Inhibition of Non-Homologous End Joining and integration of DNA upon transformation of Rhizopus oryzae |
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Authors: | Christopher?D.?SkoryEmail author |
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Affiliation: | (1) Bioproducts and Biocatalysis Research Unit, USDA, Agricultural Research Service, National Center for Agricultural Utilization Research, 1815 N. University Street, Peoria, IL 61604, USA |
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Abstract: | Site-directed integration of DNA in the fungus Rhizopus has long been problematic because linearized plasmids used for transformation tend to replicate in high-molecular-weight
concatenated structures, and rarely integrate into the chromosome. This work examines the methods that might interfere with
the multimerization process, select against plasmids that had recircularized, and encourage strand invasion, hopefully leading
to plasmid integration. In vitro methods were used to determine if the structure of the double-strand break had any effect
on the ability to rejoin plasmid ends. In cell-free extracts, little difference in end-joining activity was found between
linearized plasmids with 5′ overhangs, 3′ overhangs, or blunt ends. In addition, dephosphorylation of ends had no effect.
Transformation of plasmids prepared in the same ways confirmed that they were easily religated in vivo, with almost all prototrophic
isolates retaining autonomously replicated plasmids. It was possible to block religation by modifying the free ends of the
linearized plasmids using oligonucleotide adapters which were blocked at the 3′-OH position and contained phosphorothioate
nucleotides to make them nuclease-resistant. However, gene replacement, with repair of the auxotrophic mutation in the host
chromosome, was the predominant event observed upon the transformation of these plasmids. The highest rates of integration
were obtained with a plasmid containing a truncated, non-functional pyrG gene. Autonomous replication of this plasmid did not support prototrophic growth, but homologous recombination into the chromosome
restored the function of the endogenous pyrG gene. All of the transformants obtained with this selective construct were found to have integrated the plasmid, with multicopy
insertion being common.
Names are necessary to report factually on available data; however, the USDA neither guarantees nor warrants the standard
of the product, and the use of the name by USDA implies no approval of the product to the exclusion of others that may also
be suitable. |
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Keywords: | Rhizopus Transformation Gene replacement Integration |
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