Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism
<p>Abstract</p> <p>Background</p> <p>Arginine vasopressin (AVP) has been hypothesized to play a role in aetiology of autism based on a demonstrated involvement in the regulation of social behaviours. The arginine vasopressin receptor 1A gene (<it>AVPR1A</it>...
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doaj-2982d727529141368ddff179733d483f2020-11-25T00:23:16ZengBMCMolecular Autism2040-23922011-03-0121310.1186/2040-2392-2-3Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autismTansey Katherine EHill Matthew JCochrane Lynne EGill MichaelAnney Richard JLGallagher Louise<p>Abstract</p> <p>Background</p> <p>Arginine vasopressin (AVP) has been hypothesized to play a role in aetiology of autism based on a demonstrated involvement in the regulation of social behaviours. The arginine vasopressin receptor 1A gene (<it>AVPR1A</it>) is widely expressed in the brain and is considered to be a key receptor for regulation of social behaviour. Moreover, genetic variation at <it>AVPR1A </it>has been reported to be associated with autism. Evidence from non-human mammals implicates variation in the 5'-flanking region of <it>AVPR1A </it>in variable gene expression and social behaviour.</p> <p>Methods</p> <p>We examined four tagging single nucleotide polymorphisms (SNPs) (rs3803107, rs1042615, rs3741865, rs11174815) and three microsatellites (RS3, RS1 and AVR) at the <it>AVPR1A </it>gene for association in an autism cohort from Ireland. Two 5'-flanking region polymorphisms in the human <it>AVPR1A</it>, RS3 and RS1, were also tested for their effect on relative promoter activity.</p> <p>Results</p> <p>The short alleles of RS1 and the SNP rs11174815 show weak association with autism in the Irish population (<it>P </it>= 0.036 and <it>P </it>= 0.008, respectively). Both RS1 and RS3 showed differences in relative promoter activity by length. Shorter repeat alleles of RS1 and RS3 decreased relative promoter activity in the human neuroblastoma cell line SH-SY5Y.</p> <p>Conclusions</p> <p>These aligning results can be interpreted as a functional route for this association, namely that shorter alleles of RS1 lead to decreased <it>AVPR1A </it>transcription, which may proffer increased susceptibility to the autism phenotype.</p> http://www.molecularautism.com/content/2/1/3 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tansey Katherine E Hill Matthew J Cochrane Lynne E Gill Michael Anney Richard JL Gallagher Louise |
spellingShingle |
Tansey Katherine E Hill Matthew J Cochrane Lynne E Gill Michael Anney Richard JL Gallagher Louise Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism Molecular Autism |
author_facet |
Tansey Katherine E Hill Matthew J Cochrane Lynne E Gill Michael Anney Richard JL Gallagher Louise |
author_sort |
Tansey Katherine E |
title |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism |
title_short |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism |
title_full |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism |
title_fullStr |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism |
title_full_unstemmed |
Functionality of promoter microsatellites of arginine vasopressin receptor 1A (AVPR1A): implications for autism |
title_sort |
functionality of promoter microsatellites of arginine vasopressin receptor 1a (avpr1a): implications for autism |
publisher |
BMC |
series |
Molecular Autism |
issn |
2040-2392 |
publishDate |
2011-03-01 |
description |
<p>Abstract</p> <p>Background</p> <p>Arginine vasopressin (AVP) has been hypothesized to play a role in aetiology of autism based on a demonstrated involvement in the regulation of social behaviours. The arginine vasopressin receptor 1A gene (<it>AVPR1A</it>) is widely expressed in the brain and is considered to be a key receptor for regulation of social behaviour. Moreover, genetic variation at <it>AVPR1A </it>has been reported to be associated with autism. Evidence from non-human mammals implicates variation in the 5'-flanking region of <it>AVPR1A </it>in variable gene expression and social behaviour.</p> <p>Methods</p> <p>We examined four tagging single nucleotide polymorphisms (SNPs) (rs3803107, rs1042615, rs3741865, rs11174815) and three microsatellites (RS3, RS1 and AVR) at the <it>AVPR1A </it>gene for association in an autism cohort from Ireland. Two 5'-flanking region polymorphisms in the human <it>AVPR1A</it>, RS3 and RS1, were also tested for their effect on relative promoter activity.</p> <p>Results</p> <p>The short alleles of RS1 and the SNP rs11174815 show weak association with autism in the Irish population (<it>P </it>= 0.036 and <it>P </it>= 0.008, respectively). Both RS1 and RS3 showed differences in relative promoter activity by length. Shorter repeat alleles of RS1 and RS3 decreased relative promoter activity in the human neuroblastoma cell line SH-SY5Y.</p> <p>Conclusions</p> <p>These aligning results can be interpreted as a functional route for this association, namely that shorter alleles of RS1 lead to decreased <it>AVPR1A </it>transcription, which may proffer increased susceptibility to the autism phenotype.</p> |
url |
http://www.molecularautism.com/content/2/1/3 |
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