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. Author manuscript; available in PMC: 2018 Oct 1.
Published in final edited form as: Trends Endocrinol Metab. 2017 Sep 7;28(10):722–734. doi: 10.1016/j.tem.2017.07.004

Table 1.

Upregulation and sequence alterations of DNA repair genes in long-lived species

Mechanisms Genes Alterations Species Control
species
Refs
DNA damage response TP53 upregulation Human and naked mole rat Mouse [60]
Chek1, Rif1 upregulation Long-lived bats and rodents Short-lived counterparts [61]
Base excision repair MBD4, MUTYH, NEIL1, NEIL2, TDG, POLL upregulation Human and naked mole rat Mouse [60]
Nucleotide excision repair Ercc1 upregulation Long-lived bats and rodents Short-lived counterparts [61]
Mutations Bowhead whale 9 mammals [63]
Ercc3 Positive selection Bowhead whale Minke whale, cow, and dolphin [63]
DNA Mismatch repair MSH3 upregulation Human and naked mole rat Mouse [60]
Msh6, Pms2 upregulation Long-lived bats and rodents Short-lived counterparts [61]
DNA double strand break repair NHEJ1, XRCC6, POLL upregulation Human and naked mole rat Mouse [60]
Pnkp, Rad51b, Prpf19, Slx4 upregulation Long-lived bats and rodents Short-lived counterparts [61]
ATM, PRKDC, RAD50, KU80 Positive selection Myotis davidii, Pteropus alecto 8 non-bat mammals [64]
Fanconi anemia DNA repair Faap100, Fancg upregulation Long-lived bats and rodents Short-lived counterparts [61]