CMV-encoded GPCRs in infection, disease, and pathogenesis.

2区 医学 Q1 Medicine
Advances in Virus Research Pub Date : 2024-01-01 Epub Date: 2024-02-21 DOI:10.1016/bs.aivir.2024.01.001
William E Miller, Christine M O'Connor
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引用次数: 0

Abstract

G protein coupled receptors (GPCRs) are seven-transmembrane domain proteins that modulate cellular processes in response to external stimuli. These receptors represent the largest family of membrane proteins, and in mammals, their signaling regulates important physiological functions, such as vision, taste, and olfaction. Many organisms, including yeast, slime molds, and viruses encode GPCRs. Cytomegaloviruses (CMVs) are large, betaherpesviruses, that encode viral GPCRs (vGPCRs). Human CMV (HCMV) encodes four vGPCRs, including UL33, UL78, US27, and US28. Each of these vGPCRs, as well as their rodent and primate orthologues, have been investigated for their contributions to viral infection and disease. Herein, we discuss how the CMV vGPCRs function during lytic and latent infection, as well as our understanding of how they impact viral pathogenesis.

CMV 编码的 GPCR 在感染、疾病和发病机制中的作用。
G 蛋白偶联受体(GPCRs)是一种七跨膜结构域蛋白,可调节细胞过程以响应外部刺激。这些受体是最大的膜蛋白家族,在哺乳动物中,它们的信号调节着重要的生理功能,如视觉、味觉和嗅觉。包括酵母、粘菌和病毒在内的许多生物都编码 GPCR。巨细胞病毒(CMV)是一种大型 beta 型疱疹病毒,编码病毒 GPCR(vGPCR)。人类 CMV(HCMV)编码四个 vGPCR,包括 UL33、UL78、US27 和 US28。这些 vGPCR 及其啮齿动物和灵长类动物的直向同源物对病毒感染和疾病的作用都进行了研究。在此,我们将讨论 CMV vGPCR 在溶解和潜伏感染期间如何发挥作用,以及我们对它们如何影响病毒致病机理的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.10
自引率
0.00%
发文量
7
审稿时长
>12 weeks
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