Development of a tightly regulated copper-inducible transient gene expression system in Nicotiana benthamiana incorporating a suicide exon and Cre recombinase

被引:2
作者
Chiang, Bing-Jen [1 ]
Lin, Kuan-Yu [1 ]
Chen, Yi-Feng [1 ]
Huang, Ching-Yi [1 ]
Goh, Foong-Jing [1 ]
Huang, Lo-Ting [2 ]
Chen, Li-Hung [2 ,3 ]
Wu, Chih-Hang [1 ]
机构
[1] Acad Sinica, Inst Plant & Microbial Biol, Taipei 115?201, Taiwan
[2] Natl Chung Hsing Univ, Dept Plant Pathol, Taichung 402?202, Taiwan
[3] Natl Chung Hsing Univ, Adv Plant & Food Crop Biotechnol Ctr, Taichung 402?202, Taiwan
关键词
cell death assays; copper; Cre-LoxP recombination; inducible gene expression system; Nicotiana benthamiana; suicide exon; PLANT; PROMOTER;
D O I
10.1111/nph.20021
中图分类号
Q94 [植物学];
学科分类号
071001 ;
摘要
Chemical-inducible gene expression systems are commonly used to regulate gene expression for functional genomics in various plant species. However, a convenient system that can tightly regulate transgene expression in Nicotiana benthamiana is still lacking. In this study, we developed a tightly regulated copper-inducible system that can control transgene expression and conduct cell death assays in N. benthamiana. We tested several chemical-inducible systems using Agrobacterium-mediated transient expression and found that the copper-inducible system exhibited the least concerns regarding leakiness in N. benthamiana. Although the copper-inducible system can control the expression of some tested reporters, it is not sufficiently tight to regulate certain tested hypersensitive cell death responses. Using the MoClo-based synthetic biology approach, we incorporated the suicide exon HyP5SM/OsL5 and Cre/LoxP as additional regulatory elements to enhance the tightness of the regulation. This new design allowed us to tightly control the hypersensitive cell death induced by several tested leucine-rich repeat-containing proteins and their matching avirulence factors, and it can be easily applied to regulate the expression of other transgenes in transient expression assays. Our findings offer new approaches for both fundamental and translational studies in plant functional genomics.
引用
收藏
页码:318 / 331
页数:14
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