| Literature DB >> 29874042 |
Esmi L Zajaczkowski1, Qiong-Yi Zhao1, Zong Hong Zhang1, Xiang Li1, Wei Wei1, Paul R Marshall1, Laura J Leighton1, Sarah Nainar, Chao Feng, Robert C Spitale, Timothy W Bredy1.
Abstract
Transcriptome-wide expression profiling of neurons has provided important insights into the underlying molecular mechanisms and gene expression patterns that transpire during learning and memory formation. However, there is a paucity of tools for profiling stimulus-induced RNA within specific neuronal cell populations. A bioorthogonal method to chemically label nascent (i.e., newly transcribed) RNA in a cell-type-specific and temporally controlled manner, which is also amenable to bioconjugation via click chemistry, was recently developed and optimized within conventional immortalized cell lines. However, its value within a more fragile and complicated cellular system such as neurons, as well as for transcriptome-wide expression profiling, has yet to be demonstrated. Here, we report the visualization and sequencing of activity-dependent nascent RNA derived from neurons using this labeling method. This work has important implications for improving transcriptome-wide expression profiling and visualization of nascent RNA in neurons, which has the potential to provide valuable insights into the mechanisms underlying neural plasticity, learning, and memory.Entities:
Keywords: CuAAC; Nascent RNA; UPRT; neuron; transcriptome-wide profiling
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Year: 2018 PMID: 29874042 PMCID: PMC6272126 DOI: 10.1021/acschemneuro.8b00197
Source DB: PubMed Journal: ACS Chem Neurosci ISSN: 1948-7193 Impact factor: 4.418