January 13-17, 2007
Town & Country Convention Center
San Diego, CA
Elizabeth G Boulding1 , Keng Pee Ang2 , Paul R. Berg3 , Ian A. Fleming4 , Brian Glebe5 , Sigbjørn Lien3,6 , Danielle MacDonald7,8 , Thomas Moen3,9 , Paloma Moràn10 , Patrick O’Reilly8 , Patricia M. Schulte11
Many Atlantic salmon (Salmo salar) populations in eastern Canada and the United States are endangered and many rivers have lost their indigenous, locally adapted river-specific juveniles. Therefore, it is critical to document differences among populations at the whole genome level both to aid conservation efforts and to enable allele mining for introgression into aquacultural strains. Genome Canada’s new GRASP gene expression microarray is allowing us to assay 16,000 different genes from each fish but does not tell us how much of the observed variation in gene expression among different salmon populations is genetic. We have created four backcrosses by crossing Trans-Atlantic F1 males to a female from either the European or the North American parental populations. These four large full sib research families are segregating for the alleles that are unique to each of the original parental strains and enable us to identify genes whose expression level is strongly correlated with morphological, behavioral, or life history traits. To verify that these correlations have a genetic basis we are genotyping the families for several hundred SNPs (single nucleotide polymorphisms) from expressed sequence tags on a Norwegian SNP linkage map. We will then use SNP markers linked to quantitative trait loci (QTLs) for traits under selection to genotype tail clips from endangered wild Atlantic salmon that are held in a common hatchery environment. This will enable us to document the genetic differences in functional traits among these endangered salmon populations and may assist in their conservation.