<script type="text/javascript">
<!--
document.write('<div id="oa_widget"></div>');
document.write('<script type="text/javascript" src="https://www.openaire.eu/index.php?option=com_openaire&view=widget&format=raw&projectId=undefined&type=result"></script>');
-->
</script>Degradation of high affinity HuD targets releases Kv1.1 mRNA from miR-129 repression by mTORC1
Degradation of high affinity HuD targets releases Kv1.1 mRNA from miR-129 repression by mTORC1
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.
- University of New Mexico United States
- The University of Texas at Austin United States
- Texas A&M Health Science Center United States
- University of New Mexico
- University of New Mexico Health Sciences Center United States
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
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
28 Research products, page 1 of 3
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
- 2017IsRelatedTo
chevron_left - 1
- 2
- 3
chevron_right
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).106 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.Top 10% influence This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).Top 10% impulse This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.Top 1%
