C9orf72 dipeptides disrupt the nucleocytoplasmic transport machinery and cause TDP-43 mislocalisation to the cytoplasm
Abstract A repeat expansion in C9orf72 is the major cause of both frontotemporal dementia and amyotrophic lateral sclerosis, accounting for approximately 1 in 12 cases of either disease. The expansion is translated to produce five dipeptide repeat proteins (DPRs) which aggregate in patient brain and...
Main Authors: | Sarah Ryan, Sara Rollinson, Eleanor Hobbs, Stuart Pickering-Brown |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Portfolio
2022-03-01
|
Series: | Scientific Reports |
Online Access: | https://doi.org/10.1038/s41598-022-08724-w |
Similar Items
-
p62 overexpression induces TDP-43 cytoplasmic mislocalisation, aggregation and cleavage and neuronal death
by: A. D. Foster, et al.
Published: (2021-06-01) -
Unraveling the impact of disrupted nucleocytoplasmic transport systems in C9orf72-associated ALS
by: Philip McGoldrick, et al.
Published: (2023-08-01) -
Traumatic injury compromises nucleocytoplasmic transport and leads to TDP-43 pathology
by: Eric N Anderson, et al.
Published: (2021-06-01) -
The role of mitochondrial dysfunction and ER stress in TDP-43 and C9ORF72 ALS
by: Dafinca, R, et al.
Published: (2021) -
The pathophysiological role of TDP-43 in amyotrophic lateral sclerosis due to C9orf72 mutations
by: Scaber, J
Published: (2017)