The use of genomic DNA-based techniques in ecological and evolutionary
studies has been limited by the availability of suitable probes for s
pecies of interest due to the technical difficulty of isolating and ap
plying such probes. We have developed a simple technique that directs
polymerase chain reaction (PCR) amplification to regions rich in varia
ble number of tandem repeats (VNTRs). By using published VNTR core seq
uences as primers in PCRs, fragments were amplified that showed little
variation within a species, but did show differences between species.
When the amplified fragments were used as probes with genomic DNA Sou
thern blots they produced hypervariable single-locus or few-locus patt
erns in fish, birds, and humans. We have named this procedure as Direc
ted Amplification of Minisatellite-region DNA (DAMD).