Department of Botany, University of British Columbia, 3156-6270 University Boulevard, Vancouver, BC, Canada.
Department of Chemistry, University of Northern British Columbia, 3333 University Way, Prince George, BC, Canada.
J Eukaryot Microbiol. 2021 May;68(3):e12844. doi: 10.1111/jeu.12844. Epub 2021 Mar 12.
Pre-mRNA splicing is a highly conserved eukaryotic process, but our understanding of it is limited by a historical focus on well-studied organisms such as humans and yeast. There is considerable diversity in mechanisms and components of pre-mRNA splicing, especially in lineages that have evolved under the pressures of genome reduction. The ancestor of red algae is thought to have undergone genome reduction prior to the lineage's radiation, resulting in overall gene and intron loss in extant groups. Previous studies on the extremophilic red alga Cyanidioschyzon merolae revealed an intron-sparse genome with a highly reduced spliceosome. To determine whether these features applied to other red algae, we investigated multiple aspects of pre-mRNA splicing in the mesophilic red alga Porphyridium purpureum. Through strand-specific RNA-Seq, we observed high levels of intron retention across a large number of its introns, and nearly half of the transcripts for these genes are not spliced at all. We also discovered a relationship between variability of 5' splice site sequences and levels of splicing. To further investigate the connections between intron retention and splicing machinery, we bioinformatically assembled the P. purpureum spliceosome, and biochemically verified the presence of snRNAs. While most other core spliceosomal components are present, our results suggest highly divergent or missing U1 snRNP proteins, despite the presence of an uncharacteristically long U1 snRNA. These unusual aspects highlight the diverse nature of pre-mRNA splicing that can be seen in lesser-studied eukaryotes, raising the importance of investigating fundamental eukaryotic processes outside of model organisms.
前体 mRNA 剪接是一种高度保守的真核生物过程,但我们对它的理解受到历史上对人类和酵母等研究充分的生物的关注的限制。前体 mRNA 剪接的机制和组成存在相当大的多样性,尤其是在经历了基因组减少压力的进化支系中。红藻的祖先被认为在谱系辐射之前经历了基因组减少,导致现存群体的总体基因和内含子丢失。以前对极端嗜热红藻 Cyanidioschyzon merolae 的研究表明,其内含子稀疏的基因组具有高度简化的剪接体。为了确定这些特征是否适用于其他红藻,我们研究了中嗜热红藻 Porphyridium purpureum 中前体 mRNA 剪接的多个方面。通过链特异性 RNA-Seq,我们观察到大量内含子的内含子保留水平很高,而这些基因的近一半转录本根本没有剪接。我们还发现了 5'剪接位点序列的可变性与剪接水平之间的关系。为了进一步研究内含子保留和剪接机制之间的联系,我们生物信息学组装了 P. purpureum 的剪接体,并通过生化方法验证了 snRNA 的存在。虽然存在大多数其他核心剪接体成分,但我们的结果表明 U1 snRNP 蛋白高度分化或缺失,尽管存在异常长的 U1 snRNA。这些不寻常的方面突出了在研究较少的真核生物中可以看到的前体 mRNA 剪接的多样性,这提高了在非模式生物中研究基本真核生物过程的重要性。