A cluster of palmitoylated cysteines are essential for aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis

Tools

Diez Ardanuy, Cinta and Greaves, Jennifer and Munro, Kevin R. and Tomkinson, Nicholas C.O. and Chamberlain, Luke H. (2017) A cluster of palmitoylated cysteines are essential for aggregation of cysteine-string protein mutants that cause neuronal ceroid lipofuscinosis. Scientific Reports. 10. ISSN 2045-2322 (https://doi.org/10.1038/s41598-017-00036-8)

[thumbnail of Diez-Ardanuy-etal-SR-2016-A-cluster-of-palmitoylated-cysteines-are-essential]
Preview
 Text. Filename: Diez_Ardanuy_etal_SR_2016_A_cluster_of_palmitoylated_cysteines_are_essential.pdf
Final Published Version
License: Creative Commons Attribution 4.0 logo
Download (2MB)| Preview

Abstract

Autosomal-dominant adult-onset neuronal cero id lipofuscinosis (ANCL) is caused by mutation of the DNAJC5 gene encoding cysteine string protein alpha (CSP α ). The disease- causing mutations, which result in substituti on of leucine-115 with an arginine (L115R) or deletion of the neig hbouring leucine-116 ( Δ L116) in the cysteine-string domain cause CSP α to form high molecular weight SDS-resistant aggregates, which are also present in post- mortem brain tissue from patients. Formation and stability of these mutant aggregates is linked to palmitoylation of the cysteine-str ing domain, however the regions of the mutant proteins that drive aggregatio n have not been determined. The importance of specific residues in the cysteine-string domain was in vestigated, revealing that a central core of palmitoylated cysteines is essential for aggregation of ANCL CSP α mutants. Interestingly, palmitoylated monomers of ANCL CSP α mutants were shown to be short-lived compared with wild-type CSP α, suggesting that the mutants eith er have a faster rate of depalmitoylation or that they are consumed in a time-dependent manner into high molecular weight aggregates. These findings provide new insight into the features of CSP α that promote aggregation in the presence of L115R/ Δ L116 mutations and reveal a change in the lifetime of palmitoyla ted monomers of the mutant proteins.

ORCID iDs

Diez Ardanuy, Cinta ORCID logoORCID: https://orcid.org/0000-0003-0808-0108, Greaves, Jennifer ORCID logoORCID: https://orcid.org/0000-0001-8445-789X, Munro, Kevin R. ORCID logoORCID: https://orcid.org/0000-0003-2345-8308, Tomkinson, Nicholas C.O. ORCID logoORCID: https://orcid.org/0000-0002-5509-0133 and Chamberlain, Luke H. ORCID logoORCID: https://orcid.org/0000-0002-8701-4995;
CORE (COnnecting REpositories)