Solis-Escalante Daniel, van den Broek Marcel, Kuijpers Niels G A, Pronk Jack T, Boles Eckhard, Daran Jean-Marc, Daran-Lapujade Pascale
Department of Biotechnology, Delft University of Technology Julianalaan 67, 2628 BC Delft, The Netherlands.
Department of Biotechnology, Delft University of Technology Julianalaan 67, 2628 BC Delft, The Netherlands Platform Green Synthetic Biology, Julianalaan 67, 2628 BC Delft, The Netherlands.
FEMS Yeast Res. 2015 Mar;15(2). doi: 10.1093/femsyr/fou004.
Saccharomyces cerevisiae harbours a large group of tightly controlled hexose transporters with different characteristics. Construction and characterization of S. cerevisiae EBY.VW4000, a strain devoid of glucose import, was a milestone in hexose-transporter research. This strain has become a widely used platform for discovery and characterization of transporters from a wide range of organisms. To abolish glucose uptake, 21 genes were knocked out, involving 16 successive deletion rounds with the LoxP/Cre system. Although such intensive modifications are known to increase the risk of genome alterations, the genome of EBY.VW4000 has hitherto not been characterized. Based on a combination of whole genome sequencing, karyotyping and molecular confirmation, the present study reveals that construction of EBY.VW4000 resulted in gene losses and chromosomal rearrangements. Recombinations between the LoxP scars have led to the assembly of four neo-chromosomes, truncation of two chromosomes and loss of two subtelomeric regions. Furthermore, sporulation and spore germination are severely impaired in EBY.VW4000. Karyotyping of the EBY.VW4000 lineage retraced its current chromosomal architecture to four translocations events occurred between the 6th and the 12th rounds of deletion. The presented data facilitate further studies on EBY.VW4000 and highlight the risks of genome alterations associated with repeated use of the LoxP/Cre system.
酿酒酵母含有一大组受到严格调控且具有不同特性的己糖转运蛋白。酿酒酵母EBY.VW4000是一种缺乏葡萄糖摄取能力的菌株,其构建和特性研究是己糖转运蛋白研究中的一个里程碑。该菌株已成为一个广泛用于发现和表征来自多种生物体的转运蛋白的平台。为了消除葡萄糖摄取,敲除了21个基因,涉及使用LoxP/Cre系统进行16轮连续缺失。尽管已知这种密集修饰会增加基因组改变的风险,但迄今为止尚未对EBY.VW4000的基因组进行表征。基于全基因组测序、核型分析和分子确认相结合的方法,本研究揭示EBY.VW4000的构建导致了基因丢失和染色体重排。LoxP疤痕之间的重组导致了四条新染色体的组装、两条染色体的截短以及两个亚端粒区域的丢失。此外,EBY.VW4000的孢子形成和孢子萌发严重受损。对EBY.VW4000谱系的核型分析将其当前的染色体结构追溯到在第6轮和第12轮缺失之间发生的四次易位事件。所呈现的数据有助于对EBY.VW4000进行进一步研究,并突出了与重复使用LoxP/Cre系统相关的基因组改变风险。