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Isolation and functional analysis of cotton universal stress protein promoter in response to phytohormones and abiotic stresses

机译:棉花通用胁迫蛋白启动子对植物激素和非生物胁迫响应的分离及功能分析

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摘要

The 949 bp promoter fragment upstream from the translation initiation site of the GUSP gene encoding a universal stress protein was isolated from the genomic DNA of Gossypium arboreum. Some putative cis-acting elements involved in stress responses including E-box, ABRE, DPBF-box, and MYB-core elements were found in the promoter region. In an Agrobacterium-mediated transient expression assay, strong activation of the GUSP full promoter region occurred in tobacco leaves following dehydration, abscisic acid, salt, heavy metal, gibberellic acid and dark treatments. Deletion analysis of the promoter revealed that the dehydration, abscisic acid and salt responses were affected by the deletion between -208 and -949 bp and showed 2-4-fold induction. However, in response to dark, gibberellic acid and heavy metals the induction was only 2-fold. These findings further our understanding of the regulation of GUSP expression. This is an important study as no report of this universal stress protein promoter is available in literature. [PUBLICATION ABSTRACT]
机译:从植物棉的基因组DNA中分离出编码通用应激蛋白的GUSP基因翻译起始位点上游的949 bp启动子片段。在启动子区域发现了一些与应激反应有关的推测的顺式作用元件,包括E-box,ABRE,DPBF-box和MYB-核心元件。在农杆菌介导的瞬时表达测定中,在脱水,脱落酸,盐,重金属,赤霉素和深色处理后,烟叶中发生了GUSP全启动子区的强烈活化。启动子的缺失分析表明,脱水,脱落酸和盐反应受-208和-949 bp之间的缺失影响,并显示出2-4倍的诱导。然而,响应于深色,赤霉素和重金属,诱导仅为2倍。这些发现进一步加深了我们对GUSP表达调控的理解。这是一项重要的研究,因为在文献中没有关于这种通用应激蛋白启动子的报道。 [出版物摘要]

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