The germline, uniquely amongst the lineages of the embryo, carries the
genome from generation to generation and is therefore the only lineag
e which retains true developmental totipotency. Paradoxically, when mo
use primordial germ cells (PGCs) are introduced into a host blastocyst
, they do not contribute to either the germline or the soma, suggestin
g that they are restricted in developmental potency. Conversely, in vi
vo PGCs give rise to embryonal carcinoma (EC) cells, the pluripotent s
tem cells of teratomas, benign tumors containing derivatives of the th
ree primary germ layers. Similarly, PGCs can be converted in vitro int
o embryonic germ (EG) cells, pluripotent stem cells capable of giving
rise to somatic and germline chimeras. The ability of PGCs to form EC
cells in vivo and EG cells in vitro suggests that developmental potenc
y of PGCs is regulateable. The molecular mechanisms controlling PGC gr
owth and differentiation are gradually being elucidated through the ch
aracterization of sterile mutants and through the use of in vitro cult
ure systems. Understanding how a PGC can give rise to a pluripotent st
em cell could give significant insights into the regulation of develop
mental totipotency as well as having important implications for male f
ertility and the etiology of testicular cancer.