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April 17, 2026Science Advances2 citationsOpen Access

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

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TSTea ShavlakadzeKXKun XiongRDRomain Donné

Key Points

  • The aim is to map genes and pathways that change consistently during rodent aging across multiple tissues and time points.
  • Created a high N atlas profiling gene expression across 28 tissues in mice and 32 in rats.
  • Analyzed more than 5000 samples from both species.
  • Examined early, mid, late, and linear age-related gene changes.
  • Identified linear genes prevalent in many tissues with some spared from changes.
  • Found common and distinct aging features between different tissues, sexes, and species.
  • Provided a comprehensive resource for studying age-related gene changes.

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.

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Cite This Study

Shavlakadze et al. (2026) studied this question.

synapsesocial.com/papers/69e1cf7b5cdc762e9d858725https://doi.org/10.1126/sciadv.ady8401
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  5. 5Transcriptomic Profile of Mouse Brain Ageing in Early Developmental Stages2024 · 1 citations