Chemical Genomics Research Group, RIKEN Center for Sustainable Resource Science, 2-1, Hirosawa, Wako, Saitama, 351-0198, Japan.
Laboratory of Microbiology, Department of Biotechnology, Graduate School of Agricultural and Life Sciences, The University of Tokyo, Tokyo, 113-8657, Japan.
Sci Rep. 2023 Jun 8;13(1):9295. doi: 10.1038/s41598-023-36267-1.
The expression of heterologous genes is an important technique in yeast genetics. In fission yeast, the leu1 and ura4 genes have been used mainly as selectable markers for heterologous expression. To expand the repertoire of selection markers available for heterologous expression of genes, here we developed new host-vector systems employing lys1 and arg3. By employing genome editing with the CRISPR/Cas9 system, we isolated several alleles of lys1 and arg3, each having a critical mutation in the ORF region. In parallel, we developed a set of vectors that complement the amino acid auxotrophy of lys1 and arg3 mutants when integrated into each locus. Using these vectors in combination with the previously developed integration vector pDUAL, we successfully observed the localization of three proteins in a cell simultaneously by fusing them with different fluorescent proteins. Thus, these vectors enable combinatorial expression of heterologous genes, which addresses increasingly diverse experimental challenges.
外源基因的表达是酵母遗传学中的一项重要技术。在裂殖酵母中,leu1 和 ura4 基因主要被用作外源表达的可选择标记。为了扩大可用于基因异源表达的选择标记的范围,我们在这里开发了新的基于 lys1 和 arg3 的宿主载体系统。通过使用 CRISPR/Cas9 系统进行基因组编辑,我们分离了几个 lys1 和 arg3 的等位基因,每个等位基因在 ORF 区域都有一个关键突变。同时,我们开发了一组载体,当整合到每个基因座时,这些载体可以弥补 lys1 和 arg3 突变体的氨基酸营养缺陷。我们使用这些载体与之前开发的整合载体 pDUAL 相结合,成功地观察到三个蛋白质在一个细胞中的定位,它们通过与不同的荧光蛋白融合而被观察到。因此,这些载体可以实现异源基因的组合表达,这可以应对越来越多样化的实验挑战。