Demographic History and Genomic Response to Environmental Changes in a Rapid Radiation of Wild Rats

Author:

Ge Deyan1ORCID,Feijó Anderson1,Wen Zhixin1,Abramov Alexei V23,Lu Liang4,Cheng Jilong1,Pan Shengkai5,Ye Sicheng6,Xia Lin1,Jiang Xuelong7,Vogler Alfried P89,Yang Qisen1

Affiliation:

1. Key Laboratory of Zoological Systematics and Evolution, Institute of Zoology, Chinese Academy of Sciences, Chaoyang District, Beijing, China

2. Zoological Institute, Russian Academy of Sciences, Saint Petersburg, Russia

3. Joint Russian-Vietnamese Tropical Research and Technological Centre, Hanoi, Vietnam

4. State Key Laboratory for Infectious Diseases Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing, China

5. CAS Key Lab of Animal Ecology and Conservation Biology, Institute of Zoology, Chinese Academy of Sciences, Beijing, China

6. Center for Computational Genomics, Beijing Institute of Genomics, Chinese Academy of Sciences, Beijing, China

7. State Key Laboratory of Genetic Resources and Evolution, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming, Yunnan, China

8. Department of Life Sciences, Natural History Museum, London, United Kingdom

9. Department of Life Sciences, Imperial College London, Silwood Park Campus, Ascot, United Kingdom

Abstract

Abstract For organisms to survive and prosper in a harsh environment, particularly under rapid climate change, poses tremendous challenges. Recent studies have highlighted the continued loss of megafauna in terrestrial ecosystems and the subsequent surge of small mammals, such as rodents, bats, lagomorphs, and insectivores. However, the ecological partitioning of these animals will likely lead to large variation in their responses to environmental change. In the present study, we investigated the evolutionary history and genetic adaptations of white-bellied rats (Niviventer Marshall, 1976), which are widespread in the natural terrestrial ecosystems in Asia but also known as important zoonotic pathogen vectors and transmitters. The southeastern Qinghai-Tibet Plateau was inferred as the origin center of this genus, with parallel diversification in temperate and tropical niches. Demographic history analyses from mitochondrial and nuclear sequences of Niviventer demonstrated population size increases and range expansion for species in Southeast Asia, and habitat generalists elsewhere. Unexpectedly, population increases were seen in N. eha, which inhabits the highest elevation among Niviventer species. Genome scans of nuclear exons revealed that among the congeneric species, N. eha has the largest number of positively selected genes. Protein functions of these genes are mainly related to olfaction, taste, and tumor suppression. Extensive genetic modification presents a major strategy in response to global changes in these alpine species.

Funder

Second Tibetan Plateau Scientific Expedition and Research Program

National Nature Science Fund of China

Newton Advanced Fellowship

Royal Society

International Fellowship for Distinguished Scientists, Chinese Academy of Sciences

Ministry of Science and Higher Education of Russian

Chinese Academy of Sciences President’s International Fellowship Initiative

Publisher

Oxford University Press (OUP)

Subject

Genetics,Molecular Biology,Ecology, Evolution, Behavior and Systematics

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