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NUCLEASE FUSIONS FOR ENHANCING GENOME EDITING BY HOMOLOGY-DIRECTED TRANSGENE INTEGRATION

机译:核酸融合技术,通过同源基因定向转基因整合增强基因组编辑

摘要

The present invention relates to nuclease protein fusions for enhancing genome editing by homology-directed transgene integration (HDI). The inventors found that the rate of HDI mediated by the CRISPR/Cas9 system may be substantially improved by providing the Cas9 nuclease in the form of a fusion protein with at least the N-terminal domain of the CtIP protein. CtIP proteins are involved in the early steps of homologous recombination. In addition, the inventors identified the subdomains of the N-terminal domain of the CtIP protein that are important for improving the HDI rate. Thus, the invention relates to fusion proteins comprising a Cas9 protein, a tetramerization domain of a CtIP protein and a dimerization domain of a CtIP protein. Particularly, the inventors have tested these fusion proteins HEK293 cells, RG37DR cells and Sprague-Dawley rats.
机译:本发明涉及核酸酶蛋白融合体,其用于通过同源性定向转基因整合(HDI)来增强基因组编辑。发明人发现,通过以至少具有CtIP蛋白的N末端结构域的融合蛋白形式提供Cas9核酸酶,可以实质上提高由CRISPR / Cas9系统介导的HDI的速率。 CtIP蛋白参与同源重组的早期步骤。另外,发明人鉴定了CtIP蛋白的N-末端结构域的亚结构域,其对于提高HDI速率是重要的。因此,本发明涉及包含Cas9蛋白,CtIP蛋白的四聚结构域和CtIP蛋白的二聚结构域的融合蛋白。特别地,发明人已经测试了这些融合蛋白HEK293细胞,RG37DR细胞和Sprague-Dawley大鼠。

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