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Proteomic analysis from haploid and diploid embryos of Quercus suber L. identifies qualitative and quantitative differential expression patterns

机译:拟南芥单倍体和二倍体胚胎的蛋白质组学分析确定了定性和定量差异表达模式

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摘要

Quercus suber L. is a Mediterranean forest species with ecological, social and economic value. Clonal propagation of Q. suber elite trees has been successfully obtained from in vitro-derived somatic and gametic embryos. These clonal lines play a main role in breeding and genetic studies of Q. suber. To aid in unravelling diverse genetic and biological unknowns, a proteomic approach is proposed. The proteomic analysis of Q. suber somatic and gametic in vitro culture-derived embryos, based on DIGE and MALDI-MS, has produced for the first time proteomic data on this species. Seventeen differentially expressed proteins have been identified which display significantly altered levels between gametic and somatic embryos. These proteins are involved in a variety of cellular processes, most of which had been neither previously associated with embryo development nor identified in the genus Quercus. Some of these proteins are involved in stress and pollen development and others play a role in the metabolism of tannins and phenylpropanoids, which represent two of the major pathways for the synthesis of cork chemical components. Furthermore, the augmented expression levels found for specific proteins are probably related to the homozygous state of a doubled-haploid sample. Proteins involved in synthesis of cork components can be detected at such early stages of development, showing the potential of the method to be useful in searching for biomarkers related to cork quality.
机译:栎(Suber L.)是具有生态,社会和经济价值的地中海森林物种。已成功从体外来源的体细胞和配子胚中获得了优良的Q. suber优树的克隆繁殖。这些无性系在苏百克的繁殖和遗传研究中起主要作用。为了帮助解决各种遗传和生物学未知问题,提出了一种蛋白质组学方法。基于DIGE和MALDI-MS的Q.suber体细胞和配子体体外培养胚胎的蛋白质组学分析首次产生了该物种的蛋白质组学数据。已经鉴定出十七种差异表达的蛋白质,其在配子和体细胞胚之间显示出显着改变的水平。这些蛋白质参与多种细胞过程,其中大多数以前既未与胚胎发育相关,也未在栎属中鉴定。这些蛋白质中的一些参与应激和花粉的发育,而其他一些则在单宁和苯基丙烷的代谢中起作用,它们代表了软木化学成分合成的两个主要途径。此外,发现特定蛋白质的增强表达水平可能与双单倍体样品的纯合状态有关。可以在开发的早期阶段检测到与软木塞成分合成有关的蛋白质,这表明该方法有潜力用于寻找与软木塞质量有关的生物标记。

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