Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
. 1992 Dec;102(1):60-5.
doi: 10.1007/BF00352291.

Sensitive period for the induction of endoreduplication by rotenone in cultured Chinese hamster cells

Affiliations

Sensitive period for the induction of endoreduplication by rotenone in cultured Chinese hamster cells

K Matsumoto et al. Chromosoma. 1992 Dec.

Abstract

Rotenone-induced endoreduplication was investigated in Chinese hamster CHL cells. Cell cycle analyses, using 5-bromo-2'-deoxyuridine (BrdU) labeling, revealed that endoreduplication was induced between the G2-phase and mitotic metaphase. Morphological studies indicated that the chromosomes of cells in metaphase at the time of rotenone exposure immediately aggregated. Within 1 h, however, the aggregated chromosomes began to decondense forming telophase nuclei. Cells with aggregated chromosomes were collected by mitotic selection using the mitotic arrestant TN-16 and then cultured for 30 h following rotenone administration. This population of cells demonstrated an extremely high frequency of endoreduplicated metaphases. Further analysis by BrdU labeling indicated that the aggregated metaphases underwent only one round of DNA replication before endoreduplicated metaphases were formed. The most sensitive period for the induction of endoreduplication by rotenone occurs during mitotic metaphase.

PubMed Disclaimer

Similar articles

Cited by

References

    1. Exp Cell Res. 1965 Dec;40(3):673-7 - PubMed
    1. Exp Cell Res. 1974 Mar 30;85(1):41-6 - PubMed
    1. Cancer Res. 1974 Oct;34(10):2615-23 - PubMed
    1. J Natl Cancer Inst. 1953 Aug;14(1):1-43 - PubMed
    1. Mutat Res. 1988 Jul;208(3-4):213-8 - PubMed