胰岛素信号介导鳞翅目昆虫玻璃体前发育并增强幼年激素介导的玻璃体生成。

Q2 Biochemistry, Genetics and Molecular Biology
Md Abdullah Al Baki, Dae-Weon Lee, Jin Kyo Jung, Yonggyun Kim
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引用次数: 0

摘要

背景:胰岛素/胰岛素样生长肽信号(IIS)可下调血淋巴糖水平,促进大豆豆荚螟(Maruca vitrata)幼虫的生长。本研究的目的是确定黄豆荚螟的类生长肽信号是否能介导成年雌虫的卵巢发育:结果:大豆荚螟的一对卵巢由 8 个卵裂室组成,每个卵裂室又分为远端胚芽室和近端卵黄室。在胚芽鞘中,卵母细胞的发育伴随着活跃的有丝分裂活动。成虫出现后不久就开始了前胚乳发育和随后的卵黄发生。它们随着雌性年龄的增加而继续进行。卵黄素(Vg)和 Vg 受体(VgR)基因表达的上调促进了卵母细胞的发育。幼虫日粮对卵巢发育有明显影响,因为不同营养日粮处理的幼虫卵母细胞发育随蛹的大小而变化。它的卵巢发育依赖于来自头部的内分泌信号,因为在成虫出壳后不久斩首会阻止卵子发生和随后的卵黄发生,同时 Vg 和 VgR 的表达也会明显减少。局部施用幼年激素(JH)可明显恢复其卵巢发育,而法尼酸(JH生物合成的前体)或20-羟基蜕皮激素处理则不能。JH能刺激卵黄发生和绒毛发生,但不能刺激前卵黄发生。相反,向断头雌鼠注射胰岛素可刺激卵母细胞分化和卵黄发生,同时增加 Vg 和 VgR 的表达。为了进一步分析胰岛素对卵巢发育的影响,研究人员通过 RNA 干扰来控制四种 IIS 成分(InR、FOXO、Akt 和 TOR)基因的表达。血凝注射基因特异性双链RNA可显著降低其靶基因的mRNA水平,并干扰卵巢的发育。在对断头雌鱼进行JH处理时加入胰岛素,可通过刺激卵子生成增强JH的促性腺作用:结论:胰岛素促性腺激素(IIS)在卵黄发生前的发育过程中起着关键作用。结论:IIS在介导卵黄发生前发育过程中对营养信号起着关键作用,它还能增强JH II对卵黄发生的促性腺作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Insulin signaling mediates previtellogenic development and enhances juvenile hormone-mediated vitellogenesis in a lepidopteran insect, Maruca vitrata.

Insulin signaling mediates previtellogenic development and enhances juvenile hormone-mediated vitellogenesis in a lepidopteran insect, Maruca vitrata.

Insulin signaling mediates previtellogenic development and enhances juvenile hormone-mediated vitellogenesis in a lepidopteran insect, Maruca vitrata.

Insulin signaling mediates previtellogenic development and enhances juvenile hormone-mediated vitellogenesis in a lepidopteran insect, Maruca vitrata.

Background: Insulin/insulin-like growth peptide signaling (IIS) down-regulates hemolymph sugar level and facilitates larval growth in the soybean pod borer, Maruca vitrata. The objective of this study is to determine whether IIS of M. vitrata can mediate ovarian development of adult females.

Results: A pair of ovaries consists of 8 ovarioles, each of which is separated into distal germarium and proximal vitellarium in M. vitrata. In the germarium, oocyte development occurred with active mitotic activity which was visible by incorporating bromodeoxyribose uridine. Previtellogenic development and subsequent vitellogenesis began soon after adult emergence. They continued with increase of female age. Oocyte development was facilitated by up-regulation of vitellogenin (Vg) and Vg receptor (VgR) gene expression. Larval diets significantly influenced on ovarian development of M. vitrata because oocyte development varied with pupal size derived from larvae treated with different nutritional diets. Its ovarian development was dependent on endocrine signal(s) from the head because decapitation soon after adult emergence prevented oogenesis and subsequent vitellogenesis along with marked reduction of Vg and VgR expression. Topical application of juvenile hormone (JH) significantly recovered its ovarian development whereas farnesoic acid (a precursor of JH biosynthesis) or 20-hydroxyecdysone treatment did not. JH stimulated vitellogenesis and choriogenesis, but not previtellogenic development. In contrast, insulin injection to decapitated females stimulated oocyte differentiation and vitellogenesis along with increase of Vg and VgR expression. To further analyze the effect of insulin on ovarian development, expression of four IIS components (InR, FOXO, Akt, and TOR) genes was manipulated by RNA interference. Hemocoelic injection of gene-specific double stranded RNAs significantly reduced their target gene mRNA levels and interfered with ovarian development. An addition of insulin to JH treatment against decapitated females enhanced the gonadotropic effect of JH by stimulating oogenesis.

Conclusions: IIS plays crucial role in mediating previtellogenic development of M. vitrata in response to nutrient signal. It also enhances the gonadotropic effect of JH II on vitellogenesis.

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BMC Developmental Biology
BMC Developmental Biology 生物-发育生物学
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期刊介绍: BMC Developmental Biology is an open access, peer-reviewed journal that considers articles on the development, growth, differentiation and regeneration of multicellular organisms, including molecular, cellular, tissue, organ and whole organism research.
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