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

清脆的 生物 Cas9 遗传学 基因组编辑 基因座(遗传学) 基因组 计算生物学 引导RNA 同源重组 基因 CRISPR干扰
作者
Veronika Schusterbauer,Jasmin E. Fischer,Sarah Gangl,Lisa Schenzle,Claudia Rinnofner,Martina Geier,Christian Sailer,Anton Glieder,Gerhard G. Thallinger
出处
期刊:Journal of Fungi [Multidisciplinary Digital Publishing Institute]
卷期号:8 (10): 992-992 被引量:2
标识
DOI:10.3390/jof8100992
摘要

The industrially important non-conventional yeast Komagataella phaffii 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 de novo off-target mutations were rare and randomly distributed, with no apparent connection to unspecific CRISPR/Cas9 off-target binding sites.
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