先天性免疫中鸟苷酸结合蛋白的跨物种功能保护。

IF 5.5 3区 医学 Q1 IMMUNOLOGY Medical Microbiology and Immunology Pub Date : 2023-04-01 Epub Date: 2022-04-13 DOI:10.1007/s00430-022-00736-7
Luca Schelle, João Vasco Côrte-Real, Pedro José Esteves, Joana Abrantes, Hanna-Mari Baldauf
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引用次数: 0

摘要

鸟苷酸结合蛋白(GBPs)是一个进化古老的蛋白家族,广泛分布于真核生物中。它们是干扰素(IFN)诱导的鸟苷酸三磷酸酶,属于达纳敏超家族。众所周知,GBPs 在细胞自主的先天性免疫反应中对细菌、寄生虫和病毒感染起着重要作用,而且还参与炎性体的激活。进化研究表明,GBPs 在每个家族中都呈现出基因增减的模式,一些基因被假基因化,而另一些基因则更加分化,这表明了生死进化过程。大多数物种都蕴藏着大型 GBP 基因簇,编码多个旁系亲属。以前的功能研究主要集中在小鼠和人类的 GBP 上,但现在有越来越多的数据可供使用,从而拓宽了人们对这一多功能蛋白家族的了解。在这篇综述中,我们将提供新的见解,并概述GBP在所有研究物种(包括植物、无脊椎动物和脊椎动物)中的进化、保护及其作用,揭示所描述的GBP特征在多大程度上可以转移到其他物种中。
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Functional cross-species conservation of guanylate-binding proteins in innate immunity.

Guanylate binding proteins (GBPs) represent an evolutionary ancient protein family widely distributed among eukaryotes. They are interferon (IFN)-inducible guanosine triphosphatases that belong to the dynamin superfamily. GBPs are known to have a major role in the cell-autonomous innate immune response against bacterial, parasitic and viral infections and are also involved in inflammasome activation. Evolutionary studies depicted that GBPs present a pattern of gain and loss of genes in each family with several genes pseudogenized and some genes more divergent, indicative for the birth-and-death evolution process. Most species harbor large GBP gene clusters encoding multiple paralogs. Previous functional studies mainly focused on mouse and human GBPs, but more data are becoming available, broadening the understanding of this multifunctional protein family. In this review, we will provide new insights and give a broad overview about GBP evolution, conservation and their roles in all studied species, including plants, invertebrates and vertebrates, revealing how far the described features of GBPs can be transferred to other species.

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来源期刊
CiteScore
10.60
自引率
0.00%
发文量
29
审稿时长
1 months
期刊介绍: Medical Microbiology and Immunology (MMIM) publishes key findings on all aspects of the interrelationship between infectious agents and the immune system of their hosts. The journal´s main focus is original research work on intrinsic, innate or adaptive immune responses to viral, bacterial, fungal and parasitic (protozoan and helminthic) infections and on the virulence of the respective infectious pathogens. MMIM covers basic, translational as well as clinical research in infectious diseases and infectious disease immunology. Basic research using cell cultures, organoid, and animal models are welcome, provided that the models have a clinical correlate and address a relevant medical question. The journal also considers manuscripts on the epidemiology of infectious diseases, including the emergence and epidemic spreading of pathogens and the development of resistance to anti-infective therapies, and on novel vaccines and other innovative measurements of prevention. The following categories of manuscripts will not be considered for publication in MMIM: submissions of preliminary work, of merely descriptive data sets without investigation of mechanisms or of limited global interest, manuscripts on existing or novel anti-infective compounds, which focus on pharmaceutical or pharmacological aspects of the drugs, manuscripts on existing or modified vaccines, unless they report on experimental or clinical efficacy studies or provide new immunological information on their mode of action, manuscripts on the diagnostics of infectious diseases, unless they offer a novel concept to solve a pending diagnostic problem, case reports or case series, unless they are embedded in a study that focuses on the anti-infectious immune response and/or on the virulence of a pathogen.
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