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评估基因与基因之间的相互作用作为揭示诵读困难中缺失遗传力的一种工具。

An assessment of gene-by-gene interactions as a tool to unfold missing heritability in dyslexia.

作者信息

Mascheretti S, Bureau A, Trezzi V, Giorda R, Marino C

机构信息

Child Psychopathology Unit, Scientific Institute, IRCCS Eugenio Medea, Bosisio Parini, Lecco, 23842, Italy,

出版信息

Hum Genet. 2015 Jul;134(7):749-60. doi: 10.1007/s00439-015-1555-4. Epub 2015 Apr 28.

Abstract

Even if substantial heritability has been reported and candidate genes have been identified extensively, all known marker associations explain only a small proportion of the phenotypic variance of developmental dyslexia (DD) and related quantitative phenotypes. Gene-by-gene interaction (also known as "epistasis"--G × G) triggers a non-additive effect of genes at different loci and should be taken into account in explaining part of the missing heritability of this complex trait. We assessed potential G × G interactions among five DD candidate genes, i.e., DYX1C1, DCDC2, KIAA0319, ROBO1, and GRIN2B, upon DD-related neuropsychological phenotypes in 493 nuclear families with DD, by implementing two complementary regression-based approaches: (1) a general linear model equation whereby the trait is predicted by the main effect of the number of rare alleles of the two genes and by the effect of the interaction between them, and (2) a family-based association test to detect G × G interactions between two unlinked markers by splitting up the association effect into a between- and a within-family genetic orthogonal components. After applying 500,000 permutations and correcting for multiple testing, both methods show that G × G effects between markers within the DYX1C1, KIAA0319/TTRAP, and GRIN2B genes lower the memory letters composite z-score of on average 0.55 standard deviation. We provided initial evidence that the effects of familial transmission of synergistic interactions between genetic risk variants can be exploited in the study of the etiology of DD, explain part of its missing heritability, and assist in designing customized charts of individualized neurocognitive impairments in complex disorders, such as DD.

摘要

即使已有大量关于遗传力的报道且广泛鉴定出了候选基因,但所有已知的标记关联仅解释了发育性阅读障碍(DD)及相关定量表型的一小部分表型变异。基因与基因之间的相互作用(也称为“上位性”——G×G)会引发不同基因座上基因的非加性效应,在解释这一复杂性状部分缺失的遗传力时应予以考虑。我们通过实施两种基于回归的互补方法,评估了493个患有DD的核心家庭中,五个DD候选基因(即DYX1C1、DCDC2、KIAA0319、ROBO1和GRIN2B)之间潜在的G×G相互作用对与DD相关的神经心理学表型的影响:(1)一个一般线性模型方程,通过两个基因稀有等位基因数量的主效应及其相互作用的效应来预测性状;(2)一种基于家系的关联测试,通过将关联效应分解为家系间和家系内遗传正交成分,来检测两个不连锁标记之间的G×G相互作用。在进行500,000次排列并校正多重检验后,两种方法均表明,DYX1C1、KIAA0319/TTRAP和GRIN2B基因内标记之间的G×G效应平均使记忆字母综合z分数降低0.55个标准差。我们提供了初步证据,表明遗传风险变异之间协同相互作用的家族传递效应可用于DD病因学研究,解释其部分缺失的遗传力,并有助于设计复杂疾病(如DD)中个性化神经认知障碍的定制图表。

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