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用于丽蝇蛹集金小蜂基因组操作的胚胎显微注射和移植技术。

Embryo Microinjection and Transplantation Technique for Nasonia vitripennis Genome Manipulation.

作者信息

Li Ming, Bui Michelle, Akbari Omar S

机构信息

Department of Entomology and Riverside Center of Disease Vector Research, Institute for Integrative Genome Biology, University of California, Riverside; Section of Cell and Developmental Biology, Division of Biological Sciences, University of California, San Diego.

Department of Entomology and Riverside Center of Disease Vector Research, Institute for Integrative Genome Biology, University of California, Riverside; Section of Cell and Developmental Biology, Division of Biological Sciences, University of California, San Diego;

出版信息

J Vis Exp. 2017 Dec 25(130):56990. doi: 10.3791/56990.

Abstract

The jewel wasp Nasonia vitripennis has emerged as an effective model system for the study of processes including sex determination, haplo-diploid sex determination, venom synthesis, and host-symbiont interactions, among others. A major limitation of working with this organism is the lack of effective protocols to perform directed genome modifications. An important part of genome modification is delivery of editing reagents, including CRISPR/Cas9 molecules, into embryos through microinjection. While microinjection is well established in many model organisms, this technique is particularly challenging to perform in N. vitripennis primarily due to its small embryo size, and the fact that embryonic development occurs entirely within a parasitized blowfly pupa. The following procedure overcomes these significant challenges while demonstrating a streamlined, visual procedure for effectively removing wasp embryos from parasitized host pupae, microinjecting them, and carefully transplanting them back into the host for continuation and completion of development. This protocol will strongly enhance the capability of research groups to perform advanced genome modifications in this organism.

摘要

丽蝇蛹集金小蜂已成为一个有效的模型系统,用于研究包括性别决定、单倍体-二倍体性别决定、毒液合成以及宿主-共生体相互作用等过程。使用这种生物进行研究的一个主要限制是缺乏进行定向基因组修饰的有效方案。基因组修饰的一个重要部分是通过显微注射将编辑试剂(包括CRISPR/Cas9分子)导入胚胎。虽然显微注射在许多模式生物中已得到广泛应用,但在丽蝇蛹集金小蜂中执行该技术特别具有挑战性,主要原因是其胚胎尺寸小,且胚胎发育完全发生在被寄生的蝇蛹内。以下步骤克服了这些重大挑战,同时展示了一种简化的可视化程序,用于有效地从被寄生的宿主蛹中取出黄蜂胚胎、对其进行显微注射,并小心地将它们重新移植回宿主中以继续并完成发育。该方案将极大地增强研究小组对这种生物进行高级基因组修饰的能力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/11e3/5908372/791d392e0052/jove-130-56990-0.jpg

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