The cloning of large chromosomal fragments is required for the physical mapping and sequencing of large genomes, particularly those of various mammals including humans. Systems developed in yeast that are based on artificial chromosome vectors (YACs) have provided the means for isolating the requisite large DNAs. It is essential for the accurate chracterization and manipulation of genomic material that the DNA within YACs be accurate, that there not be cloning artifacts and that the YACs be stable within yeast. However, two major categories of errors have been shown to arise during the development and the maintenance of human YAC libraries. It is estimated that 10 to 60% of clones in existing libraries represent co-cloned DNA sequences. A second category of errors resulting from internal rearrangements and deletions in YACs also limits the utility of YAC systems. Many deletions in YACs containing human DNA could arise during transformation by recombination between repeated DNAs that may be diverged. We are examining the contribution of yeast transformation to YAC rearrangements. We have shown that mitotically stable YACs can exhibit frequent internal deletions upon retransformation. Our observations with YACs are comparable to results with plasmids containing homologous and diverged repeat DNAs. Recombination during transformation of covalently closed circular plasmids was over 50-fold more frequent than during mitotic growth. When present in the repeats, unique single-strand breaks that are ligatable lead to a high level of recombination between diverged and identical repeats. Based on the results with model plasmids, we propose that internal deletions in YACs observed in retransformation experiments are due to recombination induced by nicks in the YAC DNA. While it remains to be determined, recombination could occur between Alu's. A high level of transformation-associated deletions in the human YACs as well as in plasmids was reduced when the host was a recombination-deficient strain deleted for the RAD52 gene.

Agency
National Institute of Health (NIH)
Institute
National Institute of Environmental Health Sciences (NIEHS)
Type
Intramural Research (Z01)
Project #
1Z01ES065072-04
Application #
3755484
Study Section
Project Start
Project End
Budget Start
Budget End
Support Year
4
Fiscal Year
1994
Total Cost
Indirect Cost
City
State
Country
United States
Zip Code
Storici, Francesca; Bebenek, Katarzyna; Kunkel, Thomas A et al. (2007) RNA-templated DNA repair. Nature 447:338-41
Storici, Francesca; Resnick, Michael A (2006) The delitto perfetto approach to in vivo site-directed mutagenesis and chromosome rearrangements with synthetic oligonucleotides in yeast. Methods Enzymol 409:329-45
Storici, Francesca; Snipe, Joyce R; Chan, Godwin K et al. (2006) Conservative repair of a chromosomal double-strand break by single-strand DNA through two steps of annealing. Mol Cell Biol 26:7645-57
Storici, Francesca; Resnick, Michael A (2003) Delitto perfetto targeted mutagenesis in yeast with oligonucleotides. Genet Eng (N Y) 25:189-207
Storici, Francesca; Durham, Christopher L; Gordenin, Dmitry A et al. (2003) Chromosomal site-specific double-strand breaks are efficiently targeted for repair by oligonucleotides in yeast. Proc Natl Acad Sci U S A 100:14994-9
Storici, F; Lewis, L K; Resnick, M A (2001) In vivo site-directed mutagenesis using oligonucleotides. Nat Biotechnol 19:773-6
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