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全基因组研究揭示了阿尔茨海默病极端表型所特有的罕见 CNVs。

A genome-wide study reveals rare CNVs exclusive to extreme phenotypes of Alzheimer disease.

机构信息

Inserm U614, Faculté de Médecine, Rouen, France.

出版信息

Eur J Hum Genet. 2012 Jun;20(6):613-7. doi: 10.1038/ejhg.2011.225. Epub 2011 Dec 14.

Abstract

Studying rare extreme forms of Alzheimer disease (AD) may prove to be a useful strategy in identifying new genes involved in monogenic determinism of AD. Amyloid precursor protein (APP), PSEN1, and PSEN2 mutations account for only 85% of autosomal dominant early-onset AD (ADEOAD) families. We hypothesised that rare copy number variants (CNVs) could be involved in ADEOAD families without mutations in known genes, as well as in rare sporadic young-onset AD cases. Using high-resolution array comparative genomic hybridisation, we assessed the presence of rare CNVs in 21 unrelated ADEOAD cases, having no alteration on known genes, and 12 sporadic AD cases, with an age of onset younger than 55 years. The analysis revealed the presence of 7 singleton CNVs (4 in ADEOAD and 3 in sporadic cases) absent in 1078 controls and 912 late-onset AD cases. Strikingly, 4 out of 7 rearrangements target genes (KLK6, SLC30A3, MEOX2, and FPR2) encoding proteins that are tightly related to amyloid-β peptide metabolism or signalling. Although these variants are individually rare and restricted to particular subgroups of patients, these findings support the causal role, in human pathology, of a set of genes coding for molecules suspected for a long time to modify Aβ metabolism or signalling, and for which animal or cellular models have already been developed.

摘要

研究罕见的阿尔茨海默病(AD)极端形式可能被证明是一种有用的策略,可以确定涉及 AD 单基因决定因素的新基因。淀粉样前体蛋白(APP)、PSEN1 和 PSEN2 突变仅占常染色体显性早发性 AD(ADEOAD)家族的 85%。我们假设,罕见的拷贝数变异(CNV)可能与没有已知基因突变的 ADEOAD 家族以及罕见的散发性早发性 AD 病例有关。使用高分辨率阵列比较基因组杂交,我们评估了 21 个无已知基因改变的不相关 ADEOAD 病例和 12 个发病年龄小于 55 岁的散发性 AD 病例中罕见 CNV 的存在。分析显示,在 1078 名对照和 912 名晚发性 AD 病例中不存在 7 个单体 CNV(4 个在 ADEOAD 中,3 个在散发性病例中)。引人注目的是,7 个重排中有 4 个针对编码与淀粉样β肽代谢或信号密切相关的蛋白质的基因(KLK6、SLC30A3、MEOX2 和 FPR2)。尽管这些变体在个体中是罕见的,并且仅限于特定的患者亚组,但这些发现支持了一组编码分子的因果作用,这些分子长期以来被怀疑可以改变 Aβ代谢或信号,并且已经为其开发了动物或细胞模型。

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