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Reconstruction of Protein-Protein Interaction Network of Insulin Signaling in Homo Sapiens

机译:智人胰岛素信号的蛋白质-蛋白质相互作用网络的重建

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摘要

Diabetes is one of the most prevalent diseases in the world. Type 1 diabetes is characterized by the failure of synthesizing and secreting of insulin because of destroyed pancreatic β-cells. Type 2 diabetes, on the other hand, is described by the decreased synthesis and secretion of insulin because of the defect in pancreatic β-cells as well as by the failure of responding to insulin because of malfunctioning of insulin signaling. In order to understand the signaling mechanisms of responding to insulin, it is necessary to identify all components in the insulin signaling network. Here, an interaction network consisting of proteins that have statistically high probability of being biologically related to insulin signaling in Homo sapiens was reconstructed by integrating Gene Ontology (GO) annotations and interactome data. Furthermore, within this reconstructed network, interacting proteins which mediate the signal from insulin hormone to glucose transportation were identified using linear paths. The identification of key components functioning in insulin action on glucose metabolism is crucial for the efforts of preventing and treating type 2 diabetes mellitus.
机译:糖尿病是世界上最流行的疾病之一。 1型糖尿病的特征是由于胰岛β细胞被破坏而无法合成和分泌胰岛素。另一方面,由于胰腺β细胞缺陷以及胰岛素信号功能异常导致对胰岛素的反应失败,导致胰岛素的合成和分泌减少,描述了2型糖尿病。为了了解胰岛素响应的信号传导机制,有必要确定胰岛素信号传导网络中的所有成分。在这里,通过整合基因本体论(GO)注释和交互基因组数据,重建了一个相互作用网络,该相互作用网络由具有与智人的胰岛素信号传导生物学相关的统计学上高概率的蛋白质组成。此外,在该重建的网络中,使用线性路径鉴定了介导从胰岛素激素到葡萄糖转运的信号的相互作用蛋白。识别在胰岛素对葡萄糖代谢中起作用的关键成分对于预防和治疗2型糖尿病至关重要。

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