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    • 2. 发明申请
    • CHEMICALLY-INDUCIBLE ARABIDOPSIS PR-1 PROMOTER
    • 化学诱导性ARABIDOPSIS PR-1 PROMOTER
    • WO1998003536A1
    • 1998-01-29
    • PCT/US1997012626
    • 1997-07-18
    • NOVARTIS CORPORATIONLEBEL, Edouard, GuillaumeRYALS, John, AndrewTHORNE, LeighUKNES, Scott, JosephWARD, Eric, Russell
    • NOVARTIS CORPORATION
    • C07H21/04
    • C12N15/8238C07K14/415
    • The nucleic acid sequence of the full-length, chemically inducible Arabidopsis PR-1 promoter has been discovered and is disclosed herein. Furthermore, cis-acting regulatory elements in the Arabidopsis PR-1 promoter involved in chemical induction have been characterized using deletion and linker-scanning mutagenesis and in vivo footprinting. It has been discovered that at least a portion of the region of promoter between positions -698 and -621 (relative to the transcription start site of the PR-1 gene) is required for induction of gene expression by chemicals. Two 10-bp linker-scanning mutations centered at 640-bp and 610-bp upstream from the transcription start site abolish the inducibility of the promoter while another 10-bp mutation centered at -670 bp results in average induced expression levels 4-fold higher than the unmutated promoter. Additionally, inducible in vivo footprints are located at positions -629 and -628 and at position -604 on the coding strand and at position -641 on the non-coding strand. The use of chemically inducible Arabidopsis PR-1 promoter fragments to regulate gene expression in plants in the presence of inducing chemicals such as SA, INA, and BTH is disclosed, as well as the use of these elements for the isolation of transcriptional regulatory proteins involved in the promoter regulation and for the construction of inducible hybrid promoters.
    • 已经发现了全长化学诱导型拟南芥PR-1启动子的核酸序列,并在此公开。 此外,参与化学诱导的拟南芥PR-1启动子中的顺式作用调节元件已经使用缺失和连接物扫描诱变和体内足迹进行表征。 已经发现,通过化学物质诱导基因表达需要至少部分-698和-621位点之间的启动子区域(相对于PR-1基因的转录起始位点)。 以转录起始位点上游640-bp和610-bp为中心的两个10-bp接头扫描突变消除了启动子的诱导性,而另一个以-670bp为中心的10-bp突变导致平均诱导的表达水平高4倍 比未突变的启动子。 此外,可诱导的体内足迹位于编码链上的位置-629和-628,位置-604位于非编码链上-641位。 公开了使用化学诱导型拟南芥PR-1启动子片段在诱导化学物质如SA,INA和BTH存在下调节植物中的基因表达,以及这些元件用于分离涉及转录调节蛋白的用途 在启动子调节和诱导型杂合启动子的构建中。
    • 3. 发明申请
    • MANIPULATION OF PROTOPORPHYRINOGEN OXIDASE ENZYME ACTIVITY IN EUKARYOTIC ORGANISMS
    • 原核生物有机体中原生质体氧化酶酶活性的操作
    • WO1995034659A1
    • 1995-12-21
    • PCT/IB1995000452
    • 1995-06-08
    • CIBA-GEIGY AGWARD, Eric, RussellVOLRATH, Sandra
    • CIBA-GEIGY AG
    • C12N15/53
    • C12Y103/03004C12N5/04C12N9/001C12N15/8274C12Q1/6895
    • The present invention provides novel eukaryotic DNA sequences coding for native protoporphyrinogen oxidase (protox) or modified forms of the enzyme which are herbicide tolerant. Plants having altered protox activity which confers tolerance to herbicides are also provided. These plants may be bred or engineered for resistance to protox inhibitors via mutation of the native protox gene to a resistant form or through increased levels of expression of the native protox gene, or they may be transformed with modified eukaryotic or prokaryotic protox coding sequences or wild type prokaryotic protox sequences which are herbicide tolerant. Diagnostic and other uses for the novel eukaryotic protox sequence are also described. Plant genes encoding wild-type and altered protox, purified plant protox, methods of isolating protox from plants, and methods of using protox-encoding genes are also disclosed.
    • 本发明提供编码天然原卟啉原氧化酶(protox)或耐除草剂的酶的修饰形式的新型真核DNA序列。 还提供了赋予除草剂耐受性的具有改变的排毒活性的植物。 这些植物可以通过将天然protox基因突变为抗性形式或通过增加天然protox基因的表达水平培育或设计用于抵抗前毒素抑制剂,或者可以用经修饰的真核或原核protox编码序列或野生型 类型的原核生殖毒素序列是耐除草剂。 还描述了用于新型真核毒素序列的诊断和其它用途。 还公开了编码野生型和改变的protox的植物基因,纯化的植物protox,从植物中分离protox的方法,以及使用protox编码基因的方法。