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Proteome approaches to characterize seed storage proteins related to ditelocentric chromosomes in common wheat (Triticum aestivum L.)

机译:蛋白质组学方法表征与普通小麦(Triticum aestivum L.)的双端中心染色体相关的种子贮藏蛋白

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Changes in protein composition of wheat endosperm proteome were investigated in 39 ditelocentric chromosome lines of common wheat (Triticum aestivum L.) cv. Chinese Spring. Two-dimensional gel electrophoresis followed by Coomassie Brilliant Blue staining has resolved a total of 105 protein spots in gel. Quantitative image analysis of protein spots was performed by PDQuest. Variations in protein spots between the euploid and the 39 ditelocentric lines were evaluated by spot number, appearance, disappearance and intensity. A specific spot present in all gels was taken as an internal standard, and the intensity of all other spots was calculated as the ratio of the internal standard. Our of the 1755 major spots detected in 39 ditelocentric lines, 1372 (78%) spots were found variable in different spot parameters: 147 (11%) disappeared, 978 (71%) up-regulated and 247 (18%) down-regulated. Correlation studies in changes in protein intensities among 24 protein spots across the ditelocentric lines were performed. High correlation in changes of protein intensities were observed among the proteins encoded by genes located in the homologous arms. Locations of structural genes controlling 26 spots were identified in 10 chromosomal arms. Multiple regulators of the same protein located at various chromosomal arms were also noticed. Identification of structural genes for most of the proteins was found difficult due to multiple regulators encoding the same protein. Two novel subunits (1B_Z, 1BD_Z), the structure of which are very similar to the high molecular weight glutenin subunit 12, were identified, and the chromosome arm location of these subunits were assigned.
机译:在39个普通小麦(Triticum aestivum L.)cv的双端染色体系中研究了小麦胚乳蛋白质组蛋白质组成的变化。中国春天。二维凝胶电泳,然后进行考马斯亮蓝染色,已经解析了凝胶中总共105个蛋白质斑点。蛋白质斑点的定量图像分析由PDQuest进行。通过斑点数目,外观,消失和强度来评估整倍体和39个双端中心线之间的蛋白质斑点的变化。将所有凝胶中存在的特定斑点作为内标,并将所有其他斑点的强度计算为内标的比率。在39个双中心线中检测到的1755个主要斑点中,有1372个(78%)斑点在不同的斑点参数中变化:147(11%)消失,978(71%)上调和247(18%)下调。进行了跨双心轴系的24个蛋白质斑点之间蛋白质强度变化的相关性研究。在位于同源臂中的基因编码的蛋白质中,观察到蛋白质强度变化的高度相关性。在10个染色体臂中鉴定了控制26个斑点的结构基因的位置。还注意到位于多个染色体臂的同一蛋白的多个调节子。由于编码同一蛋白质的多个调节子,发现鉴定大多数蛋白质的结构基因很困难。确定了两个新的亚基(1B_Z,1BD_Z),它们的结构与高分子量谷蛋白亚基12非常相似,并指定了这些亚基的染色体臂位置。

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