Literature DB >> 31658403

Genetic, Structural, and Functional Evidence Link TMEM175 to Synucleinopathies.

Lynne Krohn1,2, Tuğba Nur Öztürk3,4,5, Benoît Vanderperre2,6, Bouchra Ouled Amar Bencheikh2,6, Jennifer A Ruskey2,6, Sandra B Laurent2,6, Dan Spiegelman2,6, Ronald B Postuma2,6, Isabelle Arnulf7, Michele T M Hu8,9, Yves Dauvilliers10, Birgit Högl11, Ambra Stefani11, Christelle Charley Monaca12, Giuseppe Plazzi13,14, Elena Antelmi13,14, Luigi Ferini-Strambi15, Anna Heidbreder16, Uladzislau Rudakou1,2, Valérie Cochen De Cock17,18, Peter Young16, Pavlina Wolf19, Petra Oliva19, Xiaokui Kate Zhang19, Lior Greenbaum20,21,22, Christopher Liong23, Jean-François Gagnon24,25, Alex Desautels24,26, Sharon Hassin-Baer22,23,27, Jacques Y Montplaisir24,28, Nicolas Dupré29,30, Guy A Rouleau1,2,6, Edward A Fon2,6, Jean-François Trempe31, Guillaume Lamoureux3,4,5,32,33, Roy N Alcalay23,34, Ziv Gan-Or1,2,6.   

Abstract

OBJECTIVE: The TMEM175/GAK/DGKQ locus is the 3rd strongest risk locus in genome-wide association studies of Parkinson disease (PD). We aimed to identify the specific disease-associated variants in this locus, and their potential implications.
METHODS: Full sequencing of TMEM175/GAK/DGKQ followed by genotyping of specific associated variants was performed in PD (n = 1,575) and rapid eye movement sleep behavior disorder (RBD) patients (n = 533) and in controls (n = 1,583). Adjusted regression models and a meta-analysis were performed. Association between variants and glucocerebrosidase (GCase) activity was analyzed in 715 individuals with available data. Homology modeling, molecular dynamics simulations, and lysosomal localization experiments were performed on TMEM175 variants to determine their potential effects on structure and function.
RESULTS: Two coding variants, TMEM175 p.M393T (odds ratio [OR] = 1.37, p = 0.0003) and p.Q65P (OR = 0.72, p = 0.005), were associated with PD, and p.M393T was also associated with RBD (OR = 1.59, p = 0.001). TMEM175 p.M393T was associated with reduced GCase activity. Homology modeling and normal mode analysis demonstrated that TMEM175 p.M393T creates a polar side-chain in the hydrophobic core of the transmembrane, which could destabilize the domain and thus impair either its assembly, maturation, or trafficking. Molecular dynamics simulations demonstrated that the p.Q65P variant may increase stability and ion conductance of the transmembrane protein, and lysosomal localization was not affected by these variants.
INTERPRETATION: Coding variants in TMEM175 are likely to be responsible for the association in the TMEM175/GAK/DGKQ locus, which could be mediated by affecting GCase activity. ANN NEUROL 2020;87:139-153.
© 2019 American Neurological Association.

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Year:  2019        PMID: 31658403     DOI: 10.1002/ana.25629

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  19 in total

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Journal:  Lancet Neurol       Date:  2021-08       Impact factor: 44.182

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