Max Planck Institute of Molecular Biology and Genetics, Pfotenhauerstrasse 108, 01307 Dresden, Germany.
Mol Cell. 2010 Nov 24;40(4):571-81. doi: 10.1016/j.molcel.2010.11.004.
Pre-mRNA splicing is catalyzed by the spliceosome, which can assemble on pre-mRNA cotranscriptionally. However, whether splicing generally occurs during transcription has not been addressed. Indeed, splicing catalysis is expected to occur posttranscriptionally in yeast, where the shortness of terminal exons should leave insufficient time for splicing. Here, we isolate endogenous S. cerevisiae nascent RNA and determine gene-specific splicing efficiencies and transcription profiles, using high-density tiling microarrays. Surprisingly, we find that splicing occurs cotranscriptionally for the majority of intron-containing genes. Analysis of transcription profiles reveals Pol II pausing within the terminal exons of these genes. Intronless and inefficiently spliced genes lack this pause. In silico simulations of transcription and splicing kinetics confirm that this pausing event provides sufficient time for splicing before termination. The discovery of terminal exon pausing demonstrates functional coupling of transcription and splicing near gene ends.
前体 mRNA 剪接由剪接体催化,剪接体可以在 pre-mRNA 共转录时组装。然而,剪接是否通常发生在转录过程中尚未得到解决。事实上,在酵母中,剪接催化预计是在转录后发生的,因为末端外显子的长度较短,应该没有足够的时间进行剪接。在这里,我们使用高密度平铺微阵列分离内源 S. cerevisiae 新生 RNA,并确定基因特异性剪接效率和转录谱。令人惊讶的是,我们发现大多数含有内含子的基因的剪接都是共转录的。对转录谱的分析揭示了这些基因的末端外显子中 Pol II 的暂停。无内含子和剪接效率低的基因则没有这种暂停。转录和剪接动力学的计算机模拟证实,这种暂停事件在终止前为剪接提供了足够的时间。末端外显子暂停的发现证明了转录和剪接在基因末端附近的功能耦合。