首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Identification of a MYB3R gene involved in drought, salt and cold stress in wheat (Triticum aestivum L.).
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Identification of a MYB3R gene involved in drought, salt and cold stress in wheat (Triticum aestivum L.).

机译:鉴定涉及小麦(Triticum aestivum L.)干旱,盐和冷胁迫的MYB3R基因。

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Abiotic stress seriously affects crop growth and productivity. To better understand the mechanisms plant uses to cope with drought, cold and salt stress, it is necessary to isolate and characterize important regulators response to these stresses. In this study, we cloned a MYB gene from wheat (Triticum aestivum L.) and designated it as TaMYB3R1 based on its conserved three repeats in MYB domain. The sequence of TaMYB3R1 protein shares high identity to other plant MYB3R proteins. Subcellular localization experiment in onion epidermal cells proved that TaMYB3R1 localized in the nucleus. Trans-activation essays in yeast cells confirmed that TaMYB3R1 was a transcriptional activator, and only C-terminal region was able to activate the expression of beta-galactosidase. DNA-binding test showed the MSA cis element-binding activity of TaMYB3R1. After exogenous application of phytohormone ABA, the expression of TaMYB3R1 was induced, and its transcripts accumulated up to 24h; this is also the case for MeJA treatment, but after it peaked at 4h, it decreased to low levels. However, either SA or ET had no obvious effect on the expression of TaMYB3R1. Furthermore, the TaMYB3R1 was initially expressed at low levels and was gradually induced following treatment with salt, and continued to increase up to 72 h. This was similar for the cold treatment. In contrast, the peak appeared at 6h of the PEG treatment, and then gradually decreased to low levels. Our results suggest that TaMYB3R1 is potentially involved in wheat response to drought, salt and cold stress.
机译:非生物胁迫严重影响作物的生长和生产力。为了更好地理解植物应对干旱,寒冷和盐胁迫的机制,有必要对重要的调节剂进行分离并表征其对这些胁迫的响应。在这项研究中,我们从小麦(Triticum aestivum L.)中克隆了一个MYB基因,并根据其在MYB域中的三个保守重复序列将其命名为TaMYB3R1。 TaMYB3R1蛋白的序列与其他植物MYB3R蛋白具有高度同一性。洋葱表皮细胞的亚细胞定位实验证明TaMYB3R1定位在细胞核中。酵母细胞中的反式激活文章证实TaMYB3R1是一种转录激活剂,只有C端能够激活β-半乳糖苷酶的表达。 DNA结合试验显示TaMYB3R1的MSA顺式元件结合活性。外源施用植物激素ABA后,诱导了TaMYB3R1的表达,其转录本积累长达24h。 MeJA处理也是如此,但在4h达到峰值后,下降到较低水平。但是,SA或ET对TaMYB3R1的表达均无明显影响。此外,TaMYB3R1最初以低水平表达,并在用盐处理后逐渐诱导,并持续增加至72小时。这与冷处理相似。相反,该峰在PEG处理的6小时出现,然后逐渐降低至低水平。我们的结果表明,TaMYB3R1可能参与小麦对干旱,盐分和寒冷胁迫的反应。

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