A Gateway-based platform for multigene plant transformation

被引:76
作者
Chen, Qi-Jun
Zhou, Hai-Meng
Chen, Jia
Wang, Xue-Chen [1 ]
机构
[1] China Agr Univ, Coll Biol Sci, State Key Lab Plant Physiol & Biochem, Beijing 100094, Peoples R China
[2] Tsinghua Univ, Dept Biol Sci & Biotechnol, Beijing, Peoples R China
关键词
gateway vectors; multigene plant transformation; MultiRound Gateway;
D O I
10.1007/s11103-006-9065-3
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
The post-genomic era offers unrivalled opportunities for genetic manipulation of polygenic traits, multiple traits, and multiple gene products. However, remaining technical hurdles make the manipulation of multiple genes in plants difficult. Here we describe a Gateway-based vector system to enable multiple transgenes to be directly linked or fused. The vector system consists of a destination vector and two special attL-flanked entry vectors each containing an attR cassette incompatible with the attL. By multiple rounds of LR recombination reactions, which we call MultiRound Gateway, multiple transgenes can be delivered sequentially and indefinitely into the Gateway-compatible destination vector through alternate use of the two special entry vectors. In our proof-of-principle experiments we have used this vector system to construct a plant transformation vector containing seven functional DNA fragments, including a screening marker gene, two reporter genes and four matrix attachment region sequences. This system provides a platform for fully realizing the potential of plant genetic manipulation.
引用
收藏
页码:927 / 936
页数:10
相关论文
共 37 条
[1]   Use of matrix attachment regions (MARs) to minimize transgene silencing [J].
Allen, GC ;
Spiker, S ;
Thompson, WF .
PLANT MOLECULAR BIOLOGY, 2000, 43 (2-3) :361-376
[2]   POSITIVE-SELECTION VECTORS USING THE F-PLASMID CCDB KILLER GENE [J].
BERNARD, P ;
GABANT, P ;
BAHASSI, EM ;
COUTURIER, M .
GENE, 1994, 148 (01) :71-74
[3]   Simultaneous accumulation of multiple viral coat proteins from a TEV-NIa based expression vector [J].
Ceriani, MF ;
Marcos, JF ;
Hopp, HE ;
Beachy, RN .
PLANT MOLECULAR BIOLOGY, 1998, 36 (02) :239-248
[4]   Expression and inheritance of multiple transgenes in rice plants [J].
Chen, LL ;
Marmey, P ;
Taylor, NJ ;
Brizard, JP ;
Espinoza, C ;
D'Cruz, P ;
Huet, H ;
Zhang, SP ;
de Kochko, A ;
Beachy, RN ;
Fauquet, CM .
NATURE BIOTECHNOLOGY, 1998, 16 (11) :1060-1064
[5]   Concerted assembly and cloning of multiple DNA segments using in vitro site-specific recombination: Functional analysis of multi-segment expression clones [J].
Cheo, DL ;
Titus, SA ;
Byrd, DRN ;
Hartley, JL ;
Temple, GF ;
Brasch, MA .
GENOME RESEARCH, 2004, 14 (10B) :2111-2120
[6]   Engineered GFP as a vital reporter in plants [J].
Chiu, WL ;
Niwa, Y ;
Zeng, W ;
Hirano, T ;
Kobayashi, H ;
Sheen, J .
CURRENT BIOLOGY, 1996, 6 (03) :325-330
[7]   Floral dip:: a simplified method for Agrobacterium-mediated transformation of Arabidopsis thaliana [J].
Clough, SJ ;
Bent, AF .
PLANT JOURNAL, 1998, 16 (06) :735-743
[8]   A gateway cloning vector set for high-throughput functional analysis of genes in planta [J].
Curtis, MD ;
Grossniklaus, U .
PLANT PHYSIOLOGY, 2003, 133 (02) :462-469
[9]   Iterative in vivo assembly of large and complex transgenes by combining the activities of φC31 integrase and Cre recombinase -: art. no. e189 [J].
Dafhnis-Calas, F ;
Xu, ZY ;
Haines, S ;
Malla, SK ;
Smith, MCM ;
Brown, WRA .
NUCLEIC ACIDS RESEARCH, 2005, 33 (22) :e189
[10]  
Daniell H, 2005, METH MOL B, V286, P111