betta 鱼的遗传操作。

IF 4.9 Q1 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Frontiers in genome editing Pub Date : 2023-07-21 eCollection Date: 2023-01-01 DOI:10.3389/fgeed.2023.1167093
Alec Palmiotti, Madison R Lichak, Pei-Yin Shih, Young Mi Kwon, Andres Bendesky
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摘要

Betta splendens,又名暹罗斗鱼或 "betta",是一种淡水鱼类,因其惊人的形态多样性和极端的攻击行为而闻名于世。尽管我们最近在了解 betta 的遗传学和神经生物学方面取得了进展,但由于缺乏操纵其基因组的工具,阻碍了其在功能和机理层面的进展。在本研究中,我们概述了三种基因操作技术的使用情况,并对其进行了优化,以便在鲶鱼中使用:CRISPR/Cas9 介导的基因敲除、CRISPR/Cas9 介导的基因敲入和 Tol2 介导的转基因。我们敲除了三个基因:alkal2l、bco1l 和 mitfa,并分析了它们对存活率和色素沉着的影响。此外,我们还在 mitfa 基因座中敲入了荧光蛋白,这是这项强大技术在 betta 中的原理验证实验。最后,我们利用 Tol2 介导的转基因技术创造出了普遍表达 GFP 的鱼类,然后又开发出了一种心脏特异性表达红色荧光蛋白的双螺旋质粒,作为转基因成功的可见标记。我们的工作凸显了对 betta 进行遗传操作的潜力,为在这种动物模型中有效利用遗传工具提供了宝贵的资源。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Genetic manipulation of betta fish.

Betta splendens, also known as Siamese fighting fish or "betta," is a freshwater fish species renowned for its astonishing morphological diversity and extreme aggressive behavior. Despite recent advances in our understanding of the genetics and neurobiology of betta, the lack of tools to manipulate their genome has hindered progress at functional and mechanistic levels. In this study, we outline the use of three genetic manipulation technologies, which we have optimized for use in betta: CRISPR/Cas9-mediated knockout, CRISPR/Cas9-mediated knockin, and Tol2-mediated transgenesis. We knocked out three genes: alkal2l, bco1l, and mitfa, and analyzed their effects on viability and pigmentation. Furthermore, we knocked in a fluorescent protein into the mitfa locus, a proof-of-principle experiment of this powerful technology in betta. Finally, we used Tol2-mediated transgenesis to create fish with ubiquitous expression of GFP, and then developed a bicistronic plasmid with heart-specific expression of a red fluorescent protein to serve as a visible marker of successful transgenesis. Our work highlights the potential for the genetic manipulation of betta, providing valuable resources for the effective use of genetic tools in this animal model.

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CiteScore
7.00
自引率
0.00%
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0
审稿时长
13 weeks
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