Mayerhofer R, Koncz-Kalman Z, Nawrath C, Bakkeren G, Crameri A, Angelis K, Redei G P, Schell J, Hohn B, Koncz C
Max-Planck-Institut für Züchtungsforschung, Köln, FRG.
EMBO J. 1991 Mar;10(3):697-704. doi: 10.1002/j.1460-2075.1991.tb07999.x.
Transferred DNA (T-DNA) insertions of Agrobacterium gene fusion vectors and corresponding insertional target sites were isolated from transgenic and wild type Arabidopsis thaliana plants. Nucleotide sequence comparison of wild type and T-DNA-tagged genomic loci showed that T-DNA integration resulted in target site deletions of 29-73 bp. In those cases where integrated T-DNA segments turned out to be smaller than canonical ones, the break-points of target deletions and T-DNA insertions overlapped and consisted of 5-7 identical nucleotides. Formation of precise junctions at the right T-DNA border, and DNA sequence homology between the left termini of T-DNA segments and break-points of target deletions were observed in those cases where full-length canonical T-DNA inserts were very precisely replacing plant target DNA sequences. Aberrant junctions were observed in those transformants where termini of T-DNA segments showed no homology to break-points of target sequence deletions. Homology between short segments within target sites and T-DNA, as well as conversion and duplication of DNA sequences at junctions, suggests that T-DNA integration results from illegitimate recombination. The data suggest that while the left T-DNA terminus and both target termini participate in partial pairing and DNA repair, the right T-DNA terminus plays an essential role in the recognition of the target and in the formation of a primary synapsis during integration.
从转基因和野生型拟南芥植株中分离出农杆菌基因融合载体的转移DNA(T-DNA)插入片段及其相应的插入靶点。野生型和T-DNA标签基因组位点的核苷酸序列比较表明,T-DNA整合导致靶点缺失29 - 73 bp。在那些整合的T-DNA片段比标准片段小的情况下,靶点缺失和T-DNA插入的断点重叠,且由5 - 7个相同的核苷酸组成。在全长标准T-DNA插入片段非常精确地取代植物靶点DNA序列的情况下,观察到在T-DNA右边界形成了精确的连接,以及T-DNA片段左末端与靶点缺失断点之间的DNA序列同源性。在那些T-DNA片段末端与靶点序列缺失断点无同源性的转化体中观察到异常连接。靶点位点内短片段与T-DNA之间的同源性,以及连接点处DNA序列的转换和重复,表明T-DNA整合是由异常重组导致的。数据表明,虽然T-DNA左末端和两个靶点末端参与部分配对和DNA修复,但T-DNA右末端在靶点识别以及整合过程中初级联会的形成中起关键作用。