Genetic mutations in RNA-binding proteins and their roles in ALS.
Katannya Kapeli, Fernando J Martinez, Gene W Yeo
Human genetics · 2017 · Vol. 136 (9) · pp. 1193-1214
Abstract
Mutations in genes that encode RNA-binding proteins (RBPs) have emerged as critical determinants of neurological diseases, especially motor neuron disorders such as amyotrophic lateral sclerosis (ALS). RBPs are involved in all aspects of RNA processing, controlling the life cycle of RNAs from synthesis to degradation. Hallmark features of RBPs in neuron dysfunction include misregulation of RNA processing, mislocalization of RBPs to the cytoplasm, and abnormal aggregation of RBPs. Much progress has been made in understanding how ALS-associated mutations in RBPs drive pathogenesis. Here, we focus on several key RBPs involved in ALS-TDP-43, HNRNP A2/B1, HNRNP A1, FUS, EWSR1, and TAF15-and review our current understanding of how mutations in these proteins cause disease.
Funding 8 grants
| Grant | Funder |
|---|---|
| R01 HG004659 | NHGRI NIH HHS (United States) |
| T32 GM008666 | NIGMS NIH HHS (United States) |
| U54 HG007005 | NHGRI NIH HHS (United States) |
| HG004659 | NIH HHS (United States) |
| R01 NS075449 | NINDS NIH HHS (United States) |
| HG007005 | NIH HHS (United States) |
| NS075449 | NIH HHS (United States) |
| T32GM008666 | National Institutes of Health (US) (International) |