bioRxivSynthetic BiologyPreprint
CRISPR-Cas9-assisted genome editing in E. coli elevates the frequency of unintended mutations
Karl A. WidneyiD, Dongdong YangiD, Leo M. RuschiD, Shelley D. CopleyiD
Abstract
Cas-assisted lambda Red recombineering techniques have rapidly become a mainstay of bacterial genome editing. Such techniques have been used to construct both individual mutants and massive libraries to assess the effects of genomic changes. We have found that a commonly used Cas9-assisted editing method results in unintended mutations elsewhere in the genome in 26% of edited clones. The unintended mutations are frequently found over 200 kb from the intended edit site and even over 10 kb from potential off-target sites. We attribute the high frequency of unintended mutations to error-prone polymerases expressed in response to dsDNA breaks introduced at the edit site. Most unintended mutations occur in regulatory or coding regions and thus may have phenotypic effects. Our findings highlight the risks associated with genome editing techniques involving dsDNA breaks in E. coli and likely other bacteria and emphasize the importance of sequencing the genomes of edited cells to ensure the absence of unintended mutations. GRAPHICAL ABSTRACT O_FIG O_LINKSMALLFIG WIDTH=200 HEIGHT=61 SRC="FIGDIR/small/584922v1_ufig1.gif" ALT="Figure 1"> View larger version (15K): org.highwire.dtl.DTLVardef@476263org.highwire.dtl.DTLVardef@8c891eorg.highwire.dtl.DTLVardef@7e32b4org.highwire.dtl.DTLVardef@132d3fc_HPS_FORMAT_FIGEXP M_FIG C_FIG
- organism: E. coli
- assay: whole-genome sequencing
- research focus: variant calling
- research focus: variant effect prediction
- approach: experimental assay
- Citations
- 1
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