Data from: A migration-associated supergene reveals loss of biocomplexity in Atlantic cod

Chromosome structural variation may underpin ecologically-important intraspecific diversity by reducing recombination within supergenes containing linked, co-adapted alleles. Here, we confirm that an ancient chromosomal rearrangement is strongly associated with migratory phenotype and individual gen...

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Bibliographic Details
Main Authors: Kess, Tony, Bentzen, Paul, Lehnert, Sarah J., Sylvester, Emma V. A., Lien, Sigbjørn, Kent, Matthew P., Sinclair-Waters, Marion, Morris, Corey J., Regular, Paul, Fairweather, Robert, Bradbury, Ian R.
Format: Dataset
Language:unknown
Published: 2019
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Online Access:https://zenodo.org/record/4934051
https://doi.org/10.5061/dryad.p6m4340
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Summary:Chromosome structural variation may underpin ecologically-important intraspecific diversity by reducing recombination within supergenes containing linked, co-adapted alleles. Here, we confirm that an ancient chromosomal rearrangement is strongly associated with migratory phenotype and individual genetic structure in Atlantic cod (Gadus morhua) across the Northwest Atlantic. We reconstruct trends in effective population size over the last century, and for the first time reveal declines in effective population size matching onset of industrialized harvest (post 1950). We find different demographic trajectories between individuals homozygous for the chromosomal rearrangement relative to heterozygous or homozygous individuals for the non-inverted haplotype, suggesting different selective histories across the last 150 years. These results illustrate how chromosomal structural diversity can mediate fine-scale genetic, phenotypic and demographic variation in a highly connected marine species, and show how overfishing may have led to loss of biocomplexity within Northern cod. Kess et al 2019 Northern Cod Collapse Dryad dataAtlantic cod SNP chip genotypes at 6669 SNP loci, in plink (.ped, .map) and genepop (.gen) format. Lists of SNPs from the chip found within rearranged genomic regions on LG1 and LG12. Complete table of inversion genotype assignments and migratory phenotype assignments.