首页> 外国专利> Methods and compositions for transposition using minimal segments of the eukaryotic transformation vector piggyBac

Methods and compositions for transposition using minimal segments of the eukaryotic transformation vector piggyBac

机译:使用真核转化载体piggyBac的最小片段进行转座的方法和组合物

摘要

The present invention provides a method for transforming an insect genome that has a much enhanced transformation frequency. The vectors and plasmids employed in the method are further described as transposition vectors that include a minimal amount of nucleotide sequence homologous to a 5′ region and a 3′ region of a native piggyBac nucleic acid sequence. The transformed cells or embryos may also be developed into transgenic organisms. Disclosed are minimal piggyBac-based plasmid constructs that comprises a minimal nucleic acid sequence homologous to a 5′ end of a piggyBac nucleic acid sequence (about 60-80 bp, particularly 66 bp) and a relatively long (300 to about 380 bp, particularly 311 bp or 378 bp) continuous nucleic acid sequence homologous to a 3′ end of a piggyBac native nucleic acid sequence. Methods employing these constructs include the use of a helper plasmid. Transformation frequencies employing the constructs are enhanced 100-fold or higher over that transformation frequency obtained using other than the herein described constructs.
机译:本发明提供了用于转化具有大大提高的转化频率的昆虫基因组的方法。该方法中使用的载体和质粒进一步描述为转座载体,其包括与天然piggyBac核酸序列的5'区域和3'区域同源的最小量的核苷酸序列。转化的细胞或胚​​胎也可以发育成转基因生物。公开了最小的基于piggyBac的质粒构建体,其包含与piggyBac核酸序列的5'端同源的最小核酸序列(约60-80bp,特别是66bp)和相对长的(300-约380bp,特别是与piggyBac天然核酸序列的3'端同源的311bp或378bp的连续核酸序列。采用这些构建体的方法包括使用辅助质粒。与使用除本文所述的构建体以外的构建体获得的转化频率相比,采用构建体的转化频率提高了100倍或更高。

著录项

  • 公开/公告号US10087463B2

    专利类型

  • 公开/公告日2018-10-02

    原文格式PDF

  • 申请/专利权人 MALCOLM J. FRASER;XU LI;

    申请/专利号US20060454947

  • 发明设计人 MALCOLM J. FRASER;XU LI;

    申请日2006-06-19

  • 分类号C12N15/85;C12N15/90;

  • 国家 US

  • 入库时间 2022-08-21 13:05:10

相似文献

  • 专利
  • 外文文献
  • 中文文献
获取专利

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号