Abstract
Long-term memory requires the activity-dependent reorganization of the synaptic proteome to modulate synaptic efficacy and consequently consolidate memory. Activity-regulated RNA translation can change the protein composition at the stimulated synapse. Cytoplasmic polyadenylation element-binding protein 3 (CPEB3) is a sequence-specific RNA-binding protein that represses translation of its target mRNAs in neurons, while activation of N-methyl-d-aspartic acid (NMDA) receptors alleviates this repression. Although recent research has revealed the mechanism of CPEB3-inhibited translation, how NMDA receptor signaling modulates the translational activity of CPEB3 remains unclear. This study shows that the repressor CPEB3 is degraded in NMDA-stimulated neurons and that the degradation of CPEB3 is accompanied by the elevated expression of CPEB3's target, epidermal growth factor receptor (EGFR), mostly at the translational level. Using pharmacological and knockdown approaches, we have identified that calpain 2, activated by the influx of calcium through NMDA receptors, proteolyzes the N-terminal repression motif but not the C-terminal RNA-binding domain of CPEB3. As a result, the calpain 2-cleaved CPEB3 fragment binds to RNA but fails to repress translation. Therefore, the cleavage of CPEB3 by NMDA-activated calpain 2 accounts for the activity-related translation of CPEB3-targeted RNAs.
SUPPLEMENTAL MATERIAL
Supplemental material for this article may be found at http://dx.doi.org/10.1128/MCB.00296-12.
ACKNOWLEDGMENTS
We thank Sheau-Yann Shieh for the p53 construct and Woan-Yuh Tarn for the cDNA3.1-flag plasmid. We appreciate Fu-Ann Lee in the institutional core for conducting LC-MS/MS analysis and the RNAi Core in Academia Sinica for the Capns1 shRNA clones.
This work was supported by grants from the National Science Council (NSC 99-2311-B-001-020-MY3), National Health Research Institute (NHRI-EX101-9814NI), and Academia Sinica (AS-100-TP-B09) in Taiwan. The RNAi Core, which is supported by the National Research Program for Genomic Medicine grants, is also gratefully acknowledged.