Wellcome Centre for Cell Biology, School of Biological Sciences, University of Edinburgh, Edinburgh EH9 3BF, United Kingdom.
RNA. 2019 Oct;25(10):1298-1310. doi: 10.1261/rna.070425.119. Epub 2019 Jul 9.
There is increasing evidence from yeast to humans that pre-mRNA splicing occurs mainly cotranscriptionally, such that splicing and transcription are functionally coupled. Currently, there is little insight into the contribution of the core transcription elongation machinery to cotranscriptional spliceosome assembly and pre-mRNA splicing. Spt5 is a member of the core transcription elongation machinery and an essential protein, whose absence in budding yeast causes defects in pre-mRNA splicing. To determine how Spt5 affects pre-mRNA splicing, we used the auxin-inducible degron system to conditionally deplete Spt5 in and assayed effects on cotranscriptional spliceosome assembly and splicing. We show that Spt5 is needed for efficient splicing and for the accumulation of U5 snRNPs at intron-containing genes, and therefore for stable cotranscriptional assembly of spliceosomes. The defect in cotranscriptional spliceosome assembly can explain the relatively mild splicing defect as being a consequence of the failure of cotranscriptional splicing. Coimmunoprecipitation of Spt5 with core spliceosomal proteins and all spliceosomal snRNAs suggests a model whereby Spt5 promotes cotranscriptional pre-mRNA splicing by stabilizing the association of U5 snRNP with spliceosome complexes as they assemble on the nascent transcript. If this phenomenon is conserved in higher eukaryotes, it has the potential to be important for cotranscriptional regulation of alternative splicing.
越来越多的酵母到人类的证据表明,前体 mRNA 剪接主要发生在共转录过程中,使得剪接和转录在功能上偶联。目前,对于核心转录延伸机制对共转录剪接体组装和前体 mRNA 剪接的贡献了解甚少。Spt5 是核心转录延伸机制的成员,也是一种必需蛋白,其在芽殖酵母中的缺失会导致前体 mRNA 剪接缺陷。为了确定 Spt5 如何影响前体 mRNA 剪接,我们使用了生长素诱导的去稳定系统在 中条件性耗尽 Spt5,并检测了对共转录剪接体组装和剪接的影响。我们表明,Spt5 对于有效的剪接和带有内含子的基因中 U5 snRNP 的积累是必需的,因此对于剪接体的稳定共转录组装也是必需的。共转录剪接体组装的缺陷可以解释相对温和的剪接缺陷是由于共转录剪接的失败造成的。Spt5 与核心剪接体蛋白和所有剪接体 snRNA 的共免疫沉淀表明了一种模型,即 Spt5 通过稳定 U5 snRNP 与剪接体复合物的结合来促进共转录前体 mRNA 剪接,因为它们在前体转录物上组装。如果这种现象在高等真核生物中保守,那么它有可能对共转录调控可变剪接很重要。