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      High-quality haploid genomes corroborate 29 chromosomes and highly conserved synteny of genes in Hyles hawkmoths (Lepidoptera: Sphingidae)

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          Abstract

          Background

          Morphological and traditional genetic studies of the young Pliocene genus Hyles have led to the understanding that despite its importance for taxonomy, phenotypic similarity of wing patterns does not correlate with phylogenetic relationship. To gain insights into various aspects of speciation in the Spurge Hawkmoth ( Hyles euphorbiae), we assembled a chromosome-level genome and investigated some of its characteristics.

          Results

          The genome of a male H. euphorbiae was sequenced using PacBio and Hi-C data, yielding a 504 Mb assembly (scaffold N50 of 18.2 Mb) with 99.9% of data represented by the 29 largest scaffolds forming the haploid chromosome set. Consistent with this, FISH analysis of the karyotype revealed n = 29 chromosomes and a WZ/ZZ (female/male) sex chromosome system. Estimates of chromosome length based on the karyotype image provided an additional quality metric of assembled chromosome size. Rescaffolding the published male H. vespertilio genome resulted in a high-quality assembly (651 Mb, scaffold N50 of 22 Mb) with 98% of sequence data in the 29 chromosomes. The larger genome size of H. vespertilio (average 1C DNA value of 562 Mb) was accompanied by a proportional increase in repeats from 45% in H. euphorbiae (measured as 472 Mb) to almost 55% in H. vespertilio. Several wing pattern genes were found on the same chromosomes in the two species, with varying amounts and positions of repetitive elements and inversions possibly corrupting their function.

          Conclusions

          Our two-fold comparative genomics approach revealed high gene synteny of the Hyles genomes to other Sphingidae and high correspondence to intact Merian elements, the ancestral linkage groups of Lepidoptera, with the exception of three simple fusion events. We propose a standardized approach for genome taxonomy using nucleotide homology via scaffold chaining as the primary tool combined with Oxford plots based on Merian elements to infer and visualize directionality of chromosomal rearrangements. The identification of wing pattern genes promises future understanding of the evolution of forewing patterns in the genus Hyles, although further sequencing data from more individuals are needed. The genomic data obtained provide additional reliable references for further comparative studies in hawkmoths (Sphingidae).

          Supplementary Information

          The online version contains supplementary material available at 10.1186/s12864-023-09506-y.

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          Most cited references78

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          The Sequence Alignment/Map format and SAMtools

          Summary: The Sequence Alignment/Map (SAM) format is a generic alignment format for storing read alignments against reference sequences, supporting short and long reads (up to 128 Mbp) produced by different sequencing platforms. It is flexible in style, compact in size, efficient in random access and is the format in which alignments from the 1000 Genomes Project are released. SAMtools implements various utilities for post-processing alignments in the SAM format, such as indexing, variant caller and alignment viewer, and thus provides universal tools for processing read alignments. Availability: http://samtools.sourceforge.net Contact: rd@sanger.ac.uk
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            BUSCO: assessing genome assembly and annotation completeness with single-copy orthologs.

            Genomics has revolutionized biological research, but quality assessment of the resulting assembled sequences is complicated and remains mostly limited to technical measures like N50.
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              QUAST: quality assessment tool for genome assemblies.

              Limitations of genome sequencing techniques have led to dozens of assembly algorithms, none of which is perfect. A number of methods for comparing assemblers have been developed, but none is yet a recognized benchmark. Further, most existing methods for comparing assemblies are only applicable to new assemblies of finished genomes; the problem of evaluating assemblies of previously unsequenced species has not been adequately considered. Here, we present QUAST-a quality assessment tool for evaluating and comparing genome assemblies. This tool improves on leading assembly comparison software with new ideas and quality metrics. QUAST can evaluate assemblies both with a reference genome, as well as without a reference. QUAST produces many reports, summary tables and plots to help scientists in their research and in their publications. In this study, we used QUAST to compare several genome assemblers on three datasets. QUAST tables and plots for all of them are available in the Supplementary Material, and interactive versions of these reports are on the QUAST website. http://bioinf.spbau.ru/quast . Supplementary data are available at Bioinformatics online.
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                Author and article information

                Contributors
                anna.hundsdoerfer@senckenberg.de
                Journal
                BMC Genomics
                BMC Genomics
                BMC Genomics
                BioMed Central (London )
                1471-2164
                7 August 2023
                7 August 2023
                2023
                : 24
                : 443
                Affiliations
                [1 ]GRID grid.512720.3, ISNI 0000 0000 9326 155X, Senckenberg Natural History Collections Dresden, ; Königsbrücker Landstr. 159, 01109 Dresden, Germany
                [2 ]GRID grid.511284.b, ISNI 0000 0004 8004 5574, LOEWE-Centre for Translational Biodiversity Genomics (LOEWE-TBG), ; Frankfurt Am Main, Germany
                [3 ]GRID grid.10306.34, ISNI 0000 0004 0606 5382, Tree of Life, , Wellcome Sanger Institute, ; Cambridge, CB10 1SA UK
                [4 ]Biology Centre of the Czech Academy of Sciences, Institute of Entomology, Branišovská 31, 370 05 České Budějovice, Czech Republic
                [5 ]GRID grid.419537.d, ISNI 0000 0001 2113 4567, Max Planck Institute of Molecular Cell Biology and Genetics, ; Pfotenhauerstraße 108, 01307 Dresden, Germany
                [6 ]GRID grid.517093.9, ISNI 0000 0005 0294 9006, Centre for Molecular Biodiversity Research, , Leibniz Institute for the Analysis of Biodiversity Change, ; Adenauerallee 127, 53113 Bonn, Germany
                [7 ]GRID grid.495510.c, ISNI 0000 0004 9335 670X, Center for Systems Biology Dresden, ; Pfotenhauerstr. 108, 01307 Dresden, Germany
                [8 ]GRID grid.8993.b, ISNI 0000 0004 1936 9457, Department of Cell and Molecular Biology, , Uppsala University, ; Husargatan 3, Uppsala, 751 23 Sweden
                Article
                9506
                10.1186/s12864-023-09506-y
                10405479
                37550607
                d60f005c-0286-4f4d-89b8-cbbd2eba054d
                © BioMed Central Ltd., part of Springer Nature 2023

                Open Access This 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
                : 15 March 2023
                : 5 July 2023
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100001659, Deutsche Forschungsgemeinschaft;
                Award ID: HU 1561/5-2
                Award ID: HU 1561/5-2
                Award ID: HU 1561/5-2
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/100010269, Wellcome Trust;
                Award ID: 206194 and 218328
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100001824, Grantová Agentura České Republiky;
                Award ID: 20-13784S
                Award ID: 20-13784S
                Award Recipient :
                Funded by: FundRef http://dx.doi.org/10.13039/501100002347, Bundesministerium für Bildung und Forschung;
                Award ID: 01IS18026C
                Award Recipient :
                Funded by: Senckenberg Naturhistorische Sammlungen Dresden (3507)
                Categories
                Research
                Custom metadata
                © BioMed Central Ltd., part of Springer Nature 2023

                Genetics
                karyotype,chromosome-level scaffolding,wing pattern genes,optix,wnt,cortex,aristaless,distal-less,p supergene

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