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.

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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

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article

Multitissue, multi–time point transcriptomic atlas of aging in mice and rats

Matthew Wakai, Kun Xiong, Corissa McEwen, David J. Glass et al.
Science Advances
Genetics, Aging, and Longevity in Model Organisms
article

Multitissue, multi–time point transcriptomic atlas of aging in mice and rats

Matthew Wakai, Kun Xiong, Corissa McEwen, David J. Glass, Romain Donné, Abhilash Gadi, Nicole Negron, Yu Bai, Tea Shavlakadze, H. A. Salmon, Jacob Treinish, Larry Proctor, Yi Wei, Elias Pavlopoulos, Min Ni, Shuo Li
article en

Abstract

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.

Science AdvancesVol. 12(16)
Regeneron (United States) (US)
Regeneron Pharmaceuticals
Openalex Percentile: Top 20%
Genetics, Aging, and Longevity in Model Organisms
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