Genomic convergence underlying high‐altitude adaptation in alpine plants

Author:

Zhang Xu12,Kuang Tianhui3,Dong Wenlin124,Qian Zhihao124,Zhang Huajie12,Landis Jacob B.56,Feng Tao12,Li Lijuan124,Sun Yanxia12,Huang Jinling378,Deng Tao3,Wang Hengchang12,Sun Hang3

Affiliation:

1. CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, The Chinese Academy of Sciences Wuhan Botanical Garden Wuhan 430074 China

2. Center of Conservation Biology, Core Botanical Gardens The Chinese Academy of Sciences Wuhan 430074 China

3. Yunnan International Joint Laboratory for Biodiversity of Central Asia, Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany The Chinese Academy of Sciences Kunming 650201 China

4. University of Chinese Academy of Sciences Beijing 100049 China

5. School of Integrative Plant Science, Section of Plant Biology and the L. H. Bailey Hortorium Cornell University Ithaca New York 14850 USA

6. BTI Computational Biology Center Boyce Thompson Institute Ithaca New York 14853 USA

7. State Key Laboratory of Crop Stress Adaptation and Improvement, School of Life Sciences Henan University Kaifeng 475004 China

8. Department of Biology East Carolina University Greenville North Carolina 27858 USA

Abstract

ABSTRACTEvolutionary convergence is one of the most striking examples of adaptation driven by natural selection. However, genomic evidence for convergent adaptation to extreme environments remains scarce. Here, we assembled reference genomes of two alpine plants,Saussurea obvallata(Asteraceae) andRheum alexandrae(Polygonaceae), with 37,938 and 61,463 annotated protein‐coding genes. By integrating an additional five alpine genomes, we elucidated genomic convergence underlying high‐altitude adaptation in alpine plants. Our results detected convergent contractions of disease‐resistance genes in alpine genomes, which might be an energy‐saving strategy for surviving in hostile environments with only a few pathogens present. We identified signatures of positive selection on a set of genes involved in reproduction and respiration (e.g.,MMD1, NBS1, andHPR), and revealed signatures of molecular convergence on genes involved in self‐incompatibility, cell wall modification, DNA repair and stress resistance, which may underlie adaptation to extreme cold, high ultraviolet radiation and hypoxia environments. Incorporating transcriptomic data, we further demonstrated that genes associated with cuticular wax and flavonoid biosynthetic pathways exhibit higher expression levels in leafy bracts, shedding light on the genetic mechanisms of the adaptive “greenhouse” morphology. Our integrative data provide novel insights into convergent evolution at a high‐taxonomic level, aiding in a deep understanding of genetic adaptation to complex environments.

Publisher

Wiley

Subject

Plant Science,General Biochemistry, Genetics and Molecular Biology,Biochemistry

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