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GABRB3 基因变异与 Asperger 综合征及与自闭症相关的多种内表型有关。

Genetic variation in GABRB3 is associated with Asperger syndrome and multiple endophenotypes relevant to autism.

机构信息

Department of Psychiatry, Autism Research Centre, University of Cambridge, Cambridgeshire, UK.

出版信息

Mol Autism. 2013 Dec 9;4(1):48. doi: 10.1186/2040-2392-4-48.

Abstract

BACKGROUND

Autism spectrum conditions (ASC) are associated with deficits in social interaction and communication, alongside repetitive, restricted, and stereotyped behavior. ASC is highly heritable. The gamma-aminobutyric acid (GABA)-ergic system has been associated consistently with atypicalities in autism, in both genetic association and expression studies. A key component of the GABA-ergic system is encoded by the GABRB3 gene, which has been previously implicated both in ASC and in individual differences in empathy.

METHODS

In this study, 45 genotyped single nucleotide polymorphisms (SNPs) within GABRB3 were tested for association with Asperger syndrome (AS), and related quantitative traits measured through the following tests: the Empathy Quotient (EQ), the Autism Spectrum Quotient (AQ), the Systemizing Quotient-Revised (SQ-R), the Embedded Figures Test (EFT), the Reading the Mind in the Eyes Test (RMET), and the Mental Rotation Test (MRT). Two-loci, three-loci, four-loci haplotype analyses, and one seven-loci haplotype analysis were also performed in the AS case-control sample.

RESULTS

Three SNPs (rs7180158, rs7165604, rs12593579) were significantly associated with AS, and two SNPs (rs9806546, rs11636966) were significantly associated with EQ. Two SNP-SNP pairs, rs12438141-rs1035751 and rs12438141-rs7179514, showed significant association with variation in the EFT scores. One SNP-SNP pair, rs7174437-rs1863455, was significantly associated with variation in the MRT scores. Additionally, a few haplotypes, including a 19 kb genomic region that formed a linkage disequilibrium (LD) block in our sample and contained several nominally significant SNPs, were found to be significantly associated with AS.

CONCLUSION

The current study confirms the role of GABRB3 as an important candidate gene in both ASC and normative variation in related endophenotypes.

摘要

背景

自闭症谱系障碍(ASC)与社交互动和沟通障碍有关,同时还伴有重复、受限和刻板的行为。ASC 具有高度遗传性。γ-氨基丁酸(GABA)能系统与自闭症的非典型性一直存在关联,无论是在遗传关联还是表达研究中都有发现。GABA 能系统的一个关键组成部分由 GABRB3 基因编码,该基因先前与 ASC 以及同理心的个体差异有关。

方法

在这项研究中,测试了 GABRB3 内的 45 个已基因分型的单核苷酸多态性(SNP)与阿斯伯格综合征(AS)的关联,并通过以下测试来测量相关的定量特征:共情商数(EQ)、自闭症谱系商数(AQ)、系统思维商数修订版(SQ-R)、嵌入式图形测试(EFT)、读心测试(RMET)和心理旋转测试(MRT)。在 AS 病例对照样本中还进行了两、三、四基因座单体型分析以及一个七基因座单体型分析。

结果

三个 SNP(rs7180158、rs7165604、rs12593579)与 AS 显著相关,两个 SNP(rs9806546、rs11636966)与 EQ 显著相关。两个 SNP-SNP 对 rs12438141-rs1035751 和 rs12438141-rs7179514 与 EFT 评分的变化显著相关。一个 SNP-SNP 对 rs7174437-rs1863455 与 MRT 评分的变化显著相关。此外,在我们的样本中形成一个连锁不平衡(LD)块的包含几个名义上显著 SNP 的一个 19 kb 基因组区域的几个单体型与 AS 显著相关。

结论

本研究证实了 GABRB3 作为 ASC 和相关表型的正常变异的重要候选基因的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df3a/3903107/d2cbf6527260/2040-2392-4-48-1.jpg

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