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Molecular cloning and expression analysis of the MaASR1 gene in banana and functional characterization under salt stress

机译:盐胁迫下香蕉MaASR1基因的分子克隆,表达分析及功能表征

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Background: Abscisic acid (ABA)-, stress- and ripening-induced protein (ASR) is plant-specific hydrophilic transcriptional regulators involved in sucrose stress and wounding in banana. However, it is not known whether banana ASR genes confer salt stress tolerance. The contexts of the study was to analysis the sequence characterization of banana ASR1, and identify its expression patterns and function under salt stress using quantitative real-time PCR (qPCR) and overexpression in Arabidopsis. The purpose was to evaluate the role of banana ASR1 to salt stress tolerance employed by plants. ? Results: A full-length cDNA isolated from banana fruit was named MaASR1, and it had a 432 bp open reading frame (ORF) encoding 143 amino acids. MaASR1 was preferential expression in roots and leaves compared to low expression in fruits, rhizomes and flowers. Under salt stress, the expression of MaASR1 quickly increased and highest expression level was detected in roots and leaves at 4 h, and then gradually decreased. These results suggested that MaASR1 expression was induced under salt stress. MaASR1 protein was localized in the nucleus and plasma membrane. MaASR1 was transformed to Arabidopsis and verified by Southern and northern analysis, transgenic lines L14 and L38 integrated one and two copies of MaASR1, respectively, while overexpression in transgenic lines provided evidence for the role of MaASR1 to salt stress tolerance. Conclusions: This study demonstrated that overexpression of MaASR1 in Arabidopsis confers salt stress tolerance by reducing the expression of ABA/stress-responsive genes, but does not affect the expression of the ABA-independent pathway and biosynthesis pathway genes.
机译:背景:脱落酸(ABA),胁迫和成熟诱导蛋白(ASR)是植物特有的亲水性转录调节因子,参与蔗糖胁迫和香蕉伤害。但是,尚不知道香蕉ASR基因是否赋予盐胁迫耐受性。该研究的背景是分析香蕉ASR1的序列特征,并使用定量实时PCR(qPCR)和拟南芥中的过表达来鉴定其在盐胁迫下的表达模式和功能。目的是评估香蕉ASR1对植物采用的耐盐胁迫的作用。 ?结果:从香蕉果实中分离出的全长cDNA命名为MaASR1,具有432 bp的开放阅读框(ORF),编码143个氨基酸。与在水果,根茎和花中低表达相比,MaASR1在根和叶中优先表达。在盐胁迫下,MaASR1的表达迅速升高,并在4 h时在根和叶中检测到最高表达水平,然后逐渐下降。这些结果表明在盐胁迫下诱导了MaASR1表达。 MaASR1蛋白位于细胞核和质膜中。将MaASR1转化为拟南芥并通过Southern和Northern分析验证,转基因品系L14和L38分别整合了一个和两个拷贝的MaASR1,而在转基因品系中的过表达为MaASR1对盐胁迫耐性的作用提供了证据。结论:这项研究表明,拟南芥中MaASR1的过表达通过降低ABA /胁迫响应基因的表达而赋予了盐胁迫耐受性,但并不影响ABA非依赖性途径和生物合成途径基因的表达。

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