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首页> 外文期刊>Molecular Biology Reports >Cloning and characterization of a SnRK1-encoding gene from Malus hupehensis Rehd. and heterologous expression in tomato
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Cloning and characterization of a SnRK1-encoding gene from Malus hupehensis Rehd. and heterologous expression in tomato

机译:平邑甜茶SnRK1编码基因的克隆与鉴定。和异源表达在番茄中

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Sucrose non-fermenting-1-related protein kinase-1 (SnRK1) plays an important role in metabolic regulation in plant. To understand the molecular mechanism of amino acids and carbohydrate metabolism in Malus hupehensis Rehd. var. pinyiensis Jiang (Pingyi Tiancha, PYTC), a full-length cDNA clone encoding homologue of SnRK1 was isolated from PYTC by Rapid Amplification of cDNA Ends (RACE). The clone, designated as MhSnRK1, contains 2063 nucleotides with an open reading frame of 1548 nucleotides. The deduced 515 amino acids showed high identities with other plant SnRK1 genes. Quantitative real-time PCR analysis revealed this gene was expressed in roots, stems and leaves. Exposing seedlings to nitrate caused and initial decrease in expression of the MhSnRK1 gene in roots, leaves and stems in short term. Ectopic expression of MhSnRK1 in tomato mainly resulted in higher starch content in leaf and red-ripening fruit than wild-type plants. This result supports the hypothesis that overexpression of SnRK1 causes the accumulation of starch in plant cells. All the results suggest that MhSnRK1 may play important roles in carbohydrate and amino acid metabolisms. Keywords Apple - Clone - Gene expression - MhSnRK1 - Starch All authors contributed equally to the paper.
机译:蔗糖非发酵-1相关蛋白激酶1(SnRK1)在植物的代谢调控中起着重要作用。了解平邑甜茶中氨基酸和碳水化合物代谢的分子机制。变种通过快速扩增cDNA末端(RACE)从PYTC中分离出编码SnRK1同源物的全长cDNA克隆pinyiensis Jiang(平邑天茶,PYTC)。命名为MhSnRK1的克隆包含2063个核苷酸,开放阅读框为1548个核苷酸。推断的515个氨基酸与其他植物SnRK1基因具有高度同一性。实时定量PCR分析表明该基因在根,茎和叶中表达。短期使幼苗暴露于硝酸盐中会导致MhSnRK1基因在根,叶和茎中的表达并开始减少。 MhSnRK1在番茄中的异位表达主要导致叶片和成熟红色果实中的淀粉含量高于野生型植物。该结果支持以下假设:SnRK1的过表达导致淀粉在植物细胞中的积累。所有结果表明,MhSnRK1可能在碳水化合物和氨基酸代谢中起重要作用。关键词苹果-克隆-基因表达-MhSnRK1-淀粉所有作者对本文的贡献均相等。

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