首页> 外文期刊>Plant Growth Regulation: An International Journal on Natural and Synthetic Regulators >A comparative proteomic approach to identify defence-related proteins between resistant and susceptible rice cultivars challenged with the fungal pathogen Rhizoctonia solani
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A comparative proteomic approach to identify defence-related proteins between resistant and susceptible rice cultivars challenged with the fungal pathogen Rhizoctonia solani

机译:一种对比较蛋白质组学方法,以鉴定无敏感的水稻品种与真菌病原体Rhizoctonia solani挑战的抗性和易感水稻品种之间的蛋白质组

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摘要

Rice sheath blight, caused by Rhizoctonia solani, is a major worldwide rice disease for which little is known about the molecular mechanisms of host immunity to infection. In the present study, a comparative proteomic analysis of two rice cultivars, Teqing (resistant) and Lemont (susceptible), inoculated with R. solani was conducted using an eight-plex iTRAQ (isobaric tags for relative and absolute quantitation) technique, resulting in the identification and quantification of 6560 proteins. A total of 755 proteins showed significant changes in abundance between plants infected with R. solani and control plants, based on an error factor < 2 and a more than 1.5-fold or less than 0.67-fold quantitative difference. The differentially abundant proteins were mainly involved in glyoxylate and dicarboxylate metabolism; glycine, serine and threonine metabolism; unsaturated fatty acid biosynthesis; and glycolysis/gluconeogenesis regulation pathways (p < 0.01). In addition, the expression levels of the genes encoding selected proteins were tested by qRT-PCR, and their functions were tested in Nicotiana benthamiana via agroinfiltration. Based on these proteomic and experimental data, a putative model of the regulation of rice immunity under R. solani infection is proposed. The proteins identified in the present study provide a basis for elucidating the molecular mechanisms underlying rice immunity to infection by R. solani.
机译:米鞘枯萎,由Rhizoctonia Solani引起的,是全球性稻米病,对宿主免疫感染的分子机制很少。在本研究中,使用八个Plex ITRAQ(用于相对定量的异常定量)技术进行了接种与R.Solani的两种水稻品种,Teqing(抗性)和羊膜(易感)的比较蛋白质组学分析,导致6560蛋白的鉴定和定量。基于误差因子<2和超过1.5倍或小于0.67倍的定量差异,共755蛋白蛋白质在感染的植物之间的丰富变化显着变化。差异丰富的蛋白质主要参与乙氧基化物和二羧酸酯代谢;甘氨酸,丝氨酸和苏氨酸代谢;不饱和脂肪酸生物合成;和糖酵解/葡糖生成调节途径(P <0.01)。此外,通过QRT-PCR测试编码所选蛋白质的基因的表达水平,并通过农药在尼古利氏植物嗜烟醛测试中测试它们的功能。基于这些蛋白质组学和实验数据,提出了R.Solani感染下水稻免疫调节的推定模型。本研究中鉴定的蛋白质为阐明稻免疫豁免潜免疫的分子机制提供了基础,通过R.Solani感染。

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