npj Parkinson s DiseaseGenomicsPeer-reviewed journal article
Moving beyond neurons: the role of cell type-specific gene regulation in Parkinson’s disease heritability
Regina Hertfelder ReynoldsiD, Juan Antonio BotíaiD, Mike A. NallsiD, Alastair John NoyceiD, Aude NicolasiD, Mark CooksoniD, Sara Bandrés‐CigaiD, Jesse Raphael GibbsiD, Dena G. HernandeziD, Andrew SingletoniD, Xylena ReediD, Hampton L. LeonardiD, Cornelis BlauwendraatiD, Faraz FaghriiD, José BrásiD, Rita João GuerreiroiD, Arianna TucciiD, Demis A. Kia, Henry HouldeniD, Hélène Plun‐FavreauiD, Kin Ying MokiD, Nicholas William WoodiD, Ruth C. LoveringiD, Lea R’BiboiD, Mie RizigiD, , Oriol Dols‐IcardoiD
Abstract
Parkinsons disease (PD), with its characteristic loss of nigrostriatal dopaminergic neurons and deposition of -synuclein in neurons, is often considered a neuronal disorder. However, in recent years substantial evidence has emerged to implicate glial cell types, such as astrocytes and microglia. In this study, we used stratified LD score regression and expression-weighted cell-type enrichment together with several brain-related and cell-type-specific genomic annotations to connect human genomic PD findings to specific brain cell types. We found that PD heritability does not enrich in global and regional brain annotations or brain-related cell-type-specific annotations. Likewise, we found no enrichment of PD susceptibility genes in brain-related cell types. In contrast, we demonstrated a significant enrichment of PD heritability in a curated lysosomal gene set specifically expressed in astrocytic and microglial subtypes. Our results suggest that PD risk loci do not lie in specific cell types or individual brain regions, but rather in global cellular processes to which cell types may have varying vulnerability.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
- Citations
- 100
- FWCI
- 10.80
- Field percentile
- top 1%
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