W13
Recent efforts in gene mapping of Penaied shrimp have met with a number
of obstacles. Chief amongst these has been the difficulty in characterising
large numbers of highly variable markers such as DNA microsatellites.
These difficulties stem from the high number, length and complexity of
sample sequence repeats present in these organisms. Unique flanking
sequence suitable for PCR primer design has thus been difficult to obtain.
An alternative approach utilising amplified fragment length polymorphisms
(AFLPs) has been successfully applied to gene mapping in P. japonicus.
This technique has allowed the rapid construction of a genetic map for this
species. Both AFLP markers and those microsatellite markers which have
been isolated from various species of Penaeus are, to a large degree,
species specific. Cultured shrimp, however, comprise a number of species
including P. vanameii, P. monodon, P. japonicus, P. chinesis and
P. stylirostris. Faced with the prospect that genetic maps using
highly variable markers will be species specific, methodologies must be
established for integrating such maps and optimising the utility of QTL
data gathered in any one species. Such strategies include mapping more
conserved sequence elements such as transcribed sequences, which will
enable PCR based mapping across species.