Chromosome-level genome assembly of a benthic associated Syngnathiformes species: the common dragonet, Callionymus lyra

Author:

Winter Sven12ORCID,Prost Stefan34ORCID,de Raad Jordi123ORCID,Coimbra Raphael T. F.12ORCID,Wolf Magnus12ORCID,Nebenführ Marcel1,Held Annika1,Kurzawe Melina1,Papapostolou Ramona1,Tessien Jade1,Bludau Julian1,Kelch Andreas1ORCID,Gronefeld Sarah1,Schöneberg Yannis1ORCID,Zeitz Christian1,Zapf Konstantin1,Prochotta David1,Murphy Maximilian1,Sheffer Monica M.5ORCID,Sonnewald Moritz6,Nilsson Maria A.23ORCID,Janke Axel123ORCID

Affiliation:

1. Institute for Ecology, Evolution and Diversity, Goethe University, Frankfurt am Main, Germany

2. Senckenberg Biodiversity and Climate Research Centre, Frankfurt am Main, Germany

3. LOEWE-Centre for Translational Biodiversity Genomics, Frankfurt am Main, Germany

4. South African National Biodiversity Institute, National Zoological Garden, Pretoria, South Africa

5. Zoological Institute and Museum, University of Greifswald, Greifswald, Germany

6. Senckenberg Research Institute, Department of Marine Zoology, Section Ichthyology, Frankfurt am Main, Germany

Abstract

Background The common dragonet, Callionymus lyra, is one of three Callionymus species inhabiting the North Sea. All three species show strong sexual dimorphism. The males show strong morphological differentiation, e.g., species-specific colouration and size relations, while the females of different species have few distinguishing characters. Callionymus belongs to the ‘benthic associated clade’ of the order Syngnathiformes. The ‘benthic associated clade’ so far is not represented by genome data and serves as an important outgroup to understand the morphological transformation in ‘long-snouted’ syngnatiformes such as seahorses and pipefishes. Findings Here, we present the chromosome-level genome assembly of C. lyra. We applied Oxford Nanopore Technologies’ long-read sequencing, short-read DNBseq, and proximity-ligation-based scaffolding to generate a high-quality genome assembly. The resulting assembly has a contig N50 of 2.2 Mbp and a scaffold N50 of 26.7 Mbp. The total assembly length is 568.7 Mbp, of which over 538 Mbp were scaffolded into 19 chromosome-length scaffolds. The identification of 94.5% complete BUSCO genes indicates high assembly completeness. Additionally, we sequenced and assembled a multi-tissue transcriptome with a total length of 255.5 Mbp that was used to aid the annotation of the genome assembly. The annotation resulted in 19,849 annotated transcripts and identified a repeat content of 27.7%. Conclusions The chromosome-level assembly of C. lyra provides a high-quality reference genome for future population genomic, phylogenomic, and phylogeographic analyses.

Publisher

GigaScience Press

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