Multitissue, multi–time point transcriptomic atlas of aging in mice and rats
To determine the genes and pathways that are up- or down-regulated in a consistent manner throughout the rodent lifespan, we generated a high N age-related gene expression atlas in mice and rats, by profiling 28 tissues in male and female C57BL/6J mice and 32 tissues in male Sprague Dawley rats (>5000 samples) over multiple time points. We identified age-related genes and pathways that change either early in life, at mid-age, late in life, or linearly throughout the animals' lifespan. Linear genes dominated many but not all tissues, and certain tissues were relatively spared from age-related changes. We explored common and different features of aging between tissues, sexes, and species. Given the expanse of our transcriptomic dataset, we believe that this study will serve as a useful resource for understanding the timing, tissue specificity, sex-specificity, and species specificity of age-related gene and pathway changes in mice and rats.
Authors
- Matthew Wakai
- Kun Xiong (ORCID: https://orcid.org/0000-0003-1431-6586)
- Corissa McEwen
- David J. Glass (ORCID: https://orcid.org/0000-0001-6187-4164)
- Romain Donné (ORCID: https://orcid.org/0000-0002-8152-1283)
- Abhilash Gadi
- Nicole Negron
- Yu Bai (ORCID: https://orcid.org/0000-0003-1447-0209)
- Tea Shavlakadze
- H. A. Salmon
- Jacob Treinish
- Larry Proctor (ORCID: https://orcid.org/0009-0003-5995-508X)
- Yi Wei
- Elias Pavlopoulos
- Min Ni
- Shuo Li
Institutions
- Regeneron (United States) (US)
Publication Details
- Journal
- Science Advances
- Published
- 2026-04-15
- DOI
- https://doi.org/10.1126/sciadv.ady8401
- Primary Topic
- Genetics, Aging, and Longevity in Model Organisms
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- Regeneron Pharmaceuticals