RNA polymerase II stalling at pre-mRNA splice sites is enforced by ubiquitination of the catalytic subunit

被引:17
作者
Milligan, Laura [1 ]
Sayou, Camille [1 ]
Tuck, Alex [2 ]
Aauchynnikava, Tatsiana [1 ]
Reid, Jane E. A. [1 ]
Alexander, Ross [1 ,5 ]
Alves, Flavia de Lima [1 ]
Allshire, Robin [1 ]
Spanos, Christos [1 ]
Rappsilber, Juri [1 ,3 ]
Beggs, Jean D. [1 ]
Kudla, Grzegorz [4 ]
Tollervey, David [1 ]
机构
[1] Univ Edinburgh, Wellcome Trust Ctr Cell Biol, Edinburgh, Midlothian, Scotland
[2] Friedrich Miescher Inst Biomed Res, Basel, Switzerland
[3] Tech Univ Berlin, Inst Biotechnol, Berlin, Germany
[4] Univ Edinburgh, Inst Genet & Mol Med, MRC Human Genet Unit, Edinburgh, Midlothian, Scotland
[5] Heriotwatt Univ, Inst Life & Earth Sci, Edinburgh, Midlothian, Scotland
基金
英国医学研究理事会; 英国惠康基金;
关键词
DEUBIQUITINATING ENZYME; RIBOSOMAL-RNA; GLOBAL ANALYSIS; NUCLEAR-RNA; TRANSCRIPTION; PROTEIN; DEGRADATION; COMPLEX; UBIQUITYLATION; IDENTIFICATION;
D O I
10.7554/eLife.27082
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Numerous links exist between co-transcriptional RNA processing and the transcribing RNAPII. In particular, pre-mRNA splicing was reported to be associated with slowed RNAPII elongation. Here, we identify a site of ubiquitination (K1246) in the catalytic subunit of RNAPII close to the DNA entry path. Ubiquitination was increased in the absence of the Bre5-Ubp3 ubiquitin protease complex. Bre5 binds RNA in vivo, with a preference for exon 2 regions of intron-containing pre-mRNAs and poly(A) proximal sites. Ubiquitinated RNAPII showed similar enrichment. The absence of Bre5 led to impaired splicing and defects in RNAPII elongation in vivo on a splicing reporter construct. Strains expressing RNAPII with a K1246R mutation showed reduced co-transcriptional splicing. We propose that ubiquinitation of RNAPII is induced by RNA processing events and linked to transcriptional pausing, which is released by Bre5-Ubp3 associated with the nascent transcript.
引用
收藏
页数:27
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