Science. 1988 Apr 22;240(4851):501-4. doi: 10.1126/science.240.4851.501.
The transfer process of T (transfer)-DNA of Agrobacterium tumefaciens is activated after the induction of the expression of the Ti plasmid virulence (vir) loci by plant signal molecules such as acetosyringone. The vir gene products then act to generate a free transferable single-stranded copy of the T-DNA, designated the T-strand. Although some vir proteins are responsible for the synthesis of the T-strand, others may mediate T-strand transfer to plant cells as part of a DNA-protein complex. Here, a novel 69-kilodalton vir-specific single-stranded DNA binding protein is identified in Agrobacterium harboring a nopaline-type Ti plasmid. This protein binds single-stranded but not double-stranded DNA regardless of nucleotide sequence composition. The molecular size of the vir-specific single-stranded DNA binding protein and its relative abundance in acetosyringone-induced Agrobacterium suggested that it might be the product of the virE locus; molecular cloning and expression of the virE region in Escherichia coli confirmed this prediction.
根癌农杆菌 T-DNA 的转移过程是在植物信号分子(如乙酰丁香酮)诱导 Ti 质粒毒力(vir)基因座表达后被激活的。然后,vir 基因产物作用于产生 T-DNA 的可自由转移的单链拷贝,称为 T 链。尽管一些 vir 蛋白负责 T 链的合成,但其他蛋白可能作为 DNA-蛋白复合物的一部分介导 T 链向植物细胞的转移。在这里,在含有胭脂碱型 Ti 质粒的根癌农杆菌中鉴定到一种新型的 69 千道尔顿的 vir 特异性单链 DNA 结合蛋白。该蛋白结合单链但不结合双链 DNA,无论核苷酸序列组成如何。vir 特异性单链 DNA 结合蛋白的分子量及其在乙酰丁香酮诱导的根癌农杆菌中的相对丰度表明,它可能是 virE 基因座的产物;virE 区在大肠杆菌中的分子克隆和表达证实了这一预测。