W9
Inheritance studies with marine bivalve molluscs, including the American
and Pacific oysters Crassostrea virginica and C. gigas, often
detect departures from Mendelian segregation. In controlled, pair-crosses,
about half of the genetic markers, whether protein or DNA polymorphisms,
show significant discrepancies between observed and expected genotypic
proportions in the resulting progeny. Discrepancies are evident during
larval development but are especially marked at the juvenile or adult
stages; they arise in random-bred progenies but are striking in inbred
families. The loci affected vary from cross to cross. These deviations
from normal Mendelian segregation, whatever their cause, necessitate
modifications of standard methods of linkage or QTL mapping. While
statistical corrections are available for cases of zygotic or gametic
selection, another approach is to examine segregation in very early life
stages, in haploid embryos, even in gametes directly. It is possible to
make haploid oyster embryos, which survive for 6-8 hrs, producing enough
template for 20-40 PCR reactions. We successfully amplified
microsatellites from 6 hr old haploid and diploid Pacific oyster embryos,
and preliminary data for one microsatellite locus suggest that segregation,
in both male and female parents, and genotypic proportions of progeny are
normal in three families. One female parent is hypothesized to carry a
null allele. Further studies involving more loci and parents are needed to
confirm that segregation distortion is consistently absent in early haploid
or diploid stages. A second problem in genetic mapping is the complete
interference that has been reported in studies of gene-centromere
recombination in triploids made by inhibition of the second polar body.
Whether large blocks of genes remain linked because of stereotypical sites
for crossing-over remains a concern in constructing a linkage map for oysters.