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        <identifier>oai:figshare.com:article/34004685</identifier>
        <datestamp>2026-09-27T11:26:28Z</datestamp>
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          <dc:title>Synapse-enriched lncRNAs are required for local translation and hippocampal-dependent fear memory</dc:title>
          <dc:creator>Sarbani Samaddar (9292799)</dc:creator>
          <dc:creator>Balakumar Srinivasan (9271115)</dc:creator>
          <dc:creator>Kamakshi Garg (21375442)</dc:creator>
          <dc:creator>Nandu Raj (25115814)</dc:creator>
          <dc:creator>Sania Sultana (18838432)</dc:creator>
          <dc:creator>Utsav Mukherjee (25115820)</dc:creator>
          <dc:creator>Dipanjana Banerjee (12487291)</dc:creator>
          <dc:creator>Wei-Siang Liau (17278144)</dc:creator>
          <dc:creator>Jian Xue (145753)</dc:creator>
          <dc:creator>Yangxi Lin (25115836)</dc:creator>
          <dc:creator>Dasaradhi Palakodeti (173941)</dc:creator>
          <dc:creator>Timothy W. Bredy (24667027)</dc:creator>
          <dc:creator>Sourav Banerjee (18838420)</dc:creator>
          <dc:subject>Behavioural neuroscience</dc:subject>
          <dc:subject>Neurosciences not elsewhere classified</dc:subject>
          <dc:subject>long non-coding RNAs(lncRNAs)</dc:subject>
          <dc:subject>RNA binding proteins (RBPs)</dc:subject>
          <dc:subject>Local translation</dc:subject>
          <dc:subject>Synapse development</dc:subject>
          <dc:subject>Memory</dc:subject>
          <dc:description>&lt;p dir="ltr"&gt;Studies on neuronal long noncoding RNAs (lncRNAs) have remained predominantly nucleus-centric, leaving the identity and the functional landscape of synapse-enriched lncRNAs underexplored.We identify 95 synapse-enriched lncRNAs in the adult mouse hippocampus and outline the physiological roles of the synaptic lncRNAs Pvt1,Pantr1and a  previously uncharacterized synaptic lncRNA 241000H16Rik (which we call SynLAMP), in contexts of synapse development, synaptic plasticity and memory. Pvt1 exclusively regulates excitatory synapse development, and its synapse-specific loss alters synaptic activity keeping fear-memory unaltered. Contrastingly, SynLAMP demonstrates a more synapse-centric role in activity-dependent translation and fear memory. Fear-conditioning enhances SynLAMP abundance in the dendrites, where it promotes local translation by sequestering the translation inhibitor FUS. Synaptic loss of SynLAMP, or disruption in its FUS interaction impairs fear-memory and the activity-dependent local translation of CaMK2α, a FUS target. Enhanced allocation of SynLAMP to the synapse and its dynamic interaction with FUS suggests that SynLAMP behaves as an activity-dependent, synapse-localized molecular decoy that bolsters fear memory. Collectively, this study provides a mechanistic introspection on the pervasive influence of synapse-localized lncRNAs in aspects of synapse development, activity-dependent local translation, and memory formation, highlighting a stronger demand to understand the role of localized lncRNAs in broader cellular contexts.&lt;/p&gt;</dc:description>
          <dc:date>2026-09-27T11:26:28Z</dc:date>
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          <dc:identifier>10.6084/m9.figshare.34004685.v1</dc:identifier>
          <dc:relation>https://figshare.com/articles/dataset/Synapse-enriched_lncRNAs_are_required_for_local_translation_and_hippocampal-dependent_fear_memory/34004685</dc:relation>
          <dc:rights>CC BY 4.0</dc:rights>
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