Literature DB >> 18786617

Transcriptome analysis identifies genes with enriched expression in the mouse central extended amygdala.

J A J Becker1, K Befort, C Blad, D Filliol, A Ghate, D Dembele, C Thibault, M Koch, J Muller, A Lardenois, O Poch, B L Kieffer.   

Abstract

The central extended amygdala (EAc) is an ensemble of highly interconnected limbic structures of the anterior brain, and forms a cellular continuum including the bed nucleus of the stria terminalis (BNST), the central nucleus of the amygdala (CeA) and the nucleus accumbens shell (AcbSh). This neural network is a key site for interactions between brain reward and stress systems, and has been implicated in several aspects of drug abuse. In order to increase our understanding of EAc function at the molecular level, we undertook a genome-wide screen (Affymetrix) to identify genes whose expression is enriched in the mouse EAc. We focused on the less-well known BNST-CeA areas of the EAc, and identified 121 genes that exhibit more than twofold higher expression level in the EAc compared with whole brain. Among these, 43 genes have never been described to be expressed in the EAc. We mapped these genes throughout the brain, using non-radioactive in situ hybridization, and identified eight genes with a unique and distinct rostro-caudal expression pattern along AcbSh, BNST and CeA. Q-PCR analysis performed in brain and peripheral organ tissues indicated that, with the exception of one (Spata13), all these genes are predominantly expressed in brain. These genes encode signaling proteins (Adora2, GPR88, Arpp21 and Rem2), a transcription factor (Limh6) or proteins of unknown function (Rik130, Spata13 and Wfs1). The identification of genes with enriched expression expands our knowledge of EAc at a molecular level, and provides useful information to toward genetic manipulations within the EAc.

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Year:  2008        PMID: 18786617      PMCID: PMC2629946          DOI: 10.1016/j.neuroscience.2008.07.070

Source DB:  PubMed          Journal:  Neuroscience        ISSN: 0306-4522            Impact factor:   3.590


  73 in total

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3.  Identification of novel striatal genes by expression profiling in adult mouse brain.

Authors:  A Ghate; K Befort; J A J Becker; D Filliol; C Bole-Feysot; D Demebele; B Jost; M Koch; B L Kieffer
Journal:  Neuroscience       Date:  2007-03-29       Impact factor: 3.590

4.  The transcriptome and metabolic gene signature of protoplasmic astrocytes in the adult murine cortex.

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6.  Mu-opioid receptor activation induces transcriptional plasticity in the central extended amygdala.

Authors:  K Befort; D Filliol; A Ghate; E Darcq; A Matifas; J Muller; A Lardenois; C Thibault; D Dembele; J Le Merrer; J A J Becker; O Poch; B L Kieffer
Journal:  Eur J Neurosci       Date:  2008-06       Impact factor: 3.386

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8.  Microarray analysis reveals distinctive signaling between the bed nucleus of the stria terminalis, nucleus accumbens, and dorsal striatum.

Authors:  Christopher M Olsen; Yong Huang; Shirlean Goodwin; Daniel C Ciobanu; Lu Lu; Thomas R Sutter; Danny G Winder
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  31 in total

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2.  Mice Lacking GPR88 Show Motor Deficit, Improved Spatial Learning, and Low Anxiety Reversed by Delta Opioid Antagonist.

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6.  The guanine nucleotide exchange factor (GEF) Asef2 promotes dendritic spine formation via Rac activation and spinophilin-dependent targeting.

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8.  Mapping GPR88-Venus illuminates a novel role for GPR88 in sensory processing.

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9.  Rem2 in the bullfrog (Rana catesbeiana): Patterns of expression within the central nervous system and brain expression at different ontogenetic stages.

Authors:  Megan M DeRocher; Faris H Armaly; Cara J Lepore; David M Hollis
Journal:  Gene       Date:  2014-02-24       Impact factor: 3.688

10.  Localization of rem2 in the central nervous system of the adult rainbow trout (Oncorhynchus mykiss).

Authors:  Anna G Downs; Katie R Scholles; David M Hollis
Journal:  J Chem Neuroanat       Date:  2016-09-04       Impact factor: 3.052

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