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本文引用的文献

1
Native molecule sequencing by nano-ID reveals synthesis and stability of RNA isoforms.纳米 ID 对天然分子进行测序揭示了 RNA 异构体的合成和稳定性。
Genome Res. 2020 Sep;30(9):1332-1344. doi: 10.1101/gr.257857.119. Epub 2020 Sep 4.
2
Post-transcriptional splicing of nascent RNA contributes to widespread intron retention in plants.新生 RNA 的转录后剪接导致植物中广泛的内含子保留。
Nat Plants. 2020 Jul;6(7):780-788. doi: 10.1038/s41477-020-0688-1. Epub 2020 Jun 15.
3
Using TT-seq for profiling nascent transcription and measuring transcript elongation.使用 TT-seq 进行新生转录谱分析和测量转录延伸。
Nat Protoc. 2020 Feb;15(2):604-627. doi: 10.1038/s41596-019-0262-3. Epub 2020 Jan 8.
4
Splicing Kinetics and Coordination Revealed by Direct Nascent RNA Sequencing through Nanopores.通过纳米孔直接新生 RNA 测序揭示的剪接动力学和协调。
Mol Cell. 2020 Mar 5;77(5):985-998.e8. doi: 10.1016/j.molcel.2019.11.017. Epub 2019 Dec 12.
5
Nanopore native RNA sequencing of a human poly(A) transcriptome.人 poly(A) 转录组的纳米孔天然 RNA 测序。
Nat Methods. 2019 Dec;16(12):1297-1305. doi: 10.1038/s41592-019-0617-2. Epub 2019 Nov 18.
6
A comprehensive examination of Nanopore native RNA sequencing for characterization of complex transcriptomes.对纳米孔天然 RNA 测序进行全面考察,以对复杂转录组进行特征分析。
Nat Commun. 2019 Jul 31;10(1):3359. doi: 10.1038/s41467-019-11272-z.
7
Long-read sequencing of nascent RNA reveals coupling among RNA processing events.长读测序技术对新生 RNA 进行测序,揭示了 RNA 加工事件之间的偶联。
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8
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9
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Nat Methods. 2018 Mar;15(3):221-225. doi: 10.1038/nmeth.4582. Epub 2018 Jan 22.
10
Highly parallel direct RNA sequencing on an array of nanopores.基于纳米孔阵列的高通量直接 RNA 测序。
Nat Methods. 2018 Mar;15(3):201-206. doi: 10.1038/nmeth.4577. Epub 2018 Jan 15.

利用纳米共聚焦光漂白技术揭示新生 RNA 加工动力学。

Revealing nascent RNA processing dynamics with nano-COP.

机构信息

Department of Genetics, Harvard Medical School, Boston, MA, USA.

Ontario Institute for Cancer Research, Toronto, Ontario, Canada.

出版信息

Nat Protoc. 2021 Mar;16(3):1343-1375. doi: 10.1038/s41596-020-00469-y. Epub 2021 Jan 29.

DOI:10.1038/s41596-020-00469-y
PMID:33514943
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8713461/
Abstract

During maturation, eukaryotic precursor RNAs undergo processing events including intron splicing, 3'-end cleavage, and polyadenylation. Here we describe nanopore analysis of co-transcriptional processing (nano-COP), a method for probing the timing and patterns of RNA processing. An extension of native elongating transcript sequencing, which quantifies transcription genome-wide through short-read sequencing of nascent RNA 3' ends, nano-COP uses long-read nascent RNA sequencing to observe global patterns of RNA processing. First, nascent RNA is stringently purified through a combination of 4-thiouridine metabolic labeling and cellular fractionation. In contrast to cDNA or short-read-based approaches relying on reverse transcription or amplification, the sample is sequenced directly through nanopores to reveal the native context of nascent RNA. nano-COP identifies both active transcription sites and splice isoforms of single RNA molecules during synthesis, providing insight into patterns of intron removal and the physical coupling between transcription and splicing. The nano-COP protocol yields data within 3 d.

摘要

在成熟过程中,真核生物前体 RNA 经历多种加工事件,包括内含子剪接、3'-末端切割和多聚腺苷酸化。本文描述了共转录加工的纳米孔分析(nano-COP),这是一种探测 RNA 加工时间和模式的方法。该方法是对自然延伸转录测序的扩展,通过对新生 RNA 3'末端的短读测序来全面量化转录,nano-COP 则利用长读新生 RNA 测序来观察 RNA 加工的全局模式。首先,通过 4-硫代尿嘧啶代谢标记和细胞分馏来严格纯化新生 RNA。与依赖逆转录或扩增的 cDNA 或短读测序方法不同,该样品通过纳米孔直接测序,以揭示新生 RNA 的天然结构。nano-COP 可在合成过程中鉴定单个 RNA 分子的活性转录位点和剪接异构体,从而深入了解内含子去除的模式以及转录和剪接之间的物理偶联。nano-COP 方案在 3 天内生成数据。