We have developed a method for production of transgenic chickens by DN
A microinjection of chick zygotes followed by ex vivo embryo culture.
The fate of plasmid DNA microinjected into the germinal disc of zygote
s was analyzed in embryos which survived for at least 12 days in cultu
re. Approximately half of the embryos contained plasmid DNA, 6% at a l
evel equivalent to one copy per cell in all tissues analyzed. Seven ch
icks, 5.5% of the total number of injected ova, survived to sexual mat
urity. One of these, a cockerel, transmitted the exogenous DNA to 3.4%
of his offspring. These G1 birds have reached sexual maturity and hav
e been bred to produce transgenic offspring, demonstrating that stable
transmission of foreign DNA can be obtained by our method.