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NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure
The neuronal RNA binding protein NOVA regulates splicing, shuttles to the cytoplasm, and co-localizes with target transcripts in dendrites, suggesting links between splicing and local translation. Here we identified >200 transcripts showing NOVA-dependent changes in abundance, but, surprisingly,...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
eLife Sciences Publications, Ltd
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552424/ https://www.ncbi.nlm.nih.gov/pubmed/23359859 http://dx.doi.org/10.7554/eLife.00178 |
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author | Eom, Taesun Zhang, Chaolin Wang, Huidong Lay, Kenneth Fak, John Noebels, Jeffrey L Darnell, Robert B |
author_facet | Eom, Taesun Zhang, Chaolin Wang, Huidong Lay, Kenneth Fak, John Noebels, Jeffrey L Darnell, Robert B |
author_sort | Eom, Taesun |
collection | PubMed |
description | The neuronal RNA binding protein NOVA regulates splicing, shuttles to the cytoplasm, and co-localizes with target transcripts in dendrites, suggesting links between splicing and local translation. Here we identified >200 transcripts showing NOVA-dependent changes in abundance, but, surprisingly, HITS-CLIP revealed NOVA binds these RNAs in introns rather than 3′ UTRs. This led us to discover NOVA-regulated splicing of cryptic exons within these introns. These exons triggered nonsense mediated decay (NMD), as UPF1 and protein synthesis were required for NOVA's effect on RNA levels. Their regulation was dynamic and physiologically relevant. The NMD exons were regulated by seizures, which also induced changes in Nova subcellular localization and mediated large changes in synaptic proteins, including proteins implicated in familial epilepsy. Moreover, Nova haploinsufficient mice had spontaneous epilepsy. The data reveal a hidden means of dynamic RNA regulation linking electrical activity to splicing and protein output, and of mediating homeostatic excitation/inhibition balance in neurons. DOI: http://dx.doi.org/10.7554/eLife.00178.001 |
format | Online Article Text |
id | pubmed-3552424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | eLife Sciences Publications, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-35524242013-01-28 NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure Eom, Taesun Zhang, Chaolin Wang, Huidong Lay, Kenneth Fak, John Noebels, Jeffrey L Darnell, Robert B eLife Biochemistry The neuronal RNA binding protein NOVA regulates splicing, shuttles to the cytoplasm, and co-localizes with target transcripts in dendrites, suggesting links between splicing and local translation. Here we identified >200 transcripts showing NOVA-dependent changes in abundance, but, surprisingly, HITS-CLIP revealed NOVA binds these RNAs in introns rather than 3′ UTRs. This led us to discover NOVA-regulated splicing of cryptic exons within these introns. These exons triggered nonsense mediated decay (NMD), as UPF1 and protein synthesis were required for NOVA's effect on RNA levels. Their regulation was dynamic and physiologically relevant. The NMD exons were regulated by seizures, which also induced changes in Nova subcellular localization and mediated large changes in synaptic proteins, including proteins implicated in familial epilepsy. Moreover, Nova haploinsufficient mice had spontaneous epilepsy. The data reveal a hidden means of dynamic RNA regulation linking electrical activity to splicing and protein output, and of mediating homeostatic excitation/inhibition balance in neurons. DOI: http://dx.doi.org/10.7554/eLife.00178.001 eLife Sciences Publications, Ltd 2013-01-22 /pmc/articles/PMC3552424/ /pubmed/23359859 http://dx.doi.org/10.7554/eLife.00178 Text en © 2013, Eom et al http://creativecommons.org/licenses/by/3.0/ This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits unrestricted use and redistribution provided that the original author and source are credited. |
spellingShingle | Biochemistry Eom, Taesun Zhang, Chaolin Wang, Huidong Lay, Kenneth Fak, John Noebels, Jeffrey L Darnell, Robert B NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure |
title | NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure |
title_full | NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure |
title_fullStr | NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure |
title_full_unstemmed | NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure |
title_short | NOVA-dependent regulation of cryptic NMD exons controls synaptic protein levels after seizure |
title_sort | nova-dependent regulation of cryptic nmd exons controls synaptic protein levels after seizure |
topic | Biochemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3552424/ https://www.ncbi.nlm.nih.gov/pubmed/23359859 http://dx.doi.org/10.7554/eLife.00178 |
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