Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.714701
Title: Palmitoylation in neurodegeneration : analysis of cysteine-string protein mutants linked with neuronal ceroid lipofuscinosis
Author: Diez-Ardanuy, Cinta
Awarding Body: University of Strathclyde
Current Institution: University of Strathclyde
Date of Award: 2017
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Abstract:
Neuronal Ceroid Lipofuscinoses (NCLs) are neurodegenerative lysosomal-storage disorders characterized by intracellular accumulation of autofluorescent material. Mutations in the DNAJC5 gene encoding Cysteine-String Protein alpha (CSPα) cause autosomal-dominant adult-onset NCL (ANCL). The disease-causing mutations occur within the cysteine-stringdomain (CSD), a region of the protein that is extensively palmitoylated. It has been shown that the ANCL CSPα mutants form aggregates and that this is dependent on palmitoylation. As aggregation is a common feature of neurodegenerative disorders, aggregates formed in ANCL are likely to contribute, together with loss-of-function effects, to disease pathology. The aims of this project were to: (i) investigate features of CSPα that are important for aggregate formation; (ii) identify molecular changes that occur in ANCL; and (iii) identify mechanisms regulating CSPα turnover to provide insight into pathways that might be perturbed in ANCL. A cluster of palmitoylated cysteines in the CSD were identified as essential for aggregation of the ANCL CSPα mutants, further supporting an association between palmitoylation and aggregation. Analysis of the expression levels of different proteins in post-mortem brain revealed a massive increase in expression of the palmitoyl thioesterase enzyme PPT1 in ANCL samples, which is intriguing as PPT1 functions to depalmitoylate proteins during their degradation and mutations in the PPT1 gene cause infantile NCL. Further analysis identified several other proteins that had altered expression levels including α-synuclein. Degradation of both wild-type and mutant CSPα proteins was mediated by the proteasome but was independent of lysine ubiquitination. This pathway mediated rapid degradation of non-palmitoylated protein, and blocking proteasome activity enhanced the formation of mutant aggregates. It will be important in future work to determine how mutations in CSPα affect protein degradation pathways to cause the characteristic NCL lysosomal morphology, and whether there is a role for the lysosome in degradation of palmitoylated or aggregated CSPα.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.714701  DOI: Not available
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