A heat-inducible expression system for external control of gene expression in plastids

被引:3
|
作者
Xu, Wenbo [1 ]
Li, Shengchun [1 ]
Bock, Ralph [2 ]
Zhang, Jiang [1 ,3 ]
机构
[1] Hubei Univ, Sch Life Sci, Hubei Hongshan Lab, State Key Lab Biocatalysis & Enzyme Engn, Wuhan, Peoples R China
[2] Max Planck Inst Mol Pflanzenphysiol, Potsdam, Germany
[3] Chinese Acad Agr Sci, Agr Genom Inst Shenzhen, Minist Agr & Rural Affairs, Shenzhen Branch,Guangdong Lab Lingnan Modern Agr,K, Shenzhen, Peoples R China
基金
中国国家自然科学基金;
关键词
plastid transformation; pL/pR; cI857; heat-inducible expression; T7 RNA polymerase; Nicotiana tabacum; BASIC RESEARCH; TOBACCO; TRANSGENE; TRANSFORMATION; CHLOROPLASTS; PROTEINS; GROWTH; TISSUE;
D O I
10.1111/pbi.14238
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Inducible expression systems can overcome the trade-off between high-level transgene expression and its pleiotropic effects on plant growth. In addition, they can facilitate the expression of biochemical pathways that produce toxic metabolites. Although a few inducible expression systems for the control of transgene expression in plastids have been developed, they all depend on chemical inducers and/or nuclear transgenes. Here we report a temperature-inducible expression system for plastids that is based on the bacteriophage lambda leftward and rightward promoters (pL/pR) and the temperature-sensitive repressor cI857. We show that the expression of green fluorescent protein (GFP) in plastids can be efficiently repressed by cI857 under normal growth conditions, and becomes induced over time upon exposure to elevated temperatures in a light-dependent process. We further demonstrate that by introducing into plastids an expression system based on the bacteriophage T7 RNA polymerase, the temperature-dependent accumulation of GFP increased further and was similar to 24 times higher than expression driven by the pL/pR promoter alone, reaching similar to 0.48% of the total soluble protein. In conclusion, our heat-inducible expression system provides a new tool for the external control of plastid (trans) gene expression that is cost-effective and does not depend on chemical inducers.
引用
收藏
页码:960 / 969
页数:10
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