Autoren:	Aslam, Muhammad Kandasamy, Nirosiya Ullah, Anwar Paramasivam, Nagarajan Öztürk, Mehmet Ali Naureen, Saima Arshad, Abida Badshah, Mazhar Khan, Kafaitullah Wajid, Muhammad Abbasi, Rashda Ilyas, Muhammad Eils, Roland Schlesner, Matthias Wade, Rebecca C. Ahmad, Nafees Engelhardt, Jakob von
Titel:	Putative second hit rare genetic variants in families with seemingly GBA-associated Parkinson’s disease
Online-Publikationsdatum:	24-Sep-2021
Erscheinungsdatum:	2021
Sprache des Dokuments:	Englisch
Zusammenfassung/Abstract:	Rare variants in the beta-glucocerebrosidase gene (GBA1) are common genetic risk factors for alpha synucleinopathy, which often manifests clinically as GBA-associated Parkinson’s disease (GBA-PD). Clinically, GBA-PD closely mimics idiopathic PD, but it may present at a younger age and often aggregates in families. Most carriers of GBA variants are, however, asymptomatic. Moreover, symptomatic PD patients without GBA variant have been reported in families with seemingly GBA-PD. These observations obscure the link between GBA variants and PD pathogenesis and point towards a role for unidentified additional genetic and/or environmental risk factors or second hits in GBA-PD. In this study, we explored whether rare genetic variants may be additional risk factors for PD in two families segregating the PD-associated GBA1 variants c.115+1G>A (ClinVar ID: 93445) and p.L444P (ClinVar ID: 4288). Our analysis identified rare genetic variants of the HSP70 co-chaperone DnaJ homolog subfamily B member 6 (DNAJB6) and lysosomal protein prosaposin (PSAP) as additional factors possibly influencing PD risk in the two families. In comparison to the wild-type proteins, variant DNAJB6 and PSAP proteins show altered functions in the context of cellular alpha-synuclein homeostasis when expressed in reporter cells. Furthermore, the segregation pattern of the rare variants in the genes encoding DNAJB6 and PSAP indicated a possible association with PD in the respective families. The occurrence of second hits or additional PD cosegregating rare variants has important implications for genetic counseling in PD families with GBA1 variant carriers and for the selection of PD patients for GBA targeted treatments.
DDC-Sachgruppe:	610 Medizin 610 Medical sciences
Veröffentlichende Institution:	Johannes Gutenberg-Universität Mainz
Organisationseinheit:	FB 04 Medizin
Veröffentlichungsort:	Mainz
ROR:	https://ror.org/023b0x485
DOI:	http://doi.org/10.25358/openscience-6366
Version:	Published version
Publikationstyp:	Zeitschriftenaufsatz
Nutzungsrechte:	CC BY
Informationen zu den Nutzungsrechten:	https://creativecommons.org/licenses/by/4.0/
Zeitschrift:	npj Genomic Medicine 6
Seitenzahl oder Artikelnummer:	2
Verlag:	Nature Publ. Group
Verlagsort:	London
Erscheinungsdatum:	2021
ISSN:	2056-7944
URL der Originalveröffentlichung:	https://doi.org/10.1038/s41525-020-00163-8
DOI der Originalveröffentlichung:	10.1038/s41525-020-00163-8
Enthalten in den Sammlungen:	JGU-Publikationen