The Cre/lox system was used to obtain targeted integration of an Agrobacterium T-DNA at a lox site in the genome of Arabidopsis thaliana. Site-specific recombinants, and not random events, were preferentially selected by activation of a silent lox-neomycin phosphotransferase (nptII) target gene. To analyse the effectiveness of Agrobacterium-mediated transfer we used T-DNA Vectors harbouring a single lex sequence (this vector had to circularize at the T-DNA left- and right-border sequences prior to site-specific integration) or two lex sequences (this vector allowed circularization at the lex sequences within the T-DNA either prior to or after random integration, followed by targeting of the circularized vector), respectively. Furthermore, to control the reversibility of the integration reaction, Cre recombinase was provided transiently by using a cotransformation approach. One precise stable integrant was found amongst the recombinant calli obtained after transformation with a double-lex T-DNA vector. The results indicate that Agrobacterium-mediated transformation can be used as a tool to obtain site-specific integration.
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Department of Biology, New York University, New York, NY 10003
Department of Molecular Biology, Princeton University, PrincetonDepartment of Biology, New York University, New York, NY 10003
Oberstein A.
Pare A.
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Department of Biology, New York University, New York, NY 10003Department of Biology, New York University, New York, NY 10003
Pare A.
Kaplan L.
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Department of Biology, New York University, New York, NY 10003Department of Biology, New York University, New York, NY 10003
Kaplan L.
Small S.
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Department of Biology, New York University, New York, NY 10003Department of Biology, New York University, New York, NY 10003
机构:Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA
Trinh, KR
Morrison, SL
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Univ Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USAUniv Calif Los Angeles, Dept Microbiol & Mol Genet, Los Angeles, CA 90095 USA