TcCYP4C1与海藻糖联合作用对褐藻高co2胁迫的影响。

IF 2.3 2区 农林科学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY
Xinyu Zhang, Liwen Guan, Yuya Zhang, Fan Zhong, Yuhang Xie, Yi Zhang, Xinyi Zhang, Min Zhou, Can Li, Bin Tang
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引用次数: 0

摘要

细胞色素P450单加氧酶(Cytochrome P450 monooxygenase, CYP)是昆虫体内重要的解毒酶,参与了外源化合物和内源物质的代谢和降解。探讨castaneum TcCYP4C1基因参与高CO2环境下昆虫解毒代谢及海藻糖对低氧胁迫的保护作用。在本研究中,通过双链RNA(dsRNA)成功沉默castaneum的TcCYP4C1基因后,将幼虫暴露于95%的CO2中。这种暴露导致幼虫死亡率显著增加,羧酸酯酶(CarE)活性显著升高。注射dsRNA后,投喂海藻糖可使幼虫死亡率降低18.15% ~ 11.24%。此外,海藻糖代谢途径相关基因TRE1-3、TRE1-4和TPS2的基因表达量在95% CO2处理后显著上调。综上所述,TcCYP4C1基因在castaneum对高CO2的适应性反应中发挥了关键作用。海藻糖能有效减轻甘蔗TcCYP4C1基因沉默和暴露于高CO2胁迫下所造成的有害影响。我们的研究结果不仅为开发适合低氧储粮环境的新型农药奠定了理论基础,而且为储粮领域创新的、环境可持续的有害生物治理策略提供了启发。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
TcCYP4C1 in combination with trehalose to cope with high-CO2 stress in Tribolium castaneum (Coleoptera).

Cytochrome P450 monooxygenase (CYP), an important detoxifying enzyme in insects, is involved in the metabolism and degradation of both exogenous compounds and endogenous substances. To investigate the involvement of the T. castaneum TcCYP4C1 gene in detoxification metabolism under high CO2 and the protective role of trehalose against hypoxic stress in insects. In the present study, after successfully silencing the TcCYP4C1 gene of T. castaneum by double-stranded RNA(dsRNA), the larvae were exposed to 95% CO2. This exposure resulted in a statistically significant increase in larval mortality and a significant elevation in the activity of the carboxylesterase enzyme (CarE). However, a decrease in mortality from 18.15% to 11.24% was observed when larvae were fed trehalose after dsRNA injection. In addition, the gene expression levels of the trehalose metabolism pathway related genes TRE1-3, TRE1-4 and TPS2 were significantly up-regulated after 95% CO2 treatment. In summary, the TcCYP4C1 gene emerges as a pivotal factor in the adaptive response of T. castaneum to high CO2. Trehalose effectively mitigates the detrimental effects resulting from the silencing of TcCYP4C1 and exposure to high CO2 stress in T. castaneum. Our findings not only establish a theoretical foundation for the development of novel pesticides tailored for low-oxygen grain storage environments but also inspire innovative, environmentally sustainable pest management strategies in the grain storage sector.

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来源期刊
Insect Molecular Biology
Insect Molecular Biology 生物-昆虫学
CiteScore
4.80
自引率
3.80%
发文量
68
审稿时长
6-12 weeks
期刊介绍: Insect Molecular Biology has been dedicated to providing researchers with the opportunity to publish high quality original research on topics broadly related to insect molecular biology since 1992. IMB is particularly interested in publishing research in insect genomics/genes and proteomics/proteins. This includes research related to: • insect gene structure • control of gene expression • localisation and function/activity of proteins • interactions of proteins and ligands/substrates • effect of mutations on gene/protein function • evolution of insect genes/genomes, especially where principles relevant to insects in general are established • molecular population genetics where data are used to identify genes (or regions of genomes) involved in specific adaptations • gene mapping using molecular tools • molecular interactions of insects with microorganisms including Wolbachia, symbionts and viruses or other pathogens transmitted by insects Papers can include large data sets e.g.from micro-array or proteomic experiments or analyses of genome sequences done in silico (subject to the data being placed in the context of hypothesis testing).
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