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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.


ABSTRACT:

Background

Whole-exome sequencing (WES) has been successful in identifying genes that cause familial Parkinson's disease (PD). However, until now this approach has not been deployed to study large cohorts of unrelated participants. To discover rare PD susceptibility variants, we performed WES in 1148 unrelated cases and 503 control participants. Candidate genes were subsequently validated for functions relevant to PD based on parallel RNA-interference (RNAi) screens in human cell culture and Drosophila and C. elegans models.

Results

Assuming autosomal recessive inheritance, we identify 27 genes that have homozygous or compound heterozygous loss-of-function variants in PD cases. Definitive replication and confirmation of these findings were hindered by potential heterogeneity and by the rarity of the implicated alleles. We therefore looked for potential genetic interactions with established PD mechanisms. Following RNAi-mediated knockdown, 15 of the genes modulated mitochondrial dynamics in human neuronal cultures and four candidates enhanced ?-synuclein-induced neurodegeneration in Drosophila. Based on complementary analyses in independent human datasets, five functionally validated genes-GPATCH2L, UHRF1BP1L, PTPRH, ARSB, and VPS13C-also showed evidence consistent with genetic replication.

Conclusions

By integrating human genetic and functional evidence, we identify several PD susceptibility gene candidates for further investigation. Our approach highlights a powerful experimental strategy with broad applicability for future studies of disorders with complex genetic etiologies.

SUBMITTER: Jansen IE 

PROVIDER: S-EPMC5282828 | biostudies-literature | 2017 Jan

REPOSITORIES: biostudies-literature

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Discovery and functional prioritization of Parkinson's disease candidate genes from large-scale whole exome sequencing.

Jansen Iris E IE   Ye Hui H   Heetveld Sasja S   Lechler Marie C MC   Michels Helen H   Seinstra Renée I RI   Lubbe Steven J SJ   Drouet Valérie V   Lesage Suzanne S   Majounie Elisa E   Gibbs J Raphael JR   Nalls Mike A MA   Ryten Mina M   Botia Juan A JA   Vandrovcova Jana J   Simon-Sanchez Javier J   Castillo-Lizardo Melissa M   Rizzu Patrizia P   Blauwendraat Cornelis C   Chouhan Amit K AK   Li Yarong Y   Yogi Puja P   Amin Najaf N   van Duijn Cornelia M CM   Morris Huw R HR   Brice Alexis A   Singleton Andrew B AB   David Della C DC   Nollen Ellen A EA   Jain Shushant S   Shulman Joshua M JM   Heutink Peter P  

Genome biology 20170130 1


<h4>Background</h4>Whole-exome sequencing (WES) has been successful in identifying genes that cause familial Parkinson's disease (PD). However, until now this approach has not been deployed to study large cohorts of unrelated participants. To discover rare PD susceptibility variants, we performed WES in 1148 unrelated cases and 503 control participants. Candidate genes were subsequently validated for functions relevant to PD based on parallel RNA-interference (RNAi) screens in human cell culture  ...[more]

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