The highest-elevation frog provides insights into mechanisms and evolution of defenses against high UV radiation

Author:

Fu Ting-Ting123,Sun Yan-Bo1,Gao Wei1,Long Cheng-Bo4,Yang Chun-Hua12,Yang Xin-Wang4,Zhang Yi12,Lan Xin-Qiang24,Huang Song5,Jin Jie-Qiong1,Murphy Robert W.16,Zhang Yun47ORCID,Lai Ren4ORCID,Hillis David M.3,Zhang Ya-Ping17ORCID,Che Jing17ORCID

Affiliation:

1. State Key Laboratory of Genetic Resource and Evolution & Yunnan Key Laboratory of Biodiversity and Ecological Security of Gaoligong Mountain, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China

2. Kunming College of Life Science, University of Chinese Academy of Sciences, Kunming 650204, China

3. Department of Integrative Biology and Biodiversity Center, University of Texas at Austin, Austin, TX 78712, U.S.A.

4. Key Laboratory of Animal Models and Human Disease Mechanisms of Chinese Academy of Sciences/Key Laboratory of Bioactive Peptides of Yunnan Province, Kunming Institute of Zoology, Chinese Academy of Sciences, Kunming 650223, China

5. College of Life Sciences, Anhui Normal University, Wuhu 241000, China

6. Centre for Biodiversity and Conservation Biology, Royal Ontario Museum, Toronto, ON M5S 2C6, Canada

7. Center for Excellence in Animal Evolution and Genetics, Chinese Academy of Sciences, Kunming 650223, China

Abstract

Defense against ultraviolet (UV) radiation exposure is essential for survival, especially in high-elevation species. Although some specific genes involved in UV response have been reported, the full view of UV defense mechanisms remains largely unexplored. Herein, we used integrated approaches to analyze UV responses in the highest-elevation frog, Nanorana parkeri . We show less damage and more efficient antioxidant activity in skin of this frog than those of its lower-elevation relatives after UV exposure. We also reveal genes related to UV defense and a corresponding temporal expression pattern in N. parkeri . Genomic and metabolomic analysis along with large-scale transcriptomic profiling revealed a time-dependent coordinated defense mechanism in N. parkeri . We also identified several microRNAs that play important regulatory roles, especially in decreasing the expression levels of cell cycle genes. Moreover, multiple defense genes (i.e., TYR for melanogenesis) exhibit positive selection with function-enhancing substitutions. Thus, both expression shifts and gene mutations contribute to UV adaptation in N. parkeri . Our work demonstrates a genetic framework for evolution of UV defense in a natural environment.

Funder

CAS | Strategic Priority Research Program

CAS | The Second Tibetan Plateau Scientific Expedition abd Reseach Program

CAS | Strategic Priority Reseach Program

Natural Science Foundation of China

Yunnan Fundamental Research Projects

State Key Laboratory of Genetic Resources and Evolution

Chinese Academy of Sciences, President's International Fellowship Initiative

National Sciences and Engineering Research Council of Canada, Discovery Grant

China Scholarshio Council

Publisher

Proceedings of the National Academy of Sciences

Subject

Multidisciplinary

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3