PXD074595 is an
original dataset announced via ProteomeXchange.
Dataset Summary
| Title | Pathogenic POLRMT variants in mice impair mtDNA transcription and affect perinatal survival |
| Description | Mitochondrial gene expression is essential for oxidative phosphorylation (OXPHOS) that generates the bulk of the cellular ATP, and dysfunctional mitochondria is a common cause of human metabolic diseases. Recently, the first pathogenic variants in the only known mitochondrial RNA polymerase (POLRMT) were described. Patients present with a wide variety of clinical manifestations, such as hypotonia, short stature and developmental delay. Here, we modeled two human pathogenic POLRMT variants by creating the corresponding substitutions in mice: the dominant S582F and the recessive R984C variant. Mice homozygous for the R984C variant showed perinatal lethality without apparent embryonic developmental defects, thus showing that POLRMT has a critical role in the transition to oxidative metabolism at birth. Mice carrying the S582F variant were viable and exhibited decreased mitochondrial transcript levels due to impaired de novo transcription. However, mtDNA levels and in organello mtDNA replication remained normal, which recapitulates the molecular phenotypes observed in the patients. Altogether, our findings indicate that the conserved arginine near the active site is essential for POLRMT function, while the serine in the intercalating hairpin of the N-terminal domain is required for transcription but not primase activity. This study highlights genotype–phenotype differences and provides new insights into POLRMT function. |
| HostingRepository | PRIDE |
| AnnounceDate | 2026-05-13 |
| AnnouncementXML | Submission_2026-05-13_08:49:05.754.xml |
| DigitalObjectIdentifier | |
| ReviewLevel | Peer-reviewed dataset |
| DatasetOrigin | Original dataset |
| RepositorySupport | Unsupported dataset by repository |
| PrimarySubmitter | Akos Vegvari |
| SpeciesList | scientific name: Mus musculus (Mouse); NCBI TaxID: NEWT:10090; |
| ModificationList | iodoacetamide derivatized residue |
| Instrument | timsTOF HT |
Dataset History
| Revision | Datetime | Status | ChangeLog Entry |
| 0 | 2026-02-18 10:47:24 | ID requested | |
| ⏵ 1 | 2026-05-13 08:49:06 | announced | |
Publication List
| Dataset with its publication pending |
Keyword List
| submitter keyword: mouse models, mtDNA, mitochondria,POLRMT |
Contact List
| Akos Vegvari |
| contact affiliation | Karolinska Institutet, Stockholm, Sweden |
| contact email | akos.vegvari@ki.se |
| lab head | |
| Akos Vegvari |
| contact affiliation | Karolinska Institutet |
| contact email | akos.vegvari@ki.se |
| 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/2026/05/PXD074595 |
| PRIDE project URI |
Repository Record List
[ + ]
[ - ]
- PRIDE
- PXD074595
- Label: PRIDE project
- Name: Pathogenic POLRMT variants in mice impair mtDNA transcription and affect perinatal survival