Meiotic gynogens were produced using hybrid striped bass (female white
bass, Morone chrysops, x male striped bass, M. saxatilis) eggs and wh
ite perch M. americana UV-irradiated sperm. Diploidy of the fertilized
eggs was restored by application of hydrostatic pressure, which induc
ed retention of the second polar body. Use of white perch sperm provid
ed an unmistakable marker for detection of a paternal genetic contribu
tion. Two assays were developed using the polymerase chain reaction (P
CR) to amplify specific regions of the Morone genome. Primers for gene
amplification were developed based on the DNA sequence of the striped
bass growth hormone gene (SB-GH) or an anonymous striped bass locus (
SB1-10). Control experiments using DNA from the three Morone species d
emonstrated that gene amplification yielded species-specific patterns
of DNA fragments for both of these loci. Therefore, any progeny with a
paternal contribution of a set of white perch chromosomes could be id
entified. Using these assays, we demonstrated that greater than 75% of
the progeny obtained from successful experiments were true gynogens.
These striped bass hybrid gynogens will provide the basis for future e
fforts to calculate gene-centromere distances and to identify markers
linked to specific traits of interest to aquaculture.