Plastid NDH Pseudogenization and Gene Loss in a Recently Derived Lineage from the Largest Hemiparasitic Plant Genus Pedicularis (Orobanchaceae)

Author:

Li Xin123,Yang Jun-Bo4,Wang Hong5,Song Yu126,Corlett Richard T12,Yao Xin12,Li De-Zhu4ORCID,Yu Wen-Bin126ORCID

Affiliation:

1. Center for Integrative Conservation, Xishuangbanna Tropical Botanical Garden, Chinese Academy of Sciences, Mengla, Yunnan 666303, China

2. Center of Conservation Biology, Core Botanical Gardens, Chinese Academy of Sciences, Mengla, Yunnan 666303, China

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

4. Plant Germplasm and Genomics Center, Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan 650201, China

5. Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan 650201, China

6. Southeast Asia Biodiversity Research Institute, Chinese Academy of Sciences, Yezin, Nay Pyi Taw 05282, Myanmar

Abstract

Abstract The plastid genome (plastome) is highly conserved in both gene order and content and has a lower mutation rate than the nuclear genome. However, the plastome is more variable in heterotrophic plants. To date, most such studies have investigated just a few species or only holoheterotrophic groups, and few have examined plastome evolution in recently derived lineages at an early stage of transition from autotrophy to heterotrophy. In this study, we investigated the evolutionary dynamics of plastomes in the monophyletic and recently derived Pedicularis sect. Cyathophora (Orobanchaceae). We obtained 22 new plastomes, 13 from the six recognized species of section Cyathophora, six from hemiparasitic relatives and three from autotrophic relatives. Comparative analyses of gene content, plastome structure and selection pressure showed dramatic differences among species in section Cyathophora and in Pedicularis as a whole. In comparison with autotrophic relatives and other Pedicularis spp., we found that the inverted repeat (IR) region in section Cyathophora had expansions to the small single-copy region, with a large expansion event and two independent contraction events. Moreover, NA(D)H dehydrogenase, accD and ccsA have lost function multiple times, with the function of accD being replaced by nuclear copies of an accD-like gene in Pedicularis spp. The ccsA and ndhG genes may have evolved under selection in association with IR expansion/contraction events. This study is the first to report high plastome variation in a recently derived lineage of hemiparasitic plants and therefore provides evidence for plastome evolution in the transition from autotrophy to heterotrophy.

Funder

National Natural Science Foundation China

Strategic Priority Research Program of the Chinese Academy of Sciences

Large-scale Scientific Facilities of the Chinese Academy of Sciences

Chinese Academy of Sciences 135 Program

Germplasm Bank of Wild Species, Kunming Institute of Botany, Chinese Academy of Sciences

Yunnan for Top-notch Young Talents

Publisher

Oxford University Press (OUP)

Subject

Cell Biology,Plant Science,Physiology,General Medicine

Reference70 articles.

1. Caught in action: fine-scale plastome evolution in the parasitic plants of Cuscuta section Ceratophorae (Convolvulaceae);Banerjee;Plant Mol. Biol.,2019

2. Study of Epichloe endophyte-grass symbionts on photosynthetic characteristics of hemiparasitic plant;Bao;Chinese Qighai J. Anim. Veter. Sci.,2020

3. Investigating the path of plastid genome degradation in an early-transitional clade of heterotrophic orchids, and implications for heterotrophic angiosperms;Barrett;Mol. Biol. Evol.,2014

4. Unprecedented parallel photosynthetic losses in a heterotrophic orchid genus;Barrett;Mol. Biol. Evol.,2019

5. Constructing confidence sets using rank statistics;Bauer;J. Am. Stat. Assoc.,1972

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