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Delta spike P681R mutation enhances SARS-CoV-2 fitness over Alpha variant.德尔塔刺突 P681R 突变增强了 SARS-CoV-2 对阿尔法变体的适应能力。
Cell Rep. 2022 May 17;39(7):110829. doi: 10.1016/j.celrep.2022.110829. Epub 2022 Apr 29.
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Enhanced fusogenicity and pathogenicity of SARS-CoV-2 Delta P681R mutation.SARS-CoV-2 Delta 突变株 P681R 增强了融合性和致病性。
Nature. 2022 Feb;602(7896):300-306. doi: 10.1038/s41586-021-04266-9. Epub 2021 Nov 25.
3
Furin cleavage of the SARS-CoV-2 spike is modulated by -glycosylation.弗林蛋白酶切割 SARS-CoV-2 刺突受糖基化修饰调节。
Proc Natl Acad Sci U S A. 2021 Nov 23;118(47). doi: 10.1073/pnas.2109905118.
4
The PCSK9 discovery, an inactive protease with varied functions in hypercholesterolemia, viral infections, and cancer.载脂蛋白 B 降解酶 9 的发现,一种在高胆固醇血症、病毒感染和癌症中有多种功能的无活性蛋白酶。
J Lipid Res. 2021;62:100130. doi: 10.1016/j.jlr.2021.100130. Epub 2021 Oct 2.
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The Mechanism and Consequences of SARS-CoV-2 Spike-Mediated Fusion and Syncytia Formation.SARS-CoV-2 刺突介导的融合和合胞体形成的机制和后果。
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D614G Substitution of SARS-CoV-2 Spike Protein Increases Syncytium Formation and Virus Titer via Enhanced Furin-Mediated Spike Cleavage.SARS-CoV-2 刺突蛋白 D614G 取代增加合胞体形成和病毒滴度通过增强的弗林蛋白酶介导的刺突裂解。
mBio. 2021 Aug 31;12(4):e0058721. doi: 10.1128/mBio.00587-21. Epub 2021 Jul 27.
7
Platelet Activation and Plasma Levels of Furin Are Associated With Prognosis of Patients With Coronary Artery Disease and COVID-19.血小板活化和弗林蛋白酶的血浆水平与冠心病和 COVID-19 患者的预后相关。
Arterioscler Thromb Vasc Biol. 2021 Jun;41(6):2080-2096. doi: 10.1161/ATVBAHA.120.315698. Epub 2021 Apr 29.
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The furin cleavage site in the SARS-CoV-2 spike protein is required for transmission in ferrets.SARS-CoV-2 刺突蛋白中的弗林裂解位点是在雪貂中传播所必需的。
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9
Lung expression of genes putatively involved in SARS-CoV-2 infection is modulated in cis by germline variants.先天遗传变异可在顺式调控与 SARS-CoV-2 感染相关的基因在肺部的表达。
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10
Common Genetic Variation in Humans Impacts In Vitro Susceptibility to SARS-CoV-2 Infection.人类常见遗传变异影响体外 SARS-CoV-2 感染易感性。
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FURIN 基因变异(rs6224/rs4702)作为严重 COVID-19 患者死亡和心血管特征的潜在标志物。

FURIN gene variants (rs6224/rs4702) as potential markers of death and cardiovascular traits in severe COVID-19.

机构信息

Genética Molecular, Hospital Universitario Central Asturias, Oviedo, Spain.

Instituto de Investigación Sanitaria del Principado deAsturias, ISPA, Oviedo, Spain.

出版信息

J Med Virol. 2022 Aug;94(8):3589-3595. doi: 10.1002/jmv.27748. Epub 2022 Apr 12.

DOI:10.1002/jmv.27748
PMID:35355278
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9088626/
Abstract

Furin is a protease that plays a key role in the infection cycle of SARS-CoV-2 by cleaving the viral proteins during the virus particle assembly. In addition, Furin regulates several physiological processes related to cardio-metabolic traits. DNA variants in the FURIN gene are candidates to regulate the risk of developing these traits as well as the susceptibility to severe COVID-19. We genotyped two functional FURIN variants (rs6224/rs4702) in 428 COVID-19 patients in the intensive care unit. The association with death (N = 106) and hypertension, diabetes, and hyperlipidaemia was statistically evaluated. The risk of death was associated with age, hypertension, and hypercholesterolemia. The two FURIN alleles linked to higher expression (rs6224 T and rs4702 A) were significantly increased in the death cases (odds ratio= 1.40 and 1.43). Homozygosis for the two high expression genotypes (rs6224 TT and rs4702 AA) and for the T-A haplotype was associated with an increased risk of hypercholesterolemia. In the multiple logistic regression both, hypercholesterolemia and the TT + AA genotype were significantly associated with death. In conclusion, besides its association with hypercholesterolemia, FURIN variants might be independent risk factors for the risk of death among COVID-19 patients.

摘要

弗林蛋白酶在 SARS-CoV-2 的感染周期中起着关键作用,它在病毒颗粒组装过程中切割病毒蛋白。此外,弗林蛋白酶还调节与心脏代谢特征相关的几种生理过程。FURIN 基因中的 DNA 变体是调节这些特征发生风险以及对严重 COVID-19 易感性的候选物。我们在重症监护病房的 428 名 COVID-19 患者中对两个功能性 FURIN 变体(rs6224/rs4702)进行了基因分型。统计评估了与死亡(N=106)以及高血压、糖尿病和高脂血症的相关性。死亡风险与年龄、高血压和高胆固醇血症有关。与更高表达相关的两个 FURIN 等位基因(rs6224 T 和 rs4702 A)在死亡病例中显著增加(比值比=1.40 和 1.43)。两种高表达基因型(rs6224 TT 和 rs4702 AA)以及 T-A 单倍型的纯合性与高胆固醇血症风险增加相关。在多因素逻辑回归中,高胆固醇血症和 TT+AA 基因型与死亡显著相关。总之,除了与高胆固醇血症相关外,FURIN 变体可能是 COVID-19 患者死亡风险的独立危险因素。