medRxivGenetic & Genomic MedicinePreprint
Age-Associated Expression of DIMT1 (Dimethyladenosine Transferase) in Human Mesenchymal Stromal Cells: A Candidate for Multi-Gene Aging Signatures
Abstract
BackgroundDIMT1 is a highly conserved methyltransferase that functions as an N6,N6-dimethyladenosine transferase responsible for modifying two adjacent adenosines in the 18S rRNA. This protein is also a crucial, yet catalytically independent, ribosome maturation factor essential for the biogenesis of the 40S small ribosomal subunit. Given the established roles of ribosome biogenesis and methylation dynamics in biological aging, we investigated the relationship between DIMT1 expression and chronological donor age in Mesenchymal Stromal Cells (MSCs). MethodsTranscriptomic data for DIMT1 from a publicly available human MSC dataset (n = 61 donors, age range: 17-84 years) were analyzed. Pearson correlation and simple linear regression were performed to assess the association between normalized gene expression and donor age. ResultsA statistically significant positive correlation was identified between DIMT1 expression and donor age (Pearson r = 0.4282, R2 = 0.183, p = 0.0006). Linear regression modeling demonstrated that expression increases with advancing age, exhibiting a slope of 0.0045. ConclusionDIMT1 expression demonstrates a statistically significant positive correlation with donor age in MSCs, though age explains only 18.3% of expression variance. This relationship warrants further investigation of DIMT1 as a component of multi-gene aging signatures. The observed pattern may reflect compensatory responses in ribosome biogenesis or altered methylation dynamics associated with aging, though mechanistic validation is required.
- organism: human
- assay: bulk RNA-seq
- research focus: differential expression
- approach: statistical model
- Citations
- 0
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- The 18S rRNA Methyltransferase DIMT-1 Regulates Lifespan in the Germline Later in Life
M. Hafiz Rothi, Gautam Chandra Sarkar, … Eric Lieberman Greer·Nature CommunicationsPeer-reviewed·Jul 28, 2025
- Multi-faceted deregulation of gene expression and protein synthesis with age
Aleksandra S. Anisimova, Mark Meerson, … Vadim N. Gladyshev·Proceedings of the National Academy of SciencesPeer-reviewed·Jun 23, 2020
- Expression of Most Retrotransposons in Human Blood Correlates with Biological Aging
Yi-Ting Tsai, Nogayhan Seymen, … Mohammad Mahdi Karimi·eLifePeer-reviewed·Oct 17, 2024
- Chronological Aging Stiffens Cells, Alters Mitochondria, and Impairs Mitochondrial Mechanical Responsiveness in Mesenchymal Stem Cells
Omar Faruq, N.N. Nikitina, … Gunes Uzer·bioRxiv·Feb 26, 2026
- Deregulated mito-nuclear communication alters chromatin plasticity and differentiation potential of mesenchymal stem cells upon ageing
A. Pouikli, S. Parekh, … P. Tessarz·bioRxiv·Apr 2, 2020
- Single-cell profiling reveals a novel RAB13+ endothelial subpopulation and profibrotic mesenchymal cells in the aged human bone marrow
Itziar Cenzano, Miguel Cócera, … Felipe Prósper·bioRxiv·Jan 28, 2025