Fully degenerate polymersae chain reaction (PCR) primers, designed to repre
sent amino-acid conserved regions between transposase genes of the Drosophi
la mauritiana Tsacas & David and Hyalophora cecropia (L.) mariner transposa
ble elements, were used to screen genomic DNA of 17 insect cell lines for a
possible mariner-like element. All cell lines except that of Aedes albopic
tus (Skuse) were positive, yielding a single appropriately sized band of 49
0 bp. This PCR product from 2 of the cell lines, Heliothis subflexa (Guenee
) and Heliothis virescens (F.),was further characterized by cloning and dir
ect sequencing of PCR-amplified DNA products to confirm whether the product
was a mariner-like transposon element. Alignment of the direct sequenced P
CR-amplified DNA mariner-like element showed an amino acid identity of 43%
to the mariner transposase gene of the Surinam cockroach, Pycnocelus surina
mensis (L.).