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      Molecular footprints of selection effects and whole genome duplication (WGD) events in three blueberry species: detected by transcriptome dataset

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          Abstract

          Background

          Both selection effects and whole genome duplication played very important roles in plant speciation and evolution, and to decipher the corresponding molecular footprint has always been a central task of geneticists. Vaccinium is species rich genus that comprised of about 450 species, and blueberry is one of the most important species of Vaccinium genus, which is gaining popularity because of high healthful value. In this article, we aimed to decipher the molecular footprints of natural selection on the single copy genes and WGD events occur in the evolutionary history of blueberry species.

          Results

          We identified 30,143, 29,922 and 28,891 putative protein coding sequences from 45,535, 42,914 and 43,630 unigenes assembled from the leaves’ transcriptome assembly of 19 rabbiteye (T1), 13 southern highbush (T2) and 22 northern highbush (T3) blueberry cultivars. A total of 17, 21 and 27 single copy orthologs were found to undergone positive selection in T1 versus T2, T1 versus T3, and T2 versus T3, respectively, and these orthologs were enriched in metabolic pathways including “Terpenoid backbone biosynthesis”, “Valine, leucine and isoleucine biosynthesis”, “Butanoate metabolism”, “C5-Branched dibasic acid metabolism” “Pantothenate and CoA biosynthesis”. We also detected significant molecular footprints of a recent (about 9.04 MYA), medium (about 43.44 MYA) and an ancient (about 116.39 MYA) WGD events that occurred in the evolutionary history of three blueberry species.

          Conclusion

          Some important functional genes revealed positive selection effect in blueberry. At least three rounds of WGD events were detected in the evolutionary history of blueberry species. Our work provides insights about the genetic mechanism of adaptive evolution in blueberry and species radiation of Vaccinium in short geological scale time.

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          Most cited references74

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          Evolution by gene duplication: an update

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            The Ka/Ks ratio: diagnosing the form of sequence evolution

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              Natural selection on protein-coding genes in the human genome.

              Comparisons of DNA polymorphism within species to divergence between species enables the discovery of molecular adaptation in evolutionarily constrained genes as well as the differentiation of weak from strong purifying selection. The extent to which weak negative and positive darwinian selection have driven the molecular evolution of different species varies greatly, with some species, such as Drosophila melanogaster, showing strong evidence of pervasive positive selection, and others, such as the selfing weed Arabidopsis thaliana, showing an excess of deleterious variation within local populations. Here we contrast patterns of coding sequence polymorphism identified by direct sequencing of 39 humans for over 11,000 genes to divergence between humans and chimpanzees, and find strong evidence that natural selection has shaped the recent molecular evolution of our species. Our analysis discovered 304 (9.0%) out of 3,377 potentially informative loci showing evidence of rapid amino acid evolution. Furthermore, 813 (13.5%) out of 6,033 potentially informative loci show a paucity of amino acid differences between humans and chimpanzees, indicating weak negative selection and/or balancing selection operating on mutations at these loci. We find that the distribution of negatively and positively selected genes varies greatly among biological processes and molecular functions, and that some classes, such as transcription factors, show an excess of rapidly evolving genes, whereas others, such as cytoskeletal proteins, show an excess of genes with extensive amino acid polymorphism within humans and yet little amino acid divergence between humans and chimpanzees.
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                Author and article information

                Contributors
                wys3269@126.com
                1134477929@qq.com
                qasim@scau.edu.cn
                balochfaheem13@gmail.com
                Journal
                BMC Plant Biol
                BMC Plant Biol
                BMC Plant Biology
                BioMed Central (London )
                1471-2229
                3 June 2020
                3 June 2020
                2020
                : 20
                : 250
                Affiliations
                [1 ]GRID grid.440813.a, ISNI 0000 0004 1757 633X, College of Health and Life Science, , Kaili University, ; Kaili City, 556011 Guizhou Province China
                [2 ]Biological institute of Guizhou Province, Guiyang City, 556000 Guizhou Province China
                [3 ]GRID grid.20561.30, ISNI 0000 0000 9546 5767, State Key Laboratory for Conservation and Utilization of Subtropical Agro-Bioresources, , South China Agricultural University, ; Guangzhou, 510642 China
                [4 ]GRID grid.20561.30, ISNI 0000 0000 9546 5767, Guangdong Provincial Key Laboratory of Plant Molecular Breeding, , South China Agricultural University, ; Guangzhou, 510642 China
                [5 ]GRID grid.20561.30, ISNI 0000 0000 9546 5767, College of Agriculture, , South China Agricultural University, ; Guangzhou, 510642 Guangdong Province China
                [6 ]GRID grid.411082.e, ISNI 0000 0001 0720 3140, Department of Field Crops, Faculty of Agricultural and Natural Sciences, , Abant İzzet Baysal University, ; Bolu, Turkey
                Author information
                https://orcid.org/0000-0002-0595-5661
                https://orcid.org/0000-0002-6767-4355
                Article
                2461
                10.1186/s12870-020-02461-w
                7268529
                32493212
                7a76829a-077f-42b5-83f3-46c5c58887e9
                © The Author(s) 2020

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

                History
                : 28 December 2019
                : 24 May 2020
                Funding
                Funded by: Education Department of Guizhou Province
                Award ID: KY(2013)186
                Award Recipient :
                Funded by: Science Department of Guizhou Province
                Award ID: [(2015)6013]
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001809, National Natural Science Foundation of China;
                Award ID: 31560091
                Award Recipient :
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2020

                Plant science & Botany
                adaptive evolution,phylogenetic analysis,polyploid,unigene,vaccinium
                Plant science & Botany
                adaptive evolution, phylogenetic analysis, polyploid, unigene, vaccinium

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