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Abstract
Caloric restriction (CR) reduces genome-wide somatic mutation burdens by varying degrees across different tissues in mice.
- Somatic mutations accumulate in cells throughout life, contributing to aging and genomic instability.
- CR leads to a decrease in both substitution and insertion/deletion mutation burdens.
- The effects of CR on mutation reduction vary depending on the tissue type examined.
- CR significantly decreases the activity of the single-base substitution mutational process SBS5, which is responsible for most mutations in mammals.
- The most substantial reduction in mutation burden from CR occurs in transcriptionally inactive regions of the genome.
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