Nucleic Acids Research, 2001, Vol. 29, No. 19 3975-3981
© 2001 Oxford University Press
Promiscuous patching of broken chromosomes in mammalian cells with extrachromosomal DNA
Department of Biological Sciences, University of South Carolina, 700 Sumter Street, Columbia, SC 29208, USA
To study double-strand break (DSB)-induced mutations in mammalian chromosomes, we stably transfected thymidine kinase (tk)-deficient mouse fibroblasts with a DNA substrate containing a recognition site for yeast endonuclease I-SceI embedded within a functional tk gene. Cells were then electroporated with a plasmid expressing endonuclease I-SceI to induce a DSB, and clones that had lost tk function were selected. In a previous study of DSB-induced tk-deficient clones, we found that
8% of recovered tk mutations involved the capture of one or more DNA fragments at the DSB site. Almost half of the DNA capture events involved the I-SceI expression plasmid, and several events involved retrotransposable elements. To learn whether only certain DNA sequences or motifs are efficiently captured, in the current work we electroporated an I-SceI expression plasmid along with HaeIII fragments of
X174 genomic DNA. We report that 18 out of 132 tk-deficient clones recovered had captured DNA fragments, and 14 DNA capture events involved one or more fragments of
X174 DNA. Microhomology existed at most junctions between
X174 DNA and genomic sequences. Our work suggests that virtually any extrachromosomal DNA molecule may be recruited for the patching of DSBs in a mammalian genome.
* To whom correspondence should be addressed. Tel: +1 803 777 8405; Fax: +1 803 777 4002; Email: awaldman{at}sc.edu
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