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利用 CRISPR-Cas9 核糖核蛋白复合物在农业害虫地中海实蝇中进行高效无 DNA 的基因敲除。

Highly efficient DNA-free gene disruption in the agricultural pest Ceratitis capitata by CRISPR-Cas9 ribonucleoprotein complexes.

机构信息

Department of Biology, University of Naples "Federico II", 80126, Napoli, Italy.

Institute of Biostructures and Bioimaging (IBB), CNR, 80134, Naples, Italy.

出版信息

Sci Rep. 2017 Aug 30;7(1):10061. doi: 10.1038/s41598-017-10347-5.

Abstract

The Mediterranean fruitfly Ceratitis capitata (medfly) is an invasive agricultural pest of high economic impact and has become an emerging model for developing new genetic control strategies as an alternative to insecticides. Here, we report the successful adaptation of CRISPR-Cas9-based gene disruption in the medfly by injecting in vitro pre-assembled, solubilized Cas9 ribonucleoprotein complexes (RNPs) loaded with gene-specific single guide RNAs (sgRNA) into early embryos. When targeting the eye pigmentation gene white eye (we), a high rate of somatic mosaicism in surviving G0 adults was observed. Germline transmission rate of mutated we alleles by G0 animals was on average above 52%, with individual cases achieving nearly 100%. We further recovered large deletions in the we gene when two sites were simultaneously targeted by two sgRNAs. CRISPR-Cas9 targeting of the Ceratitis ortholog of the Drosophila segmentation paired gene (Ccprd) caused segmental malformations in late embryos and in hatched larvae. Mutant phenotypes correlate with repair by non-homologous end-joining (NHEJ) lesions in the two targeted genes. This simple and highly effective Cas9 RNP-based gene editing to introduce mutations in C. capitata will significantly advance the design and development of new effective strategies for pest control management.

摘要

地中海实蝇(medfly)是一种具有高度经济影响的入侵农业害虫,已成为开发新型遗传控制策略的新兴模式,作为杀虫剂的替代品。在这里,我们报告了通过将体外预组装的、可溶的 Cas9 核糖核蛋白复合物(RNP)加载带有基因特异性单指导 RNA(sgRNA)注入早期胚胎,成功地适应了地中海实蝇中的基于 CRISPR-Cas9 的基因敲除。当靶向眼睛色素基因白眼(we)时,在幸存的 G0 成虫中观察到很高的体嵌合率。通过 G0 动物传递突变 we 等位基因的生殖系传递率平均高于 52%,个别情况达到近 100%。当两个 sgRNA 同时靶向两个位点时,我们进一步在 we 基因中恢复了大片段缺失。Cas9 在果蝇体节配对基因(Ccprd)的 Ceratitis 同源物上的靶向导致晚期胚胎和孵化幼虫的节段畸形。突变表型与两个靶向基因中同源重组修复(NHEJ)损伤的修复相关。这种简单而高效的基于 Cas9 RNP 的基因编辑方法可在 C. capitata 中引入突变,将极大地推进害虫管理的新有效控制策略的设计和开发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0b68/5577161/84e5f6a87f98/41598_2017_10347_Fig1_HTML.jpg

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