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      Plastome structure, evolution, and phylogeny of Selaginella.

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          Abstract

          As one of the earliest land plant lineages, Selaginella is important for studying land plant evolution. It is the largest genus of lycophytes containing 700-800 species. Some unique characters of Selaginella plastomes have been reported, but based only on 20 species. There have been no plastome phylogenies of Selaginella based on a relatively large sampling, and no efforts have been made to resolve the phylogeny of the enigmatic Sinensis group whose relationships have been unclear based on small datasets. Here we investigated the structures of 59 plastomes representing 51 species covering all six subgenera and 18 sections of Selaginella except two sections and including the intriguing Sinensis group for the first time. Our major results include: (1) the plastome size of Selaginella ranges tremendously from 78,492 bp to 187,632 bp; (2) there are numerous gene losses in Selaginella comparing with other lycophytes, Isoëtaceae and Lycopodiaceae; (3) the gene contents and plastome structures in Selaginella vary lineage-specifically and all infrageneric taxa are well supported in the plastome phylogeny; (4) the ndh gene family tends to lose or pseudogenize in those species with DR structure and without other short or medium repeats; (5) the short and medium repeat regions in SC mediate many conformations causing diverse and complex plastome structures, and six new conformations are discovered; (6) forty-eight species sampled have high GC content (>50%) but three species in the Sinensis group have ∼ 30% GC content in plastomes, similar to most vascular plants; (7) the Sinensis group is monophyletic, includes at least two subgroups, and has the smallest plastomes in land plants except some parasitic plants, and their plastomes do not contain any tRNAs; (8) the younger lineages in Selaginella tend to have higher GC content, whereas the older lineages tend to have lower GC content; and (9) because of incomplete genomic data and abnormal structures or some unknown reasons, even the concatenated plastomes could not well resolve the phylogenetic relationships in Selaginella with confidence, highlighting the difficulty in resolving the phylogeny and evolution of this particularly important land plant lineage.

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          Author and article information

          Journal
          Mol Phylogenet Evol
          Molecular phylogenetics and evolution
          Elsevier BV
          1095-9513
          1055-7903
          April 2022
          : 169
          Affiliations
          [1 ] School of Ecology and Environmental Science, Yunnan University, Kunming, Yunnan 650091, China.
          [2 ] School of Life Sciences, Yunnan University, East Outer Ring Road, Chenggong District, Kunming, Yunnan 650500, China.
          [3 ] Meise Botanic Garden, Nieuwelaan 38, 1860 Meise, Belgium; Fédération Wallonie-Bruxelles, Service Général de l'Enseignement supérieur et de la Recherche scientifique, 1 rue A. Lavallée, 1080 Brussels, Belgium.
          [4 ] Key Laboratory for Plant Diversity and Biogeography of East Asia, Kunming Institute of Botany, Chinese Academy of Sciences, Kunming, Yunnan 650201, China.
          [5 ] School of Life Sciences, Yunnan University, East Outer Ring Road, Chenggong District, Kunming, Yunnan 650500, China. Electronic address: zhrhe@ynu.edu.cn.
          [6 ] Missouri Botanical Garden, 4344 Shaw Blvd, St. Louis, MO 63110, USA; Chengdu Institute of Biology, Chinese Academy of Sciences, P.O. Box 416, Chengdu, Sichuan 610041, China. Electronic address: Libing.Zhang@mobot.org.
          Article
          S1055-7903(22)00023-9
          10.1016/j.ympev.2022.107410
          35031459
          4ccb5033-0188-42d8-95e2-417d7a44fb0b
          History

          Selaginella sinensis and allies,Conformation,Evolution of GC content,Gene loss,Lycophyte plastomes,Plastome organization

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