Machine learning nominates the inositol pathway and novel genes in Parkinson's disease

被引:8
|
作者
Yu, Eric [1 ,2 ]
Lariviere, Roxanne [3 ]
Thomas, Rhalena A. [3 ,4 ]
Liu, Lang [1 ,2 ]
Senkevich, Konstantin [2 ,5 ]
Rahayel, Shady [6 ,7 ]
Trempe, Jean-Francois [8 ]
Fon, Edward A. [3 ,4 ]
Gan-Or, Ziv [1 ,2 ,3 ,9 ]
机构
[1] McGill Univ, Dept Human Genet, Montreal, PQ H3A 0G4, Canada
[2] Neuro Montreal Neurol Inst Hosp, Montreal, PQ H3A 2B4, Canada
[3] McGill Univ, Dept Neurol & Neurosurg, Montreal, PQ H3A 0G4, Canada
[4] Montreal Neurol Inst Hosp, Early Drug Discovery Unit EDDU, Montreal, PQ H3A 2B4, Canada
[5] Hop Sacre Coeur Montreal, Ctr Adv Res Sleep Med, Montreal, PQ H4J 1C5, Canada
[6] Univ Montreal, Dept Med, Montreal, PQ H3C 3J7, Canada
[7] McGill Univ, Dept Pharmacol & Therapeut, Montreal, PQ H3A 0G4, Canada
[8] McGill Univ, Ctr Rech Biol Structurale, Montreal, PQ H3A 0G4, Canada
[9] McGill Univ, Montreal Neurol Inst, 1033 Av Pins O,Room 312, Montreal, PQ H3A 1A1, Canada
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
Parkinson's disease; GWAS; machine learning; gene prioritization; ALPHA-SYNUCLEIN AGGREGATION; MAX; IDENTIFICATION; METAANALYSIS; VARIANTS; INSIGHTS; NETWORK; BRAIN; RISK; LOCI;
D O I
10.1093/brain/awad345
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
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. Yu et al. train 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. They propose candidate genes for each locus, and identify novel pathways that may be involved in Parkinson's disease.
引用
收藏
页码:887 / 899
页数:13
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