A highly efficient and reproducible transformation system for oat (Avena sativa L. cv. GAF/Park-1) was developed using microprojectile bombardment of highly regenerative tissues derived from mature seeds. Callus was induced under dim light conditions on medium containing 2,4-dichlorophenoxyacetic acid (2,4-D), 6-benzylaminopurine (BAP) and high cupric sulfate. Highly regenerative tissues, generated from embryogenic callus, were used as a transformation target. From 327 individual explants bombarded with the β-glucuronidase gene (uidA; gus) and a hygromycin phosphotransferase gene (hpt), 84 independent transgenic events were obtained after an 8-12-week selection period on hygromycin. All events were regenerable, giving an effective transformation frequency of 26%; co-expression of GUS activity occurred in 70% of the independent events. Presence of the foreign genes in DNA from leaf samples of T 0 and T 1 plants was confirmed by polymerase chain reaction (PCR) amplification and/or DNA blot hybridization. Fertility of the plants from the transgenic lines was 63% (24/38) and the transgene(s) was stably transmitted to T 1 and T 2 progeny.