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Differences in the Lolium rigidum Embryo Proteome of Seeds with a High (Light-insensitive) and Low (Light-sensitive) Level of Dormancy

机译:Holim rentidum胚胎蛋白质组的差异,高(光不振)和低(光敏)休眠水平

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A preliminary study of changes in the proteome of annual ryegrass (Lolium rigidum Gaud.) seeds during dormancy release is described in this chapter. Highly dormant seeds (i.e. light-insensitive, unable to germinate under light or dark conditions) wereprepared by stratification in darkness at 20 deg C for 2 days. Seeds with a low level of dormancy (i.e. light-sensitive, able to germinate under light but not dark conditions) were prepared by stratification in darkness at 20 deg C for 35 days. 2D gel electrophoresis (2D-PAGE) was performed using excised embryos. Only six proteins were found to differ in abundance between light-insensitive and light-sensitive embryos. Spots 1 and 2 were too low to be analysed in light-insensitive embryos but were present in light-sensitive embryos, representing at least a 20-fold induction. Spots 3 and 4 were three- to fivefold more abundant in light-insensitive compared with light-sensitive embryos. Spots 5 and 6 were more abundant in light-sensitive embryo samples,but this difference was less than twofold. The six protein spots of interest were excised from the gels, digested with trypsin and analysed by tandem mass spectrometry (MS/MS). Spots 1 and 2 gave significant matches with glyceral-dehyde 3-phosphate dehydrogenases (GAPDH). Spot 4 could not be matched either against the NCBInr Viridiplantae (Green Plants) or a translation of the Lolium gene index from The Institute for Genomic Research (TIGR). De novo sequencing of two peptides was performed, but matchingof these sequences to Lolium or total plant protein data-sets with the basic local alignment search tool (BLAST) has been unsuccessful. Data from spots 3, 5 and 6 were not sufficient to allow pattern matching identification, or successful de novo sequencing analysis, and remain unidentified.
机译:本章描述了临床释放年度黑麦草蛋白质组(Lolium Rentidum Gaud。)种子的初步研究。高度休眠的种子(即,在光或黑暗条件下不能发芽的光不溶,不能发芽)通过在20℃下的黑暗中的分层进行2天。休眠水平低的种子(即光敏感,能够在光下发芽,但不是黑暗的条件)通过在20℃下的黑暗中以20℃进行35天来制备。使用切除的胚胎进行2D凝胶电泳(2D-PAGE)。发现只有六种蛋白质在光不敏感和光敏胚胎之间的丰度不同。斑点1和2太低,不能在光不溶的胚胎中分析,但存在于光敏胚胎中,其表示至少20倍的诱导。与光敏胚胎相比,斑点3和4在光不分敏感方面是三到五倍。斑点5和6在光敏胚胎样品中更丰富,但这种差异小于双重。感兴趣的六种蛋白质斑点从凝胶中切除,用胰蛋白酶消化并通过串联质谱(MS / MS)分析。斑点1和2与甘硅-Deyde 3-磷酸脱氢酶(GAPDH)进行了显着的比赛。 SPOT 4不能与NCBINR VIRIDIMPLANTAE(绿色植物)或从基因组研究所(TIGR)的Lolium基因指数的翻译匹配。进行两种肽的Novo测序,但与基本局部对准搜索工具(BLAST)的基本局部对准搜索工具(BLAST)与Lolim或总植物蛋白质数据集匹配。来自斑点3,5和6的数据不足以允许模式匹配鉴定或成功的Novo测序分析,并保持身份定值。

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