| Literature DB >> 9729329 |
W F Morgan1, J Corcoran, A Hartmann, M I Kaplan, C L Limoli, B Ponnaiya.
Abstract
DNA double-strand breaks can lead to chromosomal rearrangements at the first mitosis after exposure to the DNA strand-breaking agent. The evidence suggests a number of different pathways for DNA double-strand break rejoining in mammalian cells, but it is unclear what factors determine the fate of the induced break and whether or not it will lead to chromosomal rearrangement. If a cell does survive and proliferate after DNA cleavage, delayed chromosomal instability can be observed in the clonal descendants of the exposed cell. Most, but not all DNA double-strand breaking agents are effective at inducing this delayed chromosomal instability. In this paper, we review the evidence for the role of the DNA double-strand break in directly induced and delayed chromosomal rearrangements. Copyright 1998 Elsevier Science B.V.Entities:
Keywords: Non-programmatic
Mesh:
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Year: 1998 PMID: 9729329 DOI: 10.1016/s0027-5107(98)00104-3
Source DB: PubMed Journal: Mutat Res ISSN: 0027-5107 Impact factor: 2.433