LRRK2
全基因组关联研究
帕金森病
疾病
生物
基因座(遗传学)
遗传学
候选基因
基因
转录组
遗传关联
神经科学
单核苷酸多态性
医学
突变
基因型
基因表达
病理
作者
Eric Yu,Roxanne Larivière,Rhalena A. Thomas,Lang Liu,Konstantin Senkevich,Shady Rahayel,Jean‐François Trempe,Edward A. Fon,Ziv Gan‐Or
出处
期刊:Brain
[Oxford University Press]
日期:2023-10-06
卷期号:147 (3): 887-899
被引量:17
标识
DOI:10.1093/brain/awad345
摘要
Abstract 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.
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