Chromosome counts of 338 mouse zygotes at late prophase and metaphase of the first cleavage division revealed 96.4% diploidy, 1.8% hypodiploidy, 1.2% triploidy, and 0.3% tetraploidy. One The first cleavage division is especially crucial in embryonic development. Subsequent to sperm penetration and completion of meiosis in the egg, the male-and female-derived nuclei form pronuclei, replicate their DNA, and then simultaneously enter first cleavage prophase. The two prophase chromosome groups remain physically separated until they combine to form first cleavage metaphase (1). If any one of these events is aberrant, one or both of the two daughter cells and their descendents may carry chromosomal anomalies. Abnormalities arising at later cleavage stages would presumably contribute less to the total embryo.The few chromosome studies of mammalian embryos before uterine attachment have all been conducted on blastocysts (2). In the mouse, 2.6% of day-3 blastocysts were found to be chromosomally abnormal (3). The were at late prophase, where the separateness of the male-and female-derived chromosome groups is maintained.
Origin of pronucleiThroughout their lifespan, the pronuclei are of unequal size; the chromatin strands are more condensed in the smaller than in the larger pronucleus (1). Differential condensation is retained through most of first cleavage prophase (Fig. 1) and is present in about 50% of the zygotes at late prophase when chromosomes can be counted, providing the basis for identifying the origin of the different sized pronuclei. In 74 Abbreviation: HCG, human chorionic gonadotrophin.