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Cathepsin B p.Gly284Val Variant in Parkinson's Disease Pathogenesis
LM. Milanowski, X. Hou, JM. Bredenberg, FC. Fiesel, LT. Cocker, AI. Soto-Beasley, RL. Walton, AJ. Strongosky, AH. Faroqi, M. Barcikowska, M. Boczarska-Jedynak, J. Dulski, L. Fedoryshyn, P. Janik, A. Potulska-Chromik, K. Karpinsky, A....
Language English Country Switzerland
Document type Journal Article
Grant support
RF1 NS085070
NINDS NIH HHS - United States
U54 NS110435
NINDS NIH HHS - United States
1U19AG063911
NIH HHS - United States
NLK
Free Medical Journals
from 2000
Freely Accessible Science Journals
from 2000
PubMed Central
from 2007
Europe PubMed Central
from 2007
ProQuest Central
from 2000-03-01
Open Access Digital Library
from 2000-01-01
Open Access Digital Library
from 2007-01-01
Health & Medicine (ProQuest)
from 2000-03-01
ROAD: Directory of Open Access Scholarly Resources
from 2000
PubMed
35806091
DOI
10.3390/ijms23137086
Knihovny.cz E-resources
- MeSH
- Genotype MeSH
- Heterozygote MeSH
- Cathepsin B genetics metabolism MeSH
- Humans MeSH
- Parkinson Disease * genetics MeSH
- Penetrance MeSH
- Check Tag
- Humans MeSH
- Publication type
- Journal Article MeSH
Parkinson's disease (PD) is generally considered a sporadic disorder, but a strong genetic background is often found. The aim of this study was to identify the underlying genetic cause of PD in two affected siblings and to subsequently assess the role of mutations in Cathepsin B (CTSB) in susceptibility to PD. A typical PD family was identified and whole-exome sequencing was performed in two affected siblings. Variants of interest were validated using Sanger sequencing. CTSB p.Gly284Val was genotyped in 2077 PD patients and 615 unrelated healthy controls from the Czech Republic, Ireland, Poland, Ukraine, and the USA. The gene burden analysis was conducted for the CTSB gene in an additional 769 PD probands from Mayo Clinic Florida familial PD cohort. CTSB expression and activity in patient-derived fibroblasts and controls were evaluated by qRT-PCR, western blot, immunocytochemistry, and enzymatic assay. The CTSB p.Gly284Val candidate variant was only identified in affected family members. Functional analysis of CTSB patient-derived fibroblasts under basal conditions did not reveal overt changes in endogenous expression, subcellular localization, or enzymatic activity in the heterozygous carrier of the CTSB variant. The identification of the CTSB p.Gly284Val may support the hypothesis that the CTSB locus harbors variants with differing penetrance that can determine the disease risk.
Bielanski Hospital 01 809 Warsaw Poland
Department of Clinical Genomics Mayo Clinic Florida Jacksonville FL 32224 USA
Department of Medical Genetics Institute of Mother and Child 01 211 Warsaw Poland
Department of Neurology Faculty of Health Science Medical University of Warsaw 02 091 Warsaw Poland
Department of Neurology Jagiellonian University Medical College 31 008 Krakow Poland
Department of Neurology Mayo Clinic Florida Jacksonville FL 32224 USA
Department of Neurology St Adalbert Hospital Copernicus PL Ltd 80 462 Gdansk Poland
Department of Neuroscience Mayo Clinic Florida Jacksonville FL 32224 USA
Institute of Genetics and Biotechnology Faculty of Biology University of Warsaw 00 927 Warsaw Poland
Lviv Regional Clinical Hospital 79010 Lviv Ukraine
Neuroscience PhD Program Mayo Graduate School Mayo Clinic Florida Jacksonville FL 32224 USA
School of Medicine and Medical Science University College Dublin D04 V1W8 Dublin Ireland
St Anne's University Hospital and Faculty of Medicine Masaryk University 601 77 Brno Czech Republic
The Dublin Neurological Institute Mater Misericordiae University Hospital D07 W7XF Dublin Ireland
Uzhhorod National University 88 000 Uzhhorod Ukraine
Uzhhorod Regional Clinical Centre of Neurosurgery and Neurology 88018 Uzhhorod Ukraine
References provided by Crossref.org
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