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      Molecular phylogenomics of the tribe Shoreeae (Dipterocarpaceae) using whole plastid genomes

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          Abstract

          Background and Aims

          Phylogenetic relationships within tribe Shoreeae, containing the main elements of tropical forests in Southeast Asia, present a long-standing problem in the systematics of Dipterocarpaceae. Sequencing whole plastomes using next-generation sequencing- (NGS) based genome skimming is increasingly employed for investigating phylogenetic relationships of plants. Here, the usefulness of complete plastid genome sequences in resolving phylogenetic relationships within Shoreeae is evaluated.

          Methods

          A pipeline to obtain alignments of whole plastid genome sequences across individuals with different amounts of available data is presented. In total, 48 individuals, representing 37 species and four genera of the ecologically and economically important tribe Shoreeae sensu Ashton, were investigated. Phylogenetic trees were reconstructed using maximum parsimony, maximum likelihood and Bayesian inference.

          Key Results

          Here, the first fully sequenced plastid genomes for the tribe Shoreeae are presented. Their size, GC content and gene order are comparable with those of other members of Malvales. Phylogenomic analyses demonstrate that whole plastid genomes are useful for inferring phylogenetic relationships among genera and groups of Shorea (Shoreeae) but fail to provide well-supported phylogenetic relationships among some of the most closely related species. Discordance in placement of Parashorea was observed between phylogenetic trees obtained from plastome analyses and those obtained from nuclear single nucleotide polymorphism (SNP) data sets identified in restriction-site associated sequencing (RADseq).

          Conclusions

          Phylogenomic analyses of the entire plastid genomes are useful for inferring phylogenetic relationships at lower taxonomic levels, but are not sufficient for detailed phylogenetic reconstructions of closely related species groups in Shoreeae. Discordance in placement of Parashorea was further investigated for evidence of ancient hybridization.

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          Most cited references50

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          MRBAYES: Bayesian inference of phylogenetic trees.

          The program MRBAYES performs Bayesian inference of phylogeny using a variant of Markov chain Monte Carlo. MRBAYES, including the source code, documentation, sample data files, and an executable, is available at http://brahms.biology.rochester.edu/software.html.
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            ARAGORN, a program to detect tRNA genes and tmRNA genes in nucleotide sequences.

            A computer program, ARAGORN, identifies tRNA and tmRNA genes. The program employs heuristic algorithms to predict tRNA secondary structure, based on homology with recognized tRNA consensus sequences and ability to form a base-paired cloverleaf. tmRNA genes are identified using a modified version of the BRUCE program. ARAGORN achieves a detection sensitivity of 99% from a set of 1290 eubacterial, eukaryotic and archaeal tRNA genes and detects all complete tmRNA sequences in the tmRNA database, improving on the performance of the BRUCE program. Recently discovered tmRNA genes in the chloroplasts of two species from the 'green' algae lineage are detected. The output of the program reports the proposed tRNA secondary structure and, for tmRNA genes, the secondary structure of the tRNA domain, the tmRNA gene sequence, the tag peptide and a list of organisms with matching tmRNA peptide tags.
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                Author and article information

                Journal
                Ann Bot
                Ann. Bot
                annbot
                Annals of Botany
                Oxford University Press (UK )
                0305-7364
                1095-8290
                May 2019
                12 December 2018
                12 December 2018
                : 123
                : 5
                : 857-865
                Affiliations
                [1 ]University of Vienna, Department of Botany and Biodiversity Research, Rennweg, Vienna, Austria
                [2 ]Senckenberg Research Institute and Natural History Museum Frankfurt, Senckenberganlage, Frankfurt am Main, Germany
                [3 ]Jodrell Laboratory, Royal Botanic Gardens, Kew, Richmond, UK
                [4 ]Department of Environment and Agriculture, Curtin University, Bently, WA, Australia
                [5 ]Harvard University, Department of Organismic and Evolutionary Biology, Cambridge, MA, USA
                [6 ]University of Brunei Darussalam, Environmental and Life Sciences, Faculty of Science, Gadong, Brunei Darussalam
                Author notes
                Article
                mcy220
                10.1093/aob/mcy220
                6526321
                30541053
                02d94b6c-10fc-4326-a30e-0c87e49f5eb4
                © The Author(s) 2018. Published by Oxford University Press on behalf of the Annals of Botany Company.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 25 August 2018
                : 11 October 2018
                : 12 November 2018
                Page count
                Pages: 9
                Funding
                Funded by: Austrian Science Fund 10.13039/501100002428
                Award ID: P26548-B22
                Categories
                Original Articles

                Plant science & Botany
                plastid genomes,dipterocarpaceae,genome skimming,hopea,next-generation sequencing,parashorea,phylogenomics,shorea,shoreeae

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