The genetic variation of RELN expression in schizophrenia and bipolar disorder.

Reelin plays an important role in the development and function of the brain and has been linked to different neuropsychiatric diseases. To further clarify the connection between reelin and psychiatric disorders, we studied the factors that influence the expression of reelin gene (RELN) and its diffe...

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Main Authors: Galit Ovadia, Sagiv Shifman
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2011-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3095646?pdf=render
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spelling doaj-a430cdf86b7843a38ec7d89a447f4e462020-11-25T02:03:33ZengPublic Library of Science (PLoS)PLoS ONE1932-62032011-01-0165e1995510.1371/journal.pone.0019955The genetic variation of RELN expression in schizophrenia and bipolar disorder.Galit OvadiaSagiv ShifmanReelin plays an important role in the development and function of the brain and has been linked to different neuropsychiatric diseases. To further clarify the connection between reelin and psychiatric disorders, we studied the factors that influence the expression of reelin gene (RELN) and its different isoforms. We examined the total expression of RELN, allelic expression, and two alternative RELN isoforms in postmortem brain samples from patients with schizophrenia and bipolar disorder, as well as unaffected controls. We did not find a significant reduction in the total expression of RELN in schizophrenia or bipolar disorder. However, we did find a significant reduction of the proportion of the short RELN isoform, missing the C-terminal region in bipolar disorder, and imbalance in the allelic expression of RELN in schizophrenia. In addition, we tested the association between variation in RELN expression and rs7341475, an intronic SNP that was found to be associated with schizophrenia in women. We did not find an association between rs7341474 and the total expression of RELN either in women or in the entire sample. However, we observed a nominally significant effect of genotype-by-sex interaction on the variation in microexon skipping. Women with the risk genotype of rs7341475 (GG) had a higher proportion of microexon skipping, which is the isoform predominant in tissues outside the brain, while men had the opposite trend. Finally, we tested 83 SNPs in the gene region for association with expression variation of RELN, but none were significant. Our study further supports the connection between RELN dysfunction and psychiatric disorders, and provides a possible functional role for a schizophrenia associated SNP. Nevertheless, the positive associations observed in this study needs further replication as it may have implications for understanding the biological causes of schizophrenia and bipolar disorder.http://europepmc.org/articles/PMC3095646?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Galit Ovadia
Sagiv Shifman
spellingShingle Galit Ovadia
Sagiv Shifman
The genetic variation of RELN expression in schizophrenia and bipolar disorder.
PLoS ONE
author_facet Galit Ovadia
Sagiv Shifman
author_sort Galit Ovadia
title The genetic variation of RELN expression in schizophrenia and bipolar disorder.
title_short The genetic variation of RELN expression in schizophrenia and bipolar disorder.
title_full The genetic variation of RELN expression in schizophrenia and bipolar disorder.
title_fullStr The genetic variation of RELN expression in schizophrenia and bipolar disorder.
title_full_unstemmed The genetic variation of RELN expression in schizophrenia and bipolar disorder.
title_sort genetic variation of reln expression in schizophrenia and bipolar disorder.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2011-01-01
description Reelin plays an important role in the development and function of the brain and has been linked to different neuropsychiatric diseases. To further clarify the connection between reelin and psychiatric disorders, we studied the factors that influence the expression of reelin gene (RELN) and its different isoforms. We examined the total expression of RELN, allelic expression, and two alternative RELN isoforms in postmortem brain samples from patients with schizophrenia and bipolar disorder, as well as unaffected controls. We did not find a significant reduction in the total expression of RELN in schizophrenia or bipolar disorder. However, we did find a significant reduction of the proportion of the short RELN isoform, missing the C-terminal region in bipolar disorder, and imbalance in the allelic expression of RELN in schizophrenia. In addition, we tested the association between variation in RELN expression and rs7341475, an intronic SNP that was found to be associated with schizophrenia in women. We did not find an association between rs7341474 and the total expression of RELN either in women or in the entire sample. However, we observed a nominally significant effect of genotype-by-sex interaction on the variation in microexon skipping. Women with the risk genotype of rs7341475 (GG) had a higher proportion of microexon skipping, which is the isoform predominant in tissues outside the brain, while men had the opposite trend. Finally, we tested 83 SNPs in the gene region for association with expression variation of RELN, but none were significant. Our study further supports the connection between RELN dysfunction and psychiatric disorders, and provides a possible functional role for a schizophrenia associated SNP. Nevertheless, the positive associations observed in this study needs further replication as it may have implications for understanding the biological causes of schizophrenia and bipolar disorder.
url http://europepmc.org/articles/PMC3095646?pdf=render
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