利用 CRISPR/Cas9 对主要家畜害虫 Cochliomyia hominivorax 和 Lucilia cuprina 进行特异性基因破坏。

Q4 Engineering
Daniel F Paulo, Megan E Williamson, Alex P Arp, Fang Li, Agustin Sagel, Steven R Skoda, Joel Sanchez-Gallego, Mario Vasquez, Gladys Quintero, Adalberto A Pérez de León, Esther J Belikoff, Ana M L Azeredo-Espin, W Owen McMillan, Carolina Concha, Maxwell J Scott
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引用次数: 32

摘要

Cochliomyia hominivorax 和 Lucilia cuprina 是家畜的主要害虫。它们的幼虫侵染温血脊椎动物,以宿主的组织为食,造成严重的产业损失。由于它们是严重的害虫,人们一直在努力开发基因组资源和功能工具,以改善对它们的管理和控制。在此,我们报告了通过建立高效的 CRISPR/Cas9 方案,在这些苍蝇的基因组中产生定向和可遗传的修饰,从而大大增加了基因组操作工具的数量。在 C hominivorax 和 L cuprina 黄色基因(ChY 和 LcY)中引入了定点突变,产生了轻度色素沉着的成虫。向胚胎注射预先与高浓度引导 RNA(sgRNA)组装在一起的 Cas9 核糖核蛋白复合物(RNPs),可诱导高比例的体细胞嵌合。携带被破坏的黄色等位基因的成蝇缺乏正常的色素沉着(棕色体表型),并将突变的等位基因有效地传递给下一代,从而可以快速创建同基因品系,对候选基因座进行反向遗传。接下来,我们利用已建立的CRISPR协议破坏了C hominivorax变体基因(Chtra)。携带 Chtra 基因座突变的存活雌虫出现了具有雄性生殖器特征的转化卵器镶嵌表型,同时表现出异常的生殖组织。本文所描述的 CRISPR 方案是对现有马蹄虫分子方法工具包的重大改进。我们的研究结果还表明,针对 Chtra 和 Lctra 的基于 Cas9 的系统可以成为控制这些重要害虫自然种群的有效手段。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Specific Gene Disruption in the Major Livestock Pests Cochliomyia hominivorax and Lucilia cuprina Using CRISPR/Cas9.

Cochliomyia hominivorax and Lucilia cuprina are major pests of livestock. Their larvae infest warm-blooded vertebrates and feed on host's tissues, resulting in severe industry losses. As they are serious pests, considerable effort has been made to develop genomic resources and functional tools aiming to improve their management and control. Here, we report a significant addition to the pool of genome manipulation tools through the establishment of efficient CRISPR/Cas9 protocols for the generation of directed and inheritable modifications in the genome of these flies. Site-directed mutations were introduced in the C hominivorax and L cuprina yellow genes (ChY and LcY) producing lightly pigmented adults. High rates of somatic mosaicism were induced when embryos were injected with Cas9 ribonucleoprotein complexes (RNPs) pre-assembled with guide RNAs (sgRNAs) at high concentrations. Adult flies carrying disrupted yellow alleles lacked normal pigmentation (brown body phenotype) and efficiently transmitted the mutated alleles to the subsequent generation, allowing the rapid creation of homozygous strains for reverse genetics of candidate loci. We next used our established CRISPR protocol to disrupt the C hominivorax transformer gene (Chtra). Surviving females carrying mutations in the Chtra locus developed mosaic phenotypes of transformed ovipositors with characteristics of male genitalia while exhibiting abnormal reproductive tissues. The CRISPR protocol described here is a significant improvement on the existing toolkit of molecular methods in calliphorids. Our results also suggest that Cas9-based systems targeting Chtra and Lctra could be an effective means for controlling natural populations of these important pests.

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来源期刊
Journal of the Illuminating Engineering Institute of Japan (Shomei Gakkai Shi)
Journal of the Illuminating Engineering Institute of Japan (Shomei Gakkai Shi) Engineering-Electrical and Electronic Engineering
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