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首页> 外文期刊>BMC Plant Biology >Identification of transcription factors interacting with a 1274?bp promoter of MaPIP1;1 which confers high-level gene expression and drought stress Inducibility in transgenic Arabidopsis thaliana
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Identification of transcription factors interacting with a 1274?bp promoter of MaPIP1;1 which confers high-level gene expression and drought stress Inducibility in transgenic Arabidopsis thaliana

机译:鉴定与MAPIP1的1274磅BP启动子相互作用的转录因子; 1赋予转基因拟南芥的高级基因表达和干旱胁迫诱导性

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Drought stress can severely affect plant growth and crop yield. The cloning and identification of drought-inducible promoters would be of value for genetically-based strategies to improve resistance of crops to drought. Previous studies showed that the MaPIP1;1 gene encoding an aquaporin is involved in the plant drought stress response. In this study, the promoter pMaPIP1;1, which lies 1362?bp upstream of the MaPIP1;1 transcriptional initiation site, was isolated from the banana genome..And the transcription start site(A) is 47?bp before the ATG. To functionally validate the promoter, various lengths of pMaPIP1;1 were deleted and fused to GUS to generate pMaPIP1;1::GUS fusion constructs that were then transformed into Arabidopsis to generate four transformants termed M-P1, M-P2, M-P3 and M-P4.Mannitol treatment was used to simulate drought conditions. All four transformants reacted well to mannitol treatment. M-P2 (??1274?bp to ??1) showed the highest transcriptional activity among all transgenic Arabidopsis tissues, indicating that M-P2 was the core region of pMaPIP1;1. This region of the promoter also confers high levels of gene expression in response to mannitol treatment. Using M-P2 as a yeast one-hybrid bait, 23 different transcription factors or genes that interacted with MaPIP1;1 were screened. In an dual luciferase assay for complementarity verification, the transcription factor MADS3 positively regulated MaPIP1;1 transcription when combined with the banana promoter. qRT-PCR showed that MADS3 expression was similar in banana leaves and roots under drought stress. In banana plants grown in 45% soil moisture to mimic drought stress, MaPIP1;1 expression was maximized, which further demonstrated that the MADS3 transcription factor can synergize with MaPIP1;1. Together our results revealed that MaPIP1;1 mediates molecular mechanisms associated with drought responses in banana, and will expand our understanding of how AQP gene expression is regulated. The findings lay a foundation for genetic improvement of banana drought resistance.
机译:干旱胁迫会严重影响植物生长和作物产量。干旱诱导型启动子的克隆和鉴定将是基于基于遗传学的策略的价值,从而改善农作物的抗旱性。以前的研究表明,MAPIP1; 1个基因编码了水通蛋白的基因涉及植物干旱应激反应。在该研究中,启动子PMAPIP1; 1,其在MAPIP1的上游呈1362℃; 1转录引发位点,从香蕉基因组分离出。转录开始部位(A)是ATG之前的47bp。为了在功能上验证启动子,删除各种长度的PMAPIP1; 1被删除并融合给GUS以产生PMAPIP1; 1 :: GUS融合构建体然后转化为拟南芥,产生四种转化体M-P1,M-P2,M-P3。和M-P4.ManNitol治疗用于模拟干旱条件。所有四种转化体都反应甘露醇治疗良好。 M-P2(?? 1274?bp至10)显示所有转基因拟南芥组织中的最高转录活性,表明M-P2是PMAPIP1的核心区域; 1。该区域的启动子也赋予甘露醇治疗的高水平基因表达。使用M-P2作为酵母单杂交诱饵,23种不同的转录因子或与MAPIP1相互作用的基因;筛选1。在双荧光素酶测定中进行互补验证,转录因子MADS3积极调节MAPIP1; 1转录与香蕉启动子结合。 QRT-PCR显示疯子3表达在干旱胁迫下的香蕉叶和根中类似。在香蕉植物中生长45%的土壤水分以模仿干旱胁迫,MAPIP1; 1表达最大化,这进一步证明了MADS3转录因子可以用MAPIP1协同增量; 1。我们的结果表明,MAPIP1; 1介导与香蕉中干旱反应相关的分子机制,并将扩大我们对AQP基因表达如何调节的理解。该研究结果为香蕉抗旱的遗传改善奠定了基础。

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