Once a specific number of cells have been produced in the early Xenopu
s laevis embryo, replicon size during the S phase of the cell cycle in
creases. Here, it is reported that similar increase in replicon size o
ccurred when the concentration of nuclei in replication-competent Xeno
pus egg extracts exceeded a critical threshold. In this system, the or
igin recognition complex (ORC) did not become stoichiometrically limit
ing for initiation, and similar amounts of this complex bound to chrom
atin regardless of replicon size. These data suggest that in early dev
elopment, an unidentified factor controls how many preformed ORC-DNA c
omplexes initiate DNA replication.