4.8 Article

A single nucleotide mutation in the dual-oxidase 2 (DUOX2) gene causes some of the panda's unique metabolic phenotypes

Journal

NATIONAL SCIENCE REVIEW
Volume 9, Issue 2, Pages -

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/nsr/nwab125

Keywords

giant panda; DUOX2 mutation; metabolic rate; thyroid hormones; DUOX2; mice and microbiota

Funding

  1. Strategic Priority Research Program of the Chinese Academy of Sciences [XDB13030100, XDB29020000]
  2. Creative Research Group Project of National Natural Science Foundation of China [31821001]
  3. Key Project of the Chinese Academy of Sciences [QYZDB-SSWSMC047]
  4. National Key Research and Development Program of China [2018YFC2000500]
  5. Chinese Academy of Sciences President's International Fellowship Initiative Postdoctoral Fellowship
  6. President's International Fellowship Initiative Professorial and Wolfson Merit Award

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This study demonstrates the profound effects of a single-nucleotide mutation in a key endocrine-related gene on the metabolic phenotype, including changes in body size, energy expenditure, organ sizes, and gut microbiota, in both giant pandas and mice. The findings have significant implications for ecology and evolution.
The giant panda (Ailuropoda melanoleuca) is an iconic bear native to China, famous for eating almost exclusively bamboo. This unusual dietary behavior for a carnivore is enabled by several key adaptations including low physical activity, reduced organ sizes and hypothyroidism leading to lowered energy expenditure. These adaptive phenotypes have been hypothesized to arise from a panda-unique single-nucleotide mutation in the dual-oxidase 2 (DUOX2) gene, involved in thyroid hormone synthesis. To test this hypothesis, we created genome-edited mice carrying the same point mutation as the panda and investigated its effect on metabolic phenotype. Homozygous mice were 27% smaller than heterozygous and wild-type ones, had 13% lower body mass-adjusted food intake, 55% decreased physical activity, lower mass of kidneys (11%) and brain (5%), lower serum thyroxine (T4: 36%), decreased absolute (12%) and mass-adjusted (5%) daily energy expenditure, and altered gut microbiota. Supplementation with T4 reversed the effects of the mutation. This work uses a state-of-the-art genome editing approach to demonstrate the link between a single-nucleotide mutation in a key endocrine-related gene and profound adaptive changes in the metabolic phenotype, with great importance in ecology and evolution.

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