microRNA-Seq reveals cocaine-regulated expression of striatal microRNAs

Jodi E. Eipper-Mains, Drew D. Kiraly, Dasaradhi Palakodeti, Richard E. Mains, Betty A. Eipper, Brenton R. Graveley

Research output: Contribution to journalArticlepeer-review

119 Scopus citations

Abstract

MicroRNAs (miRNAs) are small RNAs that modulate gene expression by binding target mRNAs. The hundreds of miRNAs expressed in the brain are critical for synaptic development and plasticity. Drugs of abuse cause lasting changes in the limbic regions of the brain that process reward, and addiction is viewed as a form of aberrant neuroplasticity. Using next-generation sequencing, we cataloged miRNA expression in the nucleus accumbens and at striatal synapses in control and chronically cocaine-treated mice. We identified cocaine-responsive miRNAs, synaptically enriched and depleted miRNA families, and confirmed cocaine-induced changes in protein expression for several predicted synaptic target genes. The miR-8 family, known for its roles in cancer, is highly enriched and cocaine regulated at striatal synapses, where its members may affect expression of cell adhesion molecules. Synaptically enriched cocaine-regulated miRNAs may contribute to long-lasting drug-induced plasticity through fine-tuning regulatory pathways that modulate the actin cytoskeleton, neurotransmitter metabolism, and peptide hormone processing. Published by Cold Spring Harbor Laboratory Press.

Original languageEnglish
Pages (from-to)1529-1543
Number of pages15
JournalRNA
Volume17
Issue number8
DOIs
StatePublished - Aug 2011
Externally publishedYes

Keywords

  • Bioinformatics
  • Cocaine
  • Deep sequencing
  • RNA-Seq
  • microRNA

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