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AP2/EREBP转录因子OPBP1的过表达增强了烟草的抗病性和耐盐性。

Overexpression of the AP2/EREBP transcription factor OPBP1 enhances disease resistance and salt tolerance in tobacco.

作者信息

Guo Ze-Jian, Chen Xu-Jun, Wu Xue-Long, Ling Jian-Qun, Xu Ping

机构信息

Biotechnology Institute, Zhejiang University, Hangzhou, PR China.

出版信息

Plant Mol Biol. 2004 Jul;55(4):607-18. doi: 10.1007/s11103-004-1521-3.

Abstract

Osmotin promoter binding protein 1 (OPBP1), an AP2/EREBP-like transcription factor of tobacco (Nicotiana tabacum), was isolated using a yeast one-hybrid system. RNA gel blot analysis indicated that expression of the OPBP1 gene was induced by elicitor cryptogein, NaCl, ethephon, methyl jasmonate, as well as cycloheximide. Transient expression analysis using an OPBP1-eGFP fusion gene in onion epidermal cells revealed that the OPBP1 protein was targeted to the nuclear. Further, electrophoretic mobility shift assays demonstrated that the recombinant OPBP1 protein could bind to an oligonucleotide containing the GCC-box cis element. Transgenic tobacco plants with an over expression of the OPBP1 gene accumulated high levels of PR-1a and PR-5d genes and exhibited enhanced resistance to infection by Pseudomonas syringae pv tabaci and Phytophthora parasitica var nicotianae pathogens. They also exhibited increased tolerance to salt stress. These results suggest that OPBP1 might be a transcriptional regulator capable of regulating expression in sets of stress-related genes.

摘要

渗透素启动子结合蛋白1(OPBP1)是烟草(Nicotiana tabacum)中一种类似AP2/EREBP的转录因子,利用酵母单杂交系统分离得到。RNA凝胶印迹分析表明,OPBP1基因的表达受激发子隐地蛋白、NaCl、乙烯利、茉莉酸甲酯以及环己酰亚胺的诱导。在洋葱表皮细胞中使用OPBP1-eGFP融合基因进行瞬时表达分析,结果显示OPBP1蛋白定位于细胞核。此外,电泳迁移率变动分析表明,重组OPBP1蛋白能够与含有GCC盒顺式元件的寡核苷酸结合。OPBP1基因过表达的转基因烟草植株积累了高水平的PR-1a和PR-5d基因,并表现出对丁香假单胞菌烟草致病变种和寄生疫霉烟草变种病原体感染的抗性增强。它们对盐胁迫的耐受性也有所提高。这些结果表明,OPBP1可能是一种能够调节一组与胁迫相关基因表达的转录调节因子。

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