首页> 外文期刊>Planta >Isolation of a cDNA clone (PcSrp) encoding serine-rich-protein from Porteresia coarctata T. and its expression in yeast and finger millet (Eleusine coracana L.) affording salt tolerance
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Isolation of a cDNA clone (PcSrp) encoding serine-rich-protein from Porteresia coarctata T. and its expression in yeast and finger millet (Eleusine coracana L.) affording salt tolerance

机译:分离来自Porteresia coarctata T.的富含丝氨酸蛋白的cDNA克隆(PcSrp),并在酵母和小米(Eleusine coracana L.)中表达,从而提供耐盐性

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摘要

A 1.4 Kb cDNA clone encoding a serine-rich protein has been isolated from the cDNA library of salt stressed roots of Porteresia coarctata, and designated as P. coarctata serine-rich-protein (PcSrp) encoding gene. Northern analysis and in situ mRNA hybridization revealed the expression of PcSrp in the salt stressed roots and rhizome of P. coarctata. However, no such expression was seen in the salt stressed leaves and in the unstressed tissues of root, rhizome and leaf, indicating that PcSrp is under the control of a salt-inducible tissue-specific promoter. In yeast, the PcSrp conferred increased NaCl tolerance, implicating its role in salinity tolerance at cellular level. Further, PcSrp was cloned downstream to rice Actin-1 promoter and introduced into finger millet through particle-inflow-gun method. Transgenic plants expressing PcSrp were able to grow to maturity and set seed under 250 mM NaCl stress. The untransformed control plants by contrast failed to survive under similar salt stress. The stressed roots of transgenic plants invariably accumulated higher Na+ and K+ ion contents compared to roots of untransformed plants; whereas, shoots of transgenics accumulated lower levels of both the ions than that of untransformed plants under identical stress, clearly suggesting the involvement of PcSrp in ion homeostasis contributing to salt tolerance.
机译:一个1.4 Kb cDNA克隆,编码富含丝氨酸的蛋白已从盐胁迫的Porteresia coarctata的cDNA库中分离出来,并被命名为P. coarctata富含丝氨酸的蛋白(PcSrp)编码基因。 Northern分析和原位mRNA杂交揭示了PcSrp在盐胁迫的根和根际根中的表达。但是,在盐胁迫的叶片以及根,根茎和叶片的未胁迫组织中均未观察到这种表达,表明PcSrp受盐诱导的组织特异性启动子控制。在酵母中,PcSrp赋予NaCl耐受性增加,暗示其在细胞水平上对盐分耐受性的作用。此外,将PcSrp克隆到水稻Actin-1启动子的下游,并通过颗粒枪法引入小米。表达PcSrp的转基因植物能够生长到成熟,并将种子置于250 mM NaCl胁迫下。相反,未转化的对照植物在相似的盐胁迫下不能存活。与未转化植物的根相比,转基因植物的胁迫根始终积累较高的Na + 和K + 离子含量。相反,转基因的芽在相同的胁迫下比未转化的植物积累的离子含量要低,这清楚地表明PcSrp参与了离子稳态,从而提高了耐盐性。

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