Altered recombinases for genome modification
View Patent ↗The present invention describes methods of identifying altered recombinases and compositions thereof, wherein at least one amino acid is different from a parent, wild-type recombinase and the altered recombinase has improved recombination efficiency towards wild-type and/or pseudo att site sequences relative to the parent, wild-type recombinase. The present invention also includes methods of modifying the genomes of cells using the altered recombinases, including methods of site-specifically integrating a polynucleotide sequence of interest in a genome of a eucaryotic cell.
1. A nucleic acid encoding an altered unidirectional site-specific bacteriophage integrase chosen from the group consisting of SEQ ID NO:22, SEQ ID NO:23, and SEQ ID NO:24, that has integrase activity,
wherein said altered unidirectional site-specific bacteriophage integrase has improved recombination efficiency towards wild-type or pseudo attachment sites as compared to a corresponding wild-type unidirectional site-specific bacteriophage integrase.
2. The nucleic acid according to claim 1 , wherein said nucleic acid is isolated.
3. An expression cassette, comprising:
(a) a transcriptional initiation region functional in an expression host;
(b) a nucleic acid encoding an altered unidirectional site-specific bacteriophage integrase chosen from the group consisting of SEQ ID NO:22, SEQ ID NO:23, and SEQ ID NO:24, that has integrase activity, wherein said altered unidirectional site-specific bacteriophage integrase has improved recombination efficiency towards wild-type or pseudo attachment sites as compared to a corresponding wild-type unidirectional site-specific bacteriophage integrase, and
(c) a transcriptional termination region functional in said expression host.
4. A kit comprising: a nucleic acid encoding an altered unidirectional site-specific bacteriophage integrase chosen from the group consisting of SEQ ID NO:22, SEQ ID NO:23, and SEQ ID NO:24, that has integrase activity,
wherein said altered unidirectional site-specific bacteriophage integrase has improved recombination efficiency towards wild-type or pseudo attachment sites as compared to a corresponding wild-type unidirectional site-specific bacteriophage integrase, and instructions for using said nucleic acid.