A CRISPR-Cas assisted shotgun mutagenesis method for evolutionary genome engineering
M. Zhao, M. Gao, L. Xiong, Y. Liu, X. Tao, B. Gao, M. Liu, F.-Q. Wang, D.-Z. Wei
Abstract
Genome mutagenesis drives the evolution of organisms. Here, we developed a CRISPR-Cas assisted random mutation (CARM) technology for whole genome mutagenesis. The method leverages an entirely random gRNA library and SpCas9-NG to randomly damage genomes in a controllable shotgun-like manner that then triggers diverse and abundant mutations via low-fidelity repair. As a proof-of-principle, CARM was applied to evolve the capacity of Saccharomyces cerevisiae BY4741 to produce {beta}-carotene. After seven rounds of iterative evolution over two months, a {beta}-carotene hyper-producing strain, C7-143, was isolated with a 10.5-fold increase in {beta}-carotene production and 857 diverse genomic mutants that comprised indels, duplications, inversions, and chromosomal rearrangements. Transcriptomic analysis revealed that the expression of 2,541 genes of strain C7-143 were significantly altered, suggesting that the metabolic landscape of the strain was deeply reconstructed. In addition, CARM was applied to evolve the industrially relevant Saccharomyces cerevisiae CEN.PK2-1C, the S-adenosyl-L-methionine production of which was increased to 2.28 times after just one round. Thus, CARM is a user-friendly and practical strategy for genetic remodeling and reverse engineering to investigate complicated organismal metabolism.
02 /Specification & Classification
Click any tag to browse matching papers- Organism
- Research Focus
- Approach
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- A synthetic RNA-mediated evolution system in yeast
E. D. Jensen, M. Laloux, … J. D. Keasling·bioRxiv·Feb 27, 2021
- Selection of chromosomal DNA libraries using a multiplex CRISPR system in Saccharomyces cerevisiae
Owen W Ryan, Jeffrey M Skerker, … Jamie Cate·eLifePeer-reviewed·Aug 19, 2014
- Improved vectors for retron-mediated CRISPR-Cas9 genome editing in Saccharomyces cerevisiae
Tara N. Stuecker, Stephanie E. Hood, … Jeffrey A. Lewis·G3 Genes Genomes GeneticsPeer-reviewed·Aug 4, 2025
- CRISPR/Cas9-mediated editing of the ADE2 locus in Saccharomyces cerevisiae: targeted mutagenesis and homology-directed repair
Essa Jarra·bioRxiv·Mar 30, 2025
- Experimental Test of Evolutionary Safety of a CRISPR-Cas9 Gene-Drive Element
Michael S. Overton, Sean E. Guy, … Sergey Kryazhimskiy·G3 Genes Genomes GeneticsPeer-reviewed·Feb 18, 2026
- Rapid CRISPR-Cas9 Genome Editing in S. cerevisiae
Hosein Rostamian, Ethan W. Madden, … Brian D. Strahl·bioRxiv·Mar 30, 2026