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剪接体组装和调控:来自高度简化剪接体分析的启示。

Spliceosome assembly and regulation: insights from analysis of highly reduced spliceosomes.

机构信息

Department of Chemistry and Biochemistry, University of Northern British Columbia, Prince George, British Columbia, Canada V2N 4Z9.

Department of Anatomy and Cell Biology, McGill University, Montréal, Quebec, Canada H3A 0C7.

出版信息

RNA. 2023 May;29(5):531-550. doi: 10.1261/rna.079273.122. Epub 2023 Feb 3.

Abstract

Premessenger RNA splicing is catalyzed by the spliceosome, a multimegadalton RNA-protein complex that assembles in a highly regulated process on each intronic substrate. Most studies of splicing and spliceosomes have been carried out in human or model systems. There exists, however, a large diversity of spliceosomes, particularly in organisms with reduced genomes, that suggests a means of analyzing the essential elements of spliceosome assembly and regulation. In this review, we characterize changes in spliceosome composition across phyla, describing those that are most frequently observed and highlighting an analysis of the reduced spliceosome of the red alga We used homology modeling to predict what effect splicing protein loss would have on the spliceosome, based on currently available cryo-EM structures. We observe strongly correlated loss of proteins that function in the same process, for example, in interacting with the U1 snRNP (which is absent in ), regulation of Brr2, or coupling transcription and splicing. Based on our observations, we predict splicing in to be inefficient, inaccurate, and post-transcriptional, consistent with the apparent trend toward its elimination in this lineage. This work highlights the striking flexibility of the splicing pathway and the spliceosome when viewed in the context of eukaryotic diversity.

摘要

前信使 RNA 剪接是由剪接体催化的,剪接体是一个多亚基的 RNA-蛋白质复合物,在每个内含子底物上以高度调控的过程组装。大多数剪接和剪接体的研究都是在人类或模型系统中进行的。然而,存在着大量的剪接体多样性,特别是在基因组较小的生物体中,这表明存在一种分析剪接体组装和调节基本要素的方法。在这篇综述中,我们描述了跨门的剪接体组成的变化,描述了那些最常观察到的变化,并强调了对红藻的简化剪接体的分析。我们使用同源建模来预测根据当前可用的冷冻电镜结构,剪接蛋白缺失会对剪接体产生什么影响。我们观察到功能相同的蛋白质的强烈相关性缺失,例如与 U1 snRNP 相互作用(在 中缺失)、Brr2 的调节或转录和剪接的偶联。基于我们的观察,我们预测 在 中的剪接效率低、不准确且是转录后,与该谱系中明显的消除趋势一致。这项工作强调了在真核生物多样性的背景下,剪接途径和剪接体具有惊人的灵活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ecc2/10158995/fc32d9e9caa1/531f01.jpg

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