Mohammad Rasouli, Fatemeh Safari, Navid Sobhani, Mana Alavi, Raheleh Roudi
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引用次数: 0
摘要
几种致病细菌的效应蛋白含有 Glu-Pro-Ile-Tyr-Ala (EPIYA)基团或其他类似基团。EPIYA 基团通过 III 型和 IV 型分泌系统进入宿主细胞,通过宿主激酶对其酪氨酸残基进行磷酸化。这些基团通过酪氨酸磷酸化与多种含 Src 同源 2(SH2)结构域的哺乳动物蛋白发生非典型相互作用,从而导致多种信号级联的扰乱、感染的扩散和细菌定植的改善。有趣的是,有报道称,哺乳动物蛋白质组中存在 EPIYA(或 EPIYA-like)基序,它们调控哺乳动物细胞信号通路,导致体内平衡和疾病病理生理学。病原菌有可能利用了哺乳动物蛋白质中的 EPIYA(或 EPIYA-like)基序,而哺乳动物的 EPIYA(或 EPIYA-like)基序在进化过程中与含 SH2 结构域的蛋白质发生了高度特异性的相互作用。在这篇综述中,我们将重点讨论含有这些基序的哺乳动物蛋白对哺乳动物细胞信号通路的调控。
Regulation of Cellular-Signaling Pathways by Mammalian Proteins Containing Bacterial EPIYA or EPIYA-Like Motifs Predicted to be Phosphorylated.
The effector proteins of several pathogenic bacteria contain the Glu-Pro-Ile-Tyr-Ala (EPIYA) motif or other similar motifs. The EPIYA motif is delivered into the host cells by type III and IV secretion systems, through which its tyrosine residue undergoes phosphorylation by host kinases. These motifs atypically interact with a wide range of Src homology 2 (SH2) domain-containing mammalian proteins through tyrosine phosphorylation, which leads to the perturbation of multiple signaling cascades, the spread of infection, and improved bacterial colonization. Interestingly, it has been reported that EPIYA (or EPIYA-like) motifs exist in mammalian proteomes and regulate mammalian cellular-signaling pathways, leading to homeostasis and disease pathophysiology. It is possible that pathogenic bacteria have exploited EPIYA (or EPIYA-like) motifs from mammalian proteins and that the mammalian EPIYA (or EPIYA-like) motifs have evolved to have highly specific interactions with SH2 domain-containing proteins. In this review, we focus on the regulation of mammalian cellular-signaling pathways by mammalian proteins containing these motifs.