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Transcriptome-wide discovery of microRNA binding sites in human brain.

Neuron | 2014

The orchestration of brain function requires complex gene regulatory networks that are modulated, in part, by microRNAs (miRNAs). These noncoding RNAs associate with argonaute (Ago) proteins in order to direct posttranscriptional gene suppression via base pairing with target transcripts. In order to better understand how miRNAs contribute to human-specialized brain processes and neurological phenotypes, identifying their targets is of paramount importance. Here, we address the latter by profiling Ago2:RNA interactions using HITS-CLIP to generate a transcriptome-wide map of miRNA binding sites in human brain. We uncovered ∼ 7,000 stringent Ago2 binding sites that are highly enriched for conserved sequences corresponding to abundant brain miRNAs. This interactome points to functional miRNA:target pairs across >3,000 genes and represents a valuable resource for accelerating our understanding of miRNA functions in brain. We demonstrate the utility of this map for exploring clinically relevant miRNA binding sites that may facilitate the translation of genetic studies of complex neuropsychiatric diseases into therapeutics.

Pubmed ID: 24389009 RIS Download

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Associated grants

  • Agency: NIGMS NIH HHS, United States
    Id: R01 GM088342
  • Agency: NIEHS NIH HHS, United States
    Id: P30 ES005605
  • Agency: NHLBI NIH HHS, United States
    Id: T32 HL007121
  • Agency: NINDS NIH HHS, United States
    Id: P01 NS050210
  • Agency: NIDA NIH HHS, United States
    Id: R21 DA025132
  • Agency: NINDS NIH HHS, United States
    Id: NS50210
  • Agency: NHLBI NIH HHS, United States
    Id: HL07121
  • Agency: NIDA NIH HHS, United States
    Id: DA025132
  • Agency: NIAID NIH HHS, United States
    Id: R37 AI021640
  • Agency: NIGMS NIH HHS, United States
    Id: GM088342

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Human Gene Mutation Database (tool)

RRID:SCR_001621

Curated database of known (published) gene lesions responsible for human inherited disease.

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