Wellcome Trust Centre for Cell Biology, University of Edinburgh, Edinburgh, Scotland.
Friedrich Miescher Institute for Biomedical Research, Basel, Switzerland.
Elife. 2017 Oct 13;6:e27082. doi: 10.7554/eLife.27082.
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 KR 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.
转录过程中的 RNA 处理与正在转录的 RNAPII 之间存在着大量联系。特别是,有报道称前体 mRNA 的剪接与 RNAPII 延伸速度的减缓有关。在这里,我们在 RNAPII 的催化亚基上鉴定到了一个靠近 DNA 进入途径的泛素化位点(K1246)。在没有 Bre5-Ubp3 泛素蛋白酶复合物的情况下,泛素化增加。Bre5 在体内与 RNA 结合,优先结合包含内含子的前体 mRNA 的外显子 2 区域和 poly(A)近端位点。泛素化的 RNAPII 也表现出类似的富集。Bre5 的缺失导致剪接受损,以及在剪接报告构建体上体内 RNAPII 延伸的缺陷。在表达具有 KR 突变的 RNAPII 的菌株中,共转录剪接减少。我们提出,RNAPII 的泛素化是由 RNA 处理事件诱导的,并与转录暂停有关,而 Bre5-Ubp3 与新生转录本相关联,可释放这种暂停。