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将含正交功能化四氟苯偶氮苯的 siRNA 注入日本青鳉胚胎中,实现光控基因沉默。

Injection of Ortho-Functionalized Tetrafluorinated Azobenzene-Containing siRNAs into Japanese Medaka Embryos for Photocontrolled Gene Silencing.

机构信息

Faculty of Science, Ontario Tech University, Oshawa, Ontario, Canada.

出版信息

Curr Protoc. 2024 Nov;4(11):e70051. doi: 10.1002/cpz1.70051.

DOI:10.1002/cpz1.70051
PMID:39546401
Abstract

This article describes the detailed methodology of how to inject photoswitchable ortho-functionalized tetrafluorinated short interfering RNAs (F-siRNAs) into a single cell of stage-two Japanese medaka (Oryzias latipes) embryos and how to control gene silencing with different wavelengths of light. Many of the prior papers describing Japanese medaka embryo injections omit key information. As such, this article aims to give an in-depth explanation as to how the NanoJect III microinjector can be used for this purpose. To obtain the embryos for microinjection, adult medaka are housed under a 14-hr light, 10-hr dark cycle to mimic their natural breeding period. This induces mating at approximately the same time each day, when the lights turn on, so recently fertilized eggs can be obtained. Synthetic F-siRNAs are injected into transgenic stage-two single-cell Japanese medaka embryos expressing enhanced green fluorescent protein (eGFP). Our data demonstrate that our F-siRNAs can silence gene activity in Japanese medaka embryos expressing eGFP. Moreover, gene expression can be activated by exposing F-siRNA-injected embryos to blue light and deactivated a few days after exposure to green light. To the best of our knowledge, this marks the first reversible control of a gene-silencing oligonucleotide within an in vivo system. © 2024 The Author(s). Current Protocols published by Wiley Periodicals LLC. Basic Protocol 1: Medaka maintenance and embryo collection Basic Protocol 2: Injection of stage-two one-cell medaka embryos Basic Protocol 3: Evaluation of the F-siRNA gene-silencing ability through light activation and inactivation using blue and green light by measuring enhanced green fluorescent protein fluorescence.

摘要

这篇文章详细介绍了如何将光可切换的邻位功能化四氟短干扰 RNA(F-siRNA)注入日本青鳉(Oryzias latipes)胚胎的单细胞中,以及如何使用不同波长的光控制基因沉默。许多之前描述日本青鳉胚胎注射的论文都省略了关键信息。因此,本文旨在深入解释如何使用 NanoJect III 微量注射器来实现这一目的。为了获得用于微注射的胚胎,将成年青鳉置于 14 小时光照、10 小时黑暗的周期下,以模拟其自然繁殖期。这会诱导每天光照开启时的交配,从而获得最近受精的卵子。将合成的 F-siRNA 注入表达增强型绿色荧光蛋白(eGFP)的转基因青鳉胚胎的单细胞中。我们的数据表明,我们的 F-siRNA 可以沉默表达 eGFP 的青鳉胚胎中的基因活性。此外,通过用蓝光照射 F-siRNA 注射的胚胎,可以激活基因表达,而在暴露于绿光几天后又可以使其失活。据我们所知,这标志着在体内系统中首次可逆控制基因沉默寡核苷酸。© 2024 作者。Wiley Periodicals LLC 出版的《当代协议》。基本方案 1:青鳉的维护和胚胎收集基本方案 2:注射两细胞期的青鳉胚胎基本方案 3:通过测量增强型绿色荧光蛋白荧光,使用蓝光和绿光激活和失活来评估 F-siRNA 基因沉默能力。

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