High frequency FLP-independent homologous DNA recombination of 2 μ plasmid in the yeast Saccharomyces cerevisiae |
| |
Authors: | Carlo V. Bruschi Gregg A. Howe |
| |
Affiliation: | (1) Department of Microbiology and Immunology, School of Medicine, East Carolina University, 27858-4354 Greenville, NC, USA;(2) Present address: Department of Biology, University of California Los Angeles, 90024 Los Angeles, CA, USA |
| |
Abstract: | Summary The purpose of this work is to identify and quantitate in vivo 2 plasmid FLP-independent recombination in yeast, using a nonselective assay system for rapid detection of phenotypic expression of the recombination events. A tester plasmid was constructed such that in vivo recombination between 2 direct repeat sequences produces the resolution of the plasmid into two circular DNA molecules. This recombinational event is detected as a phenotypic shift from red to white colonies, due to the mitotic loss of the plasmid portion containing the yeast ADE8 gene in a recipient ade1 ade2 ade8 genetic background. In the absence of the 2 FLP recombinase and/or its target DNA sequence, recombination is not abolished but rather continues at a high frequency of about 17%. This suggests that the FLP-independent events are mediated by the chromosomally-encoded general homologous recombination system. We therefore conclude that the totality of 2 DNA recombination events occurring in FLP+ cells is the contribution of both FLP-mediated and FLP-independent events. |
| |
Keywords: | Saccharomyces cerevisiae Site specific recombination 2 /content/q6u52t2q263k275g/xxlarge956.gif" alt=" mgr" align=" MIDDLE" BORDER=" 0" > DNA plasmid |
本文献已被 SpringerLink 等数据库收录! |
|