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      Genomic Convergence in the Adaptation to Extreme Environments

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          Abstract

          Convergent evolution is especially common in plants that have independently adapted to the same extreme environments (i.e., extremophile plants). The recent burst of omics data has alleviated many limitations that have hampered molecular convergence studies of non-model extremophile plants. In this review, we summarize cases of genomic convergence in these taxa to examine the extent and type of genomic convergence during the process of adaptation to extreme environments. Despite being well studied by candidate gene approaches, convergent evolution at individual sites is rare and often has a high false-positive rate when assessed in whole genomes. By contrast, genomic convergence at higher genetic levels has been detected during adaptation to the same extreme environments. Examples include the convergence of biological pathways and changes in gene expression, gene copy number, amino acid usage, and GC content. Higher convergence levels play important roles in the adaptive evolution of extremophiles and may be more frequent and involve more genes. In several cases, multiple types of convergence events have been found to co-occur. However, empirical and theoretical studies of this higher level convergent evolution are still limited. In conclusion, both the development of powerful approaches and the detection of convergence at various genetic levels are needed to further reveal the genetic mechanisms of plant adaptation to extreme environments.

          Abstract

          Genomic convergence promises to be a new frontier for comparative genomic studies. This review summarizes advances in the study of plant genome convergence during adaptation to extreme environments, further explores the various levels of genomic convergence and suggests future directions for such studies.

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          Most cited references100

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          Evolution by gene duplication: an update

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            The evolutionary significance of polyploidy

            Polyploidy occurs frequently but is usually detrimental to survival; thus, few polyploids survive in the long term. Here, evidence linking the short-term evolutionary success of polyploids to environmental upheaval is reviewed and possible longer-term evolutionary benefits of polyploidy are discussed.
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              Bias in plant gene content following different sorts of duplication: tandem, whole-genome, segmental, or by transposition.

              Each mode of gene duplication (tandem, tetraploid, segmental, transpositional) retains genes in a biased manner. A reciprocal relationship exists between plant genes retained postpaleotetraploidy versus genes retained after an ancient tandem duplication. Among the models (C, neofunctionalization, balanced gene drive) and ideas that might explain this relationship, only balanced gene drive predicts reciprocity. The gene balance hypothesis explains that more "connected" genes--by protein-protein interactions in a heteromer, for example--are less likely to be retained as a tandem or transposed duplicate and are more likely to be retained postpaleotetraploidy; otherwise, selectively negative dosage effects are created. Biased duplicate retention is an instant and neutral by-product, a spandrel, of purifying selection. Balanced gene drive expanded plant gene families, including those encoding proteasomal proteins, protein kinases, motors, and transcription factors, with each paleotetraploidy, which could explain trends involving complexity. Balanced gene drive is a saltation mechanism in the mutationist tradition.
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                Author and article information

                Contributors
                Journal
                Plant Commun
                Plant Commun
                Plant Communications
                Elsevier
                2590-3462
                29 October 2020
                09 November 2020
                29 October 2020
                : 1
                : 6
                : 100117
                Affiliations
                [1]State Key Laboratory of Biocontrol, Guangdong Provincial Key Laboratory of Plant Resources, Key Laboratory of Biodiversity Dynamics and Conservation of Guangdong Higher Education Institutes, School of Life Sciences, Sun Yat-sen University, Guangzhou, Guangdong, China
                Author notes
                []Corresponding author heziwen@ 123456mail.sysu.edu.cn
                [∗∗ ]Corresponding author lssssh@ 123456mail.sysu.edu.cn
                Article
                S2590-3462(20)30148-6 100117
                10.1016/j.xplc.2020.100117
                7747959
                33367270
                22d23545-baf6-432d-9e30-02bc49c4cc17
                © 2020 The Author(s)

                This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).

                History
                : 23 August 2020
                : 12 October 2020
                : 28 October 2020
                Categories
                Review Article

                convergent evolution,plant genomes,adaptive evolution,extreme environments

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