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      Distinct Expression and Methylation Patterns for Genes with Different Fates following a Single Whole-Genome Duplication in Flowering Plants

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          Abstract

          For most sequenced flowering plants, multiple whole-genome duplications (WGDs) are found. Duplicated genes following WGD often have different fates that can quickly disappear again, be retained for long(er) periods, or subsequently undergo small-scale duplications. However, how different expression, epigenetic regulation, and functional constraints are associated with these different gene fates following a WGD still requires further investigation due to successive WGDs in angiosperms complicating the gene trajectories. In this study, we investigate lotus ( Nelumbo nucifera), an angiosperm with a single WGD during the K–pg boundary. Based on improved intraspecific-synteny identification by a chromosome-level assembly, transcriptome, and bisulfite sequencing, we explore not only the fundamental distinctions in genomic features, expression, and methylation patterns of genes with different fates after a WGD but also the factors that shape post-WGD expression divergence and expression bias between duplicates. We found that after a WGD genes that returned to single copies show the highest levels and breadth of expression, gene body methylation, and intron numbers, whereas the long-retained duplicates exhibit the highest degrees of protein–protein interactions and protein lengths and the lowest methylation in gene flanking regions. For those long-retained duplicate pairs, the degree of expression divergence correlates with their sequence divergence, degree in protein–protein interactions, and expression level, whereas their biases in expression level reflecting subgenome dominance are associated with the bias of subgenome fractionation. Overall, our study on the paleopolyploid nature of lotus highlights the impact of different functional constraints on gene fate and duplicate divergence following a single WGD in plant.

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          The grapevine genome sequence suggests ancestral hexaploidization in major angiosperm phyla.

          The analysis of the first plant genomes provided unexpected evidence for genome duplication events in species that had previously been considered as true diploids on the basis of their genetics. These polyploidization events may have had important consequences in plant evolution, in particular for species radiation and adaptation and for the modulation of functional capacities. Here we report a high-quality draft of the genome sequence of grapevine (Vitis vinifera) obtained from a highly homozygous genotype. The draft sequence of the grapevine genome is the fourth one produced so far for flowering plants, the second for a woody species and the first for a fruit crop (cultivated for both fruit and beverage). Grapevine was selected because of its important place in the cultural heritage of humanity beginning during the Neolithic period. Several large expansions of gene families with roles in aromatic features are observed. The grapevine genome has not undergone recent genome duplication, thus enabling the discovery of ancestral traits and features of the genetic organization of flowering plants. This analysis reveals the contribution of three ancestral genomes to the grapevine haploid content. This ancestral arrangement is common to many dicotyledonous plants but is absent from the genome of rice, which is a monocotyledon. Furthermore, we explain the chronology of previously described whole-genome duplication events in the evolution of flowering plants.
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            Evolution by gene duplication: an update

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              LTRharvest, an efficient and flexible software for de novo detection of LTR retrotransposons

              Background Transposable elements are abundant in eukaryotic genomes and it is believed that they have a significant impact on the evolution of gene and chromosome structure. While there are several completed eukaryotic genome projects, there are only few high quality genome wide annotations of transposable elements. Therefore, there is a considerable demand for computational identification of transposable elements. LTR retrotransposons, an important subclass of transposable elements, are well suited for computational identification, as they contain long terminal repeats (LTRs). Results We have developed a software tool LTRharvest for the de novo detection of full length LTR retrotransposons in large sequence sets. LTRharvest efficiently delivers high quality annotations based on known LTR transposon features like length, distance, and sequence motifs. A quality validation of LTRharvest against a gold standard annotation for Saccharomyces cerevisae and Drosophila melanogaster shows a sensitivity of up to 90% and 97% and specificity of 100% and 72%, respectively. This is comparable or slightly better than annotations for previous software tools. The main advantage of LTRharvest over previous tools is (a) its ability to efficiently handle large datasets from finished or unfinished genome projects, (b) its flexibility in incorporating known sequence features into the prediction, and (c) its availability as an open source software. Conclusion LTRharvest is an efficient software tool delivering high quality annotation of LTR retrotransposons. It can, for example, process the largest human chromosome in approx. 8 minutes on a Linux PC with 4 GB of memory. Its flexibility and small space and run-time requirements makes LTRharvest a very competitive candidate for future LTR retrotransposon annotation projects. Moreover, the structured design and implementation and the availability as open source provides an excellent base for incorporating novel concepts to further improve prediction of LTR retrotransposons.
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                Author and article information

                Contributors
                Role: Associate Editor
                Journal
                Mol Biol Evol
                Mol. Biol. Evol
                molbev
                Molecular Biology and Evolution
                Oxford University Press
                0737-4038
                1537-1719
                August 2020
                28 April 2020
                28 April 2020
                : 37
                : 8
                : 2394-2413
                Affiliations
                [m1 ] CAS Key Laboratory of Aquatic Botany and Watershed Ecology, Wuhan Botanical Garden, Chinese Academy of Sciences , Wuhan, China
                [m2 ] Center of Conservation Biology, Core Botanical Gardens, Chinese Academy of Sciences , Wuhan, China
                [m3 ] Department of Plant Biotechnology and Bioinformatics, Ghent University , Ghent, Belgium
                [m4 ] Appalachian Laboratory, University of Maryland Center for Environmental Science , Frostburg, MD
                [m5 ] School of Marine Sciences, Sun Yat-sen University , Guangzhou, China
                [m6 ] University of Chinese Academy of Sciences , Beijing, China
                [m7 ] Sino-African Joint Research Center, Chinese Academy of Sciences , Wuhan, China
                [m8 ] Centre for Plant Systems Biology , VIB, Ghent, Belgium
                [m9 ] Department of Biochemistry, Genetics and Microbiology, University of Pretoria , Pretoria, South Africa
                [m10 ] College of Horticulture, Nanjing Agricultural University , Nanjing, China
                [m11 ] Department of Information Technology, IDLab, IMEC, Ghent University , Ghent, Belgium
                Author notes
                Author information
                http://orcid.org/0000-0002-2169-4588
                http://orcid.org/0000-0002-3425-5939
                Article
                msaa105
                10.1093/molbev/msaa105
                7403625
                32343808
                21102719-6ac2-491a-ae80-273d7909ff88
                © The Author(s) 2020. Published by Oxford University Press on behalf of the Society for Molecular Biology and Evolution.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License ( http://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com

                History
                Page count
                Pages: 20
                Funding
                Funded by: Strategic Priority Research Program of Chinese Academy of Sciences;
                Award ID: XDB31000000
                Funded by: National Natural Science Foundation of China, DOI 10.13039/501100001809;
                Award ID: 31570220
                Award ID: 31870208
                Award ID: 31700197
                Funded by: Youth Innovation Promotion Association of Chinese Academy of Sciences, DOI 10.13039/501100004739;
                Award ID: 2019335
                Funded by: Hubei Provincial Natural Science Foundation of China;
                Award ID: 2019CFB275
                Funded by: Hubei Chenguang Talented Youth Development Foundation;
                Funded by: European Research Council, DOI 10.13039/100010663;
                Funded by: ERC, DOI 10.13039/100010663;
                Funded by: European Union’s Horizon 2020;
                Award ID: 833522
                Funded by: Ministry of Science, Research and Technology;
                Categories
                Discoveries
                AcademicSubjects/SCI01130
                AcademicSubjects/SCI01180

                Molecular biology
                whole-genome duplication,gene expression,methylation,gene balance,subgenome dominance

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