Role of Polyamine Oxidase in Apoptosis Studies with RNA Interference

多胺氧化酶在 RNA 干扰细胞凋亡研究中的作用

• 批准号: 7904715
• 负责人: GLENN D KUEHN
• 金额: $ 5.56万
• 依托单位: NEW MEXICO STATE UNIVERSITY LAS CRUCES
• 依托单位国家: 美国
• 财政年份: 2009
• 资助国家: 美国
• 起止时间: 2009-09-01 至 2010-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7904715
• 关键词: Anabolism; Animals; Apoptosis; Apoptotic; Applications Grants; Avena sativa; Base Sequence; Binding Sites; Biochemical; Biochemical Reaction; Bioinformatics; Biological; Biological Models; Catabolism; Catalysis; Cells; Copper; DNA; Development Plans; Disease; Disease Resistance; Double-Stranded RNA; Enzymes; Eukaryotic Cell; Event; Funding; Gene Expression; Genes; Genetic Transcription; Grant; Hydrogen Peroxide; Ions; Knowledge; Laboratories; Link; Literature; Location; Mediating; Messenger RNA; Methodology; Methods; NADPH Oxidase; NF-kappa B; Necrotic Lesion; Oats; Oryza sativa; Oxidative Stress; Oxygen; Pathway interactions; Peroxidases; Plant Model; Plants; Plasmid Cloning Vector; Play; Polyamine Catabolism; Polyamines; Prevention; Process; Production; Promoter Regions; Proteins; RNA Interference; Reaction; Reactive Oxygen Species; Research; Research Design; Research Personnel; Respiratory Burst; Rice; Role; Seedling; Seeds; Sequence Analysis; Signal Transduction Pathway; Site; Source; Spermidine; Spermine; System; Techniques; Time; Wound Healing; Yeasts; amine oxidase; crosslink; direct application; knock-down; oxalate oxidase; oxidation; pathogen; polyamine oxidase; promoter; rapid technique; research study; response; transcription factor

DESCRIPTION (provided by applicant): A voluminous literature documents studies that correlate the catabolism of the polyamines, spermidine and spermine, in plant and animal cells with the process of programmed cell death (apoptosis). Polyamine oxidase (PAO) catalyzes oxygen-dependent cleavage of the polyamines to form hydrogen peroxide (H2O2), among other products. Many studies indicate that the causative agent for eliciting apoptosis is oxidative stress mediated by H2O2. Our project hypothesis is: The reaction catalyzed by the enzyme PAO is the major source of cellular H2O2 that causes H2O2-mediated apoptosis in eukaryotic cells. We have gained strong evidence that PAO catalysis is indeed the major source of H2O2 in a plant model system undergoing the hypersensitive response (HR). HR is a pathogen-elicited process mediated by H2O2, which culminates in apoptosis. The origin of the H2O2 is not known. In preliminary studies, we have applied RNA interference (RNAi) methods, using a newly discovered, rapid technique for introducing double-stranded (dsRNA) into plants during HR, and have succeeded in knocking down PAO enzymatic expression with concurrent abolishment of the H2O2 burst that normally accompanies HR. The specific aims of this project are: (1) RNA interference (RNAi) methods that exploit our new technique for introducing dsRNA into plant cells will be used to silence (knockdown) PAO gene expression in Avena sativa L. (oat) seedlings. This knockdown will be shown to result in suppression of five cellular parameters: PAO mRNA levels, PAO enzymatic activity, the H2O2 burst in the HR, catabolic loss of cellular polyamines during the HR, and entry into apoptosis. (2) The existence of an NF-kB-like transcription factor in plants will be established, which may have a role in regulating the expression of PAO by pro-apoptotic, H2O2-activated pathways. The DNA nucleotide sequence (gtgaatttcc) was discovered by us in two locations of the 5'-untranslated promoter region of the PAO gene from Oryza sativa (rice). This sequence contains recognition sites for binding transcription factors that link PAO gene transcription to NF-kB-like factors. We will complete the isolation of this protein to confirm its existence in the plant kingdom. (3) Methodologies, plant seed stocks, and plasmid vectors will be developed in order to exploit a synthetic copper(ll) ion-dependent genetic promoter system, produced by our laboratory, for controlling the synthesis of trans genes in plant and yeast hosts.

描述（由申请人提供）：大量文献记录了植物和动物细胞中多胺、亚精胺和精胺的分解代谢与程序性细胞死亡（凋亡）过程之间的关系。多胺氧化酶（PAO）催化多胺的氧依赖性裂解，形成过氧化氢（H2O2）和其他产物。许多研究表明，诱导细胞凋亡的病原体是H2O2介导的氧化应激。我们的项目假设是：PAO酶催化的反应是真核细胞H2O2的主要来源，导致H2O2介导的细胞凋亡。我们已经获得了强有力的证据，证明PAO催化确实是植物模型系统中发生超敏反应（hypersensitive response， HR）的H2O2的主要来源。HR是一个由H2O2介导的病原体引发的过程，最终导致细胞凋亡。H2O2的来源尚不清楚。在初步研究中，我们应用RNA干扰（RNAi）方法，使用一种新发现的快速技术在HR期间将双链（dsRNA）引入植物，并成功地降低了PAO酶的表达，同时消除了通常伴随HR的H2O2爆发。