Genome Biology (May 2017)

Optimizing complex phenotypes through model-guided multiplex genome engineering

  • Gleb Kuznetsov,
  • Daniel B. Goodman,
  • Gabriel T. Filsinger,
  • Matthieu Landon,
  • Nadin Rohland,
  • John Aach,
  • Marc J. Lajoie,
  • George M. Church

DOI
https://doi.org/10.1186/s13059-017-1217-z
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 12

Abstract

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Abstract We present a method for identifying genomic modifications that optimize a complex phenotype through multiplex genome engineering and predictive modeling. We apply our method to identify six single nucleotide mutations that recover 59% of the fitness defect exhibited by the 63-codon E. coli strain C321.∆A. By introducing targeted combinations of changes in multiplex we generate rich genotypic and phenotypic diversity and characterize clones using whole-genome sequencing and doubling time measurements. Regularized multivariate linear regression accurately quantifies individual allelic effects and overcomes bias from hitchhiking mutations and context-dependence of genome editing efficiency that would confound other strategies.

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