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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

Yunfu Lin and Alan S. Waldman*

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 {phi}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 {phi}X174 DNA. Microhomology existed at most junctions between {phi}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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