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The Journal of Cell Biology
Article
License: CC BY NC SA
Data sources: UnpayWall
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PubMed Central
Other literature type . 2013
Data sources: PubMed Central
The Journal of Cell Biology
Article . 2013 . Peer-reviewed
Data sources: Crossref
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Degradation of high affinity HuD targets releases Kv1.1 mRNA from miR-129 repression by mTORC1

Authors: Peggy P.C. Huang; Chun Jung Chen; Luisa P. Cacheaux; Kathleen Nguyen; Nora I. Perrone-Bizzozero; Kimberly F. Raab-Graham; Natasha M. Sosanya;

Degradation of high affinity HuD targets releases Kv1.1 mRNA from miR-129 repression by mTORC1

Abstract

Little is known about how a neuron undergoes site-specific changes in intrinsic excitability during neuronal activity. We provide evidence for a novel mechanism for mTORC1 kinase–dependent translational regulation of the voltage-gated potassium channel Kv1.1 messenger RNA (mRNA). We identified a microRNA, miR-129, that repressed Kv1.1 mRNA translation when mTORC1 was active. When mTORC1 was inactive, we found that the RNA-binding protein, HuD, bound to Kv1.1 mRNA and promoted its translation. Unexpectedly, inhibition of mTORC1 activity did not alter levels of miR-129 and HuD to favor binding to Kv1.1 mRNA. However, reduced mTORC1 signaling caused the degradation of high affinity HuD target mRNAs, freeing HuD to bind Kv1.1 mRNA. Hence, mTORC1 activity regulation of mRNA stability and high affinity HuD-target mRNA degradation mediates the bidirectional expression of dendritic Kv1.1 ion channels.

Keywords

Neurons, Binding Sites, Neuronal Plasticity, RNA Stability, Proteins, ELAV-Like Protein 4, Mechanistic Target of Rapamycin Complex 1, Rats, Enzyme Activation, MicroRNAs, HEK293 Cells, ELAV Proteins, Multiprotein Complexes, Protein Biosynthesis, Proteolysis, Animals, Humans, RNA, Messenger, RNA Processing, Post-Transcriptional, Kv1.1 Potassium Channel, Research Articles

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citations
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
106
Top 10%
Top 10%
Top 1%
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