Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways
Research output: Contribution to journal › Article › peer-review
Colleges, School and Institutes
Amyotrophic lateral sclerosis (ALS) is a devastating neurological disease with no effective treatment. We report the results of a moderate-scale sequencing study aimed at increasing the number of genes known to contribute to predisposition for ALS. We performed whole-exome sequencing of 2869 ALS patients and 6405 controls. Several known ALS genes were found to be associated, and TBK1 (the gene encoding TANK-binding kinase 1) was identified as an ALS gene. TBK1 is known to bind to and phosphorylate a number of proteins involved in innate immunity and autophagy, including optineurin (OPTN) and p62 (SQSTM1/sequestosome), both of which have also been implicated in ALS. These observations reveal a key role of the autophagic pathway in ALS and suggest specific targets for therapeutic intervention.
|Number of pages||6|
|Publication status||Published - 27 Mar 2015|
- Adaptor Proteins, Signal Transducing, Adolescent, Adult, Aged, Aged, 80 and over, Amyotrophic Lateral Sclerosis, Autophagy, Exome, Female, Genes, Genetic Association Studies, Genetic Predisposition to Disease, Humans, Male, Middle Aged, Protein Binding, Protein-Serine-Threonine Kinases, Risk, Sequence Analysis, DNA, Transcription Factor TFIIIA, Young Adult