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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 mgr 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 mgr 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 mgr 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 mgr 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
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