酿酒酵母逆转录介导CRISPR-Cas9基因组编辑的改进载体

IF 2.2 3区 生物学 Q3 GENETICS & HEREDITY
Tara N Stuecker, Stephanie E Hood, Julio Molina Pineda, Sonali Lenaduwe, Joshua Winter, Meru J Sadhu, Jeffrey A Lewis
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引用次数: 0

摘要

体内位点定向诱变是一种强大的遗传工具,用于测试特定等位基因在其正常基因组环境中的作用。虽然出芽酵母酿酒酵母(Saccharomyces cerevisiae)拥有定点诱变的经典工具,但最近更有效的基于crispr的方法使用Cas“切割”与引入所需编辑的“修复”模板的同源重组相结合。然而,目前的方法仅限于完全原生营养酵母菌株,并且依赖于相对低效率的短grna克隆。因此,我们通过将gRNA及其同源修复模板顺式结合在单个寡核苷酸上来简化这一过程。此外,我们希望利用一种新的方法,即使用大肠杆菌逆转录酶(EcRT)在体内将修复模板扩增为多拷贝单链DNA,这是更有效的同源重组模板。为此,我们创建了一组表达Cas9-EcRT的质粒,允许在一个步骤中与grna -修复模板质粒共转化。我们的质粒套件包含不同的抗生素(Nat, Hyg, Kan)或营养不良(HIS3, URA3)选择标记,允许编辑完全原生营养的野生酵母菌株。除了经典的半乳糖诱导外,我们还生成了每个质粒的β-雌二醇诱导版本,以促进在半乳糖生长不良的酵母菌株中进行编辑。基于质粒的系统在最少的步骤和时间内,对点突变的编辑效率达到了95%,对无标记缺失的编辑效率达到了50%。我们为如何使用这个系统提供了详细的分步指南。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Improved vectors for retron-mediated CRISPR-Cas9 genome editing in Saccharomyces cerevisiae.

In vivo site-directed mutagenesis is a powerful genetic tool for testing the effects of specific alleles in their normal genomic context. While the budding yeast Saccharomyces cerevisiae possesses classical tools for site-directed mutagenesis, more efficient recent CRISPR-based approaches use Cas "cutting" combined with homologous recombination of a "repair" template that introduces the desired edit. However, current approaches are limited for fully prototrophic yeast strains and rely on relatively low-efficiency cloning of short gRNAs. We were thus motivated to simplify the process by combining the gRNA and its cognate repair template in cis on a single oligonucleotide. Moreover, we wished to take advantage of a new approach that uses an Escherichia coli retron (EcRT) to amplify repair templates as multi-copy single-stranded (ms)DNA in vivo, which are more efficient templates for homologous recombination. To this end, we have created a set of plasmids that express Cas9-EcRT, allowing for co-transformation with the gRNA-repair template plasmid in a single step. Our suite of plasmids contains different antibiotic (Nat, Hyg, Kan) or auxotrophic (HIS3, URA3) selectable markers, allowing for editing of fully prototrophic wild yeast strains. In addition to classic galactose induction, we generated a β-estradiol-inducible version of each plasmid to facilitate editing in yeast strains that grow poorly on galactose. The plasmid-based system results in >95% editing efficiencies for point mutations and >50% efficiencies for markerless deletions, in a minimum number of steps and time. We provide a detailed step-by-step guide on how to use this system.

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来源期刊
G3: Genes|Genomes|Genetics
G3: Genes|Genomes|Genetics GENETICS & HEREDITY-
CiteScore
5.10
自引率
3.80%
发文量
305
审稿时长
3-8 weeks
期刊介绍: G3: Genes, Genomes, Genetics provides a forum for the publication of high‐quality foundational research, particularly research that generates useful genetic and genomic information such as genome maps, single gene studies, genome‐wide association and QTL studies, as well as genome reports, mutant screens, and advances in methods and technology. The Editorial Board of G3 believes that rapid dissemination of these data is the necessary foundation for analysis that leads to mechanistic insights. G3, published by the Genetics Society of America, meets the critical and growing need of the genetics community for rapid review and publication of important results in all areas of genetics. G3 offers the opportunity to publish the puzzling finding or to present unpublished results that may not have been submitted for review and publication due to a perceived lack of a potential high-impact finding. G3 has earned the DOAJ Seal, which is a mark of certification for open access journals, awarded by DOAJ to journals that achieve a high level of openness, adhere to Best Practice and high publishing standards.
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