Hirashima Kyotaro, Iwaki Tomoko, Takegawa Kaoru, Giga-Hama Yuko, Tohda Hideki
ASPEX Division, Asahi Glass Co., Ltd Hazawa-cho, Yokohama, Kanagawa 221-8755, Japan.
Nucleic Acids Res. 2006 Jan 24;34(2):e11. doi: 10.1093/nar/gnj011.
The technologies for chromosome modification developed to date are not satisfactorily universal, owing to the typical requirements for special enzymes and sequences. In the present report, we propose a new approach for chromosome modification in Schizosaccharomyces pombe that does not involve any special enzymes or sequences. This method, designated the 'Latour system', has wide applicability with extremely high efficiency, although both the basic principle and the operation are very simple. We demonstrate the ability of the Latour system to discriminate essential genes, with a long chromosomal area of 100 kb containing 33 genes deleted simultaneously and efficiently. Since no foreign sequences are retained after deletion using the Latour system, this system can be repeatedly applied at other sites. Provided that a negative selectable marker is available, the Latour system relies solely upon homologous recombination, which is highly conserved in living organisms. For this reason, it is expected that the system will be applicable to various yeasts.
由于对特殊酶和序列的典型要求,迄今为止开发的染色体修饰技术并不具有令人满意的通用性。在本报告中,我们提出了一种用于粟酒裂殖酵母染色体修饰的新方法,该方法不涉及任何特殊酶或序列。这种方法被称为“拉图尔系统”,尽管其基本原理和操作都非常简单,但具有广泛的适用性和极高的效率。我们证明了拉图尔系统能够区分必需基因,可同时高效删除长达100 kb的染色体区域中的33个基因。由于使用拉图尔系统删除后不会保留任何外源序列,该系统可在其他位点重复应用。只要有负选择标记,拉图尔系统仅依赖同源重组,而同源重组在生物体中高度保守。因此,预计该系统将适用于各种酵母。