DNA synthesis in developing two-cell mouse embryos |
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Authors: | Frederick W. Luthardt Roger P. Donahue |
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Affiliation: | 1. Department of Psychiatry, Mental Retardation Unit, University of California, Los Angeles, California 90024 USA;2. Department of Obstetrics and Gynecology, University of Washington, Seattle, Washington 98195 USA;3. Department of Medicine, University of Washington, Seattle, Washington 98195 USA |
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Abstract: | Mated CF1 (Carworth) female mice were sacrificed at 2 hr intervals between 29 and 43 hr after human chorionic gonadotrophin (HCG) administration. One- and two-cell eggs were incubated in [3H]thymidine for 1 hr. Labeled two-cell embryos were first observed at 31 hr and reached a maximum number at 35 hr. The S period is approximately 6 hr in duration. Although both blastomeres were labeled in most cases, embryos with only one labeled blastomere were more numerous at later times. In vitro labeling was corroborated by injecting [3H]thymidine directly into the isthmic portion of the oviduct. Embryos usually complete the second cleavage division 18–20 hr after onset of DNA synthesis. The cell cycle at the two-cell stage is thus characterized by a G1 of close to 1 hr, a 6 hr S, and a G2 of about 12 hr.Embryos developing in vitro frequently fail to progress beyond the two-cell stage. The block is not due to absence of DNA synthesis since these embryos were found to incorporate [3H]thymidine. |
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