Crisis periods in development are critical periods of cell death that have
long been suggested as "epigenetic crises" which are central to normal and
abnormal embryogenesis. Under in-vitro culture conditions, there are simila
r crisis periods or Hayflick limits of culture senescence. Epigenetic modul
ations from CpG methylation coupled to DNA replication provide an alternate
timing mechanism to the telomere/telomerase biological clock. Physiologica
l cell death in both development and in in-vitro isolates is primarily apop
totic. Arguments of divergent apoptotic death commitments as caspase-depend
ent and -independent pathways seem to suggest that there is no possibility
of a global life-and-death signal. However recent reports implicating CpG-s
pecific cleavage in apoptosis implies that the powerful imprint mark that s
ilences genes, protects genes from nuclease restriction, and modulates chro
matin conformations, could provide a common commitment pathway of convergen
ce in the death cascade. If the imprint mark were central to the apoptotic
commitment, then apoptosis is Lamarckian not Darwinian.