Targeted diversification in the S. cerevisiae genome with CRISPR-guided DNA polymerase I.

ACS synthetic biology(2020)

Cited 28|Views19
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Abstract
New technologies to target nucleotide diversification are promising enabling strategies to perform directed evolution for engineering applications and forward genetics for addressing biological questions. Recently, we reported EvolvR - a system that employs CRISPR-guided Cas9 nickases fused to nick-translating, error-prone DNA polymerases to diversify targeted genomic loci - in . As CRISPR-Cas9 has shown activity across diverse cell types, EvolvR has the potential to be ported into other organisms, including eukaryotes, if nick-translating polymerases can be active across species. Here, we implement and characterize EvolvR's function in , representing a key first step to enable EvolvR-mediated mutagenesis in eukaryotes. This advance will be useful for mutagenesis of user-defined loci in the yeast chromosomes for both engineering and basic research applications, and it furthermore provides a platform to develop the EvolvR technology for performance in higher eukaryotes.
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Key words
CRISPI,mutagenesis,yeast,directed evolution,forward genetics,EvolvR
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