Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, 7 George Square, Edinburgh, EH8 9JZ, UK.
Department of Psychology, University of Edinburgh, 7 George Square, Edinburgh, EH8 9JZ, UK.
Mol Psychiatry. 2018 Dec;23(12):2347-2362. doi: 10.1038/s41380-017-0005-1. Epub 2018 Jan 10.
Pedigree-based analyses of intelligence have reported that genetic differences account for 50-80% of the phenotypic variation. For personality traits these effects are smaller, with 34-48% of the variance being explained by genetic differences. However, molecular genetic studies using unrelated individuals typically report a heritability estimate of around 30% for intelligence and between 0 and 15% for personality variables. Pedigree-based estimates and molecular genetic estimates may differ because current genotyping platforms are poor at tagging causal variants, variants with low minor allele frequency, copy number variants, and structural variants. Using ~20,000 individuals in the Generation Scotland family cohort genotyped for ~700,000 single-nucleotide polymorphisms (SNPs), we exploit the high levels of linkage disequilibrium (LD) found in members of the same family to quantify the total effect of genetic variants that are not tagged in GWAS of unrelated individuals. In our models, genetic variants in low LD with genotyped SNPs explain over half of the genetic variance in intelligence, education, and neuroticism. By capturing these additional genetic effects our models closely approximate the heritability estimates from twin studies for intelligence and education, but not for neuroticism and extraversion. We then replicated our finding using imputed molecular genetic data from unrelated individuals to show that ~50% of differences in intelligence, and ~40% of the differences in education, can be explained by genetic effects when a larger number of rare SNPs are included. From an evolutionary genetic perspective, a substantial contribution of rare genetic variants to individual differences in intelligence, and education is consistent with mutation-selection balance.
基于家系的智力分析报告称,遗传差异占表型变异的 50-80%。对于人格特质,这些影响较小,遗传差异解释了 34-48%的方差。然而,使用无关个体的分子遗传研究通常报告智力的遗传力估计值约为 30%,人格变量的遗传力估计值在 0 到 15%之间。基于家系的估计值和分子遗传估计值可能不同,因为当前的基因分型平台在标记因果变异、低频次要等位基因变异、拷贝数变异和结构变异方面效果不佳。我们利用苏格兰一代家族队列中约 20000 名个体的约 700000 个单核苷酸多态性(SNP)进行基因分型,利用同一家庭成员之间发现的高度连锁不平衡(LD)来量化 GWAS 中未标记的遗传变异的总效应在无关个体中。在我们的模型中,与基因分型 SNP 低度连锁的遗传变异解释了智力、教育和神经质的遗传变异的一半以上。通过捕获这些额外的遗传效应,我们的模型非常接近智力和教育的双胞胎研究的遗传力估计值,但不包括神经质和外向性。然后,我们使用来自无关个体的推断分子遗传数据复制了我们的发现,结果表明,当包含更多罕见 SNP 时,智力差异的约 50%和教育差异的约 40%可以用遗传效应来解释。从进化遗传的角度来看,罕见遗传变异对智力和教育个体差异的大量贡献与突变-选择平衡一致。