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Nitrogen (N) is critical for micronutrient biofortification in wheat grain and is essential for a series of nitrogenous compounds biosynthesis. This study aims to assess the role of improved N supply in iron (Fe) and zinc (Zn) enrichment and expression of genes related to Zn and Fe chelation and transport in winter wheat. Potting and hydroponic culture experiments were conducted to study the effect of increasing N application on Zn and Fe uptake and translocation from roots to leaves and the temporal and spatial gene expression profiles of the NICOTIANAMINE SYNTHASE (NAS) genes in wheat. Plants were grown with low, medium and high N supply levels. The results showed that higher N application increased Fe and Zn content in leaves, and decreased Fe and Zn content in root compared with the lower N supply. High N application also increased the distribution of Fe and Zn from roots to leaves. Expression analysis showed that increased N application resulted in up-regulation of two wheat NAS genes, TaNAS1 and TaNAS2. Highly positive response between NAS genes and increasing N application indicated that abundance nicotianamine (NA) resulted from highly expressed NAS genes might involve in the chelation of Fe and Zn in the phloem and favor Fe and Zn uptake and accumulation in wheat leaves. 相似文献
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牛TLR4基因生物信息学分析 总被引:1,自引:0,他引:1
为了更加深入地了解牛TLR4基因的功能、结构及与该基因有关联的疾病识别及其致病机理,利用牛TLR4基因的氨基酸序列对其编码蛋白的基本理化性质、蛋白质译后的磷酸化位点和糖基化位点以及跨膜结构域和蛋白质结构进行预测。结果显示,牛TLR4基因一共编码841个氨基酸,负电荷残基总和(Asp+Glu)为84,正电荷残基总和(Arg+Lys)为76,不稳定指数小于40,表明该基因编码产物稳定性较好。在该基因整个编码产物中,亲水氨基酸占比较多,平均分值为-0.011,由此得知TLR4基因编码的蛋白质是一种易溶蛋白。有9个潜在的N-糖基化位点;78个磷酸化位点以及存在一个跨膜蛋白和存在信号肽,其切割位点在第25和第26个氨基酸之间。蛋白质的二、三级结构预测结果显示,二级结构和三级结构均由α-螺旋、β-折叠和无规则卷曲组成,其在生物合成、基因表达与调控等方面有重要作用。本研究结果可为牛TLR4基因深入研究提供理论基础。 相似文献
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Inducible responses in plants against pathogen attack play a major role in resistance to disease. The defense responses are
mostly associated with the expression of various kinds of inducible genes. We employed differential hybridization to isolate
elicitor-inducible genes (EIGs) of tobacco (Nicotiana tabacum cv. Samsun NN) using the tobacco-fungal elicitor system. A cDNA library was constructed from tobacco leaves treated for 12
hr with hyphal wall components (HWC) prepared from Phytophthora infestans, and six EIGs were identified. Expression of all EIGs was induced after inoculation with the soybean pathogen Pseudomonas syringae pv. glycinea (nonpathogenic on tobacco) or treatment with salicylic acid, and a variety of expression patterns of EIG mRNAs was observed.
Sequence analysis of EIG cDNAs revealed similarities to genes for SAR8.2 (EIG-B39 and EIG-D14), glycine-rich protein (EIG-G7), extensin (EIG-I30), acyltransferase (EIG-I24) and unknown protein (EIG-J7). Possible roles of EIG products in disease resistance are discussed.
Received 30 August 2000/ Accepted in revised form 30 November 2000 相似文献
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P. Castagnone-Sereno M. Bongiovanni A. Palloix A. Dalmasso 《European journal of plant pathology / European Foundation for Plant Pathology》1996,102(6):585-590
Experiments were designed to analyze the relationships between the root-knot nematodeMeloidogyne incognita and resistant tomato and pepper genotypes. From a natural avirulent isolate, near-isogenic nematode lineages were selected with virulence either against the tomatoMi resistance gene or the pepperMe3 resistance gene. Despite the drastic selection pressure used, nematodes appeared unable to overcome the pepperMe1 gene, therefore suggesting some differences in the resistance conferred byMe1 andMe3 in this species. Nematodes virulent onMi-resistant tomatoes were not able to reproduce onMe1-resistant nor onMe3-resistant peppers, and nematodes virulent onMe3-resistant peppers were not able to reproduce onMi-resistant tomatoes nor onMe1-resistant peppers. These results clearly demonstrate the specificity ofM. incognita virulence against resistance genes from both tomato and pepper, and indirectly suggest that gene-for-gene relationships could occur between these two solanaceous crops and the nematode. 相似文献
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