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Rolf B Edvardsen

Publications and source records attributed to Rolf B Edvardsen.

2 recordsLinked to original sources

An improved genome assembly uncovers a prolific tandem repeat structure in Atlantic cod

Background: The first Atlantic cod (Gadus morhua) genome assembly published in 2011 was one of the early genome assemblies exclusively based on high-throughput 454 pyrosequencing. Since then, rapid advances in sequencing technologies have led to a multitude of assemblies generated for complex genomes, although many of these are of a fragmented nature with a significant fraction of bases in gaps. The development of long-read sequencing and improved software now enable the generation of more contiguous genome assemblies.\n\nResults: By combining data from Illumina, 454 and the longer PacBio sequencing technologies, as well as integrating the results of multiple assembly programs, we have created a substantially improved version of the Atlantic cod genome assembly. The sequence contiguity of this assembly is increased fifty-fold and the proportion of gap-bases has been reduced fifteen-fold. Compared to other vertebrates, the assembly contains an unusual high density of tandem repeats (TRs). Indeed, retrospective analyses reveal that gaps in the first genome assembly were largely associated with these TRs. We show that 21 % of the TRs across the assembly, 19 % in the promoter regions and 12 % in the coding sequences are heterozygous in the sequenced individual.\n\nConclusions: The inclusion of PacBio reads combined with the use of multiple assembly programs drastically improved the Atlantic cod genome assembly by successfully resolving long TRs. The high frequency of heterozygous TRs within or in the vicinity of genes in the genome indicate a considerable standing genomic variation in Atlantic cod populations, which is likely of evolutionary importance.

Genomics

The vgll3 locus controls age at maturity in wild and domesticated Atlantic salmon (Salmo salar L.) males

BackgroundSea age at sexual maturation displays large plasticity for wild Atlantic salmon males and varies between 1-5 years. This flexibility can also be observed in domesticated salmon. Previous studies have uncovered a genetic predisposition for age at maturity with moderate heritability, thus suggesting a polygenic nature of this trait. The aim with this study was to identify genomic regions and associated SNPs and genes conferring age at maturity in salmon.\n\nResultsWe performed a GWAS using a pool sequencing approach (n=20 per river and trait) of salmon returning as sexually mature either after one sea winter (2009) or after three sea winters (2011) in six rivers in Norway. The study revealed one major selective sweep, which covered 76 significant SNP in a 230 kb region of Chr 25. A SNP assay of other year classes of wild salmon and from cultivated fish supported this finding. The assay in cultivated fish reduced the haplotype conferring the trait to a region which covered 4 SNPs of a 2386 bp region containing the vgll3 gene. 2 of these SNPs caused miss-sense mutations in vgll3.\n\nConclusionsThis study presents a single selective region in the genome for age at maturation in male Atlantic salmon. The SNPs identified may be used as QTLs to prevent early maturity in aquaculture and in monitoring programs of wild salmon. Interestingly, the identified vgll3 gene has previously been linked to time of puberty in humans, suggesting a conserved mechanism for time of puberty in vertebrates.

Genomics