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

Abstract:

:Large-scale transcriptome analysis in the brain is a powerful approach to identify novel genes of potential interest toward understanding cerebral organization and function. We utilized the microarray technology to measure expression levels of about 24,000 genes and expressed sequence tags in mouse hippocampus, frontal cortex and striatum. Using expression profile obtained from whole brain as a reference, we categorized the genes into groups of genes either enriched in, or restricted to, one of the three areas of interest. We found enriched genes for each target area. Further, we identified 14 genes in the category of genes restricted to the striatum, among which were the orphan G protein-coupled receptor GPR88 and retinoic acid receptor-beta. These two genes were already reported to be selectively expressed in the striatum, thus validating our experimental approach. We selected 6 striatal-restricted genes, as well as 10 striatal-enriched candidates, that were previously undescribed. We analyzed their expression by in situ hybridization analysis in the brain, and quantitative RT-PCR in both brain and peripheral organs. Two of these unknown genes displayed a notable expression pattern. The striatal-restricted gene H3076B11 shows uniform expression throughout and uniquely in the striatum, representing a genuine striatal marker. The striatal-enriched gene 4833421E05Rik is preferentially expressed in the rostral striatum, and is also abundant in kidney, liver and lung. These two genes may contribute to some of the many striatal-controlled behaviors, including initiation of movement, habit formation, or reward and motivation.

journal_name

Neuroscience

journal_title

Neuroscience

authors

Ghate A,Befort K,Becker JA,Filliol D,Bole-Feysot C,Demebele D,Jost B,Koch M,Kieffer BL

doi

10.1016/j.neuroscience.2007.02.040

subject

Has Abstract

pub_date

2007-05-25 00:00:00

pages

1182-92

issue

3

eissn

0306-4522

issn

1873-7544

pii

S0306-4522(07)00239-4

journal_volume

146

pub_type

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