Use this URL to cite or link to this record in EThOS: https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.789540
Title: Exploration of the role of TBK1 in autophagy and Amyotrophic Lateral Sclerosis
Author: Davies, Maria
ISNI:       0000 0004 8501 3504
Awarding Body: University of Sheffield
Current Institution: University of Sheffield
Date of Award: 2019
Availability of Full Text:
Access from EThOS:
Full text unavailable from EThOS. Thesis embargoed until 18 Oct 2024
Access from Institution:
Abstract:
Tumor necrosis factor receptor-associated factor NF-KB (TANK) binding kinase 1 (TBK1) was recently identified as a novel Amyotrophic Lateral Sclerosis (ALS) gene in numerous independent human genetic studies. TBK1 is a non-canonical IkB kinase, playing a role in autophagy and the innate immune response. Over 150 TBK1 mutations along the entire protein length, predicted to cause TBK1 haploinsufficiency, have been found in patients with ALS and ALS-frontotemporal dementia (FTD). TBK1 mutations are found in approximately 4% of all ALS, ALS-FTD and FTD cases, but exactly how these mutations are contributing towards disease is unclear. It is hypothesised that TBK1 mutations contribute to ALS disease pathology due to impaired autophagy, in particular mitophagy. These two processes are crucial for homeostasis and are involved in numerous neurodegenerative diseases; basal autophagy levels are also high in neurons. Given that aggregate formation is a pathological feature of ALS, removal of these aggregates by autophagy is of particular relevance in this disease. The main aim of this work is to investigate pathways regulated by TBK1 in a 'neuronal-like' setting, and to elucidate how TBK1 mutations contribute to the pathogenesis of ALS. This work shows that TBK1 phosphorylation is elevated upon autophagy induction in NSC-34 cells, a cell-line commonly used in ALS research. Inhibition or depletion of TBK1 results in two distinct autophagy phenotypes - autophagy blockage and autophagy reduction. Using proteomic approaches, this work has explored the TBK1 signalling pathways further and identified a novel upstream kinase of TBK1, Nek1, another recently discovered ALS-gene. This not only links two ALS genes in the same pathway regulating autophagy, but also identifies a novel role for Nek1 in autophagy. This work has implications in the ALS field as expansion of both the potential roles of TBK1 and Nek1 mutations in ALS has been conducted, giving further insight into how they may be contributing to ALS pathology.
Supervisor: Collins, Mark Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.789540  DOI: Not available
Share: