Skip to main content

Research Repository

Advanced Search

An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of a-synuclein

Kara, E; Crimi, A; Wiedmer, A; Emmenegger, M; Manzoni, C; Bandres-Ciga, S; D’Sa, K; Reynolds, RH; Botía, JA; Losa, M; Lysenko, V; Carta, M; Heinzer, D; Avar, M; Chincisan, A; Blauwendraat, C; Ruiz, SG; Pease, D; Mottier, L; Carrella, A; Schneider, D; Magalhaes, A; Aemisegger, C; Theocharides, APA; Fan, Z; Marks, JD; Hopp, SC; Lewis, P; Ryten, Mina; Hardy, John; Hyman, Bradley T; Aguzzi, Adriano

Authors

E Kara

A Crimi

A Wiedmer

M Emmenegger

C Manzoni

S Bandres-Ciga

K D’Sa

RH Reynolds

JA Botía

M Losa

V Lysenko

M Carta

D Heinzer

M Avar

A Chincisan

C Blauwendraat

SG Ruiz

D Pease

L Mottier

A Carrella

D Schneider

A Magalhaes

C Aemisegger

APA Theocharides

Z Fan

JD Marks

SC Hopp

P Lewis

Mina Ryten

John Hardy

Bradley T Hyman

Adriano Aguzzi



Abstract

Neuropathological and experimental evidence suggests that the cell-to-cell transfer of a-synuclein has an important role in the pathogenesis of Parkinson’s disease (PD). However, the mechanism underlying this phenomenon is not fully understood. We undertook an siRNA, genome-wide high throughput screen to identify genes regulating the cell-to-cell transfer of a-synuclein. We transiently transfected HEK cells stably overexpressing a-synuclein with a construct encoding GFP-2a-aSynuclein-RFP. The cells expressing a-synuclein-RFP through transfection were double positive for GFP and RFP fluorescence, whereas the cells receiving it through transfer were positive only for RFP fluorescence. The amount of a-synuclein transfer was quantified by high content microscopy. A series of unbiased screens confirmed the involvement of 38 genes in the regulation of a-synuclein-RFP transfer. One of those hits was ITGA8, a candidate gene recently identified through a large PD genome wide association study (GWAS). Weighted gene co-expression network analysis (WGCNA) and weighted protein-protein network interaction analysis (WPPNIA) showed that the hits clustered in networks that included known PD Mendelian and GWAS risk genes more frequently than expected than random chance. Given the genetic overlap between a-synuclein transfer and PD, those findings provide supporting evidence for the importance of the cell-to-cell transfer of a-synuclein in the pathogenesis of PD, and expand our understanding of the mechanism of a-synuclein spread.

Citation

Kara, E., Crimi, A., Wiedmer, A., Emmenegger, M., Manzoni, C., Bandres-Ciga, S., …Aguzzi, A. (2019). An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of a-synuclein

Publication Date Dec 23, 2019
Deposit Date Aug 17, 2020
Book Title An integrated genomic approach to dissect the genetic landscape regulating the cell-to-cell transfer of a-synuclein
DOI https://doi.org/10.1101/2019.12.23.886838
Public URL https://rvc-repository.worktribe.com/output/1379224