Many cells contain spatially defined subcellular regions that perform specialized tasks enabled by localized proteins. The subcellular distribution of these localized proteins is often facilitated by the subcellular localization of the RNA molecules that encode them. A key question in the study of this process of RNA localization is the characterization of the transcripts present at a given subcellular location. Historically, experiments aimed at answering this question have centered upon microscopy-based techniques that target one or a few transcripts at a time. However, more recently, the advent of high-throughput RNA sequencing has allowed the transcriptome-wide profiling of the RNA content of subcellular fractions. Here, we present a protocol for the isolation of cell body and neurite fractions from neuronal cells using mechanical fractionation and characterization of their RNA content. Graphic abstract: Fractionation of neuronal cells and analysis of subcellular RNA contents.
Mechanical Fractionation of Cultured Neuronal Cells into Cell Body and Neurite Fractions.
将培养的神经元细胞机械分离成细胞体和神经突部分
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作者:Arora Ankita, Goering Raeann, Lo Hei-Yong G, Taliaferro Matthew J
| 期刊: | Bio-protocol | 影响因子: | 1.100 |
| 时间: | 2021 | 起止号: | 2021 Jun 5; 11(11):e4048 |
| doi: | 10.21769/BioProtoc.4048 | 研究方向: | 神经科学、细胞生物学 |
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