Abstract
Long-lived rodents have become an attractive model for the studies on aging. To understand evolutionary paths to long life, we prepare chromosome-level genome assemblies of the two longest-lived rodents, Canadian beaver (Castor canadensis) and naked mole rat (NMR, Heterocephalus glaber), which were scaffolded with in vitro proximity ligation and chromosome conformation capture data and complemented with long-read sequencing. Our comparative genomic analyses reveal that amino acid substitutions at “disease-causing” sites are widespread in the rodent genomes and that identical substitutions in long-lived rodents are associated with common adaptive phenotypes, e.g., enhanced resistance to DNA damage and cellular stress. By employing a newly developed substitution model and likelihood ratio test, we find that energy and fatty acid metabolism pathways are enriched for signals of positive selection in both long-lived rodents. Thus, the high-quality genome resource of long-lived rodents can assist in the discovery of genetic factors that control longevity and adaptive evolution.
| Original language | English |
|---|---|
| Article number | 107949 |
| Pages (from-to) | 107949 |
| Journal | Cell Reports |
| Volume | 32 |
| Issue number | 4 |
| DOIs | |
| State | Published - Jul 28 2020 |
| Externally published | Yes |
Keywords
- Aging/genetics
- Animals
- Genome/genetics
- Longevity/genetics
- Models, Animal
- Mole Rats/genetics
- Rodentia/genetics
- Species Specificity
- Transcriptome/genetics
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