Nature Communications (Nov 2023)

Fear extinction is regulated by the activity of long noncoding RNAs at the synapse

  • Wei-Siang Liau,
  • Qiongyi Zhao,
  • Adekunle Bademosi,
  • Rachel S. Gormal,
  • Hao Gong,
  • Paul R. Marshall,
  • Ambika Periyakaruppiah,
  • Sachithrani U. Madugalle,
  • Esmi L. Zajaczkowski,
  • Laura J. Leighton,
  • Haobin Ren,
  • Mason Musgrove,
  • Joshua Davies,
  • Simone Rauch,
  • Chuan He,
  • Bryan C. Dickinson,
  • Xiang Li,
  • Wei Wei,
  • Frédéric A. Meunier,
  • Sandra M. Fernández-Moya,
  • Michael A. Kiebler,
  • Balakumar Srinivasan,
  • Sourav Banerjee,
  • Michael Clark,
  • Robert C. Spitale,
  • Timothy W. Bredy

DOI
https://doi.org/10.1038/s41467-023-43535-1
Journal volume & issue
Vol. 14, no. 1
pp. 1 – 16

Abstract

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Abstract Long noncoding RNAs (lncRNAs) represent a multidimensional class of regulatory molecules that are involved in many aspects of brain function. Emerging evidence indicates that lncRNAs are localized to the synapse; however, a direct role for their activity in this subcellular compartment in memory formation has yet to be demonstrated. Using lncRNA capture-seq, we identified a specific set of lncRNAs that accumulate in the synaptic compartment within the infralimbic prefrontal cortex of adult male C57/Bl6 mice. Among these was a splice variant related to the stress-associated lncRNA, Gas5. RNA immunoprecipitation followed by mass spectrometry and single-molecule imaging revealed that this Gas5 isoform, in association with the RNA binding proteins G3BP2 and CAPRIN1, regulates the activity-dependent trafficking and clustering of RNA granules. In addition, we found that cell-type-specific, activity-dependent, and synapse-specific knockdown of the Gas5 variant led to impaired fear extinction memory. These findings identify a new mechanism of fear extinction that involves the dynamic interaction between local lncRNA activity and RNA condensates in the synaptic compartment.