Matsuyama Akihisa, Shirai Atsuko, Yashiroda Yoko, Kamata Ayako, Horinouchi Sueharu, Yoshida Minoru
Chemical Genetics Laboratory, RIKEN, Saitama 351-0198, Japan.
Yeast. 2004 Nov;21(15):1289-305. doi: 10.1002/yea.1181.
A novel series of plasmid vectors named pDUAL have been developed. These vectors enable one to introduce not only multicopies of genes with episomal maintenance but also a single copy with chromosomal integration into the fission yeast, Schizosaccharomyces pombe. The multicopy plasmids can be easily converted to fragments for chromosomal integration by digestion of the plasmids with a certain restriction endonuclease before transformation of the yeast cells. The resultant fragments, lacking the autonomously replicating sequence, are designed for targeting into the chromosomal leu1 locus by homologous recombination. Whether the transformants are the results of episomal maintenance of the plasmid or homologous gene targeting can be readily checked by their requirement for uracil or leucine, or by the PCR diagnostic analysis. Furthermore, we propose the use of pDUAL derivatives for PCR-based chromosomal tagging of a gene to introduce several tags into 5'-terminus of a gene, employing a set of primers. Using these all-in-one vectors, a suitable mode of expression of a cloned gene can be selected for individual analysis without any complicated subcloning processes.
已开发出一系列名为pDUAL的新型质粒载体。这些载体不仅能使携带附加型维持的多个基因拷贝导入裂殖酵母粟酒裂殖酵母,还能使携带单个基因拷贝并整合到染色体中的基因导入该酵母。多拷贝质粒在转化酵母细胞之前,通过用特定限制性内切酶消化质粒,可轻松转化为用于染色体整合的片段。所得片段缺乏自主复制序列,设计用于通过同源重组靶向染色体亮氨酸1位点。转化体是质粒附加型维持的结果还是同源基因靶向的结果,可以通过它们对尿嘧啶或亮氨酸的需求,或通过PCR诊断分析轻松检查。此外,我们建议使用pDUAL衍生物对基因进行基于PCR的染色体标记,利用一组引物将多个标签引入基因的5'端。使用这些一体化载体,可以选择合适的克隆基因表达模式进行个体分析,而无需任何复杂的亚克隆过程。