A Modular Plasmid Assembly Kit for Multigene Expression, Gene Silencing and Silencing Rescue in Plants

被引:85
作者
Binder, Andreas [1 ]
Lambert, Jayne [1 ]
Morbitzer, Robert [1 ]
Popp, Claudia [1 ]
Ott, Thomas [1 ]
Lahaye, Thomas [1 ]
Parniske, Martin [1 ]
机构
[1] Univ Munich LMU, Fac Biol, Martinsried, Germany
来源
PLOS ONE | 2014年 / 9卷 / 02期
关键词
SYNTHETIC BIOLOGY; RECOMBINANT-DNA; IN-VITRO; RESTRICTION ENZYMES; RAPID CONSTRUCTION; BINARY VECTORS; CLONING METHOD; FUSION SYSTEM; TARGET GENE; P19; PROTEIN;
D O I
10.1371/journal.pone.0088218
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
The Golden Gate (GG) modular assembly approach offers a standardized, inexpensive and reliable way to ligate multiple DNA fragments in a pre-defined order in a single-tube reaction. We developed a GG based toolkit for the flexible construction of binary plasmids for transgene expression in plants. Starting from a common set of modules, such as promoters, protein tags and transcribed regions of interest, synthetic genes are assembled, which can be further combined to multigene constructs. As an example, we created T-DNA constructs encoding multiple fluorescent proteins targeted to distinct cellular compartments (nucleus, cytosol, plastids) and demonstrated simultaneous expression of all genes in Nicotiana benthamiana, Lotus japonicus and Arabidopsis thaliana. We assembled an RNA interference (RNAi) module for the construction of intron-spliced hairpin RNA constructs and demonstrated silencing of GFP in N. benthamiana. By combination of the silencing construct together with a codon adapted rescue construct into one vector, our system facilitates genetic complementation and thus confirmation of the causative gene responsible for a given RNAi phenotype. As proof of principle, we silenced a destabilized GFP gene (dGFP) and restored GFP fluorescence by expression of a recoded version of dGFP, which was not targeted by the silencing construct.
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页数:14
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