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首页> 外文期刊>Plant molecular biology reporter >Ectopic Expression of a Proteinase Inhibitor I4 (MtPiI4) Gene from Medicago truncatula Confers Plant Resistance to Pseudomonas syringae pv. Tomato DC3000
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Ectopic Expression of a Proteinase Inhibitor I4 (MtPiI4) Gene from Medicago truncatula Confers Plant Resistance to Pseudomonas syringae pv. Tomato DC3000

机译:run藜苜蓿蛋白酶抑制剂I4(MtPiI4)基因的异位表达赋予植物对丁香假单胞菌pv的抗性。番茄DC3000

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Proteinase inhibitors (PIs) play an important role in plant responses to biotic and environmental stimuli, but little is known about the role of PIs in mediating plant immune responses to microbial infection. In this study, a gene named proteinase inhibitor I4 (MtPiI4) was isolated from Medicago truncatula and characterized as a serpin family gene with a typically conserved DUF716 domain. MtPiI4 was differentially expressed in seed, root, leaf, stem and flower tissues. Expression of MtPiI4 was induced by inoculation with a typical bacterial pathogen Pseudomonas syringae pv. tomato DC3000 strain (Pst DC3000). It was also up-regulated by methyl jasmonate (MeJA) treatment. To identify its function in regulating plant immunity against Pst DC3000, we constructed transgenic Arabidopsis plants over-expressing MtPiI4. Compared to wild type, 35S::MtPiI4 plants showed enhanced resistance to Pst DC3000. Expression of JA biosynthetic and responsive genes such as LOX2, PDF1.2, and VSP1 was depressed in 35S::MtPiI4 plants as compared to wild type, suggesting that the JA signaling response was attenuated in 35S::MtPiI4 plants upon Pst DC3000 exposure. Furthermore, over-expression of MtPiI4 led to up-regulation of NPR1 (nonexpressor of pathogenesis-related gene 1-a negative regulator of JA signaling) and down-regulation of MAPK4 (mitogen-activated protein kinase4-a positive regulator of JA signaling). These results indicate that MtPiI4 regulation of plant resistance to Pst DC3000 is involved in the JA signaling transduction pathway.
机译:蛋白酶抑制剂(PIs)在植物对生物和环境刺激的反应中起重要作用,但对PI在介导植物对微生物感染的免疫反应中的作用知之甚少。在这项研究中,从梅花苜蓿中分离出一种名为蛋白酶抑制剂I4(MtPiI4)的基因,并将其表征为带有典型DUF716结构域的丝氨酸蛋白酶抑制剂家族基因。 MtPiI4在种子,根,叶,茎和花组织中差异表达。通过接种典型的细菌病原体丁香假单胞菌PV诱导MtPiI4的表达。番茄DC3000株(Pst DC3000)。茉莉酸甲酯(MeJA)处理也上调了它。为了确定其在调节植物抗Pst DC3000免疫力中的功能,我们构建了过表达MtPiI4的转基因拟南芥植物。与野生型相比,35S :: MtPiI4植物显示出对Pst DC3000的增强抗性。与野生型相比,在35S :: MtPiI4植物中JA生物合成和响应基因如LOX2,PDF1.2和VSP1的表达被抑制,这表明在暴露于Pst DC3000的情况下,在35S :: MtPiI4植物中JA信号响应减弱了。此外,MtPiI4的过表达导致NPR1上调(致病相关基因1-a JA信号负调节子的非表达子)和MAPK4的下调(MAPK4(JA信号转导的丝裂原活化蛋白激酶4的正调节子))。 。这些结果表明,MtPiI4调节植物对Pst DC3000的抗性参与了JA信号转导途径。

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