TY - JOUR
T1 - A simple and effective chromosome modification method for large-scale deletion of genome sequences and identification of essential genes in fission yeast
AU - Hirashima, Kyotaro
AU - Iwaki, Tomoko
AU - Takegawa, Kaoru
AU - Giga-Hama, Yuko
AU - Tohda, Hideki
N1 - Funding Information:
This study was carried out as part of the project ‘Development of Technological Infrastructure for Industrial Bioprocesses on R&D of New Industrial Science and Technology Frontiers’ of the Ministry of Economy, Trade & Industry (METI), and entrusted by the New Energy and Industrial Technology Development Organization (NEDO), Japan. Funding to pay the Open Access publication charges for this article was provided by Asahi Glass Co., Ltd.
PY - 2006/2
Y1 - 2006/2
N2 - 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.
AB - 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.
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U2 - 10.1093/nar/gnj011
DO - 10.1093/nar/gnj011
M3 - Article
C2 - 16434698
AN - SCOPUS:32544461879
SN - 0305-1048
VL - 34
SP - 1
EP - 7
JO - Nucleic Acids Research
JF - Nucleic Acids Research
IS - 2
ER -