Regulatory effects of post-translational modifications on zDHHC S-acyltransferases
Zmuda, Filip and Chamberlain, Luke H. (2020) Regulatory effects of post-translational modifications on zDHHC S-acyltransferases. Journal of Biological Chemistry, 295 (43). pp. 14640-14652. ISSN 1083-351X (https://doi.org/10.1074/jbc.REV120.014717)
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Abstract
The human zDHHC S-acyltransferase family comprises 23 enzymes that mediate the S-acylation of a multitude of cellular proteins, including channels, receptors, transporters, signaling molecules, scaffolds, and chaperones. This reversible post-transitional modification (PTM) involves the attachment of a fatty acyl chain, usually derived from palmitoyl-CoA, to specific cysteine residues on target proteins, which affects their stability, localization, and function. These outcomes are essential to control many processes, including synaptic transmission and plasticity, cell growth and differentiation, and infectivity of viruses and other pathogens. Given the physiological importance of S-acylation, it is unsurprising that perturbations in this process, including mutations in ZDHHC genes, have been linked to different neurological pathologies and cancers, and there is growing interest in zDHHC enzymes as novel drug targets. Although zDHHC enzymes control a diverse array of cellular processes and are associated with major disorders, our understanding of these enzymes is surprisingly incomplete, particularly with regard to the regulatory mechanisms controlling these enzymes. However, there is growing evidence highlighting the role of different PTMs in this process. In this review, we discuss how PTMs, including phosphorylation, S-acylation, and ubiquitination, affect the stability, localization, and function of zDHHC enzymes and speculate on possible effects of PTMs that have emerged from larger screening studies. Developing a better understanding of the regulatory effects of PTMs on zDHHC enzymes will provide new insight into the intracellular dynamics of S-acylation and may also highlight novel approaches to modulate S-acylation for clinical gain.
ORCID iDs
Zmuda, Filip and Chamberlain, Luke H. ORCID: https://orcid.org/0000-0002-8701-4995;-
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Item type: Article ID code: 73637 Dates: DateEvent23 October 2020Published17 August 2020Published Online17 August 2020AcceptedSubjects: Medicine > Therapeutics. Pharmacology Department: Faculty of Science > Strathclyde Institute of Pharmacy and Biomedical Sciences Depositing user: Pure Administrator Date deposited: 18 Aug 2020 10:45 Last modified: 17 Dec 2024 01:21 URI: https://strathprints.strath.ac.uk/id/eprint/73637