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Adaptive Evolution of Antioxidase-related Genes in Hypoxia-tolerant Mammals

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Journal Front Genet
Date 2024 May 10
PMID 38725483
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Abstract

To cope with the damage from oxidative stress caused by hypoxia, mammals have evolved a series of physiological and biochemical traits, including antioxidant ability. Although numerous research studies about the mechanisms of hypoxia evolution have been reported, the molecular mechanisms of antioxidase-related genes in mammals living in different environments are yet to be completely understood. In this study, we constructed a dataset comprising 7 antioxidase-related genes (, , , , , , and ) from 43 mammalian species to implement evolutionary analysis. The results showed that six genes (, , , , , and ) have undergone divergent evolution based on the free-ratio (M1) model. Furthermore, multi-ratio model analyses uncovered the divergent evolution between hypoxic and non-hypoxic lineages, as well as various hypoxic lineages. In addition, the branch-site model identified 9 positively selected branches in 6 genes (, , , , , and ) that contained 35 positively selected sites, among which 31 positively selected sites were identified in hypoxia-tolerant branches, accounting for 89% of the total number of positively selected sites. Interestingly, 65 parallel/convergent sites were identified in the 7 genes. In summary, antioxidase-related genes are subjected to different selective pressures among hypoxia-tolerant species living in different habitats. This study provides a valuable insight into the molecular evolution of antioxidase-related genes in hypoxia evolution in mammals.

References
1.
Hu H, Li Y, Yang Y, Xu K, Yang L, Qiao S . Effect of a Plateau Environment on the Oxidation State of the Heart and Liver through AMPK/p38 MAPK/Nrf2-ARE Signaling Pathways in Tibetan and DLY Pigs. Animals (Basel). 2022; 12(9). PMC: 9104009. DOI: 10.3390/ani12091219. View

2.
Panneton W . The mammalian diving response: an enigmatic reflex to preserve life?. Physiology (Bethesda). 2013; 28(5):284-97. PMC: 3768097. DOI: 10.1152/physiol.00020.2013. View

3.
Ramirez J, Folkow L, Blix A . Hypoxia tolerance in mammals and birds: from the wilderness to the clinic. Annu Rev Physiol. 2006; 69:113-43. DOI: 10.1146/annurev.physiol.69.031905.163111. View

4.
Nathaniel T, Williams-Hernandez A, Hunter A, Liddy C, Peffley D, Umesiri F . Tissue hypoxia during ischemic stroke: adaptive clues from hypoxia-tolerant animal models. Brain Res Bull. 2015; 114:1-12. DOI: 10.1016/j.brainresbull.2015.02.006. View

5.
Shen Y, Liang L, Li G, Murphy R, Zhang Y . Parallel evolution of auditory genes for echolocation in bats and toothed whales. PLoS Genet. 2012; 8(6):e1002788. PMC: 3386236. DOI: 10.1371/journal.pgen.1002788. View