Center for Synthetic Biology Engineering Research, Shenzhen Institutes of Advanced Technology, Chinese Academy of Sciences, Shenzhen, 518055, China.
Key Laboratory of Industrial Biocatalysis (Ministry of Education) and Center for Synthetic and Systems Biology, School of Life Sciences, Tsinghua University, Beijing, 100084, China.
Nat Commun. 2018 May 22;9(1):1930. doi: 10.1038/s41467-017-00806-y.
SCRaMbLE is a novel system implemented in the synthetic yeast genome, enabling massive chromosome rearrangements to produce strains with a large genotypic diversity upon induction. Here we describe a reporter of SCRaMbLEd cells using efficient selection, termed ReSCuES, based on a loxP-mediated switch of two auxotrophic markers. We show that all randomly isolated clones contained rearrangements within the synthetic chromosome, demonstrating high efficiency of selection. Using ReSCuES, we illustrate the ability of SCRaMbLE to generate strains with increased tolerance to several stress factors, such as ethanol, heat and acetic acid. Furthermore, by analyzing the tolerant strains, we are able to identify ACE2, a transcription factor required for septum destruction after cytokinesis, as a negative regulator of ethanol tolerance. Collectively, this work not only establishes a generic platform to rapidly identify strains of interest by SCRaMbLE, but also provides methods to dissect the underlying mechanisms of resistance.
SCRaMbLE 是一种在合成酵母基因组中实现的新型系统,能够在诱导时通过大规模染色体重排产生具有大量基因型多样性的菌株。在这里,我们描述了一种使用高效选择的 SCRaMbLEd 细胞报告器,称为 ReSCuES,它基于两个营养缺陷型标记物的loxP 介导开关。我们表明,所有随机分离的克隆都在合成染色体内发生了重排,证明了选择的高效率。使用 ReSCuES,我们说明了 SCRaMbLE 能够产生对几种应激因素(如乙醇、热和乙酸)具有更高耐受性的菌株的能力。此外,通过分析耐受菌株,我们能够鉴定出 ACE2,即细胞分裂后隔膜破坏所必需的转录因子,作为乙醇耐受性的负调节剂。总的来说,这项工作不仅建立了一个通用平台,通过 SCRaMbLE 快速鉴定感兴趣的菌株,而且还提供了剖析抗性潜在机制的方法。