Cosmids are valuable tools in physical mapping of genomes. They are commonl
y used in low resolution physical mapping, as markers for Fluorescence In S
itu Hybridization (FISH) of chromosomes. In addition, they are used in high
resolution physical mapping, i.e., cosmid contigs, restriction mapping, se
quencing. With aims of physically mapping the salmon (Salmo salar) genome w
e have constructed a partial (incomplete genome coverage) salmon cosmid lib
rary. A strategy has been adopted where anonymous, randomly picked, cosmids
are isolated, characterized by partial shotgun nucleotide sequencing and u
sed as markers for FISH. By multicolour multiprobe FISH a low resolution ph
ysical map can be established. Identifying on the cosmids, genes, whose hom
ologs in other organisms are mapped, enables comparative mapping. Identifyi
ng genetic markers like microsatellites enables linkage of physical and gen
etic maps. This strategy has sofar proven to be effective: on one cosmid cl
one the salmon U2 snRNP-specific A' protein gene (U2 small nuclear ribonucl
eoprotein particle) (U2A') was identified. (This is the first identified ge
nomic sequence of a U2A' gene from any organism). In addition a tetranucleo
tide microsatellite was identified within an intron. On another cosmid clon
e the salmon RAN gene was identified. The cosmid containing the U2A' gene w
as assigned to a metacentric salmon chromosome. (C) 1999 Elsevier Science B
.V. All rights reserved.