The ability of the Hermes transposable element to function as a germ line t
ransformation vector was tested in the stable fly, Stomoxys calcitrans. Pla
smid-based transposable element mobility assays indicated moderate mobility
of Hermes in this species. Germline transformants were created using a Her
mes element containing the enhanced green fluorescent protein (EGFP) under
the regulatory control of the promoter from Actin5C gene of Drosophila mela
nogaster. Approximately 4% of the fifty-five adults that developed from the
1903 G(0) embryos injected with the vector produced transgenic progeny. In
the four transgenic lines established, the EGFP expression pattern was dis
tinctly nonuniform and levels of expression were low. Promoters other than
the one from the Actin5C gene of D. melanogaster should be considered for w
idespread, constitutive expression. All transgenic lines contained multiple
(2-4) integrated Hermes elements. Hermes integration events occurred throu
gh a canonical cut-and-paste mechanism.