Kim Sung-Ryul, Lee Jinwon, Jun Sung-Hoon, Park Sunhee, Kang Hong-Gyu, Kwon Soontae, An Gynheung
National Research Laboratory of Plant Functional Genomics, Division of Molecular and Life Sciences, Pohang University of Science and Technology (POSTECH), Pohang 790-784, Republic of Korea.
Plant Mol Biol. 2003 Jul;52(4):761-73. doi: 10.1023/a:1025093101021.
T-DNA is commonly used for delivery of foreign genes and as an insertional mutagen. Although ample information exists regarding T-DNA organization in dicotyledonous plants, little is known about the monocot rice. Here, we investigated the structure of T-DNA in a large number of transgenic rice plants. Analysis of the T-DNA borders revealed that more than half of the right ends were at the cleavage site, whereas the left ends were not conserved and were deleted up to 180 bp from the left border (LB) cleavage site. Three types of junctions were found between T-DNA and genomic DNA. In the first, up to seven nucleotide overlaps were present. The frequency of this type was much higher in the LB region than at the right border (RB). In the second type, which was more frequent in RB, the link was direct, without any overlaps or filler DNA. Finally, the third type showed filler DNA between T-DNA and the plant sequences. Out of 171 samples examined, 77 carried the vector backbone sequence, with the majority caused by the failure of T-strand termination at LB. However, a significant portion also resulted from co-integration of T-DNA and the vector backbone to a single locus. Most linkages between T-DNA and the vector backbone were formed between two 3' ends or two 5' ends of the transferred DNAs. The 3' ends were mostly linked through 3-6 bp of the complementing sequence, whereas the 5' ends were linked through either precise junctions or imprecise junctions with filler DNA.
T-DNA常用于导入外源基因并作为插入诱变剂。尽管关于双子叶植物中T-DNA的组织已有大量信息,但对于单子叶植物水稻却知之甚少。在此,我们研究了大量转基因水稻植株中T-DNA的结构。对T-DNA边界的分析表明,超过一半的右端位于切割位点,而左端并不保守,从左边界(LB)切割位点起最多缺失180 bp。在T-DNA与基因组DNA之间发现了三种类型的连接。第一种类型存在多达七个核苷酸的重叠。这种类型在LB区域的频率远高于右边界(RB)。第二种类型在RB中更常见,连接是直接的,没有任何重叠或填充DNA。最后,第三种类型在T-DNA与植物序列之间显示有填充DNA。在检测的171个样本中,77个携带载体骨架序列,大多数是由于LB处T链终止失败所致。然而,相当一部分也是由T-DNA与载体骨架共整合到单个位点引起的。T-DNA与载体骨架之间的大多数连接是在转移DNA的两个3'端或两个5'端之间形成的。3'端大多通过3 - 6 bp的互补序列连接,而5'端则通过精确连接或带有填充DNA的不精确连接相连。