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首页> 外文期刊>RSC Advances >Functional characterization and expression study of sugarcane MYB transcription factor gene PEaMYBAS1 promoter from Erianthus arundinaceus that confers abiotic stress tolerance in tobacco
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Functional characterization and expression study of sugarcane MYB transcription factor gene PEaMYBAS1 promoter from Erianthus arundinaceus that confers abiotic stress tolerance in tobacco

机译:甘蔗MYB转录因子基因磷酸盐植物的甘蔗1启动子的功能性表征及表达研究,促使烟草中非生物胁迫耐受性耐受性耐受性

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Sugarcane is a glycophyte which has to confront various biotic and abiotic stresses while standing in fields. These stresses ultimately affect the growth and sucrose contents, causing heavy losses to farmers. A genetic approach through transgenic technology offers promising avenues to counter stresses and overcome the losses in production. In this study, PEaMYBAS1 promoter from Erianthus arundinaceus , a wild relative of sugarcane, was isolated to reveal its stress tolerance mechanism at the transcriptional level. A series of PEaMYBAS1 promoter deletions constructed from the transcription start sites F1 (?161 bp), F2 (?282 bp), F3 (?554 bp), F4 (?598 bp), F5 (?714 bp), F6 (?841 bp), and F0 (?1032 bp) were fused to the uid A reporter gene (GUS) separately, and each construct was analyzed by agroinfiltration in tobacco leaves subjected independently to drought, cold, salinity and wounding. Deletion analysis of the PEaMYBAS1 promoter revealed that the F3 (?554 bp) region was required for basal expression. Interestingly, full length deletion fragment F0 (?1032 bp) showed the highest GUS activity in drought (4.9 fold), among the other abiotic stresses such as cold (3.89 fold), salinity (3.87 fold) and wounding (3.06 fold). GUS induction characterization of the promoter revealed the enhanced stress tolerance capacity against abiotic stresses in the model plant Nicotiana tabacum . Thus, the full length deletion fragment F0 (?1032) of the inducible promoter PEaMYBAS1 can be advocated as an important genetic engineering tool to develop stress tolerant plants.
机译:甘蔗是一种糖糖细胞,其在站立在田地时必须面对各种生物和非生物胁迫。这些压力最终影响了生长和蔗糖含量,对农民造成重大损失。通过转基因技术的遗传方法提供了承诺的途径来反击强调并克服生产中的损失。在本研究中,分离来自Erianthus Arundinaeus的Peamybas1启动子,甘蔗的野生相对,揭示其在转录水平下的应力耐受机制。从转录开始部位F1(α161bp),F2(α282bp),f4(α598bp),f5(α714bp),f6(α714bp),f6(? 841bp)和F0(α1032bp)分别融合给UID报告基因(GUS),并且通过在烟草叶中独立于干旱,冷,盐度和伤口的烟草叶片中的农药分析每个构建体。 PeamyBas1启动子的缺失分析显示基础表达需要F3(α554bp)区域。有趣的是,全长缺失片段F0(α1032bp)在干旱(4.9倍)中显示出最高的GUS活性,以及​​其他非生物应力,如冷(3.89倍),盐度(3.87折叠)和伤口(3.06倍)。启动子的GUS诱导表征揭示了模型植物Nicotiana Tabacum中非生物胁迫的增强的应力耐受能力。因此,诱导型启动子杆肽1的全长缺失片段F0(α1032)可以被提倡作为发展应力耐受植物的重要遗传工程工具。

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