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Nucleic Acids Research, 2000, Vol. 28, No. 17 3361-3369
© 2000 Oxford University Press

Requirements for double-strand cleavage by chimeric restriction enzymes with zinc finger DNA-recognition domains

Jeff Smith1,2, Marina Bibikova3, Frank G. Whitby3, A. R. Reddy1,4, Srinivasan Chandrasegaran1 and Dana Carroll3,*

1Department of Environmental Health Sciences, The Johns Hopkins University School of Hygiene and Public Health, 615 North Wolfe Street, Baltimore, MD 21205, USA, 2Department of Biophysics and Biophysical Chemistry, The Johns Hopkins University School of Medicine, Baltimore, MD 21205, USA, 3Department of Biochemistry, University of Utah School of Medicine, 50 North Medical Drive, Salt Lake City, UT 84132, USA and 4Department of Biological Sciences, Pondicherry University, Pondicherry 605014, India

This study concerns chimeric restriction enzymes that are hybrids between a zinc finger DNA-binding domain and the non-specific DNA-cleavage domain from the natural restriction enzyme FokI. Because of the flexibility of DNA recognition by zinc fingers, these enzymes are potential tools for cleaving DNA at arbitrarily selected sequences. Efficient double-strand cleavage by the chimeric nucleases requires two binding sites in close proximity. When cuts were mapped on the DNA strands, it was found that they occur in pairs separated by ~4 bp with a 5' overhang, as for native FokI. Furthermore, amino acid changes in the dimer interface of the cleavage domain abolished activity. These results reflect a requirement for dimerization of the cleavage domain. The dependence of cleavage efficiency on the distance between two inverted binding sites was determined and both upper and lower limits were defined. Two different zinc finger combinations binding to non-identical sites also supported specific cleavage. Molecular modeling was employed to gain insight into the precise location of the cut sites. These results define requirements for effective targets of chimeric nucleases and will guide the design of novel specificities for directed DNA cleavage in vitro and in vivo.

* To whom correspondence should be addressed. Tel: +1 801 581 5977; Fax: +1 801 581 7959; Email: carroll@medschool.med.utah.edu The authors wish it to be known that, in their opinion, the first two authors should be regarded as joint First Authors


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