| Literature DB >> 30219486 |
Anirudh Vashisht1, Svitlana V Bach2, Dustin Fetterhoff2, James W Morgan2, Maria McGee3, Ashok N Hegde4.
Abstract
Proteolysis by the ubiquitin-proteasome pathway has pleiotropic effects on both induction and maintenance of long-term synaptic plasticity. In this study, we examined the effect of proteasome inhibition on signaling to the nucleus during late-phase long-term potentiation. When a subthreshold L-LTP induction protocol was used, proteasome inhibition led to a significant increase in phosphorylated CREB (pCREB) in the nucleus. Inhibitors of cAMP-dependent protein kinase/protein kinase A, extracellular signal-regulated kinase and cGMP-dependent protein kinase/protein kinase G all blocked the proteasome-inhibition-mediated increase in nuclear pCREB after subthreshold stimulation. These results lay the groundwork for understanding a novel role for the proteasome in limiting signaling to the nucleus in the absence of adequate synaptic stimulation.Entities:
Keywords: Gene expression; Long-term potentiation; Protein degradation; Protein kinase; Transcription factor
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Year: 2018 PMID: 30219486 PMCID: PMC6231982 DOI: 10.1016/j.neulet.2018.09.017
Source DB: PubMed Journal: Neurosci Lett ISSN: 0304-3940 Impact factor: 3.046