Unravelling the Role of Insulin-Like Peptide Genes in Bombyx mori: Potential Key Regulators of Insect Metabolism

IF 1.5 4区 农林科学 Q4 BIOCHEMISTRY & MOLECULAR BIOLOGY
Creaminar D. Shira, Kanmoni Malakar, Bidyadhar Das
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Abstract

Understanding gene expression in specific tissues and their modulation under environmental stimuli, such as nutritional deficiency, reveals the key physiological regulatory mechanisms of an organism. This study examined the tissue-specific expression of insulin-like peptide (ILP) genes (BmX and BmZ) in Bombyx mori larvae and their responses to hyperglycaemia, food deprivation and hormonal (20-hydroxyecdysone and bovine insulin) treatments. mRNA expression levels of BmX and BmZ were analyzed in the brain, fat body, midgut and ovary. The results revealed that BmX was highly expressed in the fat body, while both genes were abundant in the ovary. Hyperglycaemia increased BmX mRNA expression level in the midgut (3.07-fold) and brain (7.53-fold), while BmZ mRNA expression level was increased in all tissues except the midgut. Nutrient deficiency upregulated BmX mRNA expression level (1.36-fold) in the fat body while reducing it (−0.53-fold) in the midgut. Food deprivation progressively increased (0.77-fold at 24 h and 2.34-fold at 72 h) BmX mRNA expression level in the fat body, while both BmX and BmZ transcripts declined in the midgut. Insulin suppressed BmX (−0.25-fold) and BmZ (−0.91-fold) mRNA expression levels in food-deprived larvae in the fat body, whereas 20E consistently downregulated BmX, BmZ, and BmInR (insulin receptor) mRNA expression levels in all the conditions. These findings revealed the complex interaction of gene expression, tissue specificity, and environmental factors in B. mori larvae and provided insights into adaptive responses to nutritional stress and hormonal regulation in the insect with potential applications in sericulture and agricultural biotechnology.

Abstract Image

揭示家蚕胰岛素样肽基因的作用:昆虫代谢的潜在关键调节因子
了解特定组织中的基因表达及其在营养缺乏等环境刺激下的调控,可以揭示生物体的关键生理调控机制。本研究考察了胰岛素样肽(ILP)基因(BmX和BmZ)在沙蚕幼虫体内的特异性组织表达,以及它们对高血糖、食物匮乏和激素(20-羟基蜕皮激素和牛胰岛素)处理的反应。结果显示,BmX在脂肪体中高表达,而这两个基因在卵巢中都大量表达。高血糖使中肠(3.07倍)和脑(7.53倍)中的BmX mRNA表达水平升高,而除中肠外,其他组织中的BmZ mRNA表达水平均升高。营养缺乏使脂肪体中的 BmX mRNA 表达水平升高(1.36 倍),而中肠中的表达水平降低(-0.53 倍)。食物匮乏会使脂肪体中的 BmX mRNA 表达水平逐渐升高(24 h 升高 0.77 倍,72 h 升高 2.34 倍),而中肠中的 BmX 和 BmZ 转录物均下降。胰岛素抑制了缺食幼虫脂肪体中BmX(-0.25倍)和BmZ(-0.91倍)mRNA的表达水平,而20E在所有条件下都持续下调BmX、BmZ和BmInR(胰岛素受体)mRNA的表达水平。这些发现揭示了森蝇幼虫体内基因表达、组织特异性和环境因素之间复杂的相互作用,为了解昆虫对营养胁迫的适应性反应和激素调控提供了见解,具有在养蚕业和农业生物技术中应用的潜力。
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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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