We have used hybridization analysis to detect ancient DNA in wheat see
ds collected from three archaeological sites in Europe and the Middle
East. One of these samples, carbonized T. spelta dated to the first mi
llennium BC, has yielded PCR products after amplification with primers
directed at the leader regions of the HMW (high molecular weight) glu
tenin alleles. Sequences obtained from these products suggest that the
DNA present in the Danebury seeds is chemically damaged, as expected
for ancient DNA, and also indicate that it should be possible to study
the genetic variability of archaeological wheat by ancient DNA analys
is. Finally, we describe a PCR-based system that enables tetraploid an
d hexaploid wheats to be distinguished.