Genome-wide profiling of the activity-dependent hippocampal transcriptome

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Genome-wide profiling of the activity-dependent hippocampal transcriptome. / Hermey, Guido; Mahlke, Claudia; Gutzmann, Jakob J; Schreiber, Jörg; Blüthgen, Nils; Kuhl, Franz-Dietmar.

in: PLOS ONE, Jahrgang 8, Nr. 10, 01.01.2013, S. e76903.

Publikationen: SCORING: Beitrag in Fachzeitschrift/ZeitungSCORING: ZeitschriftenaufsatzForschungBegutachtung

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@article{8ce8775114d94ffa94d92d788af837cb,
title = "Genome-wide profiling of the activity-dependent hippocampal transcriptome",
abstract = "Activity-dependent gene expression is central for sculpting neuronal connectivity in the brain. Despite the importance for synaptic plasticity, a comprehensive analysis of the temporal changes in the transcriptomic response to neuronal activity is lacking. In a genome wide survey we identified genes that were induced at 1, 4, 8, or 24 hours following neuronal activity in the hippocampus. According to their distinct expression kinetics we assigned these genes to five clusters, each containing approximately 200 genes. Using in situ hybridizations the regulated expression of 24 genes was validated. Apart from known activity-dependent genes our study reveals a large number of unknown induced genes with distinct expression kinetics. Among these we identified several genes with complex temporal expression patterns. Furthermore, our study provides examples for activity-induced exon switching in the coding region of genes and activity-induced alternative splicing of the 3'-UTR. One example is Zwint. In contrast to the constitutively expressed variant, the induced Zwint transcript harbors multiple regulatory elements in the 3'-UTR. Taken together, our study provides a comprehensive analysis of the transcriptomic response to neuronal activity and sheds new light on expression kinetics and alternative splicing events.",
keywords = "3' Untranslated Regions, Alternative Splicing, Animals, Binding Sites, Cluster Analysis, Exons, Gene Expression Profiling, Gene Expression Regulation, Genome-Wide Association Study, Hippocampus, Male, Mice, Molecular Sequence Annotation, Protein Binding, Reproducibility of Results, Transcription Factors, Transcription, Genetic, Transcriptome",
author = "Guido Hermey and Claudia Mahlke and Gutzmann, {Jakob J} and J{\"o}rg Schreiber and Nils Bl{\"u}thgen and Franz-Dietmar Kuhl",
year = "2013",
month = jan,
day = "1",
doi = "10.1371/journal.pone.0076903",
language = "English",
volume = "8",
pages = "e76903",
journal = "PLOS ONE",
issn = "1932-6203",
publisher = "Public Library of Science",
number = "10",

}

RIS

TY - JOUR

T1 - Genome-wide profiling of the activity-dependent hippocampal transcriptome

AU - Hermey, Guido

AU - Mahlke, Claudia

AU - Gutzmann, Jakob J

AU - Schreiber, Jörg

AU - Blüthgen, Nils

AU - Kuhl, Franz-Dietmar

PY - 2013/1/1

Y1 - 2013/1/1

N2 - Activity-dependent gene expression is central for sculpting neuronal connectivity in the brain. Despite the importance for synaptic plasticity, a comprehensive analysis of the temporal changes in the transcriptomic response to neuronal activity is lacking. In a genome wide survey we identified genes that were induced at 1, 4, 8, or 24 hours following neuronal activity in the hippocampus. According to their distinct expression kinetics we assigned these genes to five clusters, each containing approximately 200 genes. Using in situ hybridizations the regulated expression of 24 genes was validated. Apart from known activity-dependent genes our study reveals a large number of unknown induced genes with distinct expression kinetics. Among these we identified several genes with complex temporal expression patterns. Furthermore, our study provides examples for activity-induced exon switching in the coding region of genes and activity-induced alternative splicing of the 3'-UTR. One example is Zwint. In contrast to the constitutively expressed variant, the induced Zwint transcript harbors multiple regulatory elements in the 3'-UTR. Taken together, our study provides a comprehensive analysis of the transcriptomic response to neuronal activity and sheds new light on expression kinetics and alternative splicing events.

AB - Activity-dependent gene expression is central for sculpting neuronal connectivity in the brain. Despite the importance for synaptic plasticity, a comprehensive analysis of the temporal changes in the transcriptomic response to neuronal activity is lacking. In a genome wide survey we identified genes that were induced at 1, 4, 8, or 24 hours following neuronal activity in the hippocampus. According to their distinct expression kinetics we assigned these genes to five clusters, each containing approximately 200 genes. Using in situ hybridizations the regulated expression of 24 genes was validated. Apart from known activity-dependent genes our study reveals a large number of unknown induced genes with distinct expression kinetics. Among these we identified several genes with complex temporal expression patterns. Furthermore, our study provides examples for activity-induced exon switching in the coding region of genes and activity-induced alternative splicing of the 3'-UTR. One example is Zwint. In contrast to the constitutively expressed variant, the induced Zwint transcript harbors multiple regulatory elements in the 3'-UTR. Taken together, our study provides a comprehensive analysis of the transcriptomic response to neuronal activity and sheds new light on expression kinetics and alternative splicing events.

KW - 3' Untranslated Regions

KW - Alternative Splicing

KW - Animals

KW - Binding Sites

KW - Cluster Analysis

KW - Exons

KW - Gene Expression Profiling

KW - Gene Expression Regulation

KW - Genome-Wide Association Study

KW - Hippocampus

KW - Male

KW - Mice

KW - Molecular Sequence Annotation

KW - Protein Binding

KW - Reproducibility of Results

KW - Transcription Factors

KW - Transcription, Genetic

KW - Transcriptome

U2 - 10.1371/journal.pone.0076903

DO - 10.1371/journal.pone.0076903

M3 - SCORING: Journal article

C2 - 24146943

VL - 8

SP - e76903

JO - PLOS ONE

JF - PLOS ONE

SN - 1932-6203

IS - 10

ER -