Transgene structures in T-DNA-inserted rice plants

被引:115
作者
Kim, SR
Lee, J
Jun, SH
Park, S
Kang, HG
Kwon, S
An, G [1 ]
机构
[1] Pohang Univ Sci & Technol, Natl Res Lab Plant Funct Genom, Div Mol & Life Sci, Pohang 790784, South Korea
[2] Andong Natl Univ, Dept Hort & Breeding, Andong 760749, South Korea
关键词
border; flanking sequence; Oryza sativa; repeat; rice; T-DNA integration; vector backbone;
D O I
10.1023/A:1025093101021
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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.
引用
收藏
页码:761 / 773
页数:13
相关论文
共 53 条
[1]   NEW CLONING VEHICLES FOR TRANSFORMATION OF HIGHER-PLANTS [J].
AN, G ;
WATSON, BD ;
STACHEL, S ;
GORDON, MP ;
NESTER, EW .
EMBO JOURNAL, 1985, 4 (02) :277-284
[2]   BINARY AGROBACTERIUM VECTORS FOR PLANT TRANSFORMATION [J].
BEVAN, M .
NUCLEIC ACIDS RESEARCH, 1984, 12 (22) :8711-8721
[3]   T-DNA of Agrobacterium tumefaciens:: 25 years and counting [J].
Binns, AN .
TRENDS IN PLANT SCIENCE, 2002, 7 (05) :231-233
[4]   Plant transformation: Problems and strategies for practical application [J].
Birch, RG .
ANNUAL REVIEW OF PLANT PHYSIOLOGY AND PLANT MOLECULAR BIOLOGY, 1997, 48 :297-326
[5]   T-DNA integration into the Arabidopsis genome depends on sequences of pre-insertion sites [J].
Brunaud, V ;
Balzergue, S ;
Dubreucq, B ;
Aubourg, S ;
Samson, F ;
Chauvin, S ;
Bechtold, N ;
Cruaud, C ;
DeRose, R ;
Pelletier, G ;
Lepiniec, L ;
Caboche, M ;
Lecharny, A .
EMBO REPORTS, 2002, 3 (12) :1152-1157
[6]   T-DNA ORGANIZATION IN TUMOR CULTURES AND TRANSGENIC PLANTS OF THE MONOCOTYLEDON ASPARAGUS-OFFICINALIS [J].
BYTEBIER, B ;
DEBOECK, F ;
DEGREVE, H ;
VANMONTAGU, M ;
HERNALSTEENS, JP .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1987, 84 (15) :5345-5349
[7]   A rapid DNA minipreparation method suitable for AFLP and other PCR applications [J].
Chen, DH ;
Ronald, PC .
PLANT MOLECULAR BIOLOGY REPORTER, 1999, 17 (01) :53-57
[8]   Details of T-DNA structural organization from a transgenic Petunia population exhibiting co-suppression [J].
Cluster, PD ;
ODell, M ;
Metzlaff, M ;
Flavell, RB .
PLANT MOLECULAR BIOLOGY, 1996, 32 (06) :1197-1203
[9]  
De Buck S, 1999, PLANT J, V20, P295, DOI 10.1046/j.1365-313X.1999.t01-1-00602.x
[10]   T-DNA vector backbone sequences are frequently integrated into the genome of transgenic plants obtained by Agrobacterium-mediated transformation [J].
De Buck, S ;
De Wilde, C ;
Van Montagu, M ;
Depicker, A .
MOLECULAR BREEDING, 2000, 6 (05) :459-468