<i>Grin2b</i> 3'UTR is necessary for synaptic plasticity and spatial learning.

Abstract

Spatially precise protein synthesis is critical for synaptic plasticity and cognitive function. The <i>GRIN2B</i> transcript encodes the GluN2B subunit of N-methyl-D-aspartate (NMDA) receptors and has a 25 kb-long 3'-untranslated region (3'UTR) of unknown function. To investigate its role, we generated a ∆3'UTR mouse line by deleting the <i>Grin2b</i> 3'UTR while preserving the coding sequence. Despite unchanged <i>Grin2b</i> mRNA levels in ∆3'UTR mice, GluN2B protein was reduced 50%. In wildtype (WT) mice, <i>Grin2b</i> mRNA was enriched in synaptosomes, but this enrichment was impaired in ∆3'UTR mice along with reduced GluN2B phosphorylation. Notably, ∆3'UTR mice had no long-term potentiation (LTP) and exhibited hippocampal-dependent spatial learning impairments. Together, these findings demonstrate that the 3'UTR is critical for <i>Grin2b</i> mRNA function, ultimately influencing synaptic composition and plasticity.