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一种显著提高种系显微注射效率的简单方法。

A simple method to dramatically increase germline microinjection efficiency.

作者信息

Gibney Theresa V, Favichia Michelle, Latifi Laila, Medwig-Kinney Taylor N, Matus David Q, McIntyre Daniel C, Arrigo Angelo B, Branham Kendall R, Bubrig Louis T, Ghaddar Abbas, Jiranek Juliana A, Liu Kendra E, Marcucci Charles G, Porter Robert J, Pani Ariel M

机构信息

Department of Biology, University of Virginia, Charlottesville, VA, USA.

Department of Biochemistry & Cell Biology, Stony Brook University, Stony Brook, NY, USA.

出版信息

bioRxiv. 2023 Mar 25:2023.03.23.533855. doi: 10.1101/2023.03.23.533855.

DOI:10.1101/2023.03.23.533855
PMID:36993165
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10055348/
Abstract

Genome manipulation methods in require microinjecting DNA or ribonucleoprotein complexes into the microscopic core of the gonadal syncytium. These microinjections are technically demanding and represent a key bottleneck for all genome engineering and transgenic approaches in . While there have been steady improvements in the ease and efficiency of genetic methods for genome manipulation, there have not been comparable advances in the physical process of microinjection. Here, we report a simple and inexpensive method for handling worms using a paintbrush during the injection process that nearly tripled average microinjection rates compared to traditional worm handling methods. We found that the paintbrush increased injection throughput by substantially increasing both injection speeds and post-injection survival rates. In addition to dramatically and universally increasing injection efficiency for experienced personnel, the paintbrush method also significantly improved the abilities of novice investigators to perform key steps in the microinjection process. We expect that this method will benefit the community by increasing the speed at which new strains can be generated and will also make microinjection-based approaches less challenging and more accessible to personnel and labs without extensive experience.

摘要

线虫中的基因组操作方法需要将DNA或核糖核蛋白复合物显微注射到性腺合胞体的微观细胞核中。这些显微注射技术要求很高,是线虫所有基因组工程和转基因方法的关键瓶颈。虽然线虫基因组操作的遗传方法在简便性和效率方面一直在稳步提高,但显微注射的物理过程却没有取得类似的进展。在这里,我们报告了一种在注射过程中使用画笔处理线虫的简单且廉价的方法,与传统的线虫处理方法相比,该方法使平均显微注射率提高了近两倍。我们发现,画笔通过大幅提高注射速度和注射后存活率,从而提高了注射通量。除了显著且普遍地提高经验丰富人员的注射效率外,画笔方法还显著提高了新手研究人员执行显微注射过程关键步骤的能力。我们预计,这种方法将通过提高新菌株的产生速度而使线虫研究群体受益,并且还将使基于显微注射的方法对没有丰富经验的人员和实验室来说更具挑战性且更易于操作。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de8/10055348/7bf22b8e46a6/nihpp-2023.03.23.533855v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de8/10055348/44a840e20e5d/nihpp-2023.03.23.533855v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de8/10055348/7bf22b8e46a6/nihpp-2023.03.23.533855v1-f0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de8/10055348/44a840e20e5d/nihpp-2023.03.23.533855v1-f0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8de8/10055348/7bf22b8e46a6/nihpp-2023.03.23.533855v1-f0002.jpg

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