首页> 外文期刊>Genetics and Molecular Research >Cloning of an anthocyanidin synthase gene homolog from blackcurrant (Ribes nigrum L.) and its expression at different fruit stages
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Cloning of an anthocyanidin synthase gene homolog from blackcurrant (Ribes nigrum L.) and its expression at different fruit stages

机译:黑加仑(Ribes nigrum L.)花色苷合酶基因同源物的克隆及其在不同果期的表达

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Anthocyanidin synthase (ANS), a 2-oxoglutarate (2OG) and Fe(II)-dependent oxygenase, catalyzes the penultimate step in anthocyanin biosynthesis, from leucoanthocyanidins to anthocyanidins, the first colored compound in the anthocyanin pathway. In this study, a full-length, 1427-bp long cDNA named RnANS1, which is homologous to the anthocyanidin synthase gene, was cloned from blackcurrant using a homologous cloning strategy. RnANS1 is highly homologous to other plant ANS genes at both the nucleotide and amino acid sequence levels. The deduced protein contains domains conserved in the 2OG and Fe(II)-dependent oxygenase, and is phylogenetically closely related to Paeonia suffruticosa and Paeonia lactiflora. The expression of RnANS1 was upregulated during fruit maturation, and correlated with the accumulation of anthocyanins and soluble carbohydrates in the fruit. Further characterization of the structure and expression patterns of RnANS1 will clarify our understanding of anthocyanin biosynthesis in blackcurrant, and support the development of molecular approaches to manipulate anthocyanin production in this plant.
机译:花青素合酶(ANS)是一种2-氧代戊二酸酯(2OG)和Fe(II)依赖性加氧酶,催化花色苷生物合成中的倒数第二个步骤,从花色素苷到花色素苷,是花色素苷途径中的第一个有色化合物。在这项研究中,使用同源克隆策略从黑醋栗中克隆了与花青素合酶基因同源的全长1427 bp长的cDNA,称为RnANS1。 RnANS1在核苷酸和氨基酸序列水平上均与其他植物ANS基因高度同源。推导的蛋白质包含在2OG和依赖Fe(II)的加氧酶中保守的域,并且在系统发育上与Paeonia suffruticosa和Paeonia lactiflora密切相关。 RnANS1的表达在果实成熟过程中被上调,并与花色苷和可溶性碳水化合物在果实中的积累相关。 RnANS1的结构和表达模式的进一步表征将阐明我们对黑加仑中花色苷生物合成的理解,并支持开发控制该植物中花色苷生产的分子方法。

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