In recent years, both homing endonucleases (HEases) and zinc-finger nucleases (ZFNs) have been engineered and selected for the targeting of desired human loci for gene therapy. However, enzyme engineering is lengthy and expensive and the off-target effect of the manufactured endonucleases is difficult to predict. Moreover, enzymes selected to cleave a human DNA locus may not cleave the homologous locus in the genome of animal models because of sequence divergence, thus hampering attempts to assess the in vivo efficacy and safety of any engineered enzyme priorto its application in human trials. Here, we show that naturally occurring HEases can be found, that cleave desirable human targets. Some of these enzymes are also shown to cleave the homologous sequence in the genome of animal models. In addition, the distribution of off-target effects may be more predictable for native HEases. Based on our experimental observations, we present the HomeBase algorithm, database and web server that allow a high-throughput computational search and assignment of HEases for the targeting of specific loci in the human and other genomes. We validate experimentally the predicted target specificity of candidate fungal, bacterial and archaeal HEases using cell free, yeast and archaeal assays.
Bibliographical noteFunding Information:
The Israel Science Foundation (to M.K.); the German-Israeli Science Fund (to M.K.); the Israel Cancer Research Fund (to M.K.); the Israel Science Foundation (to T.P.); the National Evolutionary Synthesis Center (NESCent) National Science Foundation #EF-0905606t (to T.P.); the Binational Science Foundation (to U.G.); the McDonnell Research Foundation (to U.G.); fellowship of the Edmond J. Safra Bioinformatics Program (to E.P.); fellowship of the Converging Technologies Program of the Israeli Council for Higher Education (to D.B.). Funding for open access charge: the Israel Cancer Research Fund.
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