Programmed cell death AS A
MECHANISM OF NEURAL DEVELOPMENT
THE SWITCH FROM DIVISION TO APOPTOSIS OCCURS AT A DEFINED TIME POINT: new EVIDENCE in Drosophila
The original research paper (Bello B.C., et al. A
pulse of the Drosophila Hox protein Abdominal-A schedules the end of neural
proliferation via neuroblast apoptosis Neuron 37, 209-219, 2003) shows new evidence for
the role of apoptosis, or programmed cell death, in regulating neural
development by a process linked to axial patterning in Drosophila. The change
from proliferation to death doesn’t seem related to a defined phase of the cell
cycle, but it exactly occurs at one point in time during larval development.
Apoptosis was observed in abdominal neuroblasts, while their thoracic
counterpart didn’t undergo the same destiny. This regional difference seems to
depend on the control of the cell numbers linked to axial patterning
mechanisms. The authors studied through deletion and ectopic expression the abdominal
A (abdA) gene, one among Hox family of homeobox transcription factors,
concluding that abdA is probably a factor that signals immature neurons to stop
dividing.
Apoptotic control of the
neuroblast proliferation might be a widespread strategy of development in other
species.
BM&L-March 2003