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    • 82. 发明申请
    • Targeted genetic manipulation using Mu bacteriophage cleaved donor complex
    • 使用Mu噬菌体切割供体复合物进行靶向遗传操作
    • US20020132350A1
    • 2002-09-19
    • US09951856
    • 2001-09-13
    • Pioneer Hi-Bred International, Inc.
    • Hideki SuzukiLeszek Alexander Lyznik
    • C12N015/74C12N015/00
    • C12N15/8213A01K2217/05A01K2217/075C12N15/8202C12N15/8206C12N15/902
    • Compositions and methods for targeted genetic manipulation of an organism are provided. The compositions are novel integration vectors derived from the Mu bacteriophage comprising an active cleaved donor complex (CDC) and further comprising a targeting mechanism whereby integration of the Mu transposable cassette may be directed to a predetermined target site within a host organism's genome. These integration vectors comprise a Mu transposable cassette and one or more navigator elements that direct targeted insertion of the CDC. Methods of the invention utilize the integration vectors of the invention to insert the Mu transposable cassette into a target site of an organism's genome. This insertion occurs in the absence of the MuB accessory protein. The methods are useful for modulating activity of known genes and for targeting integration of nucleotide sequences of interest into a specific location of an organism's genome. Accordingly, the methods may also be used to create gene disruptions and knockouts.
    • 提供了一种用于有机体靶向遗传操作的组合物和方法。 所述组合物是衍生自包含活性切割供体复合物(CDC)的Mu噬菌体的新型整合载体,并且还包含靶向机制,由此可将Mu转座盒的整合导向宿主生物体基因组内的预定靶位点。 这些整合载体包含Mu转座盒和一个或多个引导CDC的靶向插入的导航器元件。 本发明的方法利用本发明的整合载体将Mu转座盒插入生物体基因组的靶位点。 该插入发生在没有MuB辅助蛋白的情况下。 该方法可用于调节已知基因的活性并靶向将感兴趣的核苷酸序列整合到生物体基因组的特定位置。 因此,该方法也可用于产生基因破坏和敲除。