DNA synthesis in the preimplantation mouse embryo

Author:

Barlow P.1,Owen D. A. J.1,Graham Chris1

Affiliation:

1. Paediatric Research Unit, Guy's Hospital Medical School, London, the Institute of Animal Genetics, Edinburgh and the Sir William Dunn School of Pathology, University of Oxford

Abstract

Strain PO preimplantation embryos were labelled with [3H]thymidine. The incorporation of the label was studied by autoradiography of air-dried and serially sectioned embryos. DNA amounts were measured with a microdensitometer. The following observations were made at the 5- to 16-cell stages. All nuclei contained 2C–4C amounts of DNA and all could eventually synthesize DNA. However, after short labelling intervals, unlabelled nuclei were found with 2C and AC amounts of DNA. We concluded that both the G1 and the G2 phases of the cell cycle were present at this time. Embryos were found in which the S phase of the 4th and the 5th cell cycles post fertilization overlapped. In 12- to 15-cell embryos which contained inside cells it was found that the inside cells were produced by one of the first four 8-cell-stage blastomeres to divide. The inside cells of 9- to 256-cell embryos had a significantly higher labelling index than the outside cells and the number of inside cells increased faster than the number of outside cells during development. We concluded that the inside cells were dividing faster than the outside cells. Blastocysts which had developed in vivo or in vitro contained nuclei with greater than 4C amounts of DNA. We concluded that the development of excess DNA amounts does not depend on the maternal environment. These nuclei which contained greater than 4C amounts of DNA were labelled after short exposures to radioactivity. We concluded that it was likely that they were becoming polyploid.

Publisher

The Company of Biologists

Subject

Developmental Biology,Molecular Biology

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