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GPNMB confers risk for Parkinson's disease through interaction with a-synuclein.

Diaz-Ortiz ME, Seo Y, Posavi M, Carceles Cordon M, Clark E, Jain N, Charan R, Gallagher MD, Unger TL, Amari N, Skrinak RT, Davila-Rivera R, Brody EM, Han N, Zack R, Van Deerlin VM, Tropea TF, Luk KC, Lee EB, Weintraub D, Chen-Plotkin AS. GPNMB confers risk for Parkinson's disease through interaction with a-synuclein. Science (New York, N.Y.). 2022 Aug 19; 377(6608):eabk0637.

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Many risk loci for Parkinson''s disease (PD) have been identified by genome-wide association studies (GWASs), but target genes and mechanisms remain largely unknown. We linked the GWAS-derived chromosome 7 locus (sentinel single-nucleotide polymorphism rs199347) to through colocalization analyses of expression quantitative trait locus and PD risk signals, confirmed by allele-specific expression studies in the human brain. In cells, glycoprotein nonmetastatic melanoma protein B (GPNMB) coimmunoprecipitated and colocalized with a-synuclein (aSyn). In induced pluripotent stem cell-derived neurons, loss of resulted in loss of ability to internalize aSyn fibrils and develop aSyn pathology. In 731 PD and 59 control biosamples, GPNMB was elevated in PD plasma, associating with disease severity. Thus, represents a PD risk gene with potential for biomarker development and therapeutic targeting.

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