Abstract

It has been recognized for several decades that the number of cleavage divisions which precede blastocyst formation in the mammalian embryo is rigorously fixed, such that removal of cells from the embryo, or augmentation of cell number by embryo aggregation, does not affect the timing of blastulation. Instead, embryos manipulated so as to reduce cell number form small blastocysts with fewer numbers of cells, while aggregate embryos form giant blastocysts. This tight control of the number of cleavage divisions ensures that the timing of blastocyst formation corresponds to the period of uterine receptivity for implantation. As yet, no experimental manipulation has succeeded in altering control of the number of cleavage divisions prior to blastulation, and as a consequence, the biological basis for the control mechanism is entirely obscure. We report here that removal of cytoplasm from one-celled mouse embryos does not alter the rate of cleavage, but does induce precocious formation of small blastocysts. These findings suggest that the early embryo "counts" cleavage divisions by measuring the size of its blastomeres, and that experimental reduction of cell size disturbs the counting mechanism and leads to abnormally early blastulation.

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