GATEWAY™ vectors for Agrobacterium-mediated plant transformation

被引:2947
作者
Karimi, M [1 ]
Inzé, D [1 ]
Depicker, A [1 ]
机构
[1] State Univ Ghent VIB, Dept Plant Syst Biol, B-9000 Ghent, Belgium
关键词
D O I
10.1016/S1360-1385(02)02251-3
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Agrobacterium tumefaciens is the preferred method for transformation of a wide range of plant species. Commonly, the genes to be transferred are cloned between the left and right T-DNA borders of so-called binary T-DNA vectors that can replicate both in E coli and Agrobacterium. Because these vectors are generally large, cloning can be time-consuming and laborious. Recently, the GATEWAY(TM) conversion technology has provided a fast and reliable alternative to the cloning of sequences into large acceptor plasmids.
引用
收藏
页码:193 / 195
页数:3
相关论文
共 5 条
[1]  
GALLIE DR, 1989, PLANT CELL, V1, P301, DOI 10.1105/tpc.1.3.301
[2]   THE SMALL, VERSATILE PPZP FAMILY OF AGROBACTERIUM BINARY VECTORS FOR PLANT TRANSFORMATION [J].
HAJDUKIEWICZ, P ;
SVAB, Z ;
MALIGA, P .
PLANT MOLECULAR BIOLOGY, 1994, 25 (06) :989-994
[3]   pGreen:: a versatile and flexible binary Ti vector for Agrobacterium-mediated plant transformation [J].
Hellens, RP ;
Edwards, EA ;
Leyland, NR ;
Bean, S ;
Mullineaux, PM .
PLANT MOLECULAR BIOLOGY, 2000, 42 (06) :819-832
[4]   IDENTIFICATION OF DNA-SEQUENCES REQUIRED FOR ACTIVITY OF THE CAULIFLOWER MOSAIC VIRUS-35S PROMOTER [J].
ODELL, JT ;
NAGY, F ;
CHUA, NH .
NATURE, 1985, 313 (6005) :810-812
[5]   Construct design for efficient, effective and high-throughput gene silencing in plants [J].
Wesley, SV ;
Helliwell, CA ;
Smith, NA ;
Wang, MB ;
Rouse, DT ;
Liu, Q ;
Gooding, PS ;
Singh, SP ;
Abbott, D ;
Stoutjesdijk, PA ;
Robinson, SP ;
Gleave, AP ;
Green, AG ;
Waterhouse, PM .
PLANT JOURNAL, 2001, 27 (06) :581-590