Destabilization of mutated human PUS3 protein causes intellectual disability

Lin, Ting‐Yu; Smigiel, Robert; Kuzniewska, Bozena; Chmielewska, Joanna J.; Kosińska, Joanna; Biela, Mateusz; Biela, Anna; Kościelniak, Anna; Dobosz, Dominika; Laczmanska, Izabela; Chramiec‐Głąbik, Andrzej; Jeżowski, Jakub; Nowak, Jakub; Gos, Monika; Rzonca‐Niewczas, Sylwia; Dziembowska, Magdalena; Ploski, Rafał; Glatt, Sebastian

Abstract

Pseudouridine (Ψ) is an RNA base modification ubiquitously found in many types of RNAs. In humans, the isomerization of uridine is catalyzed by different stand-alone pseudouridine synthases (PUS). Genomic mutations in the human pseudouridine synthase 3 gene (PUS3) have been identified in patients with neurodevelopmental disorders. However, the underlying molecular mechanisms that cause the disease phenotypes remain elusive. Here, we utilize exome sequencing to identify genomic variants that lead to a homozygous amino acid substitution (p.[(Tyr71Cys)];[(Tyr71Cys)]) in human PUS3 of two affected individuals and a compound heterozygous substitution (p.[(Tyr71Cys)];[(Ile299Thr)]) in a third patient. We obtain wild-type and mutated full-length human recombinant PUS3 proteins and characterize the enzymatic activity in vitro. Unexpectedly, we find that the p.Tyr71Cys substitution neither affect tRNA binding nor pseudouridylation activity in vitro, but strongly impair the thermostability profile of PUS3, while the p.Ile299Thr mutation causes protein aggregation. Concomitantly, we observe that the PUS3 protein levels as well as the level of PUS3-dependent Ψ levels are strongly reduced in fibroblasts derived from all three patients. In summary, our results directly illustrate the link between the identified PUS3 variants and reduced Ψ levels in the patient cells, providing a molecular explanation for the observed clinical phenotypes.

Citation

Lin, T., Smigiel, R., Kuzniewska, B., Chmielewska, J. J., Kosińska, J., Biela, M., …Glatt, S. (2022). Destabilization of mutated human PUS3 protein causes intellectual disability. Human Mutation: Variation, Informatics and Disease, 43(12), 2063-2078. https://doi.org/10.1002/humu.24471

• Journal Article Type: Article
• Acceptance Date: Sep 2, 2022
• Online Publication Date: Oct 2, 2022
• Publication Date: 2022-12
• Deposit Date: Nov 2, 2023
• Journal: Human Mutation: Variation, Informatics and Disease
• Print ISSN: 1059-7794
• Electronic ISSN: 1098-1004
• Publisher: Wiley
• Peer Reviewed: Peer Reviewed
• Volume: 43
• Issue: 12
• Pages: 2063-2078
• DOI: https://doi.org/10.1002/humu.24471
• Keywords: Genetics (clinical); Genetics
• Public URL: https://durham-repository.worktribe.com/output/1874992
• Additional Information: This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution-NonCommercial-NoDerivs (CC BY-NC-ND) license (https://creativecommons.org/licenses/by-nc-nd/4.0/).