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The draft genome of the endangered, relictual plant Kingdonia uniflora (Circaeasteraceae, Ranunculales) reveals potential mechanisms and perils of evolutionary specialization

Yanxia Sun, Tao Deng, Aidi Zhang, Michael J. Moore, Jacob B. Landis, Nan Lin, Huajie Zhang, Xu Zhang, Jinling Huang, Xiujun Zhang, Hang Sun, Hengchang Wang
doi: https://doi.org/10.1101/2020.01.08.898460
Yanxia Sun
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
2Center of Conservation Biology, Core Botanical Gardens, Chinese Academy of Sciences, Wuhan, Hubei, China
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Tao Deng
3Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China
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Aidi Zhang
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
4Center of Economic Botany, Core Botanical Gardens, Chinese Academy of Sciences, Wuhan, Hubei, China
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Michael J. Moore
5Department of Biology, Oberlin College, Oberlin, OH, USA
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Jacob B. Landis
6Department of Botany and Plant Sciences, University of California Riverside, Riverside, CA, USA
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Nan Lin
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
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Huajie Zhang
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
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Xu Zhang
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
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Jinling Huang
7Department of Biology, East Carolina University, Greenville, NC, USA
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Xiujun Zhang
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
4Center of Economic Botany, Core Botanical Gardens, Chinese Academy of Sciences, Wuhan, Hubei, China
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  • For correspondence: hcwang@wbgcas.cn sunhang@mail.kib.ac.cn zhangxj@wbgcas.cn
Hang Sun
3Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan, China
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  • For correspondence: hcwang@wbgcas.cn sunhang@mail.kib.ac.cn zhangxj@wbgcas.cn
Hengchang Wang
1CAS Key Laboratory of Plant Germplasm Enhancement and Specialty Agriculture, Wuhan Botanical Garden, Chinese Academy of Sciences, Wuhan, Hubei, China
2Center of Conservation Biology, Core Botanical Gardens, Chinese Academy of Sciences, Wuhan, Hubei, China
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  • For correspondence: hcwang@wbgcas.cn sunhang@mail.kib.ac.cn zhangxj@wbgcas.cn
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Abstract

Kingdonia uniflora, an alpine herb, has an extremely narrow distribution and represents a model for studying evolutionary mechanisms of species that have adapted to undisturbed environments for evolutionary long periods of time. We assembled a 1,004.7-Mb draft genome (encoding 43,301 genes) and investigated the evolutionary history of K. uniflora, along with mechanisms related to its endangered status. Phylogenomic analyses based on 497 single copy genes confirmed the sister relationship between K. uniflora and Circaeaster agrestis, which were estimated to have diverged around 52 Mya. Proliferation of LTR retrotransposons in K. uniflora is estimated to occur around 2.7 Mya, coinciding with one recent uplift of the Hengduan Mountains between the late Miocene and late Pliocene. Across 12 species of monocots, early-diverging eudicots and core eudicots, K. uniflora showed significant overrepresentation in gene families associated with DNA repair and underrepresentation in gene families associated with stress response. Most of the plastid ndh genes were found to be lost not only in the plastome but also in the nuclear genome of K. uniflora. During the evolutionary process, the overrepresentation of gene families involved in DNA repair could help asexual K. uniflora reduce the accumulation of deleterious mutations, while at the same time, reducing genetic diversity which is important in responding to environment fluctuations. The underrepresentation of gene families related to stress response and functional loss of ndh genes could be due to lack or loss of ability to respond to environmental changes caused by long-term adaptation to a relatively stable ecological environment.

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Posted January 09, 2020.
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The draft genome of the endangered, relictual plant Kingdonia uniflora (Circaeasteraceae, Ranunculales) reveals potential mechanisms and perils of evolutionary specialization
Yanxia Sun, Tao Deng, Aidi Zhang, Michael J. Moore, Jacob B. Landis, Nan Lin, Huajie Zhang, Xu Zhang, Jinling Huang, Xiujun Zhang, Hang Sun, Hengchang Wang
bioRxiv 2020.01.08.898460; doi: https://doi.org/10.1101/2020.01.08.898460
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The draft genome of the endangered, relictual plant Kingdonia uniflora (Circaeasteraceae, Ranunculales) reveals potential mechanisms and perils of evolutionary specialization
Yanxia Sun, Tao Deng, Aidi Zhang, Michael J. Moore, Jacob B. Landis, Nan Lin, Huajie Zhang, Xu Zhang, Jinling Huang, Xiujun Zhang, Hang Sun, Hengchang Wang
bioRxiv 2020.01.08.898460; doi: https://doi.org/10.1101/2020.01.08.898460

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