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一种可扩展的链特异性方案,可实现从单细胞进行全长总RNA测序。

A Scalable Strand-Specific Protocol Enabling Full-Length Total RNA Sequencing From Single Cells.

作者信息

Haile Simon, Corbett Richard D, LeBlanc Veronique G, Wei Lisa, Pleasance Stephen, Bilobram Steve, Nip Ka Ming, Brown Kirstin, Trinh Eva, Smith Jillian, Trinh Diane L, Bala Miruna, Chuah Eric, Coope Robin J N, Moore Richard A, Mungall Andrew J, Mungall Karen L, Zhao Yongjun, Hirst Martin, Aparicio Samuel, Birol Inanc, Jones Steven J M, Marra Marco A

机构信息

Canada's Michael Smith Genome Sciences Centre, BC Cancer, Vancouver, BC, Canada.

Department of Molecular Oncology, BC Cancer, Vancouver, BC, Canada.

出版信息

Front Genet. 2021 Jun 3;12:665888. doi: 10.3389/fgene.2021.665888. eCollection 2021.

DOI:10.3389/fgene.2021.665888
PMID:34149808
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8209500/
Abstract

RNA sequencing (RNAseq) has been widely used to generate bulk gene expression measurements collected from pools of cells. Only relatively recently have single-cell RNAseq (scRNAseq) methods provided opportunities for gene expression analyses at the single-cell level, allowing researchers to study heterogeneous mixtures of cells at unprecedented resolution. Tumors tend to be composed of heterogeneous cellular mixtures and are frequently the subjects of such analyses. Extensive method developments have led to several protocols for scRNAseq but, owing to the small amounts of RNA in single cells, technical constraints have required compromises. For example, the majority of scRNAseq methods are limited to sequencing only the 3' or 5' termini of transcripts. Other protocols that facilitate full-length transcript profiling tend to capture only polyadenylated mRNAs and are generally limited to processing only 96 cells at a time. Here, we address these limitations and present a novel protocol that allows for the high-throughput sequencing of full-length, total RNA at single-cell resolution. We demonstrate that our method produced strand-specific sequencing data for both polyadenylated and non-polyadenylated transcripts, enabled the profiling of transcript regions beyond only transcript termini, and yielded data rich enough to allow identification of cell types from heterogeneous biological samples.

摘要

RNA测序(RNAseq)已被广泛用于生成从细胞群体中收集的大量基因表达测量数据。直到最近,单细胞RNA测序(scRNAseq)方法才为单细胞水平的基因表达分析提供了机会,使研究人员能够以前所未有的分辨率研究细胞的异质混合物。肿瘤往往由异质细胞混合物组成,并且经常是此类分析的对象。广泛的方法开发已经产生了几种scRNAseq方案,但是由于单细胞中的RNA量很少,技术限制需要做出妥协。例如,大多数scRNAseq方法仅限于对转录本的3'或5'末端进行测序。其他有助于全长转录本分析的方案往往只能捕获多聚腺苷酸化的mRNA,并且通常一次只能处理96个细胞。在这里,我们解决了这些限制,并提出了一种新的方案,该方案允许在单细胞分辨率下对全长总RNA进行高通量测序。我们证明,我们的方法为多聚腺苷酸化和非多聚腺苷酸化转录本都产生了链特异性测序数据,能够对仅转录本末端之外的转录本区域进行分析,并产生了足够丰富的数据,以允许从异质生物样本中识别细胞类型。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/2cb0c4fdd3f1/fgene-12-665888-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/91cd34bef76f/fgene-12-665888-g001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/916373da18e2/fgene-12-665888-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/2cb0c4fdd3f1/fgene-12-665888-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/91cd34bef76f/fgene-12-665888-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/89d82dd9a72c/fgene-12-665888-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1047/8209500/916373da18e2/fgene-12-665888-g003.jpg
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1
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Nat Commun. 2020 Jan 3;11(1):90. doi: 10.1038/s41467-019-13840-9.
2
Clonal Decomposition and DNA Replication States Defined by Scaled Single-Cell Genome Sequencing.规模化单细胞基因组测序定义的克隆分解和 DNA 复制状态。
Cell. 2019 Nov 14;179(5):1207-1221.e22. doi: 10.1016/j.cell.2019.10.026.
3
Differential roles of protease isoforms in the tumor microenvironment.不同蛋白酶亚型在肿瘤微环境中的作用。
用于对多聚腺苷酸化和非多聚腺苷酸化RNA进行长读长纳米孔测序的适应性强且全面的方法。
Front Genet. 2024 Dec 2;15:1466338. doi: 10.3389/fgene.2024.1466338. eCollection 2024.
4
Full-length transcriptome analysis of the bloom-forming dinoflagellate by single-molecule real-time sequencing.通过单分子实时测序对形成水华的甲藻进行全长转录组分析。
Front Microbiol. 2022 Oct 17;13:993914. doi: 10.3389/fmicb.2022.993914. eCollection 2022.
5
Chimeric RNAs Discovered by RNA Sequencing and Their Roles in Cancer and Rare Genetic Diseases.通过 RNA 测序发现的嵌合 RNA 及其在癌症和罕见遗传疾病中的作用。
Genes (Basel). 2022 Apr 22;13(5):741. doi: 10.3390/genes13050741.
Cancer Metastasis Rev. 2019 Sep;38(3):389-415. doi: 10.1007/s10555-019-09816-2.
4
Evaluation of protocols for rRNA depletion-based RNA sequencing of nanogram inputs of mammalian total RNA.评价基于 rRNA 耗尽的哺乳动物总 RNA 纳克输入 RNA 测序的方案。
PLoS One. 2019 Oct 31;14(10):e0224578. doi: 10.1371/journal.pone.0224578. eCollection 2019.
5
SMARTer single cell total RNA sequencing.SMARTer 单细胞总 RNA 测序。
Nucleic Acids Res. 2019 Sep 19;47(16):e93. doi: 10.1093/nar/gkz535.
6
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7
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Nat Immunol. 2019 Feb;20(2):163-172. doi: 10.1038/s41590-018-0276-y. Epub 2019 Jan 14.
8
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Front Immunol. 2018 Dec 18;9:2994. doi: 10.3389/fimmu.2018.02994. eCollection 2018.
9
fastp: an ultra-fast all-in-one FASTQ preprocessor.fastp:一个超快速的一体化 FASTQ 预处理程序。
Bioinformatics. 2018 Sep 1;34(17):i884-i890. doi: 10.1093/bioinformatics/bty560.
10
Disease-specific oligodendrocyte lineage cells arise in multiple sclerosis.多发性硬化症中出现了特定于疾病的少突胶质细胞谱系细胞。
Nat Med. 2018 Dec;24(12):1837-1844. doi: 10.1038/s41591-018-0236-y. Epub 2018 Nov 12.