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EMBO Rep ; 25(7): 3008-3039, 2024 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-38831125

RESUMEN

The circular RNA (circRNA) Cdr1as is conserved across mammals and highly expressed in neurons, where it directly interacts with microRNA miR-7. However, the biological function of this interaction is unknown. Here, using primary cortical murine neurons, we demonstrate that stimulating neurons by sustained depolarization rapidly induces two-fold transcriptional upregulation of Cdr1as and strong post-transcriptional stabilization of miR-7. Cdr1as loss causes doubling of glutamate release from stimulated synapses and increased frequency and duration of local neuronal bursts. Moreover, the periodicity of neuronal networks increases, and synchronicity is impaired. Strikingly, these effects are reverted by sustained expression of miR-7, which also clears Cdr1as molecules from neuronal projections. Consistently, without Cdr1as, transcriptomic changes caused by miR-7 overexpression are stronger (including miR-7-targets downregulation) and enriched in secretion/synaptic plasticity pathways. Altogether, our results suggest that in cortical neurons Cdr1as buffers miR-7 activity to control glutamatergic excitatory transmission and neuronal connectivity important for long-lasting synaptic adaptations.


Asunto(s)
Ácido Glutámico , MicroARNs , Neuronas , Transmisión Sináptica , MicroARNs/genética , MicroARNs/metabolismo , Animales , Neuronas/metabolismo , Ratones , Ácido Glutámico/metabolismo , Transmisión Sináptica/genética , Plasticidad Neuronal/genética , ARN Circular/genética , ARN Circular/metabolismo , Sinapsis/metabolismo , ARN Largo no Codificante/genética , ARN Largo no Codificante/metabolismo , Regulación de la Expresión Génica , Células Cultivadas
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