Department of Human Genetics, McGill University, Montreal, Quebec H3A 0G4, Canada.
The Neuro (Montreal Neurological Institute-Hospital), Montreal, Quebec H3A 2B4, Canada.
Brain. 2024 Mar 1;147(3):887-899. doi: 10.1093/brain/awad345.
There are 78 loci associated with Parkinson's disease in the most recent genome-wide association study (GWAS), yet the specific genes driving these associations are mostly unknown. Herein, we aimed to nominate the top candidate gene from each Parkinson's disease locus and identify variants and pathways potentially involved in Parkinson's disease. We trained a machine learning model to predict Parkinson's disease-associated genes from GWAS loci using genomic, transcriptomic and epigenomic data from brain tissues and dopaminergic neurons. We nominated candidate genes in each locus and identified novel pathways potentially involved in Parkinson's disease, such as the inositol phosphate biosynthetic pathway (INPP5F, IP6K2, ITPKB and PPIP5K2). Specific common coding variants in SPNS1 and MLX may be involved in Parkinson's disease, and burden tests of rare variants further support that CNIP3, LSM7, NUCKS1 and the polyol/inositol phosphate biosynthetic pathway are associated with the disease. Functional studies are needed to further analyse the involvements of these genes and pathways in Parkinson's disease.
在最近的全基因组关联研究 (GWAS) 中,有 78 个与帕金森病相关的基因座,但驱动这些关联的特定基因大多未知。在此,我们旨在从帕金森病基因座中提名每个基因座的顶级候选基因,并确定可能与帕金森病相关的变异和途径。我们使用来自脑组织和多巴胺能神经元的基因组、转录组和表观基因组数据,训练了一个机器学习模型,从 GWAS 基因座预测与帕金森病相关的基因。我们在每个基因座中提名候选基因,并确定了可能与帕金森病相关的新途径,例如肌醇磷酸盐生物合成途径(INPP5F、IP6K2、ITPKB 和 PPIP5K2)。SPNS1 和 MLX 中的特定常见编码变异可能与帕金森病有关,罕见变异的负担测试进一步支持 CNIP3、LSM7、NUCKS1 和多元醇/肌醇磷酸盐生物合成途径与该疾病相关。需要进行功能研究来进一步分析这些基因和途径在帕金森病中的作用。