Genomic Mechanisms of Physiological and Morphological Adaptations of Limestone Langurs to Karst Habitats

Author:

Liu Zhijin12,Zhang Liye13,Yan Zhongze12,Ren Zhijie4,Han Fengming5,Tan Xinxin13,Xiang Zhiyuan13,Dong Fang12,Yang Zuomin16,Liu Guangjian1,Wang Ziming13,Zhang Jiali1,Que Tengcheng7,Tang Chaohui8,Li Yifeng8,Wang Song9,Wu Junyi9,Li Legong4,Huang Chengming1,Roos Christian10,Li Ming111

Affiliation:

1. CAS Key Laboratory of Animal Ecology and Conservation Biology, Institute of Zoology, Beijing 100101, China

2. Institute of Physical Science and Information Technology, Anhui University, Hefei 230601, China

3. University of Chinese Academy of Sciences, Beijing 100049, China

4. College of Life Sciences, Capital Normal University, Beijing 100048, China

5. Biomarker Technologies Corporation, Beijing 101300, China

6. School of Life Sciences, Qufu Normal University, Qufu 273165, Shandong, China

7. Guangxi Zhuang Autonomous Region Terrestrial Wildlife Medical-Aid Monitoring Epidemic Diseases Research Center, Nanning 530001, Guangxi Province, China

8. Wuzhou Langur Breeding and Research Center, Wuzhou 543002, Guangxi Province, China

9. Nanning Zoo, Nanning 530000, Guangxi Province, China

10. Gene Bank of Primates and Primate Genetics Laboratory, German Primate Center, Leibniz Institute for Primate Research, Göttingen 37077, Germany

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

Abstract

AbstractKnowledge of the physiological and morphological evolution and adaptation of nonhuman primates is critical to understand hominin origins, physiological ecology, morphological evolution, and applications in biomedicine. Particularly, limestone langurs represent a direct example of adaptations to the challenges of exploiting a high calcium and harsh environment. Here, we report a de novo genome assembly (Tfra_2.0) of a male François’s langur (Trachypithecus francoisi) with contig N50 of 16.3 Mb and resequencing data of 23 individuals representing five limestone and four forest langur species. Comparative genomics reveals evidence for functional evolution in genes and gene families related to calcium signaling in the limestone langur genome, probably as an adaptation to naturally occurring high calcium levels present in water and plant resources in karst habitats. The genomic and functional analyses suggest that a single point mutation (Lys1905Arg) in the α1c subunit of the L-type voltage-gated calcium channel Cav1.2 (CACNA1C) attenuates the inward calcium current into the cells in vitro. Population genomic analyses and RNA-sequencing indicate that EDNRB is less expressed in white tail hair follicles of the white-headed langur (T. leucocephalus) compared with the black-colored François’s langur and hence might be responsible for species-specific differences in body coloration. Our findings contribute to a new understanding of gene–environment interactions and physiomorphological adaptative mechanisms in ecologically specialized primate taxa.

Funder

Strategic Priority Research Program of the Chinese Academy of Sciences

National Natural Science Foundation of China

National Key R&D Program of China

Publisher

Oxford University Press (OUP)

Subject

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

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