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辣根潜隐病毒(HRLV)一种新型全长转录本启动子的结构特征及其受多种胁迫响应转录因子的转录调控

Structural characterization of a novel full-length transcript promoter from Horseradish Latent Virus (HRLV) and its transcriptional regulation by multiple stress responsive transcription factors.

作者信息

Khan Ahamed, Shrestha Ankita, Bhuyan Kashyap, Maiti Indu B, Dey Nrisingha

机构信息

Department of Gene Function and Regulation, Department of Biotechnology, Government of India, Institute of Life Sciences, Chandrasekharpur, Bhubaneswar, Odisha, India.

Department of Molecular Plant Virology and Plant Genetic Engineering, KTRDC, College of Agriculture, Food and Environment, University of Kentucky, Lexington, KY, 40546-0236, USA.

出版信息

Plant Mol Biol. 2018 Jan;96(1-2):179-196. doi: 10.1007/s11103-017-0693-6. Epub 2018 Jan 11.

Abstract

The promoter fragment described in this study can be employed for strong transgene expression under both biotic and abiotic stress conditions. Plant-infecting Caulimoviruses have evolved multiple regulatory mechanisms to address various environmental stimuli during the course of evolution. One such mechanism involves the retention of discrete stress responsive cis-elements which are required for their survival and host-specificity. Here we describe the characterization of a novel Caulimoviral promoter isolated from Horseradish Latent Virus (HRLV) and its regulation by multiple stress responsive Transcription factors (TFs) namely DREB1, AREB1 and TGA1a. The activity of full length transcript (Flt-) promoter from HRLV (- 677 to + 283) was investigated in both transient and transgenic assays where we identified H12 (- 427 to + 73) as the highest expressing fragment having ~ 2.5-fold stronger activity than the CaMV35S promoter. The H12 promoter was highly active and near-constitutive in the vegetative and reproductive parts of both Tobacco and Arabidopsis transgenic plants. Interestingly, H12 contains a distinct cluster of cis-elements like dehydration-responsive element (DRE-core; GCCGAC), an ABA-responsive element (ABRE; ACGTGTC) and as-1 element (TGACG) which are known to be induced by cold, drought and pathogen/SA respectively. The specific binding of DREB1, AREB1 and TGA1a to DRE, ABRE and as-1 elements respectively were confirmed by the gel-binding assays using H12 promoter-specific probes. Detailed mutational analysis of the H12 promoter suggested that the presence of DRE-core and as-1 element was indispensable for its activity which was further confirmed by the transactivation assays. Our studies imply that H12 could be a valuable genetic tool for regulated transgene expression under diverse environmental conditions.

摘要

本研究中描述的启动子片段可用于在生物和非生物胁迫条件下实现强转基因表达。侵染植物的花椰菜花叶病毒在进化过程中已进化出多种调控机制来应对各种环境刺激。其中一种机制涉及保留离散的应激反应顺式元件,这些元件是它们生存和宿主特异性所必需的。在这里,我们描述了从辣根潜伏病毒(HRLV)中分离出的一种新型花椰菜花叶病毒启动子的特性,以及它受多种应激反应转录因子(TFs)即DREB1、AREB1和TGA1a的调控。通过瞬时和转基因分析研究了HRLV(-677至+283)全长转录本(Flt-)启动子的活性,我们确定H12(-427至+73)是表达最高的片段,其活性比CaMV35S启动子强约2.5倍。H12启动子在烟草和拟南芥转基因植物的营养和生殖部分都具有高活性且近乎组成型。有趣的是,H12包含一组独特的顺式元件簇,如脱水反应元件(DRE核心;GCCGAC)、脱落酸反应元件(ABRE;ACGTGTC)和as-1元件(TGACG),已知它们分别受寒冷、干旱和病原体/水杨酸诱导。通过使用H12启动子特异性探针的凝胶结合试验证实了DREB1、AREB1和TGA1a分别与DRE、ABRE和as-1元件的特异性结合。对H12启动子的详细突变分析表明,DRE核心和as-1元件的存在对其活性不可或缺,这通过反式激活试验进一步得到证实。我们的研究表明,H12可能是一种有价值的遗传工具,用于在不同环境条件下调控转基因表达。

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