Beaver and Naked Mole Rat Genomes Reveal Common Paths to Longevity

  • Xuming Zhou
  • , Qianhui Dou
  • , Guangyi Fan
  • , Quanwei Zhang
  • , Maxwell Sanderford
  • , Alaattin Kaya
  • , Jeremy Johnson
  • , Elinor K. Karlsson
  • , Xiao Tian
  • , Aleksei Mikhalchenko
  • , Sudhir Kumar
  • , Andrei Seluanov
  • , Zhengdong D. Zhang
  • , Vera Gorbunova
  • , Xin Liu
  • , Vadim N. Gladyshev

Research output: Contribution to journalArticlepeer-review

24 Scopus citations

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 languageEnglish
Article number107949
Pages (from-to)107949
JournalCell Reports
Volume32
Issue number4
DOIs
StatePublished - Jul 28 2020
Externally publishedYes

Keywords

  • Aging/genetics
  • Animals
  • Genome/genetics
  • Longevity/genetics
  • Models, Animal
  • Mole Rats/genetics
  • Rodentia/genetics
  • Species Specificity
  • Transcriptome/genetics

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