Veluthambi K, Ream W, Gelvin S B
Department of Biological Sciences, Purdue University, West Lafayette, Indiana 47907.
J Bacteriol. 1988 Apr;170(4):1523-32. doi: 10.1128/jb.170.4.1523-1532.1988.
Agrobacterium tumefaciens transfers the T-DNA portion of its Ti plasmid to the nuclear genome of plant cells. Upon cocultivation of A. tumefaciens A348 with regenerating tobacco leaf protoplasts, six distinct single-stranded T-DNA molecules (T strands) were generated in addition to double-stranded T-DNA border cleavages which we have previously reported (K. Veluthambi, R.K. Jayaswal, and S.B. Gelvin, Proc. Natl. Acad. Sci. USA 84:1881-1885, 1987). The T region of an octopine-type Ti plasmid has four border repeats delimiting three T-DNA regions defined as T left (TL), T center (TC), and T right (TR). The six T strands generated upon induction corresponded to the TL, TC, TR, TL + TC, TC + TR, and TL + TC + TR regions, suggesting that the initiation and termination of T-strand synthesis can occur at each of the four borders. Most TL + TC + TR T-strand molecules corresponded to the top T-DNA strand, whereas the other five T strands corresponded to the bottom T-DNA strand. Generation of T strands required the virA, virG, and virD operons. Extra copies of vir genes, harbored on cosmids within derivatives of A. tumefaciens A348, enhanced production of T strands. The presence of right and left border repeats in their native orientation is important for the generation of full-length T strands. When a right border repeat was placed in the opposite orientation, single-stranded T-DNA molecules that corresponded to the top strand were generated. Deletion of overdrive, a sequence that flanks right border repeats and functions as a T-DNA transmission enhancer, reduced the level of T-strand generation. Induction of A. tumefaciens cells by regenerating tobacco protoplasts increased the copy number of the Ti plasmid relative to the bacterial chromosome.
根癌土壤杆菌将其Ti质粒的T-DNA部分转移到植物细胞的核基因组中。当根癌土壤杆菌A348与再生的烟草叶原生质体共培养时,除了我们之前报道过的双链T-DNA边界切割外,还产生了六个不同的单链T-DNA分子(T链)(K. Veluthambi、R.K. Jayaswal和S.B. Gelvin,《美国国家科学院院刊》84:1881 - 1885,1987)。章鱼碱型Ti质粒的T区域有四个边界重复序列,界定了三个T-DNA区域,分别定义为T左(TL)、T中(TC)和T右(TR)。诱导产生的六个T链对应于TL、TC、TR、TL + TC、TC + TR和TL + TC + TR区域,这表明T链合成的起始和终止可以发生在四个边界中的每一个。大多数TL + TC + TR T链分子对应于顶部T-DNA链,而其他五个T链对应于底部T-DNA链。T链的产生需要virA、virG和virD操纵子。根癌土壤杆菌A348衍生物中的粘粒携带的额外vir基因拷贝增强了T链的产生。左右边界重复序列以其天然方向存在对于全长T链的产生很重要。当一个右边界重复序列以相反方向放置时,产生了对应于顶部链的单链T-DNA分子。删除超驱动序列(一种位于右边界重复序列侧翼并作为T-DNA传递增强子起作用的序列)降低了T链产生的水平。再生烟草原生质体对根癌土壤杆菌细胞的诱导增加了Ti质粒相对于细菌染色体的拷贝数。