THE development of a multicellular organism involves a delicate balanc
e among the processes of proliferation, differentiation and death. Nat
urally occurring cell death aids tissue remodelling, eliminates supern
umerary cell populations and provides structural elements such as hair
and skin. In the nervous system, selective cell death contributes to
the formation and organization of the spinal cord and sympathetic gang
lia1, retina2 and corpus callosum3. But cell death also occurs in seve
ral neuropathological conditions, such as amyelotrophic lateral sclero
sis4 and Alzheimer's disease5. Therefore an elucidation of the mechani
sms responsible for cell death is critical for an appreciation of both
normal development and neuropathological disorders. Using a fos-lacZ
transgenic mouse6, we provide evidence showing that the continuous exp
ression of Fos beginning hours or days before the morphological demise
of the cell, appears to be a hallmark of terminal differentiation and
a harbinger of death.