CREATION AND TRANSMISSION OF MEGALOCI
    3.
    发明申请
    CREATION AND TRANSMISSION OF MEGALOCI 审中-公开
    MEGALOCI的创造和传播

    公开(公告)号:US20140283166A1

    公开(公告)日:2014-09-18

    申请号:US14209731

    申请日:2014-03-13

    CPC classification number: A01H1/02 C12N15/8213

    Abstract: The current invention provides methods for creating a block of genetically linked transgenic traits or a megalocus that can be transmitted as a single genetic unit. The present invention further provides methods for trait introgression to other plants, varieties or species using the megaloci of the invention. Also provided are plants, seeds, and plant parts comprising the megaloci.

    Abstract translation: 本发明提供了用于产生遗传连锁转基因性状的块或可作为单个遗传单位传播的巨晶的方法。 本发明还提供了使用本发明的巨球藻对其它植物,品种或物种进行性状渗入的方法。 还提供了包含巨藻的植物,种子和植物部分。

    CREATION AND TRANSMISSION OF MEGALOCI

    公开(公告)号:US20210321586A1

    公开(公告)日:2021-10-21

    申请号:US17308978

    申请日:2021-05-05

    Abstract: The current invention provides methods for creating a block of genetically linked transgenic traits or a megalocus that can be transmitted as a single genetic unit. The present invention further provides methods for trait introgression to other plants, varieties or species using the megaloci of the invention. Also provided are plants, seeds, and plant parts comprising the megaloci.

    COMPOSITIONS AND METHODS FOR CHROMOSOME REARRANGEMENT

    公开(公告)号:US20220251588A1

    公开(公告)日:2022-08-11

    申请号:US17630465

    申请日:2020-08-04

    Abstract: Methods and compositions for evaluating the efficiency of chromosomal rearrangement are provided. In some examples, systems comprising a first DNA molecule comprising the N-terminal portion of a first split reporter coding sequence linked to the C-terminal portion of a second split reporter coding sequence via a first intron, and a second DNA molecule comprising the N-terminal portion of said second split reporter coding sequence linked to the C-terminal portion of said first split reporter coding sequence via a second intron. The introns comprise at least one target site recognized by a genome editing reagent, such as a recombinase or endonuclease, such that recombination results in expression of the first or second reporter coding sequence following splicing of the introns.

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