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Proanthocyanidin accumulation and transcriptional responses in the seed coat of cranberry beans ( Phaseolus vulgaris L.) with different susceptibility to postharvest darkening

机译:蔓越莓变种后变黑敏感性不同的酸果蔓豆(菜豆)种皮中原花青素的积累和转录响应

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Background Edible dry beans ( Phaseolus vulgaris L.) that darken during postharvest storage are graded lower and are less marketable than their non-darkened counterparts. Seed coat darkening in susceptible genotypes is dependent upon the availability of proanthocyanidins, and their subsequent oxidation to reactive quinones. Mature cranberry beans lacking this postharvest darkening trait tend to be proanthocyanidin-deficient, although the underlying molecular and biochemical determinants for this metabolic phenomenon are unknown. Results Seed coat proanthocyanidin levels increased with plant maturation in a darkening-susceptible cranberry bean recombinant inbred line (RIL), whereas these metabolites were absent in seeds of the non-darkening RIL plants. RNA sequencing (RNA-seq) analysis was used to monitor changes in the seed coat transcriptome as a function of bean development, where transcript levels were measured as fragments per kilobase of exon per million fragments mapped. A total of 1336 genes were differentially expressed between darkening and non-darkening cranberry bean RILs. Structural and regulatory genes of the proanthocyanidin biosynthesis pathway were upregulated in seed coats of the darkening RIL. A principal component analysis determined that changes in transcript levels for two genes of unknown function and three proanthocyanidin biosynthesis genes, FLAVANONE 3-HYDROXYLASE 1 , DIHYDROFLAVONOL 4-REDUCTASE 1 and ANTHOCYANIDIN REDUCTASE 1 ( PvANR1 ) were highly correlated with proanthocyanidin accumulation in seed coats of the darkening-susceptible cranberry bean RIL. HPLC-DAD analysis revealed that in vitro activity of a recombinant Pv ANR1 was NADPH-dependent and assays containing cyanidin yielded epicatechin and catechin; high cyanidin substrate levels inhibited the formation of both of these products. Conclusion Proanthocyanidin oxidation is a pre-requisite for postharvest-related seed coat darkening in dicotyledonous seeds. In model plant species, the accumulation of proanthocyanidins is dependent upon upregulation of biosynthetic genes. In this study, proanthocyanidin production in cranberry bean seed coats was strongly associated with an increase in PvANR1 transcripts during seed maturation. In the presence of NADPH, Pv ANR1 converted the physiologically relevant substrate cyanidin to epicatechin and catechin.
机译:背景技术收获后储存期间变黑的可食用干豆(菜豆)比未变黑的豆品分级低,且市场销售性较差。易感基因型的种皮变黑取决于原花青素的可用性及其随后氧化为反应性醌的能力。缺乏这种采后变黑特性的成熟蔓越莓豆倾向于缺乏原花色素,尽管尚不清楚该代谢现象的潜在分子和生化决定因素。结果在变黑易感的蔓越莓重组自交系(RIL)中,种子皮的原花色素水平随植物成熟而增加,而在未变黑的RIL植物的种子中则没有这些代谢产物。 RNA测序(RNA-seq)分析用于监测种皮转录组随豆发育的变化,其中转录水平以每千个外显子每千碱基的片段数计。在变黑和不变红的蔓越莓RIL之间共有1336个基因差异表达。原花青素生物合成途径的结构和调节基因在变黑的RIL的种皮中上调。主成分分析确定,两个功能未知的基因和三个原花青素生物合成基因(黄酮3羟化酶1,二氢黄酮酚4还原酶1和原花色素还原酶1(PvANR1))的转录水平变化与种皮中原花色素的积累高度相关易变黑的蔓越莓RIL。 HPLC-DAD分析表明,重组Pv ANR1的体外活性是NADPH依赖性的,含有花青素的测定可产生表儿茶素和儿茶素;高花青素底物水平抑制了这两种产物的形成。结论原花青素氧化是双子叶种子收获后相关种皮变黑的前提。在模型植物物种中,原花色素的积累取决于生物合成基因的上调。在这项研究中,蔓越莓种皮中原花色素的产生与种子成熟过程中PvANR1转录本的增加强烈相关。在NADPH存在下,Pv ANR1将生理相关的底物花青素转化为表儿茶素和儿茶素。

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