PXD056053 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Human tRNA genes enable differential nonsense suppression in live cells and a model of frontotemporal dementia |
| Description | Nonsense mutations generate premature termination codons (PTCs) that are responsible for 11% of human genetic disease alleles. Thus, nonsense suppressor tRNAs have broad therapeutic potential. Humans encode > 600 tRNA genes with many identical or similar copies of each tRNA. We hypothesized that tRNA gene variants will enable differential nonsense suppression and developed a dual fluorescent reporter to measure suppression in live cells. The arginine (CGA) to stop (UGA) mutation is the most common PTC, and an Arg nonsense suppressor tRNAArg (G36A) is found in 0.01% of human genomes in the tRNAArg TCG-6-1 gene. In multiple mammalian cell lines, we found tRNAArgUCA promotes readthrough levels that depend on the sequence of the tRNA gene and the cell type. We tested G36A variants of all six human tRNAArgUCG isodecoders, and only the TCG-6-1 gene was unable to translate nonsense codons. With tRNA sequencing, we showed that a suppressor tRNA derived from the TCG-3-1 gene was expressed 2-fold higher and generated 3-fold more nonsense suppression than a tRNA derived from the TCG-4-1 gene. In a neuroblastoma cell model of frontotemporal dementia (FTD), we observed up to 60% readthrough of the progranulin R493X allele with a human tRNAArg suppressor. The tRNAs outperformed an aminoglycoside nonsense suppression drug (G418) in efficacy, tolerability to the cells, and translation fidelity according to mass spectrometry. Our studies show that nonsense suppressor tRNAs can correct genetic defects that cause disease. |
| HostingRepository | PRIDE |
| AnnounceDate | 2025-07-25 |
| AnnouncementXML | Submission_2025-07-25_08:50:48.078.xml |
| DigitalObjectIdentifier | https://dx.doi.org/10.6019/PXD056053 |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Supported dataset by repository |
| PrimarySubmitter | Kyle Hoffman |
| SpeciesList | scientific name: Homo sapiens (Human); NCBI TaxID: 9606; |
| ModificationList | monohydroxylated residue; deamidated residue; iodoacetamide derivatized residue |
| Instrument | Orbitrap Fusion Lumos |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2024-09-20 04:58:39 | ID requested | |
| ⏵ 1 | 2025-07-25 08:50:48 | announced | |
Publication List
Keyword List
| submitter keyword: therapeutics, live-cell fluorescent reporters,frontotemporal dementia, tRNA, nonsense suppression, progranulin, protein synthesis |
Contact List
| Patrick O'Donoghue |
| contact affiliation | Department of Biochemistry, The University of Western Ontario, London, Ontario, Canada. Department of Chemistry, The University of Western Ontario, London, Ontario, Canada. |
| contact email | podonog@uwo.ca |
| lab head | |
| Kyle Hoffman |
| contact affiliation | Bioinformatics Solutions Inc. |
| contact email | khoffman@bioinfor.com |
| dataset submitter | |
Full Dataset Link List
Dataset FTP location
NOTE: Most web browsers have now discontinued native support for FTP access within the browser window. But you can usually install another FTP app (we recommend FileZilla) and configure your browser to launch the external application when you click on this FTP link. Or otherwise, launch an app that supports FTP (like FileZilla) and use this address: ftp://ftp.pride.ebi.ac.uk/pride/data/archive/2025/07/PXD056053 |
| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD056053
- Label: PRIDE project
- Name: Human tRNA genes enable differential nonsense suppression in live cells and a model of frontotemporal dementia