Literature DB >> 29874042

Bioorthogonal Metabolic Labeling of Nascent RNA in Neurons Improves the Sensitivity of Transcriptome-Wide Profiling.

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

Mesh:

Substances:

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


  38 in total

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  2 in total

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  2 in total

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