RNA-dependent chromatin association of transcription elongation factors and Pol II CTD kinases

被引:46
作者
Battaglia, Sofia [1 ]
Lidschriber, Michael [1 ,2 ,3 ]
Baejen, Carlo [1 ]
Torkler, Phillip [1 ]
Vos, Seychelle M. [1 ]
Cramer, Patrick [1 ,2 ,3 ]
机构
[1] Max Planck Inst Biophys Chem, Dept Mol Biol, Gottingen, Germany
[2] Novum, Karolinska Inst, Dept Biosci & Nutr, Ctr Innovat Med, Huddinge, Sweden
[3] Novum, Karolinska Inst, Sci Life Lab, Huddinge, Sweden
基金
欧洲研究理事会;
关键词
CARBOXYL-TERMINAL DOMAIN; POLYMERASE-II; PAF1; COMPLEX; HISTONE H3; SACCHAROMYCES-CEREVISIAE; FACTOR RECRUITMENT; STRUCTURAL BASIS; GENE-EXPRESSION; CAPPING ENZYME; BUR1; KINASE;
D O I
10.7554/eLife.25637
中图分类号
Q [生物科学];
学科分类号
090105 [作物生产系统与生态工程];
摘要
For transcription through chromatin, RNA polymerase (Pol) II associates with elongation factors (EFs). Here we show that many EFs crosslink to RNA emerging from transcribing Pol II in the yeast Saccharomyces cerevisiae. Most EFs crosslink preferentially to mRNAs, rather than unstable non-coding RNAs. RNA contributes to chromatin association of many EFs, including the Pol II serine 2 kinases Ctkl and Burl and the histone H3 methyltransferases Setl and Set2. The Ctkl kinase complex binds RNA in vitro, consistent with direct EF-RNA interaction. Setl recruitment to genes in vivo depends on its RNA recognition motifs (RRMs). These results strongly suggest that nascent RNA contributes to EF recruitment to transcribing Pol II. We propose that EFRNA interactions facilitate assembly of the elongation complex on transcribed genes when RNA emerges from Pol II, and that loss of EF-RNA interactions upon RNA cleavage at the polyadenylation site triggers disassembly of the elongation complex.
引用
收藏
页数:26
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