Neocortical neuronogenesis occurs in the pseudostratified ventricular
epithelium (PVE) which forms the margin of the ventricular system of t
he embryonic cerebral wall. We have determined that in mouse the neuro
nogenetic interval continues 6 days and is divisible into 11 integer c
ycles. The fraction of daughter cells which leaves the cycle (Q) follo
ws a curvilinear path from 0 to 1.0 over the neuronogenetic interval.
Q reaches 0.5 in the course of cell cycle 8 at which point the number
of daughter cells which leaves the PVE is equal to the number that rem
ains to renew the proliferative process. Over the course of the neuron
ogenetic interval in mouse, the founder population is amplified 140 fo
ld. If, theoretically, the operation of the process were altered so th
at the total number of integer cycles were kept constant but that Q va
ried so that it reached 0.5 in the course of cell cycles 7, 9 and 10,
the total neuronal production from the same founder population would b
e 60%, 160% and 550%, respectively, that observed in mouse. If, on the
other hand, the number of integer cycles was varied but the relative
rate of progressin of Q with respect to the neuronogenetic interval wa
s kept the same as in mouse, the total neuronal production would be 50
% with 9 cycles, 2 fold with 13 cycles and 60 fold with 22 cycles with
respect to the 140 fold amplification of the founder population seen
in mouse. These large scale amplifications in neuronal output from the
PVE illustrate the predominant effect of the number of integer cycles
, but also the substantial effect of variations in Q as potential cont
rol parameters in the regulation of neuronogenesis.