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Widney, K. A.

Publications and source records attributed to Widney, K. A..

2 recordsLinked to original sources

A cheater founds the winning lineages during evolution of a novel metabolic pathway

Underground metabolic pathways--leaks in the metabolic network caused by promiscuous enzyme activities and non-enzymatic transformations--can provide the starting point for emergence of novel protopathways if a mutation or environmental change increases flux to a physiologically significant level. This early stage in the evolution of metabolic pathways is typically hidden from our view. We have evolved a novel protopathway in {Delta}pdxB E. coli, which lacks an enzyme required for synthesis of the essential cofactor pyridoxal 5'-phosphate (PLP). This protopathway is comprised of four steps catalyzed by promiscuous enzymes that are still serving their native functions. Complex population dynamics occurred during the evolution experiment. The dominant strain after 150 population doublings, JK1, had acquired four mutations. We constructed every intermediate between the {Delta}pdxB strain and JK1 and identified the order in which mutations arose in JK1 and the physiological effect of each. Three of the mutations together increased the PLP accumulation rate by 32-fold. The second mutation created a cheater that was less fit on its own but thrived in the population by scavenging nutrients released from the fragile parental cells. Notably, the dominant lineages at the end of the experiment all derived from this cheater strain.

evolutionary biology↗

CRISPR-Cas9-assisted genome editing in E. coli elevates the frequency of unintended mutations

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

synthetic biology↗