The terminal sequences of long-terminal repeat (LTR) retrotransposons are a
source of powerful molecular markers for linkage mapping and biodiversity
studies. The major factor limiting the widespread application of LTR retrot
ransposon-based molecular markers is the availability of new retrotransposo
n terminal sequences. We describe a PCR-based method for the rapid isolatio
n of LTR sequences of Ty1-copia group retrotransposons from the genomic DNA
of potentially any higher plant species. To demonstrate the utility of thi
s technique, we have identified a variety of new retrotransposon LTR sequen
ces from pea, broad bean and Norway spruce. Primers specific for three pea
LTRs have been used to reveal polymorphisms associated with the correspondi
ng retrotransposons within the Pisum genus.