Totipotent embryonic stem (ES) cells represent a bridge that links in vitro
and in vivo manipulations of animal genomes and have enormous potential fo
r genetic engineering of livestock. We have recently established feeder cel
l-free conditions for culturing cells of midblastula embryos (MBE) of the m
edaka (Oryzias latipes) and obtained several stable cell lines that show al
l features of mouse ES cells in vitro. One of these lines, MES1, has been d
emonstrated to retain a diploid karyotype and can be induced to differentia
te into various cell types in vitro. Upon microinjection into albino host b
lastulae, MES1 cells are able to form pigmented chimeras. Genotype-specific
PCR analysis revealed that 90% of host blastulae transplanted with MES1 ce
lls developed into chimeric fry. This high frequency was not compromised by
cryostorage or DNA transfection of the donor cells. Transplantation of gen
etically labelled MES1 cells revealed a wide contribution to numerous organ
s derived from all three germ layers and differentiation into various types
of functional cells. These ES properties of MES1 line was not abolished by
stable gene transfer and long-term selection. Thus MES1 cells may represen
t a first promising cellular vehicle for the production of genetically modi
fied fish. The genetic background has been found to have a profound effect
on the efficacy of ES cell derivation and of chimera formation.