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扩展测序:在完整生物系统中进行空间精确的原位转录组学分析。

Expansion sequencing: Spatially precise in situ transcriptomics in intact biological systems.

机构信息

Department of Media Arts and Sciences, MIT, Cambridge, MA, USA.

McGovern Institute, MIT, Cambridge, MA, USA.

出版信息

Science. 2021 Jan 29;371(6528). doi: 10.1126/science.aax2656.

Abstract

Methods for highly multiplexed RNA imaging are limited in spatial resolution and thus in their ability to localize transcripts to nanoscale and subcellular compartments. We adapt expansion microscopy, which physically expands biological specimens, for long-read untargeted and targeted in situ RNA sequencing. We applied untargeted expansion sequencing (ExSeq) to the mouse brain, which yielded the readout of thousands of genes, including splice variants. Targeted ExSeq yielded nanoscale-resolution maps of RNAs throughout dendrites and spines in the neurons of the mouse hippocampus, revealing patterns across multiple cell types, layer-specific cell types across the mouse visual cortex, and the organization and position-dependent states of tumor and immune cells in a human metastatic breast cancer biopsy. Thus, ExSeq enables highly multiplexed mapping of RNAs from nanoscale to system scale.

摘要

方法进行高多重 RNA 成像受限于空间分辨率,因此无法将转录物定位到纳米级和亚细胞隔室。我们改编了扩展显微镜,该显微镜通过物理方式扩展生物样本,用于长读长无靶向和靶向原位 RNA 测序。我们将无靶向扩展测序(ExSeq)应用于小鼠大脑,得到了数千个基因的读值,包括剪接变体。靶向 ExSeq 获得了小鼠海马体神经元中树突和棘突内 RNA 的纳米级分辨率图谱,揭示了多种细胞类型、小鼠视觉皮层中特定于层的细胞类型以及人类转移性乳腺癌活检中肿瘤和免疫细胞的组织和位置依赖性状态的模式。因此,ExSeq 能够从纳米级到系统级对 RNA 进行高度多重映射。

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