T-DNA from Agrobacterium tumefaciens as an efficient tool for gene targeting in Kluyveromyces lactis

被引:73
作者
Bundock, P
Mróczek, K
Winkler, AA
Steensma, HY
Hooykaas, PJJ
机构
[1] Inst Mol Plant Sci, Clusius Lab, NL-2333 AL Leiden, Netherlands
[2] Delft Univ Technol, Kluyver Inst Biotechnol, NL-2628 BC Delft, Netherlands
来源
MOLECULAR AND GENERAL GENETICS | 1999年 / 261卷 / 01期
基金
英国生物技术与生命科学研究理事会;
关键词
Agrobacterium tumefaciens; Kluyveromyces lactis; gene targeting; recombination;
D O I
10.1007/s004380050948
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The soil bacterium Agrobacterium tumefaciens can transfer a part of its tumour-inducing (Ti) plasmid, the T-DNA, to plant cells. The virulence (vir) genes, also located on the Ti plasmid, encode proteins involved in the transport of T-DNA into the plant cell. Once in the plant nucleus, T-DNA is able to integrate into the plant genome by an illegitimate recombination mechanism. The host range of A. tumefaciens is not restricted to plant species. A. tumefaciens is also able to transfer T-DNA to the yeast Saccharomyces cerevisiae. In this paper we demonstrate transfer of T-DNA from A. tumefaciens to the yeast Kluyveromyces lactis. Furthermore, we found that T-DNA serves as an ideal substrate for gene targeting in K. lactis. We have studied the efficiency of gene targeting at the K. lactis TRP1 locus using either direct DNA transfer (electroporation) or T-DNA transfer from Agrobacterium. We found that gene targeting using T-DNA was at least ten times more efficient than using linear double-stranded DNA introduced by electroporation. Therefore, the outcome of gene targeting experiments in some organisms may depend strongly upon the DNA substrate used.
引用
收藏
页码:115 / 121
页数:7
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