The low efficiency of transgenic animal production by microinjection h
as been a serious problem especially for the production of transgenic
livestock. We developed a method to selectively produce transgenic mic
e using green fluorescent protein (GFP) as a marker. Using this method
, we obtained eight fetuses and four live-born mice derived from 55 GF
P-positive blastocysts. PCR analysis showed II out of 12 mice (fetuses
and newborn mice) were transgenic. Southern blot analysis showed that
8 out of 12 were transgenic. GFP expression was also observed in bovi
ne blastocysts, suggesting that this method should contribute to the e
fficient production of transgenic livestock.