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利用 CRISPR 技术评估基因敲除作为蚊子遗传工程的潜在靶点

Evaluation of Gene Knockouts by CRISPR as Potential Targets for the Genetic Engineering of the Mosquito .

机构信息

Section of Cell and Developmental Biology, University of California San Diego, La Jolla, California, USA; University of Monash, Clayton, Australia.

Department of Biology, University of Hawai'i at Hilo, Hilo, Hawai'i, USA; University of Monash, Clayton, Australia.

出版信息

CRISPR J. 2021 Aug;4(4):595-608. doi: 10.1089/crispr.2021.0028. Epub 2021 Jul 19.

Abstract

mosquitoes are a globally widespread vector of several human and animal pathogens. Their biology and behavior allow them to thrive in proximity to urban areas, rendering them a constant public health threat. Their mixed bird/mammal feeding behavior further offers a vehicle for zoonotic pathogens transmission to people and, separately, poses a threat to the conservation of insular birds. The advent of CRISPR has led to the development of novel technologies for the genetic engineering of wild mosquito populations. Yet, research into has been lagging compared to other disease vectors. Here, we use this tool to disrupt a set of five pigmentation genes in that, when altered, lead to visible, homozygous-viable phenotypes. We further validate this approach in separate laboratories and in two distinct strains of that are relevant to potential future public health and bird conservation applications. We generate a double-mutant line, demonstrating the possibility of sequentially combining multiple such mutations in a single individual. Lastly, we target two loci, in the sex-determination pathway and , a hox gene, demonstrating the flexibility of these methods applied to novel targets. Our work provides a platform of seven validated loci that could be used for targeted mutagenesis in and the future development of genetic suppression strategies for this species. Furthermore, the mutant lines generated here could have widespread utility to the research community using this model organism, as they could be used as targets for transgene delivery, where a copy of the disrupted gene could be included as an easily scored transgenesis marker.

摘要

蚊子是全球广泛分布的几种人类和动物病原体的载体。它们的生物学和行为使它们能够在靠近城市的地方繁衍生息,这使它们成为持续的公共卫生威胁。它们混合的鸟类/哺乳动物的取食行为进一步为动物源性病原体向人类传播提供了途径,并且分别对岛屿鸟类的保护构成了威胁。CRISPR 的出现导致了针对野生蚊子种群的基因工程的新技术的发展。然而,与其他疾病载体相比,对 的研究一直滞后。在这里,我们使用这种工具来破坏一组五个色素基因,这些基因在改变时会导致可见的、纯合的、可行的表型。我们还在两个不同的实验室和两个与未来公共卫生和鸟类保护应用相关的 的不同品系中验证了这种方法。我们生成了一个双突变系,证明了在单个个体中依次组合多个这种突变的可能性。最后,我们针对性别决定途径中的两个基因座 和一个同源盒基因 ,证明了这些方法应用于新目标的灵活性。我们的工作提供了一个经过验证的七个基因座平台,可用于 的靶向诱变,并为该物种的遗传抑制策略的未来发展提供了基础。此外,这里生成的突变系可以广泛应用于使用该模式生物的研究社区,因为它们可以用作转基因传递的靶标,其中可以包含破坏基因的拷贝作为易于评分的转基因标记。

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