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

Esmi L. Zajaczkowski, Qiong Yi Zhao, Zong Hong Zhang, Xiang Li, Wei Wei, Paul R. Marshall, Laura J. Leighton, Sarah Nainar, Chao Feng, Robert C. Spitale*, Timothy W. Bredy

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

14 Citations (Scopus)

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.

Original languageEnglish
Pages (from-to)1858-1865
Number of pages8
JournalACS Chemical Neuroscience
Volume9
Issue number7
DOIs
Publication statusPublished - 18 Jul 2018
Externally publishedYes

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