Coping with alpine habitats: genomic insights into the adaptation strategies of Triplostegia glandulifera (Caprifoliaceae)

Author:

Zhang Jian12,Dong Kai-Lin123,Ren Miao-Zhen4,Wang Zhi-Wen5,Li Jian-Hua6,Sun Wen-Jing123,Zhao Xiang5,Fu Xin-Xing7,Ye Jian-Fei8,Liu Bing129,Zhang Da-Ming12,Wang Mo-Zhu12,Zeng Gang10,Niu Yan-Ting12,Lu Li-Min12,Su Jun-Xia11,Liu Zhong-Jian12ORCID,Soltis Pamela S13,Soltis Douglas E1314,Chen Zhi-Duan129

Affiliation:

1. Chinese Academy of Sciences State Key Laboratory of Plant Diversity and Specialty Crops & Key Laboratory of Systematic and Evolutionary Botany, Institute of Botany, , Beijing 100093, China

2. China National Botanical Garden , Beijing 100093, China

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

4. Northwest University, Xi'an 710069 Key Laboratory of Resource Biology and Biotechnology in Western China, Ministry of Education, College of Life Sciences, , China

5. PubBio-Tech Services Corporation , Wuhan 430070, China

6. Hope College Biology Department, , Holland, MI 49423, USA

7. Northwest Normal University College of Life Sciences, , Lanzhou 730070, China

8. Shenzhen Campus of Sun Yat-sen University School of Ecology, , Shenzhen 518107, China

9. Chinese Academy of Sciences Sino-Africa Joint Research Center, , Wuhan 430074, China

10. Chinese Academy of Sciences, Menglun 666303 Xishuangbanna Tropical Botanical Garden, , China

11. Shanxi Normal University School of Life Science, , Taiyuan 030031, China

12. Fujian Agriculture and Forestry University Key Laboratory of National Forestry and Grassland Administration for Orchid Conservation and Utilization, , Fuzhou 350002, China

13. University of Florida Florida Museum of Natural History, , Gainesville, FL 32611, USA

14. University of Florida Department of Biology, , Gainesville, FL 32611-7800, USA

Abstract

Abstract How plants find a way to thrive in alpine habitats remains largely unknown. Here we present a chromosome-level genome assembly for an alpine medicinal herb, Triplostegia glandulifera (Caprifoliaceae), and 13 transcriptomes from other species of Dipsacales. We detected a whole-genome duplication event in T. glandulifera that occurred prior to the diversification of Dipsacales. Preferential gene retention after whole-genome duplication was found to contribute to increasing cold-related genes in T. glandulifera. A series of genes putatively associated with alpine adaptation (e.g. CBFs, ERF-VIIs, and RAD51C) exhibited higher expression levels in T. glandulifera than in its low-elevation relative, Lonicera japonica. Comparative genomic analysis among five pairs of high- vs low-elevation species, including a comparison of T. glandulifera and L. japonica, indicated that the gene families related to disease resistance experienced a significantly convergent contraction in alpine plants compared with their lowland relatives. The reduction in gene repertory size was largely concentrated in clades of genes for pathogen recognition (e.g. CNLs, prRLPs, and XII RLKs), while the clades for signal transduction and development remained nearly unchanged. This finding reflects an energy-saving strategy for survival in hostile alpine areas, where there is a tradeoff with less challenge from pathogens and limited resources for growth. We also identified candidate genes for alpine adaptation (e.g. RAD1, DMC1, and MSH3) that were under convergent positive selection or that exhibited a convergent acceleration in evolutionary rate in the investigated alpine plants. Overall, our study provides novel insights into the high-elevation adaptation strategies of this and other alpine plants.

Publisher

Oxford University Press (OUP)

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