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

Esmi L ZajaczkowskiQiong-Yi ZhaoZong Hong ZhangXiang LiWei WeiPaul R MarshallLaura J LeightonSarah NainarChao FengRobert C SpitaleTimothy W Bredy
Published in: ACS chemical neuroscience (2018)
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.
Keyphrases
  • single cell
  • genome wide
  • gene expression
  • rna seq
  • spinal cord
  • dna methylation
  • nucleic acid
  • risk assessment
  • climate change
  • cell therapy
  • genome wide identification
  • diabetic rats
  • high glucose