Bundock P, Mróczek K, Winkler A A, Steensma H Y, Hooykaas P J
Institute of Molecular Plant Sciences, Clusius Laboratory, Leiden, The Netherlands.
Mol Gen Genet. 1999 Feb;261(1):115-21. doi: 10.1007/s004380050948.
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.
土壤细菌根癌农杆菌能够将其致瘤(Ti)质粒的一部分,即T-DNA,转移到植物细胞中。同样位于Ti质粒上的毒性(vir)基因编码参与将T-DNA转运到植物细胞中的蛋白质。一旦进入植物细胞核,T-DNA能够通过非同源重组机制整合到植物基因组中。根癌农杆菌的宿主范围并不局限于植物物种。根癌农杆菌还能够将T-DNA转移到酿酒酵母中。在本文中,我们证明了T-DNA从根癌农杆菌转移到乳酸克鲁维酵母中。此外,我们发现T-DNA是乳酸克鲁维酵母中基因打靶的理想底物。我们使用直接DNA转移(电穿孔)或来自农杆菌的T-DNA转移,研究了在乳酸克鲁维酵母TRP1基因座进行基因打靶的效率。我们发现,使用T-DNA进行基因打靶的效率比使用通过电穿孔导入的线性双链DNA至少高十倍。因此,在某些生物体中进行基因打靶实验的结果可能在很大程度上取决于所使用的DNA底物。