Diverse functions of the ecdysone receptor (EcR) in the panoistic ovary of the German cockroach

IF 3.2 2区 农林科学 Q2 BIOCHEMISTRY & MOLECULAR BIOLOGY Insect Biochemistry and Molecular Biology Pub Date : 2023-05-01 DOI:10.1016/j.ibmb.2023.103935
M. Rumbo, V. Pagone, M.D. Piulachs
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Abstract

Ecdysone regulates essential processes in insect life. Perhaps the most well-known of these are related to metamorphosis. However, ecdysone is also required to regulate the proliferation and differentiation of germ cells in the ovary. The role of ecdysone in insect oogenesis has been studied in depth in holometabolan species with meroistic ovaries, such as Drosophila melanogaster, while in hemimetabolan species with panoistic ovaries their functions are still poorly understood. In the present work, we studied the role of ecdysone in the ovary of the last nymphal instar of the cockroach Blattella germanica by using RNA interference to reduce the levels of the ecdysone receptor (EcR), and thereby deplete the expression of ecdysteroidogenic genes in the prothoracic gland. However, the expression of ecdysteroidogenic genes was upregulated in the ovary, resulting in cell overproliferation in the germarium, which appeared swollen. By analysing the expression of genes that respond to ecdysone, we found that when the source of 20E is the nymphal ovary, EcR appears to repress 20E-associated genes bypassing early genes signalling.

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蜕皮激素受体(EcR)在德国蜚蠊全卵巢中的多种功能
蜕皮激素调节昆虫生命的基本过程。也许其中最著名的是与变态有关。然而,蜕皮激素也需要调节卵巢生殖细胞的增殖和分化。蜕皮激素在昆虫卵发生中的作用已经在具有分子体的全代谢物种中得到了深入的研究,如黑腹果蝇,而在具有全卵巢的半代谢物种中,蜕皮激素的功能仍然知之甚少。本研究采用RNA干扰的方法,通过降低蜕皮激素受体(EcR)的水平,从而减少前胸腺中致蜕皮激素基因的表达,研究蜕皮激素在德国小蠊晚期若虫卵巢中的作用。而卵巢中促卵甾体基因表达上调,导致胚乳细胞过度增殖,出现肿胀。通过分析对脱皮激素有反应的基因的表达,我们发现当20E的来源是雌卵巢时,EcR似乎抑制了20E相关的基因,绕过了早期基因信号传导。
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来源期刊
CiteScore
7.40
自引率
5.30%
发文量
105
审稿时长
40 days
期刊介绍: This international journal publishes original contributions and mini-reviews in the fields of insect biochemistry and insect molecular biology. Main areas of interest are neurochemistry, hormone and pheromone biochemistry, enzymes and metabolism, hormone action and gene regulation, gene characterization and structure, pharmacology, immunology and cell and tissue culture. Papers on the biochemistry and molecular biology of other groups of arthropods are published if of general interest to the readership. Technique papers will be considered for publication if they significantly advance the field of insect biochemistry and molecular biology in the opinion of the Editors and Editorial Board.
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Identification of a gene promoter active in Lucilia sericata larval salivary glands using a rapid transient expression assay. In vivo RNAi screening identifies multiple deubiquitinases required for the maintenance of intestinal homeostasis in Drosophila. JAK and STAT5B mediate olfactory response of migratory locusts to their own volatiles. Functional redundancy of the three insulin receptors of cockroaches. Editorial Board
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