Several aspects of transposition of an in vitro modified Ds element ar
e described. This Ds element, designated Ds-r, is equipped with bacter
ial plasmid sequences and can, therefore, be rescued from the plant ge
nome. Our results indicate that the Ds-r element has a 'late' timing o
f transposition from T-DNAs. This feature of the element might be adva
ntageous for tagging experiments because it leads to independently tra
nsposed germinally transmitted elements. Furthermore, it is shown that
Ds-r transposition generates clusters of insertions, indicating that
'genes to be tagged' should be located in genomic regions covered by i
nsertions.