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Letter

Codon 104 of p53 is not an adaptively selected site for extreme environments in mammals of the Tibet plateau

Zhen Liu
PNAS June 10, 2014 111 (23) E2357; first published May 28, 2014; https://doi.org/10.1073/pnas.1323662111
Zhen Liu
State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China
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  • For correspondence: zhenliu@mail.kiz.ac.cn

This Letter has a Reply and related content. Please see:

  • Reply to Liu: Amino acid 104 asparagine/glutamic acid of p53 is an adaptively selected site for extreme environments in mammals of the Tibet plateau - May 28, 2014
  • Codon 104 variation of p53 gene provides adaptive apoptotic responses to extreme environments in mammals of the Tibet plateau - December 02, 2013
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The theories of molecular evolution are very helpful to yield insights into the genetic mechanisms for phenotypes or physiological roles that are difficult to discern in the laboratory. Mutations of functional genes that benefit fitness may experience fixation, especially when they originate in species living in challenging environments where selection may be extreme. Based on comparison of p53 sequence data and functional studies, Zhao et al. (1) conclude that asparagine-104 (104N) in the wild zokor (Myospalax baileyi) and glutamic acid-104 (104E) in root vole (Microtus oeconomus) are “adaptively variable, meeting the environment stresses of the Tibetan plateau.” I believe that this conclusion is unwarranted.

Zhao et al. (1) contend that the amino acids of 104N and 104E in p53 are an outcome of environmental adaptation and evolutionary selection to high elevation living for M. baileyi and M. oeconomus, respectively. If the independent mutations yielded advantages to stressful environments, then selection should have exclusively fixed them in taxa high elevation species. However, searching in National Center for Biotechnology Information and Ensembl databases reveals that 104N also occurs in many lowland rodents, including mouse, rat, gerbil, naked mole-rat, lesser Egyptian jerboa, degu, and chinchilla, which suggests that the mutation has already occurred in the ancestors of rodents. In addition, this mutation also occurs in more diverse lowland taxa, such as mouse lemur, hedgehog, cow, sheep, rabbit, and horseshoe bat. Similarly, 104E of p53 is not unique to M. oeconomus. This amino acid also occurs in the closely related prairie vole (Microtus ochrogaster), which lives in lowland areas (2). Its origin appears to have occurred in ancestral Microtus, if not earlier. Thus, there is no indication at the sequence level that the mutational variation of S104N/E of p53 in M. baileyi and M. oeconomus is fixed adaptively for facing the environmental stresses of the Tibetan plateau.

Zhao et al. further contend that 104N/E contributed functionally to adaptive resistance to extreme environments of the Tibet plateau. However, their data do not support that assertion. Considering phylogenetic relationships, the human control in their functional studies may have yielded misleading results caused by lineage-specific history due to long divergence times (3). Compared with the lowland relative of Gansu zokor (Myospalax cansus), M. baileyi exhibited that three (Apaf1, Bax, and Puma) of six p53 target genes were differentially expressed (figure S4 from ref. 1). However, 104N of p53 in M. baileyi does not result in their expression difference. Upon mutating 104N into 104S in M. baileyi, the expression level of Apaf1 did not increase, as it did in M. cansus, but rather it decreased; the expression levels of Bax and Puma did not change significantly (figure 2 from ref. 1). The functional experiments of Zhao et al. do not determine whether site 104 was under positive selection or not, even if this site appears to play an important role in p53 function, because most of important functional sites of genes typically tend to be under purifying and not adaptive selection (4, 5).

Footnotes

  • ↵1E-mail: zhenliu{at}mail.kiz.ac.cn.
  • Author contributions: Z.L. wrote the paper.

  • The author declares no conflict of interest.

View Abstract

References

  1. ↵
    1. Zhao Y,
    2. et al.
    (2013) Codon 104 variation of p53 gene provides adaptive apoptotic responses to extreme environments in mammals of the Tibet plateau. Proc Natl Acad Sci USA 110(51):20639–20644.
    OpenUrlAbstract/FREE Full Text
  2. ↵
    1. Getz LL
    (1985) Biology of New World Microtus, ed Tamarin R (American Society of Mammalogists, Stillwater, OK), pp 286–304.
  3. ↵
    1. Shi P,
    2. Bakewell MA,
    3. Zhang J
    (2006) Did brain-specific genes evolve faster in humans than in chimpanzees? Trends Genet 22(11):608–613.
    OpenUrlCrossRefPubMed
  4. ↵
    1. Kimura M,
    2. Ohta T
    (1974) On some principles governing molecular evolution. Proc Natl Acad Sci USA 71(7):2848–2852.
    OpenUrlAbstract/FREE Full Text
  5. ↵
    1. Thomas JW,
    2. et al.
    (2003) Comparative analyses of multi-species sequences from targeted genomic regions. Nature 424(6950):788–793.
    OpenUrlCrossRefPubMed
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104N/E of p53 is not an adaptively selected site
Zhen Liu
Proceedings of the National Academy of Sciences Jun 2014, 111 (23) E2357; DOI: 10.1073/pnas.1323662111

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104N/E of p53 is not an adaptively selected site
Zhen Liu
Proceedings of the National Academy of Sciences Jun 2014, 111 (23) E2357; DOI: 10.1073/pnas.1323662111
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