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WeightNameValue
1000 Titel
  • Neuronal activity regulates alternative exon usage
1000 Autor/in
  1. Denkena, Johanna |
  2. Zaisser, Andrea |
  3. Merz, Barbara |
  4. Klinger, Bertram |
  5. Kuhl, Dietmar |
  6. Blüthgen, Nils |
  7. Hermey, Guido |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-11-10
1000 Erschienen in
1000 Quellenangabe
  • 13(1):148
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1186/s13041-020-00685-3 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7656758/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Neuronal activity-regulated gene transcription underlies plasticity-dependent changes in the molecular composition and structure of neurons. A large number of genes regulated by different neuronal plasticity inducing pathways have been identified, but altered gene expression levels represent only part of the complexity of the activity-regulated transcriptional program. Alternative splicing, the differential inclusion and exclusion of exonic sequence in mRNA, is an additional mechanism that is thought to define the activity-dependent transcriptome. Here, we present a genome wide microarray-based survey to identify exons with increased expression levels at 1, 4 or 8 h following neuronal activity in the murine hippocampus provoked by generalized seizures. We used two different bioinformatics approaches to identify alternative activity-induced exon usage and to predict alternative splicing, ANOSVA (ANalysis Of Splicing VAriation) which we here adjusted to accommodate data from different time points and FIRMA (Finding Isoforms using Robust Multichip Analysis). RNA sequencing, in situ hybridization and reverse transcription PCR validate selected activity-dependent splicing events of previously described and so far undescribed activity-regulated transcripts, including Homer1a, Homer1d, Ania3, Errfi1, Inhba, Dclk1, Rcan1, Cda, Tpm1 and Krt75. Taken together, our survey significantly adds to the comprehensive understanding of the complex activity-dependent neuronal transcriptomic signature. In addition, we provide data sets that will serve as rich resources for future comparative expression analyses.
1000 Sacherschließung
lokal Mice, Inbred C57BL [MeSH]
lokal Exons/genetics [MeSH]
lokal Hippocampus
lokal Neurons/metabolism [MeSH]
lokal Nerve Tissue Proteins/metabolism [MeSH]
lokal Microarray
lokal Synaptic plasticity
lokal Animals [MeSH]
lokal Nerve Tissue Proteins/genetics [MeSH]
lokal Alternative Splicing/genetics [MeSH]
lokal Alternative splicing
lokal Male [MeSH]
lokal Neuronal activity
lokal Reproducibility of Results [MeSH]
lokal Transcriptome
lokal Research
lokal RNA sequencing
lokal Gene expression
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/RGVua2VuYSwgSm9oYW5uYQ==|https://frl.publisso.de/adhoc/uri/WmFpc3NlciwgQW5kcmVh|https://frl.publisso.de/adhoc/uri/TWVyeiwgQmFyYmFyYQ==|https://frl.publisso.de/adhoc/uri/S2xpbmdlciwgQmVydHJhbQ==|https://frl.publisso.de/adhoc/uri/S3VobCwgRGlldG1hcg==|https://frl.publisso.de/adhoc/uri/QmzDvHRoZ2VuLCBOaWxz|https://orcid.org/0000-0003-4762-5262
1000 Hinweis
  • DeepGreen-ID: 4579bc9aafd84daaac2a15bd899cd15c ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 Dateien
  1. Neuronal activity regulates alternative exon usage
1000 Objektart article
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1000 @id frl:6463047.rdf
1000 Erstellt am 2023-11-15T16:14:48.035+0100
1000 Erstellt von 322
1000 beschreibt frl:6463047
1000 Zuletzt bearbeitet 2023-11-30T20:55:31.780+0100
1000 Objekt bearb. Thu Nov 30 20:55:31 CET 2023
1000 Vgl. frl:6463047
1000 Oai Id
  1. oai:frl.publisso.de:frl:6463047 |
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