在全基因组范围内鉴定扁平苔癣菌的角质层蛋白超家族,为控制昆虫媒介和植物病毒提供启示。

IF 1.5 4区 农林科学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY Archives of Insect Biochemistry and Physiology Pub Date : 2024-03-19 DOI:10.1002/arch.22102
Yang Zheng, Yinghao Feng, Zhejin Li, Junwen Wang
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引用次数: 0

摘要

结构性角质层蛋白(CPs)在昆虫的发育和适应性方面发挥着重要作用。然而,尽管 CP 对植物病毒传播的重要性已逐渐受到重视,但人们对传播病毒的昆虫媒介中 CP 基因超家族的了解还很有限。本研究在西花蓟马(Frankliniella occidentalis)中对 CP 超家族进行了全基因组鉴定,西花蓟马是全球入侵害虫和植物病毒媒介害虫。该害虫在全球传播臭名昭著的番茄斑萎病毒(TSWV),对多种植物造成严重危害。本研究注释了 128 个 F. occidentalis CP 基因(FoCPs),并将其分为 10 个不同的家族,包括 68 个 CPRs、16 个 CPAP1s、6 个 CPAP3s、2 个 CPCFCs、10 个 Tweedles、4 个 CPFs、16 个 CPLCPs 和 6 个 CPGs。研究人员对西番莲不同发育阶段的系统发育关系、基因位置和基因表达谱进行了全面分析。转录组分析表明,当隐杆线虫感染 TSWV 时,超过 30% 的 FoCPs 上调至少 1.5 倍,这表明它们可能参与了 TSWV 的相互作用。我们的研究为我们提供了一个关于 F. occidentalis CP 超家族的概览。该研究使人们更好地了解了CP在发育和病毒传播中的作用,为通过沉默昆虫载体中的CP基因来减少病毒损害提供了线索。
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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Genome-wide identification of cuticle protein superfamily in Frankliniella occidentalis provide insight into the control of both insect vectors and plant virus

The structural cuticle proteins (CPs) play important roles in the development and fitness of insects. However, knowledge about CP gene superfamily is limited in virus-transmitting insect vectors, although its importance on transmission of plant virus has been gradually emphasized. In this study, the genome-wide identification of CP superfamily was conducted in western flower thrips Frankliniella occidentalis that is the globally invasive pest and plant virus vector pest. The pest transmits notorious tomato spotted wilt virus (TSWV) around the world, causing large damage to a wide array of plants. One hundred and twenty-eight F. occidentalis CP genes (FoCPs) were annotated in this study and they were classified into 10 distinct families, including 68 CPRs, 16 CPAP1s, 6 CPAP3s, 2 CPCFCs, 10 Tweedles, 4 CPFs, 16 CPLCPs, and 6 CPGs. The comprehensive analysis was performed including phylogenetic relationship, gene location and gene expression profiles during different development stages of F. occidentalis. Transcriptome analysis revealed more than 30% FoCPs were upregulated at least 1.5-fold when F. occidentalis was infected by TSWV, indicating their potential involvement in TSWV interactions. Our study provided an overview of F. occidentalis CP superfamily. The study gave a better understand of CP's role in development and virus transmission, which provided clues for reducing viral damages through silencing CP genes in insect vectors.

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来源期刊
CiteScore
4.30
自引率
4.50%
发文量
115
审稿时长
12 months
期刊介绍: Archives of Insect Biochemistry and Physiology is an international journal that publishes articles in English that are of interest to insect biochemists and physiologists. Generally these articles will be in, or related to, one of the following subject areas: Behavior, Bioinformatics, Carbohydrates, Cell Line Development, Cell Signalling, Development, Drug Discovery, Endocrinology, Enzymes, Lipids, Molecular Biology, Neurobiology, Nucleic Acids, Nutrition, Peptides, Pharmacology, Pollinators, Proteins, Toxicology. Archives will publish only original articles. Articles that are confirmatory in nature or deal with analytical methods previously described will not be accepted.
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