AT, England
来源
CELL REPORTS METHODS | 2022年 / 2卷 / 12期
基金
英国惠康基金; 欧洲研究理事会; 英国医学研究理事会; 新加坡国家研究基金会;
关键词
TRANSCRIPTION ELONGATION; CTD; PATTERNS;
D O I
10.1016/j.crmeth.2022.100368
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Transcription of protein-coding genes is regulated by dynamic association of co-factors with RNA polymerase II (RNAPII). The function of these factors and their relationship with RNAPII is often poorly understood. Here, we present an approach for elongation-factor-specific mNET capture (ELCAP) of RNAPII complexes for sequencing and mass spectrometry analysis aimed at investigating the function of such RNAPII regulatory proteins. As proof of principle, we apply ELCAP to the RNAPII-associated proteins SCAF4 and SCAF8, which share an essential role as mRNA anti-terminators but have individual roles at the 3' end of genes. Mass spectrometry analysis shows that both SCAF4 and SCAF8 are part of RNAPII elongation complexes containing 3' end processing factors but depleted of splicing components. Importantly, the ELCAP sequencing (ELCAP-seq) profiles of SCAF4- and SCAF8-RNAPII complexes nicely reflect their function as mRNA-anti-terminators and their competing functions at the end of genes, where they prevent or promote transcriptional readthrough.
引用
收藏
页数:16
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