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基于 Smart-seq3 技术进行等位基因和异构体分辨率的单细胞 RNA 计数

Single-cell RNA counting at allele and isoform resolution using Smart-seq3.

机构信息

Department of Cell and Molecular Biology, Karolinska Institutet, Stockholm, Sweden.

Integrated Cardio Metabolic Center, Karolinska Institutet, Stockholm, Sweden.

出版信息

Nat Biotechnol. 2020 Jun;38(6):708-714. doi: 10.1038/s41587-020-0497-0. Epub 2020 May 4.

Abstract

Large-scale sequencing of RNA from individual cells can reveal patterns of gene, isoform and allelic expression across cell types and states. However, current short-read single-cell RNA-sequencing methods have limited ability to count RNAs at allele and isoform resolution, and long-read sequencing techniques lack the depth required for large-scale applications across cells. Here we introduce Smart-seq3, which combines full-length transcriptome coverage with a 5' unique molecular identifier RNA counting strategy that enables in silico reconstruction of thousands of RNA molecules per cell. Of the counted and reconstructed molecules, 60% could be directly assigned to allelic origin and 30-50% to specific isoforms, and we identified substantial differences in isoform usage in different mouse strains and human cell types. Smart-seq3 greatly increased sensitivity compared to Smart-seq2, typically detecting thousands more transcripts per cell. We expect that Smart-seq3 will enable large-scale characterization of cell types and states across tissues and organisms.

摘要

对单个细胞的 RNA 进行大规模测序可以揭示不同细胞类型和状态下基因、异构体和等位基因表达的模式。然而,目前的短读长单细胞 RNA 测序方法在等位基因和异构体分辨率上对 RNA 的计数能力有限,而长读长测序技术缺乏在细胞间进行大规模应用所需的深度。在这里,我们介绍 Smart-seq3,它将全长转录组覆盖与 5'独特分子标识符 RNA 计数策略相结合,使每个细胞能够对数千个 RNA 分子进行计算机重建。在计数和重建的分子中,60%可以直接分配给等位基因起源,30-50%可以分配给特定异构体,我们发现不同小鼠品系和人类细胞类型中异构体的使用存在显著差异。与 Smart-seq2 相比,Smart-seq3 的灵敏度大大提高,通常每细胞检测到数千个更多的转录本。我们预计 Smart-seq3 将能够在组织和生物体中大规模描述细胞类型和状态。

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