Hudson Andrew J, Stark Martha R, Fast Naomi M, Russell Anthony G, Rader Stephen D
a Alberta RNA Research and Training Institute and Department of Biological Sciences ; University of Lethbridge ; Lethbridge , Alberta , Canada.
b Department of Chemistry ; University of Northern British Columbia ; Prince George , British Columbia , Canada.
RNA Biol. 2015;12(11):1-8. doi: 10.1080/15476286.2015.1094602. Epub 2015 Sep 23.
Pre-mRNA splicing has been considered one of the hallmarks of eukaryotes, yet its diversity is astonishing: the number of substrate introns for splicing ranges from hundreds of thousands in humans to a mere handful in certain parasites. The catalytic machinery that carries out splicing, the spliceosome, is similarly diverse, with over 300 associated proteins in humans to a few tens in other organisms. In this Point of View, we discuss recent work characterizing the reduced spliceosome of the acidophilic red alga Cyanidioschyzon merolae, which further highlights the diversity of splicing in that it does not possess the U1 snRNP that is characteristically responsible for 5' splice site recognition. Comparisons to other organisms with reduced spliceosomes, such as microsporidia, trypanosomes, and Giardia, help to identify the most highly conserved splicing factors, pointing to the essential core of this complex machine. These observations argue for increased exploration of important biochemical processes through study of a wider ranger of organisms.
前体信使核糖核酸(pre-mRNA)剪接一直被视为真核生物的标志之一,但其多样性令人惊讶:可供剪接的底物内含子数量从人类的数十万到某些寄生虫中的寥寥几个不等。执行剪接的催化机制——剪接体同样具有多样性,人类中有300多种相关蛋白质,而其他生物中只有几十种。在这一观点中,我们讨论了最近关于嗜酸性红藻梅氏嗜热栖热菌(Cyanidioschyzon merolae)简化剪接体的研究工作,这进一步凸显了剪接的多样性,因为它不具备通常负责识别5'剪接位点的U1小核核糖核蛋白(U1 snRNP)。与其他具有简化剪接体的生物(如微孢子虫、锥虫和贾第虫)进行比较,有助于确定最保守的剪接因子,指出这一复杂机制的核心要素。这些观察结果表明,通过研究更广泛的生物来加强对重要生化过程的探索。