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[自闭症谱系障碍的遗传学与动物模型。新进展]

[Genetics and animal modeling of autism spectrum disorders. New developments].

作者信息

Klauck S M, Poustka L, Chiocchetti A

机构信息

Abteilung Molekulare Genomanalyse, Deutsches Krebsforschungszentrum, Im Neuenheimer Feld 580, 69120, Heidelberg.

出版信息

Nervenarzt. 2011 May;82(5):553-62. doi: 10.1007/s00115-010-3241-z.

Abstract

Autism spectrum disorders (ASD) are pervasive developmental disorders with a complex phenotype in respect to communication, verbal development, and social behavior. Manifold molecular genetic analyses point towards a multifactorial genetic predisposition. For the identification of central key mechanisms large consortia have performed linkage analysis, genome-wide association, and copy number variation (CNV) studies, which led to the characterization of risk factors for ASD like CNV and single nucleotide polymorphisms but also single rare mutations. The so far associated genomic regions and candidate genes impact neuronal development especially the establishment of the synaptic cleft, secretion of surface proteins, or dendritic translation. These findings point towards deficits of translation-dependent cell-cell connectivity and synaptic plasticity for ASD. Animal models are relevant to analyze the pathomechanisms of single genetic risk variants at the cellular, tissue-specific, and behavioral levels.

摘要

自闭症谱系障碍(ASD)是一种广泛性发育障碍,在沟通、语言发展和社交行为方面具有复杂的表型。多种分子遗传学分析表明存在多因素遗传易感性。为了确定核心关键机制,大型研究联盟进行了连锁分析、全基因组关联研究和拷贝数变异(CNV)研究,这些研究导致了ASD风险因素的特征描述,如CNV和单核苷酸多态性,以及单个罕见突变。迄今为止相关的基因组区域和候选基因影响神经元发育,尤其是突触间隙的形成、表面蛋白的分泌或树突翻译。这些发现表明ASD存在翻译依赖性细胞间连接和突触可塑性缺陷。动物模型对于在细胞、组织特异性和行为水平分析单个遗传风险变异的发病机制具有重要意义。

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