Fridman Hila, Khazeeva Gelana, Levy-Lahad Ephrat, Gilissen Christian, Brunner Han G
Department of Human Genetics, Radboud Institute for Molecular Life Sciences, Radboud University Medical Center, Nijmegen, the Netherlands.
The Fuld Family Medical Genetics Institute; The Eisenberg R&D Authority, Shaare Zedek Medical Center, Jerusalem, Israel.
Nat Hum Behav. 2025 May 15. doi: 10.1038/s41562-025-02204-7.
The genetic landscape of human Mendelian diseases is shaped by mutation and selection. Although selection on heterozygotes is well-established in autosomal-dominant disorders, convincing evidence for selection in carriers of pathogenic variants associated with recessive conditions is limited. Here, we studied heterozygous pathogenic variants in 1,929 genes, which cause recessive diseases when bi-allelic, in n = 378,751 unrelated European individuals from the UK Biobank. We find evidence suggesting fitness effects in heterozygous carriers for recessive genes, especially for variants in constrained genes across a broad range of diseases. Our data suggest reproductive effects at the population level, and hence natural selection, for autosomal-recessive disease variants. Further, variants in genes that underlie intellectual disability are associated with lower educational attainment in carriers, and we observe an altered genetic landscape, characterized by a threefold reduction in the calculated frequency of bi-allelic intellectual disability in the population relative to other recessive disorders.
人类孟德尔疾病的遗传格局由突变和选择塑造。尽管杂合子选择在常染色体显性疾病中已得到充分证实,但关于与隐性疾病相关的致病变异携带者中选择的令人信服的证据有限。在这里,我们研究了来自英国生物银行的n = 378,751名不相关欧洲个体中1929个基因的杂合致病变异,这些基因在双等位基因状态下会导致隐性疾病。我们发现有证据表明隐性基因的杂合携带者存在适应性效应,特别是在广泛疾病中受约束基因的变异。我们的数据表明常染色体隐性疾病变异在群体水平上有生殖效应,因此存在自然选择。此外,导致智力残疾的基因中的变异与携带者较低的教育程度相关,并且我们观察到一种改变的遗传格局,其特征是相对于其他隐性疾病,群体中双等位基因智力残疾的计算频率降低了三倍。