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从棉花中分离三个乙烯响应元件结合因子基因的分子特征。

Molecular characterization of three ethylene responsive element binding factor genes from cotton.

机构信息

Laboratory of Molecular Biology and MOE Laboratory of Protein Science, Department of Biological Sciences and Biotechnology, Tsinghua University, Beijing 100084, China.

出版信息

J Integr Plant Biol. 2010 May;52(5):485-95. doi: 10.1111/j.1744-7909.2010.00914.x.

Abstract

Ethylene-responsive factors (ERFs) are important regulators of plant gene expression. In this study, three novel ERF genes, GhERF2, GhERF3 and GhERF6, were isolated from cotton (Gossypium hirstum) using rapid amplification of cDNA ends-polymerase chain reaction. Transient expression analysis using GhERF-green fluorescent protein fusions showed that these three proteins were targeted to the nucleus. Fusion proteins consisting of GhERF2, GhERF3 or GhERF6 coupled to the GAL4 DNA binding domain strongly activated transcription in yeast. Furthermore, GhERF6 was shown to be able to bind specifically to GCC boxes using a particle bombardment assay in tobacco cells. Semi-quantitative reverse transcription-polymerase chain reaction revealed that GhERF2 and GhERF3 are constitutively expressed in all organs, while GhERF6 is only constitutively expressed in vegetative organs. When plants were treated with ethylene, abscisic acid, salt, cold and drought, the transcripts of GhERF2, GhERF3 and GhERF6 were rapidly induced to high levels. Promoter analysis also indicated that the 5' upstream regions of the three genes possess elements induced by these physiological and environmental factors. Collectively, our data suggest that GhERF2, GhERF3 and GhERF6 might function as positive trans-acting factors in the plant responses to ethylene, abscisic acid and other stresses and provide useful clues for further research into the mechanism of them in regulating cotton multiple stress responses.

摘要

乙烯响应因子(ERFs)是植物基因表达的重要调控因子。本研究采用快速扩增 cDNA 末端-聚合酶链反应(RACE-PCR)技术,从棉花(Gossypium hirstum)中分离得到三个新的 ERF 基因,GhERF2、GhERF3 和 GhERF6。瞬时表达分析表明,这三个蛋白均定位于细胞核。GhERF2、GhERF3 或 GhERF6 与 GAL4 DNA 结合域融合的融合蛋白在酵母中强烈激活转录。此外,利用粒子轰击法在烟草细胞中证明 GhERF6 能够特异性结合 GCC 盒。半定量 RT-PCR 分析表明,GhERF2 和 GhERF3 在所有器官中均持续表达,而 GhERF6 仅在营养器官中持续表达。当植物受到乙烯、脱落酸、盐、冷和干旱处理时,GhERF2、GhERF3 和 GhERF6 的转录物迅速被诱导至高水平。启动子分析还表明,三个基因的 5'上游区域具有这些生理和环境因子诱导的元件。综上所述,我们的数据表明,GhERF2、GhERF3 和 GhERF6 可能作为植物对乙烯、脱落酸和其他胁迫反应的正调控因子发挥作用,并为进一步研究它们在调控棉花多种胁迫反应中的机制提供了有用线索。

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