Xie Ze-Xiong, Mitchell Leslie A, Liu Hui-Min, Li Bing-Zhi, Liu Duo, Agmon Neta, Wu Yi, Li Xia, Zhou Xiao, Li Bo, Xiao Wen-Hai, Ding Ming-Zhu, Wang Ying, Yuan Ying-Jin, Boeke Jef D
Key Laboratory of Systems Bioengineering (Ministry of Education), School of Chemical Engineering and Technology, Tianjin University, 300072, China.
SynBio Research Platform, Collaborative Innovation Center of Chemical Science and Engineering (Tianjin), Tianjin University, 300072, China.
G3 (Bethesda). 2018 Jan 4;8(1):173-183. doi: 10.1534/g3.117.300347.
Rapid and highly efficient mating-type switching of enables a wide variety of genetic manipulations, such as the construction of strains, for instance, isogenic haploid pairs of both mating-types, diploids and polyploids. We used the CRISPR/Cas9 system to generate a double-strand break at the locus and, in a single cotransformation, both haploid and diploid cells were switched to the specified mating-type at ∼80% efficiency. The mating-type of strains carrying either rod or ring chromosome III were switched, including those lacking α and cryptic mating loci. Furthermore, we transplanted the synthetic yeast chromosome V to build a haploid polysynthetic chromosome strain by using this method together with an endoreduplication intercross strategy. The CRISPR/Cas9 mating-type switching method will be useful in building the complete synthetic yeast (Sc2.0) genome. Importantly, it is a generally useful method to build polyploids of a defined genotype and generally expedites strain construction, for example, in the construction of fully /α/α isogenic tetraploids.
快速且高效的交配型转换能够实现多种基因操作,例如构建菌株,如两种交配型的同基因单倍体对、二倍体和多倍体。我们使用CRISPR/Cas9系统在该位点产生双链断裂,并且在一次共转化中,单倍体和二倍体细胞都以约80%的效率转换为指定的交配型。携带棒状或环状III号染色体的菌株的交配型被转换,包括那些缺乏α和隐性交配位点的菌株。此外,我们通过将这种方法与核内复制互交策略相结合,移植了合成酵母V号染色体以构建单倍体多合成染色体菌株。CRISPR/Cas9交配型转换方法将有助于构建完整的合成酵母(Sc2.0)基因组。重要的是,这是构建特定基因型多倍体的一种普遍有用的方法,并且通常会加快菌株构建速度,例如在构建完全同基因的α/α/α/α四倍体时。