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Proteomic analysis of near-isogenic sunflower varieties differing in seed oil traits

机译:不同种子油性状的近等基因向日葵品种的蛋白质组学分析

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Near-isogenic sunflower lines containing 25% (inbred RHA280) and 48% (RHA801) oil by seed dry mass were comparatively analyzed in biological triplicate at 18 days after flowering using two-dimensional (both p/3-10 and 4-7) Difference Gel Electrophoresis. Additionally, two inbred lines varying in oleic acid content, HA89 (18% oleic) and HA341 (89% oleic), were also analyzed in the same manner. Statistical analyses of these sunflower lines was performed beginning with fitting a mixed effects linear model to the log-transformed optical volume of each spot to account for gel variation, followed by testing the significance between varieties for mean transformed optical spot volumes. The p-values from the spot analysis procedures were then used to find the cutoff point for differential expression using a 10% false-discovery rate (FDR). Comparison of the oil content and oleic acid composition lines revealed 77 and 42 protein spots below the 10% FDR cutoff, respectively, and were therefore declared differentially expressed. Liquid chromatography-tandem mass spectrometry analysis of each of these protein spots resulted in assignments for 44 and 17 spots, respectively. Fructokinase, plastid phosphoglycerate kinase, and enolase proteins were determined to be up-regulated in the high oil line, while phosphofructokinase, cytosolic phosphoglucomutase, and cytsolic phosphoglycerate kinase were up-regulated in the low oil variety. Additionally, four activities involved in amino acid synthesis were up-regulated in the low oil variety in addition to 12S storage proteins and a protein similar to legumin storage protein. Interestingly, two 2-DE spots identified as 14-3-3 proteins were found to be up-regulated in high oleic acid variety. Alteration of glycolytic and amino acid biosynthetic enzymes, as well as storage protein levels, suggests seed oil content is tightly linked to carbohydrate metabolism and protein synthesis in a complex manner.
机译:在开花后第18天,使用二维方法(p / 3-10和4-7),一式三份地比较了按种子干重计含25%(自交RHA280)和48%(RHA801)油的近等基因向日葵品系。差异凝胶电泳。另外,还以相同的方式分析了油酸含量不同的两个自交系,即HA89(18%的油酸)和HA341(89%的油酸)。对这些向日葵品系进行统计分析,首先将混合效应线性模型拟合到每个斑点的对数转换光学体积以解决凝胶变化,然后测试变种之间平均转换光学斑点体积的显着性。然后,使用10%错误发现率(FDR)将来自斑点分析程序的p值用于查找差异表达的临界点。比较油含量和油酸组成谱系,分别发现FDR临界值低于10%时有77和42个蛋白点,因此被宣布为差异表达。对这些蛋白质斑点中的每一个进行液相色谱-串联质谱分析,分别得到44个和17个斑点的分配。在高油品系中,果糖激酶,质体磷酸甘油酸激酶和烯醇酶蛋白被确定为上调,而在低油品系中,磷酸果糖激酶,胞质磷酸葡糖突变酶和胞浆磷酸甘油酸激酶被上调。另外,在低油品种中,除了12S贮藏蛋白和类似于豆蛋白贮藏蛋白的蛋白外,与氨基酸合成有关的四个活性也被上调。有趣的是,发现在高油酸品种中两个被识别为14-3-3蛋白的2-DE点被上调。糖酵解和氨基酸生物合成酶的变化以及贮藏蛋白的水平表明,籽油含量以复杂的方式与碳水化合物的代谢和蛋白质的合成紧密相关。

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