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CRISPR 在实蝇科中的应用基础:开发在 Anastrepha、Bactrocera 和 Ceratitis 属中诱导可遗传突变的方法。

The ABCs of CRISPR in Tephritidae: developing methods for inducing heritable mutations in the genera Anastrepha, Bactrocera and Ceratitis.

机构信息

USDA-ARS Daniel K. Inouye US Pacific Basin Agricultural Research Center, Hilo, HI, USA.

IAEA Technical Cooperation- Latin America and Caribbean Section, Guatemala City, Guatemala.

出版信息

Insect Mol Biol. 2019 Apr;28(2):277-289. doi: 10.1111/imb.12550. Epub 2019 Jan 10.

Abstract

Tephritid fruit flies are destructive agricultural pests that are the targets of expensive population eradication and suppression efforts. Genetic pest management is one of the strategies for reducing or eliminating tephritid populations, relying upon the genetic manipulation of insects to render them sterile or capable of transmitting deleterious traits through gene drive. Currently, radiation, chemical mutagenesis, and transgenic techniques are employed to generate agents for genetic pest management, but new methods must be explored and developed for all tephritid pest species. Targeted mutagenesis induced by nonhomologous end join repair of clustered regularly interspaced short palindromic repeats and the CRISPR associated protein 9 (Cas9) (commonly known as CRISPR/Cas9) has been demonstrated to be an efficient method for creating knock-out mutants and can be utilized to create germline mutations in Tephritidae. In this paper, we describe detailed methods to knockout the white gene in three tephritid species in the genera Anastrepha, Bactrocera and Ceratitis, including the first demonstration of CRISPR/Cas9 induced mutations in the genus Anastrepha. Lastly, we discuss the variables in tephritid systems that directed method development as well as recommendations for performing injections in remote containment facilities with little molecular biology capabilities. These methods and recommendations combined can serve as a guide for others to use in pursuit of developing CRISPR/Cas9 methods in tephritid systems.

摘要

实蝇是具有破坏性的农业害虫,是昂贵的种群根除和抑制工作的目标。遗传害虫管理是减少或消除实蝇种群的策略之一,依赖于对昆虫进行遗传操作,使其不育或能够通过基因驱动传递有害性状。目前,辐射、化学诱变和转基因技术被用于生成遗传害虫管理的制剂,但必须探索和开发所有实蝇害虫物种的新方法。通过非同源末端连接修复的靶向诱变聚集的规则间隔的短回文重复序列和 CRISPR 相关蛋白 9 (Cas9)(通常称为 CRISPR/Cas9)已被证明是一种有效的方法来创建敲除突变体,并可用于在双翅目科中创建生殖系突变。在本文中,我们详细描述了在 Anastrepha、Bactrocera 和 Ceratitis 属的三个实蝇物种中敲除白色基因的方法,包括首次在 Anastrepha 属中证明 CRISPR/Cas9 诱导的突变。最后,我们讨论了实蝇系统中的变量,这些变量指导了方法的发展,并为在分子生物学能力有限的远程封闭设施中进行注射提供了建议。这些方法和建议可以作为其他人在实蝇系统中开发 CRISPR/Cas9 方法的指南。

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