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人工合成 TAL 效应因子可靶向增强植物中转基因的表达。

Synthetic TAL effectors for targeted enhancement of transgene expression in plants.

机构信息

Department of Plant Sciences, The University of Tennessee, Knoxville, TN, USA.

出版信息

Plant Biotechnol J. 2014 May;12(4):436-46. doi: 10.1111/pbi.12150. Epub 2013 Dec 23.

DOI:10.1111/pbi.12150
PMID:24373379
Abstract

Transcription activator-like effectors (TALEs), secreted by the pathogenic bacteria Xanthomonas, specifically activate expression of targeted genes in plants. Here, we designed synthetic TALEs that bind to the flanking regions of the TATA-box motif on the CaMV 35S promoter for the purpose of understanding the engineerable 'hot-spots' for increasing transgene expression. We demonstrated that transient expression of de novo-engineered TALEs using agroinfiltration could significantly increase reporter gene expression in stable transgenic tobacco expressing the orange fluorescent protein reporter gene pporRFP under the control of synthetic inducible, minimal or full-length 35S promoters. Moreover, the additive effects of a combination of two different synthetic TALEs could significantly enhance the activation effects of TALEs on reporter gene expression more than when each TALE was used individually. We also studied the effects of the C-terminal domain and the activation domain of synthetic TALEs, as well as the best 'hot-spots' on the 35S promoter on targeted transgene activation. Furthermore, TALE activation of the Arabidopsis MYB transcription factor AtPAP1 (PRODUCTION OF ANTHOCYANIN PIGMENT 1) in stable transgenic tobacco gave rise to a dark purple colour on infiltrated leaves when driven by four copies of cis-regulatory elements of pathogenesis-related gene (PR1) with enhancer motifs B and A1 from the 35S promoter. These results provide novel insights into the potential applications of synthetic TALEs for targeted gene activation of transgenes in plants.

摘要

转录激活因子样效应物(TALEs),由致病细菌黄单胞菌分泌,能够特异性激活植物中靶向基因的表达。在这里,我们设计了合成的 TALEs,使其与 CaMV35S 启动子 TATA 盒基序的侧翼区域结合,目的是了解可用于增加转基因表达的可设计“热点”。我们通过农杆菌浸润证明,使用从头设计的合成 TALEs 瞬时表达可以显著增加稳定转化烟草中报告基因的表达,该烟草表达橙色荧光蛋白报告基因 pporRFP,受合成诱导型、最小型或全长 35S 启动子的控制。此外,两种不同的合成 TALEs 的组合的累加效应可以显著增强 TALEs 对报告基因表达的激活作用,比单独使用每种 TALE 时要强。我们还研究了合成 TALEs 的 C 端结构域和激活结构域以及 35S 启动子上的最佳“热点”对靶向转基因激活的影响。此外,TALE 激活稳定转化烟草中的拟南芥 MYB 转录因子 AtPAP1(花青素合成酶 1),当由 35S 启动子中的增强子 B 和 A1 以及 PR1 基因的顺式调控元件的四个拷贝驱动时,在浸润叶片上产生深紫色。这些结果为合成 TALEs 在植物中转基因的靶向基因激活提供了新的见解。

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