P16
DNA marker analysis of genomes has revolutionized genetic
studies of organisms in the past 15 years. AFLP, RFLP and SSR
genetic maps have been developed for almost all major crops.
The recent developement of technologies for large DNA fragment
(>100 Kb) cloning, such as bacterial artificial chromosome
(BAC), BAC fingerprinting and contig assembly has provided
powerful tools to rapidly generate molecular physical maps. A
physical map integrated with the developed DNA marker genetic
maps will provide a new strategy to clone genes known only by
their phenotypes by gene golfing (Zhang and Wing 1997).
Practically, using the newly developed BAC DNA isolation and
BAC fingerprinting technologies one technicien can fingerprint
up to 40,000 clones of 150 kb per year, covering 6 x haploid
genomes of 1,000 Mb. Using the integrated physical map, DNA
molecular marker identified 10 cM away from a gene of interest
can be used to clone the target gene. Genes in regions where
repeated sequences are rich can also be cloned with the
integrated physical map, whereas it is difficult, if not
impossible, to clone the genes in such regions by the
currently used map-based cloning strategy. The development
of an integrated physical map will provide a "highway" for
isolation of large number of genes and for many other genetic
and biological studies of plant and animal genomes. Currently,
the integrated physical maps of the rice, Arabidopsis and
sorghum genomes are under development using the BAC
fingerprinting and contigs assembly technlogies. We are using
these technologies to develop the integrated physical map of
the soybean genome. We will report the progress in construction
of the soybean genome integrated physical map. A new approach
to isolate microsattelites DNA markers for gene cloning and
marker assisted selection will be also presented.