Telomere-to-telomere assembly of the genome of an individual Oikopleura dioica from Okinawa using Nanopore-based sequencing
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Abstract
Background: The larvacean Oikopleura dioica is an abundant tunicate plankton with the smallest (65-70 Mbp) non-parasitic, non-extremophile animal genome identified to date. Currently, there are two genomes available for the Bergen (OdB3) and Osaka (OSKA2016) O. dioica laboratory strains. Both assemblies have full genome coverage and high sequence accuracy. However, a chromosome-scale assembly has not yet been achieved. Results: Here, we present a chromosome-scale genome assembly (OKI2018_I69) of the Okinawan O. dioica produced using long-read Nanopore and short-read Illumina sequencing data from a single male, combined with Hi-C chromosomal conformation capture data for scaffolding. The OKI2018_I69 assembly has a total length of 64.3 Mbp distributed among 19 scaffolds. 99% of the assembly is in five megabase-scale scaffolds. We found telomeres on both ends of the two largest scaffolds, which represent assemblies of two fully contiguous autosomal chromosomes. Each of the other three large scaffolds have telomeres at one end only and we propose that they correspond to sex chromosomes split into a pseudo-autosomal region and X-specific or Y-specific regions. Indeed, these five scaffolds mostly correspond to equivalent linkage groups of OdB3, suggesting overall agreement in chromosomal organization between the two populations. At a more detailed level, the OKI2018_I69 assembly possesses similar genomic features in gene content and repetitive elements reported for OdB3. The Hi-C map suggests few reciprocal interactions between chromosome arms. At the sequence level, multiple genomic features such as GC content and repetitive elements are distributed differently along the short and long arms of the same chromosome. Conclusions: We show that a hybrid approach of integrating multiple sequencing technologies with chromosome conformation information results in an accurate de novo chromosome-scale assembly of O. dioica ’s highly polymorphic genome. This assembly will be a useful resource for genome-wide comparative studies between O. dioica and other species, as well as studies of chromosomal evolution in this lineage.Keywords
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- Published version: BMC Genomics, 22 (1), 1.
This publication has 62 references indexed in Scilit:
- STAR: ultrafast universal RNA-seq alignerBioinformatics, 2012
- Full-length transcriptome assembly from RNA-Seq data without a reference genomeNature Biotechnology, 2011
- A fast, lock-free approach for efficient parallel counting of occurrences of k-mersBioinformatics, 2011
- A new repeat-masking method enables specific detection of homologous sequencesNucleic Acids Research, 2010
- MITE-Hunter: a program for discovering miniature inverted-repeat transposable elements from genomic sequencesNucleic Acids Research, 2010
- MAKER: An easy-to-use annotation pipeline designed for emerging model organism genomesGenome Research, 2007
- Evolution of genes and genomes on the Drosophila phylogenyNature, 2007
- RNAmmer: consistent and rapid annotation of ribosomal RNA genesNucleic Acids Research, 2007
- Tunicates and not cephalochordates are the closest living relatives of vertebratesNature, 2006
- Improving the Arabidopsis genome annotation using maximal transcript alignment assembliesNucleic Acids Research, 2003