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Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types

Title: Genetic analysis of amyotrophic lateral sclerosis identifies contributing pathways and cell types
Authors: Saez-Atienzar, S; Bandres-Ciga, S; Langston, RG; Kim, JJ; Choi, SW; Reynolds, RH; International ALS Genomics Consortium; ITALSGEN; Abramzon, Y; Dewan, R; Ahmed, S; Landers, JE; Chia, R; Ryten, M; Cookson, MR; Nalls, MA; Chiò, A; Traynor, BJ
Source: Science Advances , 7 (3) , Article eabd9036. (2021)
Publication Year: 2021
Collection: University College London: UCL Discovery
Description: Despite the considerable progress in unraveling the genetic causes of amyotrophic lateral sclerosis (ALS), we do not fully understand the molecular mechanisms underlying the disease. We analyzed genome-wide data involving 78,500 individuals using a polygenic risk score approach to identify the biological pathways and cell types involved in ALS. This data-driven approach identified multiple aspects of the biology underlying the disease that resolved into broader themes, namely, neuron projection morphogenesis, membrane trafficking, and signal transduction mediated by ribonucleotides. We also found that genomic risk in ALS maps consistently to GABAergic interneurons and oligodendrocytes, as confirmed in human single-nucleus RNA-seq data. Using two-sample Mendelian randomization, we nominated six differentially expressed genes (ATG16L2, ACSL5, MAP1LC3A, MAPKAPK3, PLXNB2, and SCFD1) within the significant pathways as relevant to ALS. We conclude that the disparate genetic etiologies of this fatal neurological disease converge on a smaller number of final common pathways and cell types.
Document Type: article in journal/newspaper
File Description: text
Language: English
Relation: https://discovery.ucl.ac.uk/id/eprint/10121626/1/eabd9036.full.pdf; https://discovery.ucl.ac.uk/id/eprint/10121626/
Availability: https://discovery.ucl.ac.uk/id/eprint/10121626/1/eabd9036.full.pdf; https://discovery.ucl.ac.uk/id/eprint/10121626/
Rights: open
Accession Number: edsbas.8825EB0E
Database: BASE