利用 RNA 干扰对 Nilaparvata lugens 中的 CPSF30 进行功能分析,揭示其在发育和存活中的重要作用。

IF 2.7 2区 农林科学 Q1 ENTOMOLOGY
Insects Pub Date : 2024-11-03 DOI:10.3390/insects15110860
Shengli Jing, Jing Yang, Yali Liu, Feifei Wang, Fang Zheng, Aobo Ren, Bingbing Yu, Yue Zhao, Bing Jia, Ruixian Chen, Bin Yu, Qingsong Liu, Jingang Xu
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引用次数: 0

摘要

褐飞虱(Nilaparvata lugens)是威胁全球水稻生产的主要害虫,每年都会大幅减产。由于褐飞虱对化学农药等传统防治方法产生了越来越强的抗药性,因此迫切需要创新和可持续的害虫管理策略。裂解和多腺苷酸化特异性因子 30(CPSF30)是一种参与 mRNA 3' 端处理的关键蛋白,但其在 N. lugens 中的功能仍鲜为人知。本研究旨在阐明 CPSF30 在 N. lugens 生长发育过程中的作用,并评估其作为基于 RNA 干扰(RNAi)的害虫控制策略靶标的潜力。我们克隆并鉴定了NlCPSF30的cDNA序列,该序列编码了一个341个氨基酸的蛋白质,包含5个CCCH锌指结构域和2个CCHC锌节结构域。序列比对显示,NlCPSF30在昆虫物种间高度保守,尤其是在RNA结合和处理所必需的锌指结构域。系统进化分析表明,NlCPSF30 与其他半翅目昆虫的 CPSF30 蛋白关系密切。表达分析表明,NlCPSF30在脂肪体和成虫阶段的表达量最高,雌性的表达量明显高于雄性。通过RNAi介导的方法沉默三龄若虫的NlCPSF30会导致严重的表型异常,包括蜕皮中断和注射靶向NlCPSF30的双链RNA(dsRNA)后死亡率升高。此外,它还影响了与激素调控相关的基因(即 NlHry、NlE93 和 NlKr-h1)的表达。这些结果表明,NlCPSF30 与关键的生理过程密不可分,破坏它将导致死亡率上升。我们的研究结果表明,NlCPSF30 是 N. lugens 生存的一个重要基因,也是基于 RNAi 的害虫管理策略的一个有希望的靶标。这项研究为开发基于 RNAi 的 N. lugens 控制方法提供了有价值的分子靶标和理论见解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Functional Analysis of CPSF30 in Nilaparvata lugens Using RNA Interference Reveals Its Essential Role in Development and Survival.

The brown planthopper (Nilaparvata lugens) is a major pest threatening global rice production, significantly reducing yields annually. As N. lugens increasingly develops resistance to conventional control methods, such as chemical pesticides, there is an urgent need for innovative and sustainable pest management strategies. Cleavage and Polyadenylation Specificity Factor 30 (CPSF30) is a key protein involved in mRNA 3' end processing, yet its function in N. lugens remains poorly understood. This study aims to elucidate the role of CPSF30 in the growth and development of N. lugens and evaluate its potential as a target for RNA interference (RNAi)-based pest control strategies. We cloned and characterized the cDNA sequence of NlCPSF30, which encodes a protein of 341 amino acids containing five CCCH zinc-finger domains and two CCHC zinc-knuckle domains. Sequence alignment revealed that NlCPSF30 is highly conserved among insect species, particularly in the zinc-finger domains essential for RNA binding and processing. Phylogenetic analysis showed that NlCPSF30 is closely related to CPSF30 proteins from other hemipteran species. Expression analysis indicated that NlCPSF30 is most highly expressed in the fat body and during the adult stage, with significantly higher expression in females than in males. RNAi-mediated silencing of NlCPSF30 in third-instar nymphs resulted in severe phenotypic abnormalities, including disrupted molting and increased mortality following injection of double-stranded RNA (dsRNA) targeting NlCPSF30. Moreover, it influenced the expression of genes associated with hormone regulation, namely NlHry, NlE93, and NlKr-h1. These results suggest that NlCPSF30 is integral to critical physiological processes, with its disruption leading to increased mortality. Our findings identify NlCPSF30 as an essential gene for N. lugens' survival and a promising target for RNAi-based pest management strategies. This study provides a valuable molecular target and theoretical insights for developing RNAi-based control methods against N. lugens.

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来源期刊
Insects
Insects Agricultural and Biological Sciences-Insect Science
CiteScore
5.10
自引率
10.00%
发文量
1013
审稿时长
21.77 days
期刊介绍: Insects (ISSN 2075-4450) is an international, peer-reviewed open access journal of entomology published by MDPI online quarterly. It publishes reviews, research papers and communications related to the biology, physiology and the behavior of insects and arthropods. Our aim is to encourage scientists to publish their experimental and theoretical results in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced. Electronic files regarding the full details of the experimental procedure, if unable to be published in a normal way, can be deposited as supplementary material.
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