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精神分裂症患者中外显子新生突变率增加。

Increased exonic de novo mutation rate in individuals with schizophrenia.

机构信息

Centre of Excellence in Neuromics of Université de Montréal, Centre Hospitalier de l'Université de Montréal Research Center, Montréal, Québec, Canada.

出版信息

Nat Genet. 2011 Jul 10;43(9):860-3. doi: 10.1038/ng.886.

Abstract

Schizophrenia is a severe psychiatric disorder that profoundly affects cognitive, behavioral and emotional processes. The wide spectrum of symptoms and clinical variability in schizophrenia suggest a complex genetic etiology, which is consistent with the numerous loci thus far identified by linkage, copy number variation and association studies. Although schizophrenia heritability may be as high as ∼80%, the genes responsible for much of this heritability remain to be identified. Here we sequenced the exomes of 14 schizophrenia probands and their parents. We identified 15 de novo mutations (DNMs) in eight probands, which is significantly more than expected considering the previously reported DNM rate. In addition, 4 of the 15 identified DNMs are nonsense mutations, which is more than what is expected by chance. Our study supports the notion that DNMs may account for some of the heritability reported for schizophrenia while providing a list of genes possibly involved in disease pathogenesis.

摘要

精神分裂症是一种严重的精神疾病,深刻影响认知、行为和情感过程。精神分裂症症状的广泛谱和临床变异性表明其具有复杂的遗传病因,这与迄今为止通过连锁、拷贝数变异和关联研究确定的众多基因座一致。尽管精神分裂症的遗传率可能高达 80%左右,但负责大部分遗传率的基因仍有待确定。在这里,我们对 14 名精神分裂症先证者及其父母的外显子组进行了测序。我们在 8 名先证者中发现了 15 个新生突变(DNMs),这明显高于先前报道的 DNM 率。此外,在 15 个鉴定的 DNM 中,有 4 个是无义突变,这比随机预期的要多。我们的研究支持了 DNM 可能导致部分精神分裂症遗传率的观点,同时提供了可能参与疾病发病机制的基因列表。

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