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Whole Genome Sequencing Analysis of Effects of CRISPR/Cas9 in : A Budding Yeast in Distress

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Journal J Fungi (Basel)
Date 2022 Oct 27
PMID 36294556
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Abstract

The industrially important non-conventional yeast suffers from low rates of homologous recombination, making site specific genetic engineering tedious. Therefore, genome editing using CRISPR/Cas represents a simple and efficient alternative. To characterize on- and off-target mutations caused by CRISPR/Cas9 followed by non-homologous end joining repair, we chose a diverse set of CRISPR/Cas targets and conducted whole genome sequencing on 146 CRISPR/Cas9 engineered single colonies. We compared the outcomes of single target CRISPR transformations to double target experiments. Furthermore, we examined the extent of possible large deletions by targeting a large genomic region, which is likely to be non-essential. The analysis of on-target mutations showed an unexpectedly high number of large deletions and chromosomal rearrangements at the CRISPR target loci. We also observed an increase of on-target structural variants in double target experiments as compared to single target experiments. Targeting of two loci within a putatively non-essential region led to a truncation of chromosome 3 at the target locus in multiple cases, causing the deletion of 20 genes and several ribosomal DNA repeats. The identified off-target mutations were rare and randomly distributed, with no apparent connection to unspecific CRISPR/Cas9 off-target binding sites.

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References
1.
Thomas M, Burgio G, Adams D, Iyer V . Collateral damage and CRISPR genome editing. PLoS Genet. 2019; 15(3):e1007994. PMC: 6417652. DOI: 10.1371/journal.pgen.1007994. View

2.
Vogl T, Kickenweiz T, Pitzer J, Sturmberger L, Weninger A, Biggs B . Engineered bidirectional promoters enable rapid multi-gene co-expression optimization. Nat Commun. 2018; 9(1):3589. PMC: 6123417. DOI: 10.1038/s41467-018-05915-w. View

3.
Cleves A, Cooper D, Barondes S, Kelly R . A new pathway for protein export in Saccharomyces cerevisiae. J Cell Biol. 1996; 133(5):1017-26. PMC: 2120850. DOI: 10.1083/jcb.133.5.1017. View

4.
Seol J, Shim E, Lee S . Microhomology-mediated end joining: Good, bad and ugly. Mutat Res. 2017; 809:81-87. PMC: 6477918. DOI: 10.1016/j.mrfmmm.2017.07.002. View

5.
Rainha J, Rodrigues J, Rodrigues L . CRISPR-Cas9: A Powerful Tool to Efficiently Engineer . Life (Basel). 2020; 11(1). PMC: 7823794. DOI: 10.3390/life11010013. View