通过喂食对轮虫(Brachionus plicatilis)进行高效 RNA 干扰的方法。

IF 2 4区 生物学 Q3 BIOTECHNOLOGY & APPLIED MICROBIOLOGY Biotechnology Letters Pub Date : 2024-09-05 DOI:10.1007/s10529-024-03524-w
Yu Zhang, Dongqi Kan, Yang Zhou, Hairong Lian, Lingling Ge, Jing Shen, Zhongqi Dai, Yan Shi, Cui Han, Xiaojie Liu, Jiaxin Yang
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引用次数: 0

摘要

轮虫是一种遍布世界各地的小型无脊椎动物,已成为实验生态学、水生毒理学和环境科学领域研究分子机制的一种很有前途的模式系统。然而,由于缺乏高效的基因表达操作技术,轮虫的研究受到了阻碍。在本研究中,我们利用带有两个反向T7启动子的L4440质粒和RNase缺陷的大肠杆菌HT115,高效地产生了dsRNA,从而提出了一种高效的基于喂养的轮虫RNAi方法。我们以DNA双链断裂修复途径中的关键蛋白Bp-Ku70和Ku80为靶标,然后将轮虫置于紫外线辐射下。我们发现,RNAi导致轮虫的mRNA表达、繁殖力和存活率显著下降。总之,我们的研究结果表明,基于喂食的RNAi方法是一种简单而有效的敲除轮虫基因的工具,从而推动了轮虫作为生物研究模式生物的应用。
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Efficient RNA interference method by feeding in Brachionus plicatilis (Rotifera).

Rotifers are small, ubiquitous invertebrate animals found throughout the world and have emerged as a promising model system for studying molecular mechanisms in the fields of experimental ecology, aquatic toxicology, and geroscience. However, the lack of efficient gene expression manipulation techniques has hindered the study of rotifers. In this study, we used the L4440 plasmid with two reverse-oriented T7 promoters, along with RNase-deficient E. coli HT115, to efficiently produce dsRNA and thereby present an efficient feeding-based RNAi method in Brachionus plicatilis. We targeted Bp-Ku70 & Ku80, key proteins in the DNA double-strand breaks repair pathway, and then subjected rotifers to UV radiation. We found that the mRNA expression, fecundity, as well as survival rate diminished significantly as a result of RNAi. Overall, our results demonstrate that the feeding-based RNAi method is a simple and efficient tool for gene knockdown in B. plicatilis, advancing their use as a model organism for biological research.

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来源期刊
Biotechnology Letters
Biotechnology Letters 工程技术-生物工程与应用微生物
CiteScore
5.90
自引率
3.70%
发文量
108
审稿时长
1.2 months
期刊介绍: Biotechnology Letters is the world’s leading rapid-publication primary journal dedicated to biotechnology as a whole – that is to topics relating to actual or potential applications of biological reactions affected by microbial, plant or animal cells and biocatalysts derived from them. All relevant aspects of molecular biology, genetics and cell biochemistry, of process and reactor design, of pre- and post-treatment steps, and of manufacturing or service operations are therefore included. Contributions from industrial and academic laboratories are equally welcome. We also welcome contributions covering biotechnological aspects of regenerative medicine and biomaterials and also cancer biotechnology. Criteria for the acceptance of papers relate to our aim of publishing useful and informative results that will be of value to other workers in related fields. The emphasis is very much on novelty and immediacy in order to justify rapid publication of authors’ results. It should be noted, however, that we do not normally publish papers (but this is not absolute) that deal with unidentified consortia of microorganisms (e.g. as in activated sludge) as these results may not be easily reproducible in other laboratories. Papers describing the isolation and identification of microorganisms are not regarded as appropriate but such information can be appended as supporting information to a paper. Papers dealing with simple process development are usually considered to lack sufficient novelty or interest to warrant publication.
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