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      De novo assembly of the zucchini genome reveals a whole‐genome duplication associated with the origin of the Cucurbita genus

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          Summary

          The Cucurbita genus (squashes, pumpkins and gourds) includes important domesticated species such as C. pepo, C. maxima and C. moschata. In this study, we present a high‐quality draft of the zucchini ( C. pepo) genome. The assembly has a size of 263 Mb, a scaffold N50 of 1.8 Mb and 34 240 gene models. It includes 92% of the conserved BUSCO core gene set, and it is estimated to cover 93.0% of the genome. The genome is organized in 20 pseudomolecules that represent 81.4% of the assembly, and it is integrated with a genetic map of 7718 SNPs. Despite the small genome size, three independent lines of evidence support that the C. pepo genome is the result of a whole‐genome duplication: the topology of the gene family phylogenies, the karyotype organization and the distribution of 4 DTv distances. Additionally, 40 transcriptomes of 12 species of the genus were assembled and analysed together with all the other published genomes of the Cucurbitaceae family. The duplication was detected in all the Cucurbita species analysed, including C. maxima and C. moschata, but not in the more distant cucurbits belonging to the Cucumis and Citrullus genera, and it is likely to have occurred 30 ± 4 Mya in the ancestral species that gave rise to the genus.

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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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            The genome of the cucumber, Cucumis sativus L.

            Cucumber is an economically important crop as well as a model system for sex determination studies and plant vascular biology. Here we report the draft genome sequence of Cucumis sativus var. sativus L., assembled using a novel combination of traditional Sanger and next-generation Illumina GA sequencing technologies to obtain 72.2-fold genome coverage. The absence of recent whole-genome duplication, along with the presence of few tandem duplications, explains the small number of genes in the cucumber. Our study establishes that five of the cucumber's seven chromosomes arose from fusions of ten ancestral chromosomes after divergence from Cucumis melo. The sequenced cucumber genome affords insight into traits such as its sex expression, disease resistance, biosynthesis of cucurbitacin and 'fresh green' odor. We also identify 686 gene clusters related to phloem function. The cucumber genome provides a valuable resource for developing elite cultivars and for studying the evolution and function of the plant vascular system.
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              Isolation of plant DNA from fesh tissue

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                Author and article information

                Contributors
                mpicosi@btc.upv.es
                jcanizares@upv.es
                Journal
                Plant Biotechnol J
                Plant Biotechnol. J
                10.1111/(ISSN)1467-7652
                PBI
                Plant Biotechnology Journal
                John Wiley and Sons Inc. (Hoboken )
                1467-7644
                1467-7652
                04 December 2017
                June 2018
                : 16
                : 6 ( doiID: 10.1111/pbi.2018.16.issue-6 )
                : 1161-1171
                Affiliations
                [ 1 ] Institute for the Conservation and Breeding of Agricultural Biodiversity (COMAV‐UPV) Universitat Politècnica de València Valencia Spain
                [ 2 ] Department of Horticulture Virginia Polytechnic Institute and State University Blacksburg VA USA
                [ 3 ] Instituto Agroforestal Mediterráneo (IAM) Universitat Politècnica de València Valencia Spain
                [ 4 ] IFAPA Centro La Mojonera La Mojonera Almería Spain
                [ 5 ] Department of Biology and Geology Research Centers CIAIMBITAL and CeiA3 University of Almeria Almería Spain
                [ 6 ] Boyce Thompson Institute for Plant Research Ithaca NY USA
                Author notes
                [*] [* ] Correspondence (Tel (+34)963888470; fax (+34)963879422; emails jcanizares@ 123456upv.es (J.C.), mpicosi@ 123456btc.upv.es (B.P.))
                [†]

                Both authors contributed equally.

                Author information
                http://orcid.org/0000-0002-0864-8157
                Article
                PBI12860
                10.1111/pbi.12860
                5978595
                29112324
                b2eb41e1-b2d6-4597-960b-e0342111b1c6
                © 2017 The Authors. Plant Biotechnology Journal published by Society for Experimental Biology and The Association of Applied Biologists and John Wiley & Sons Ltd.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 June 2017
                : 17 October 2017
                : 31 October 2017
                Page count
                Figures: 3, Tables: 3, Pages: 11, Words: 10314
                Funding
                Funded by: Spanish Instituto Nacional de Investigación y Tecnología Agraria y Alimentaria (INIA)
                Award ID: RTA2011‐00044‐C02‐2
                Award ID: E‐RTA2013‐00020‐C04‐03
                Funded by: FEDER funds (EU)
                Funded by: Spanish Ministry of Economy and Competitivity
                Award ID: AGL2014‐54598‐C2‐1‐R
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                pbi12860
                June 2018
                Converter:WILEY_ML3GV2_TO_NLMPMC version:version=5.4.0 mode:remove_FC converted:31.05.2018

                Biotechnology
                genome,crop,zucchini,whole‐genome duplication,cucurbitaceae,transcriptome
                Biotechnology
                genome, crop, zucchini, whole‐genome duplication, cucurbitaceae, transcriptome

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