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通过对天然 RNA 的纳米孔测序进行异构体特异性 Poly(A) 尾长估计。

Transcript Isoform-Specific Estimation of Poly(A) Tail Length by Nanopore Sequencing of Native RNA.

机构信息

Computational Biology Unit, Department of Informatics, University of Bergen, Bergen, Norway.

Sars International Centre for Marine Molecular Biology, University of Bergen, Bergen, Norway.

出版信息

Methods Mol Biol. 2021;2284:543-567. doi: 10.1007/978-1-0716-1307-8_30.

Abstract

The poly(A) tail is a homopolymeric stretch of adenosine at the 3'-end of mature RNA transcripts and its length plays an important role in nuclear export, stability, and translational regulation of mRNA. Existing techniques for genome-wide estimation of poly(A) tail length are based on short-read sequencing. These methods are limited because they sequence a synthetic DNA copy of mRNA instead of the native transcripts. Furthermore, they can identify only a short segment of the transcript proximal to the poly(A) tail which makes it difficult to assign the measured poly(A) length uniquely to a single transcript isoform. With the introduction of native RNA sequencing by Oxford Nanopore Technologies, it is now possible to sequence full-length native RNA. A single long read contains both the transcript and the associated poly(A) tail, thereby making transcriptome-wide isoform-specific poly(A) tail length assessment feasible. We developed tailfindr-an R-based package for estimating poly(A) tail length from Oxford Nanopore sequencing data. In this chapter, we describe in detail the pipeline for transcript isoform-specific poly(A) tail profiling based on native RNA Nanopore sequencing-from library preparation to downstream data analysis with tailfindr.

摘要

多聚腺苷酸尾是成熟 RNA 转录本 3' 端的腺苷同聚物延伸,其长度在 mRNA 的核输出、稳定性和翻译调控中发挥重要作用。目前用于全基因组估计多聚腺苷酸尾长度的技术是基于短读测序的。这些方法存在局限性,因为它们对 mRNA 的合成 DNA 拷贝进行测序,而不是对天然转录本进行测序。此外,它们只能识别靠近多聚腺苷酸尾的转录本的短片段,这使得难以将测量的多聚腺苷酸长度唯一分配给单个转录本异构体。随着牛津纳米孔技术的全转录本测序的引入,现在可以对全长的天然 RNA 进行测序。单个长读长包含转录本和相关的多聚腺苷酸尾,从而使得对全转录组的异构体特异性多聚腺苷酸尾长度评估成为可能。我们开发了 tailfindr,这是一个基于 R 的用于从牛津纳米孔测序数据中估计多聚腺苷酸尾长度的软件包。在本章中,我们详细描述了基于天然 RNA 纳米孔测序的转录本异构体特异性多聚腺苷酸尾分析的工作流程,包括从文库制备到使用 tailfindr 进行下游数据分析。

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