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      Assembling large genomes: analysis of the stick insect ( Clitarchus hookeri) genome reveals a high repeat content and sex-biased genes associated with reproduction

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          Abstract

          Background

          Stick insects (Phasmatodea) have a high incidence of parthenogenesis and other alternative reproductive strategies, yet the genetic basis of reproduction is poorly understood. Phasmatodea includes nearly 3000 species, yet only the genome of Timema cristinae has been published to date. Clitarchus hookeri is a geographical parthenogenetic stick insect distributed across New Zealand. Sexual reproduction dominates in northern habitats but is replaced by parthenogenesis in the south. Here, we present a de novo genome assembly of a female C. hookeri and use it to detect candidate genes associated with gamete production and development in females and males. We also explore the factors underlying large genome size in stick insects.

          Results

          The C. hookeri genome assembly was 4.2 Gb, similar to the flow cytometry estimate, making it the second largest insect genome sequenced and assembled to date. Like the large genome of Locusta migratoria, the genome of C. hookeri is also highly repetitive and the predicted gene models are much longer than those from most other sequenced insect genomes, largely due to longer introns. Miniature inverted repeat transposable elements (MITEs), absent in the much smaller T. cristinae genome, is the most abundant repeat type in the C. hookeri genome assembly. Mapping RNA-Seq reads from female and male gonadal transcriptomes onto the genome assembly resulted in the identification of 39,940 gene loci, 15.8% and 37.6% of which showed female-biased and male-biased expression, respectively. The genes that were over-expressed in females were mostly associated with molecular transportation, developmental process, oocyte growth and reproductive process; whereas, the male-biased genes were enriched in rhythmic process, molecular transducer activity and synapse. Several genes involved in the juvenile hormone synthesis pathway were also identified.

          Conclusions

          The evolution of large insect genomes such as L. migratoria and C. hookeri genomes is most likely due to the accumulation of repetitive regions and intron elongation. MITEs contributed significantly to the growth of C. hookeri genome size yet are surprisingly absent from the T. cristinae genome. Sex-biased genes identified from gonadal tissues, including genes involved in juvenile hormone synthesis, provide interesting candidates for the further study of flexible reproduction in stick insects.

          Electronic supplementary material

          The online version of this article (10.1186/s12864-017-4245-x) contains supplementary material, which is available to authorized users.

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          Most cited references57

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          The Universal Protein Resource (UniProt)

          The Universal Protein Resource (UniProt) provides a stable, comprehensive, freely accessible, central resource on protein sequences and functional annotation. The UniProt Consortium is a collaboration between the European Bioinformatics Institute (EBI), the Protein Information Resource (PIR) and the Swiss Institute of Bioinformatics (SIB). The core activities include manual curation of protein sequences assisted by computational analysis, sequence archiving, development of a user-friendly UniProt website, and the provision of additional value-added information through cross-references to other databases. UniProt is comprised of four major components, each optimized for different uses: the UniProt Knowledgebase, the UniProt Reference Clusters, the UniProt Archive and the UniProt Metagenomic and Environmental Sequences database. UniProt is updated and distributed every three weeks, and can be accessed online for searches or download at http://www.uniprot.org.
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            The monarch butterfly genome yields insights into long-distance migration.

            We present the draft 273 Mb genome of the migratory monarch butterfly (Danaus plexippus) and a set of 16,866 protein-coding genes. Orthology properties suggest that the Lepidoptera are the fastest evolving insect order yet examined. Compared to the silkmoth Bombyx mori, the monarch genome shares prominent similarity in orthology content, microsynteny, and protein family sizes. The monarch genome reveals a vertebrate-like opsin whose existence in insects is widespread; a full repertoire of molecular components for the monarch circadian clockwork; all members of the juvenile hormone biosynthetic pathway whose regulation shows unexpected sexual dimorphism; additional molecular signatures of oriented flight behavior; microRNAs that are differentially expressed between summer and migratory butterflies; monarch-specific expansions of chemoreceptors potentially important for long-distance migration; and a variant of the sodium/potassium pump that underlies a valuable chemical defense mechanism. The monarch genome enhances our ability to better understand the genetic and molecular basis of long-distance migration. Copyright © 2011 Elsevier Inc. All rights reserved.
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              A heterozygous moth genome provides insights into herbivory and detoxification.

              How an insect evolves to become a successful herbivore is of profound biological and practical importance. Herbivores are often adapted to feed on a specific group of evolutionarily and biochemically related host plants, but the genetic and molecular bases for adaptation to plant defense compounds remain poorly understood. We report the first whole-genome sequence of a basal lepidopteran species, Plutella xylostella, which contains 18,071 protein-coding and 1,412 unique genes with an expansion of gene families associated with perception and the detoxification of plant defense compounds. A recent expansion of retrotransposons near detoxification-related genes and a wider system used in the metabolism of plant defense compounds are shown to also be involved in the development of insecticide resistance. This work shows the genetic and molecular bases for the evolutionary success of this worldwide herbivore and offers wider insights into insect adaptation to plant feeding, as well as opening avenues for more sustainable pest management.
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                Author and article information

                Contributors
                chen.wu@plantandfood.co.nz
                vtwort@gmail.com
                ross.crowhurst@plantandfood.co.nz
                richard.newcomb@plantandfood.co.nz
                BuckleyT@landcareresearch.co.nz
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                16 November 2017
                16 November 2017
                2017
                : 18
                : 884
                Affiliations
                [1 ]ISNI 0000 0004 0372 3343, GRID grid.9654.e, School of Biological Sciences, , The University of Auckland, ; Auckland, New Zealand
                [2 ]ISNI 0000 0001 0747 5306, GRID grid.419186.3, Landcare Research, ; Auckland, New Zealand
                [3 ]GRID grid.27859.31, New Zealand Institute for Plant & Food Research Ltd, ; Auckland, New Zealand
                [4 ]ISNI 0000 0001 0930 2361, GRID grid.4514.4, Department of Biology, , Lund University, ; Lund, Sweden
                Author information
                http://orcid.org/0000-0003-1499-9567
                Article
                4245
                10.1186/s12864-017-4245-x
                5691397
                29145825
                b58228e3-7404-4a68-9446-6f27c733652c
                © The Author(s). 2017

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. 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.

                History
                : 21 August 2017
                : 31 October 2017
                Funding
                Funded by: Alan Wilson Centre
                Award ID: RM 13790/24947
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2017

                Genetics
                phasmatodea,genome assembly,rna-seq,reproduction,parthenogenesis,clitarchus hookeri
                Genetics
                phasmatodea, genome assembly, rna-seq, reproduction, parthenogenesis, clitarchus hookeri

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