AMBRA1,自噬和自闭症的极端男性脑理论

B. Crespi, Silven Read, A. Ly, P. Hurd
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引用次数: 9

摘要

自闭症的极端男性脑理论认为,它的男性偏见是由在典型人群中发现的自闭症相关特征表达中男性偏见的性别差异的夸大所介导的。这一理论得到了大量表型证据的支持,但目前还没有基因被描述具有符合其预测的特性。在最近的精神分裂症GWAS研究中,自噬相关基因AMBRA1代表了全基因组中最重要的“亮点”之一,显示出性别差异表达,并与人类和小鼠的自闭症风险和特征有关,特别是在女性中。我们在一个典型人群中对AMBRA1自闭症风险SNP进行了基因分型,这些人群对自闭症和分裂型特征的维度表达进行了评分。GG基因型纯合子的女性,而不是男性,在自闭症商数-想象力分量表上的单性状得分显著增加,这在典型人群中显示出强烈的、显著的男性偏见。因此,具有这种基因型的女性在这种与自闭症相关的高度两性二态表型上与男性相似。这些发现支持了极端男性大脑假说,并表明性别特异性遗传效应可以调节自闭症风险的各个方面。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
AMBRA1, Autophagy, and the Extreme Male Brain Theory of Autism
The extreme male brain theory of autism posits that its male bias is mediated by exaggeration of male-biased sex differences in the expression of autism-associated traits found in typical populations. The theory is supported by extensive phenotypic evidence, but no genes have yet been described with properties that fit its predictions. The autophagy-associated gene AMBRA1 represents one of the top genome-wide “hits” in recent GWAS studies of schizophrenia, shows sex-differential expression, and has been linked with autism risk and traits in humans and mice, especially or exclusively among females. We genotyped the AMBRA1 autism-risk SNP in a population of typical humans who were scored for the dimensional expression of autistic and schizotypal traits. Females, but not males, homozygous for the GG genotype showed a significant increase in score for the single trait, the Autism Quotient-Imagination subscale, that exhibits a strong, significant male bias in typical populations. As such, females with this genotype resembled males for this highly sexually dimorphic, autism-associated phenotype. These findings support the extreme male brain hypothesis and indicate that sex-specific genetic effects can mediate aspects of risk for autism.
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