Suppr超能文献

使用长读长技术进行异构体年龄 - 剪接异构体分析

Isoform Age - Splice Isoform Profiling Using Long-Read Technologies.

作者信息

De Paoli-Iseppi Ricardo, Gleeson Josie, Clark Michael B

机构信息

Centre for Stem Cell Systems, Department of Anatomy and Physiology, The University of Melbourne, Parkville, VIC, Australia.

出版信息

Front Mol Biosci. 2021 Aug 2;8:711733. doi: 10.3389/fmolb.2021.711733. eCollection 2021.

Abstract

Alternative splicing (AS) of RNA is a key mechanism that results in the expression of multiple transcript isoforms from single genes and leads to an increase in the complexity of both the transcriptome and proteome. Regulation of AS is critical for the correct functioning of many biological pathways, while disruption of AS can be directly pathogenic in diseases such as cancer or cause risk for complex disorders. Current short-read sequencing technologies achieve high read depth but are limited in their ability to resolve complex isoforms. In this review we examine how long-read sequencing (LRS) technologies can address this challenge by covering the entire RNA sequence in a single read and thereby distinguish isoform changes that could impact RNA regulation or protein function. Coupling LRS with technologies such as single cell sequencing, targeted sequencing and spatial transcriptomics is producing a rapidly expanding suite of technological approaches to profile alternative splicing at the isoform level with unprecedented detail. In addition, integrating LRS with genotype now allows the impact of genetic variation on isoform expression to be determined. Recent results demonstrate the potential of these techniques to elucidate the landscape of splicing, including in tissues such as the brain where AS is particularly prevalent. Finally, we also discuss how AS can impact protein function, potentially leading to novel therapeutic targets for a range of diseases.

摘要

RNA的可变剪接(AS)是一种关键机制,它能使单个基因表达多种转录本异构体,进而增加转录组和蛋白质组的复杂性。AS的调控对于许多生物途径的正常运作至关重要,而AS的破坏在诸如癌症等疾病中可能直接致病,或导致患复杂疾病的风险。当前的短读长测序技术可实现高读长深度,但在解析复杂异构体方面能力有限。在本综述中,我们探讨了长读长测序(LRS)技术如何通过在单次读取中覆盖整个RNA序列来应对这一挑战,从而区分可能影响RNA调控或蛋白质功能的异构体变化。将LRS与单细胞测序、靶向测序和空间转录组学等技术相结合,正在产生一系列迅速扩展的技术方法,以前所未有的细节在异构体水平上分析可变剪接。此外,将LRS与基因型相结合,现在可以确定遗传变异对异构体表达的影响。最近的结果证明了这些技术在阐明剪接图谱方面的潜力,包括在AS特别普遍的脑组织等组织中。最后,我们还讨论了AS如何影响蛋白质功能,这可能为一系列疾病带来新的治疗靶点。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1a8/8364947/a8e5a955f3e4/fmolb-08-711733-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验