Protocol for isolating specific C. elegans neuron types for bulk and single-cell RNA sequencing.

IF 1.3 Q4 BIOCHEMICAL RESEARCH METHODS STAR Protocols Pub Date : 2024-12-20 Epub Date: 2024-11-06 DOI:10.1016/j.xpro.2024.103439
Seth R Taylor, Rebecca D McWhirter, Brittany K Matlock, David K Flaherty, David M Miller
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引用次数: 0

Abstract

The C. elegans nervous system is compact and well described, ideal for identifying genetic programs that drive neuron-specific development, function, and connectivity. Here, we present a protocol for isolating specific neuron types for gene expression profiling by bulk or single-cell RNA sequencing. We describe steps for worm synchronization, dissociation, and fluorescence-activated cell sorting (FACS) isolation. We then detail procedures for RNA extraction and preparing cells for single-cell sequencing. This protocol is applicable to the isolation of individual cell types from larval and adult animals. For additional details on the use and execution of this protocol, see Taylor et al.1.

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用于大量和单细胞 RNA 测序的特定秀丽隐杆线虫神经元类型分离规程。
秀丽隐杆线虫神经系统结构紧凑、描述详尽,非常适合用于鉴定驱动神经元特异性发育、功能和连接的遗传程序。在此,我们介绍了一种分离特定神经元类型的方案,以便通过大量或单细胞 RNA 测序进行基因表达谱分析。我们介绍了虫体同步、解离和荧光激活细胞分选(FACS)分离的步骤。然后我们详细介绍了提取 RNA 和准备单细胞测序细胞的步骤。该方案适用于从幼虫和成虫中分离单个细胞类型。有关本方案使用和执行的更多详情,请参阅 Taylor 等人1。
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来源期刊
STAR Protocols
STAR Protocols Biochemistry, Genetics and Molecular Biology-General Biochemistry, Genetics and Molecular Biology
CiteScore
2.00
自引率
0.00%
发文量
789
审稿时长
10 weeks
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