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Integrative genetic analysis illuminates ALS heritability and identifies risk genes

Title: Integrative genetic analysis illuminates ALS heritability and identifies risk genes
Authors: Salim Megat; Natalia Mora; Jason Sanogo; Olga Roman; Alberto Catanese; Najwa Ouali Alami; Axel Freischmidt; Xhuljana Mingaj; Hortense De Calbiac; François Muratet; Sylvie Dirrig-Grosch; Stéphane Dieterle; Nick Van Bakel; Kathrin Müller; Kirsten Sieverding; Jochen Weishaupt; Peter Munch Andersen; Markus Weber; Christoph Neuwirth; Markus Margelisch; Andreas Sommacal; Kristel R. Van Eijk; Jan H. Veldink; Project Mine Als Sequencing Consortium; Géraldine Lautrette; Philippe Couratier; Agnès Camuzat; Isabelle Le Ber; Maurizio Grassano; Adriano Chio; Tobias Boeckers; Albert C. Ludolph; Francesco Roselli; Deniz Yilmazer-Hanke; Stéphanie Millecamps; Edor Kabashi; Erik Storkebaum; Chantal Sellier; Luc Dupuis
Source: Nature Communications, Vol 14, Iss 1, Pp 1-18 (2023)
Publisher Information: Nature Portfolio, 2023.
Publication Year: 2023
Collection: LCC:Science
Subject Terms: Science
Description: Abstract Amyotrophic lateral sclerosis (ALS) has substantial heritability, in part shared with fronto-temporal dementia (FTD). We show that ALS heritability is enriched in splicing variants and in binding sites of 6 RNA-binding proteins including TDP-43 and FUS. A transcriptome wide association study (TWAS) identified 6 loci associated with ALS, including in NUP50 encoding for the nucleopore basket protein NUP50. Independently, rare variants in NUP50 were associated with ALS risk (P = 3.71.10−03; odds ratio = 3.29; 95%CI, 1.37 to 7.87) in a cohort of 9,390 ALS/FTD patients and 4,594 controls. Cells from one patient carrying a NUP50 frameshift mutation displayed a decreased level of NUP50. Loss of NUP50 leads to death of cultured neurons, and motor defects in Drosophila and zebrafish. Thus, our study identifies alterations in splicing in neurons as critical in ALS and provides genetic evidence linking nuclear pore defects to ALS.
Document Type: article
File Description: electronic resource
Language: English
ISSN: 2041-1723
Relation: https://doaj.org/toc/2041-1723
DOI: 10.1038/s41467-022-35724-1
Access URL: https://doaj.org/article/6c41a4f4e8fe4f95afcbf96cee484c70
Accession Number: edsdoj.6c41a4f4e8fe4f95afcbf96cee484c70
Database: Directory of Open Access Journals