GENETICALLY MODIFIED PLANTS WITH RESISTANCE TO XANTHOMONAS AND OTHER BACTERIAL PLANT PATHOGENS
    1.
    发明申请
    GENETICALLY MODIFIED PLANTS WITH RESISTANCE TO XANTHOMONAS AND OTHER BACTERIAL PLANT PATHOGENS 审中-公开
    遗传修饰植物对西洋参和其他细菌植物病原体的抗性

    公开(公告)号:WO2013101877A3

    公开(公告)日:2015-06-18

    申请号:PCT/US2012071722

    申请日:2012-12-27

    CPC classification number: C12N15/8281 C07K14/415 C12N9/16

    Abstract: Applicants have successfully generated heritable phenotypes in plants making them resistant to bacterial blight. TAL effector binding elements, (EBEs) of bacterial pathogen disease susceptibility genes are modified to prevent induction of expression associated with disease states caused by the bacterial pathogens. Surprisingly, Applicants have found that modifications may be made in the EBEs of these genes which prevent bacterial pathogen induction, but still allow for normal plant development and seed production. Nucleic acid sequences for generating such plants, amino acid sequences, cells, vectors and expression constructs are included as well as resistant plants, seeds and lines.

    Abstract translation: 申请人已成功地在植物中产生了遗传表型,使其对细菌性枯萎病具有抗性。 细菌病原体易感性基因的TAL效应物结合元件(EBEs)被修饰以防止与由细菌病原体引起的疾病状态相关的表达的诱导。 令人惊讶的是,申请人已经发现可以在这些基因的EBE中进行修饰,这些基因预防细菌病原体的诱导,但仍然允许正常的植物发育和种子生产。 包括用于产生这种植物,氨基酸序列,细胞,载体和表达构建体的核酸序列以及抗性植物,种子和品系。

    MONOMER ARCHITECTURE OF TAL NUCLEASE OR ZINC FINGER NUCLEASE FOR DNA MODIFICATION
    2.
    发明申请
    MONOMER ARCHITECTURE OF TAL NUCLEASE OR ZINC FINGER NUCLEASE FOR DNA MODIFICATION 审中-公开
    用于DNA修饰的TAL核酸或ZINC指纹核的单体结构

    公开(公告)号:WO2013043638A1

    公开(公告)日:2013-03-28

    申请号:PCT/US2012/055980

    申请日:2012-09-19

    Abstract: The present invention provides compositions and methods for targeted cleavage of cellular chromatin in a region of interest and/or homologous recombination at a predetermined site in cells. Compositions include fusion polypeptides comprising a TAL effector binding or a zinc finger domain and an I-TevI homing endonuclease cleavage domain as well as nucleic acid sequence encoding the same. The use of the I-TevI domain allows for monomer endonuclease sequences to achieve cleavage of cellular chromatin and represents an advantage over prior endonucleases which require self-dimerization, and two nucleases with appropriate spacers.

    Abstract translation: 本发明提供了在细胞中的预定位点处目的切割感兴趣区域和/或同源重组中的细胞染色质的组合物和方法。 组合物包括包含TAL效应物结合或锌指结构域和I-TevI​​归巢内切核酸酶切割结构域的融合多肽以及编码该融合多肽的核酸序列。 使用I-TevI​​结构域允许单体内切核酸酶序列实现细胞染色质的切割,并且代表了优于需要自身二聚化的先前核酸内切酶的优点,以及具有合适间隔物的两个核酸酶。

    GENETICALLY MODIFIED PLANTS WITH RESISTANCE TO XANTHOMONAS AND OTHER BACTERIAL PLANT PATHOGENS
    5.
    发明申请
    GENETICALLY MODIFIED PLANTS WITH RESISTANCE TO XANTHOMONAS AND OTHER BACTERIAL PLANT PATHOGENS 审中-公开
    遗传修饰植物对西洋参和其他细菌植物病原体的抗性

    公开(公告)号:WO2013101877A2

    公开(公告)日:2013-07-04

    申请号:PCT/US2012/071722

    申请日:2012-12-27

    CPC classification number: C12N15/8281 C07K14/415 C12N9/16

    Abstract: Applicants have successfully generated heritable phenotypes in plants making them resistant to bacterial blight. TAL effector binding elements, (EBEs) of bacterial pathogen disease susceptibility genes are modified to prevent induction of expression associated with disease states caused by the bacterial pathogens. Surprisingly, Applicants have found that modifications may be made in the EBEs of these genes which prevent bacterial pathogen induction, but still allow for normal plant development and seed production. Nucleic acid sequences for generating such plants, amino acid sequences, cells, vectors and expression constructs are included as well as resistant plants, seeds and lines.

    Abstract translation: 申请人已成功地在植物中产生了遗传表型,使其对细菌性枯萎病具有抗性。 细菌病原体易感性基因的TAL效应物结合元件(EBEs)被修饰以防止与由细菌病原体引起的疾病状态相关的表达的诱导。 令人惊讶的是,申请人已经发现可以在这些基因的EBE中进行修饰,这些基因预防细菌病原体的诱导,但仍然允许正常的植物发育和种子生产。 包括用于产生这种植物,氨基酸序列,细胞,载体和表达构建体的核酸序列以及抗性植物,种子和品系。

    METHOD FOR TRANSMITTING RADIO FREQUENCY SIGNAL AND BASE STATION DEVICE
    6.
    发明申请
    METHOD FOR TRANSMITTING RADIO FREQUENCY SIGNAL AND BASE STATION DEVICE 审中-公开
    用于发射无线电频率信号和基站装置的方法

    公开(公告)号:WO2011157168A3

    公开(公告)日:2012-05-03

    申请号:PCT/CN2011075273

    申请日:2011-06-03

    CPC classification number: H04B1/0475

    Abstract: The present invention provides a method for transmitting a radio frequency (RF) signal and a base station device. The method includes: controlling energy of a first RF input signal of a power amplifier (PA), transmitting a first RF output signal, and coupling part of the first RF output signal and feeding it back to a predistortion system, so as to control the energy increase of a second RF input signal inputted to the PA according to a preset energy increment. The method can realize adjustment for the interModulation Distortion (IMD) component in the RF output signal outputted from the PA in an initial phase (that is a startup phase), thereby improving linearity of the PA in the initial phase.

    Abstract translation: 本发明提供了一种用于发送射频(RF)信号和基站装置的方法。 该方法包括:控制功率放大器(PA)的第一RF输入信号的能量,发送第一RF输出信号,以及耦合第一RF输出信号的一部分并将其馈送回预失真系统,以便控制 根据预设的能量增量输入到PA的第二RF输入信号的能量增加。 该方法可以在初始阶段(即启动阶段)中实现从PA输出的RF输出信号中的调制失真(IMD)分量的调整,从而提高初始阶段的PA的线性度。

    NUCLEASE ACTIVITY OF TAL EFFECTOR AND FOKI FUSION PROTEIN
    9.
    发明申请
    NUCLEASE ACTIVITY OF TAL EFFECTOR AND FOKI FUSION PROTEIN 审中-公开
    TAL效应和FOKI融合蛋白的核苷酸活性

    公开(公告)号:WO2011159369A1

    公开(公告)日:2011-12-22

    申请号:PCT/US2011/024515

    申请日:2011-02-11

    CPC classification number: C12N9/22 C12N15/8213

    Abstract: The present invention provides compositions and methods for targeted cleavage of cellular chromatin in a region of interest and/or homologous recombination at a predetermined site in cells. Compositions include fusion polypeptides comprising a TAL effector binding domain and a cleavage domain. The cleavage domain can be from any endonuclease. In certain embodiments, the endonuclease is a Type IIS restriction endonuclease. In further embodiments, the Type IIS restriction endonuclease is Fokl.

    Abstract translation: 本发明提供了在细胞中的预定位点处目的切割感兴趣区域和/或同源重组中的细胞染色质的组合物和方法。 组合物包括包含TAL效应子结合结构域和切割结构域的融合多肽。 切割结构域可以来自任何内切核酸酶。 在某些实施方案中,内切核酸酶是IIS型限制性内切酶。 在另外的实施方案中,类型IIS限制性内切核酸酶是Fok1。

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