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Enhancing the Specificity of Recombinase-Mediated Genome Engineering through Dimer Interface Redesign
Author(s) -
Thomas Gaj,
Shan J. Sirk,
Ryan Tingle,
Andrew C. Mercer,
Mark C. Wallen,
Carlos F. Barbas
Publication year - 2014
Publication title -
journal of the american chemical society
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.115
H-Index - 612
eISSN - 1520-5126
pISSN - 0002-7863
DOI - 10.1021/ja4130059
Subject(s) - recombinase , computational biology , genome engineering , tn3 transposon , integrase , integrases , rational design , chemistry , effector , protein engineering , directed evolution , synthetic biology , cre recombinase , dna , genome , genome editing , genetics , gene , enzyme , biology , biochemistry , transposable element , transgene , recombination , genetically modified mouse , mutant
Despite recent advances in genome engineering made possible by the emergence of site-specific endonucleases, there remains a need for tools capable of specifically delivering genetic payloads into the human genome. Hybrid recombinases based on activated catalytic domains derived from the resolvase/invertase family of serine recombinases fused to Cys2-His2 zinc-finger or TAL effector DNA-binding domains are a class of reagents capable of achieving this. The utility of these enzymes, however, has been constrained by their low overall targeting specificity, largely due to the formation of side-product homodimers capable of inducing off-target modifications. Here, we combine rational design and directed evolution to re-engineer the serine recombinase dimerization interface and generate a recombinase architecture that reduces formation of these undesirable homodimers by >500-fold. We show that these enhanced recombinases demonstrate substantially improved targeting specificity in mammalian cells and achieve rates of site-specific integration similar to those previously reported for site-specific nucleases. Additionally, we show that enhanced recombinases exhibit low toxicity and promote the delivery of the human coagulation factor IX and α-galactosidase genes into endogenous genomic loci with high specificity. These results provide a general means for improving hybrid recombinase specificity by protein engineering and illustrate the potential of these enzymes for basic research and therapeutic applications.

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