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