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dc.contributor.authorWyngaard, Grace
dc.contributor.authorSkern-Mauritzen, Rasmus
dc.contributor.authorMalde, Ketil
dc.contributor.authorPrendergast, Rachel
dc.contributor.authorPeruzzi, Stefano
dc.date.accessioned2022-06-17T09:03:15Z
dc.date.available2022-06-17T09:03:15Z
dc.date.created2022-04-22T20:46:23Z
dc.date.issued2022
dc.identifier.issn2045-2322
dc.identifier.urihttps://hdl.handle.net/11250/2999261
dc.description.abstractThe genome size of organisms impacts their evolution and biology and is often assumed to be characteristic of a species. Here we present the first published estimates of genome size of the ecologically and economically important ectoparasite, Lepeophtheirus salmonis (Copepoda, Caligidae). Four independent L. salmonis genome assemblies of the North Atlantic subspecies Lepeophtheirus salmonis salmonis, including two chromosome level assemblies, yield assemblies ranging from 665 to 790 Mbps. These genome assemblies are congruent in their findings, and appear very complete with Benchmarking Universal Single-Copy Orthologs analyses finding > 92% of expected genes and transcriptome datasets routinely mapping > 90% of reads. However, two cytometric techniques, flow cytometry and Feulgen image analysis densitometry, yield measurements of 1.3–1.6 Gb in the haploid genome. Interestingly, earlier cytometric measurements reported genome sizes of 939 and 567 Mbps in L. salmonis salmonis samples from Bay of Fundy and Norway, respectively. Available data thus suggest that the genome sizes of salmon lice are variable. Current understanding of eukaryotic genome dynamics suggests that the most likely explanation for such variability involves repetitive DNA, which for L. salmonis makes up ≈ 60% of the genome assemblies.en_US
dc.language.isoengen_US
dc.titleThe salmon louse genome may be much larger than sequencing suggests.en_US
dc.title.alternativeThe salmon louse genome may be much larger than sequencing suggests.en_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.volume12en_US
dc.source.journalScientific Reportsen_US
dc.identifier.doi10.1038/s41598-022-10585-2
dc.identifier.cristin2018531
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1


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