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
. 1988 Apr;8(4):1525-33.
doi: 10.1128/mcb.8.4.1525-1533.1988.

Double minute chromosomes can be produced from precursors derived from a chromosomal deletion

Affiliations

Double minute chromosomes can be produced from precursors derived from a chromosomal deletion

S M Carroll et al. Mol Cell Biol. 1988 Apr.

Abstract

Recent experiments have shown that gene amplification can be mediated by submicroscopic, autonomously replicating, circular extrachromosomal molecules. We refer to those molecules as episomes (S. Carroll, P. Gaudray, M. L. DeRose, J. F. Emery, J. L. Meinkoth, E. Nakkim, M. Subler, D. D. Von Hoff, and G. M. Wahl, Mol. Cell. Biol. 7:1740-1750, 1987). The experiments reported in this paper explore the way episomes are formed and their fate in the cell over time. The data reveal that in our system the episomes are initially 250 kilobases, but gradually enlarge until they become double minute chromosomes. In addition, we show that episomes or double minute chromosomes can integrate into chromosomes. Our results also suggest that episomes can be produced by deletion of the corresponding sequences from the chromosome.

PubMed Disclaimer

References

    1. J Virol. 1981 Oct;40(1):11-9 - PubMed
    1. Plasmid. 1978 Sep;1(4):584-8 - PubMed
    1. Proc Natl Acad Sci U S A. 1983 Oct;80(19):5961-4 - PubMed
    1. Somatic Cell Genet. 1977 Sep;3(5):483-95 - PubMed
    1. Mol Cell Biol. 1982 Mar;2(3):308-19 - PubMed

Publication types

Substances