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人类感染新型冠状病毒(SARS-CoV-2)的基因控制

Genetic Control of Human Infection with SARS-CoV-2.

作者信息

Kucher A N, Babushkina N P, Sleptcov A A, Nazarenko M S

机构信息

Research Institute of Medical Genetics, Tomsk National Research Medical Center, Russian Academy of Sciences, 634050 Tomsk, Russia.

出版信息

Russ J Genet. 2021;57(6):627-641. doi: 10.1134/S1022795421050057. Epub 2021 Jul 3.

Abstract

In 2019, the SARS-CoV-2 beta-coronavirus, which caused a pandemic of severe acute respiratory viral infection COVID-19 (from COronaVIrus Disease 2019), was first detected. The susceptibility to SARS-CoV-2 and the nature of the course of the COVID-19 clinical picture are determined by many factors, including genetic characteristics of both the pathogen and the human. The SARS-CoV-2 genome has a similarity to the genomes of other coronaviruses, which are pathogenic for humans and cause a severe course of infection: 79% to the SARS-CoV genome and 50% to the MERS-CoV genome. The most significant differences between SARS-CoV-2 and other coronaviruses are recorded in the structure of the gene of the S protein, a key protein responsible for the virus binding to the receptor of the host organism cells. In particular, substitutions in the S protein of SARS-CoV-2, leading to the formation of the furin cleavage site that is absent in other SARS-like coronaviruses, were identified, which may explain the high pathogenicity of SARS-CoV-2. In humans, the genes that are significant for the initial stages of infection include , , (encode receptors for coronavirus binding); , , , , (encode proteases involved in the entry of the coronavirus into the cell); (the gene of ATP-dependent RNA helicase DDX1, which promotes replication of coronaviruses); and , , and (encode interferon-induced transmembrane proteins with an antiviral effect). These genes are expressed in many tissues (including those susceptible to the effects of SARS-CoV-2); rare and frequent variants that affect the structure of the encoded protein and its properties and expression level are described in them. A number of common genetic variants with proven functional significance are characterized by the variability in the allele frequency in the world's populations, which can determine interpopulation differences in the prevalence of COVID-19 and in the clinical features of the course of this pathology. The expression level of genes that are important for the formation of the susceptibility to SARS-CoV-2 is affected by epigenetic modifications, comorbidities at the time of infection, taking medications, and bad habits.

摘要

2019年,首次检测到严重急性呼吸道病毒感染新冠病毒病(COVID-19,源自2019冠状病毒病)的病原体——严重急性呼吸综合征冠状病毒2(SARS-CoV-2)β冠状病毒。对SARS-CoV-2的易感性以及COVID-19临床表现的病程性质由许多因素决定,包括病原体和人类的遗传特征。SARS-CoV-2基因组与其他对人类致病并导致严重感染病程的冠状病毒基因组具有相似性:与SARS-CoV基因组的相似性为79%,与中东呼吸综合征冠状病毒(MERS-CoV)基因组的相似性为50%。SARS-CoV-2与其他冠状病毒之间最显著的差异记录在S蛋白基因的结构中,S蛋白是负责病毒与宿主生物体细胞受体结合的关键蛋白。特别是,已鉴定出SARS-CoV-2的S蛋白中的替换,导致形成了其他类SARS冠状病毒中不存在的弗林蛋白酶切割位点,这可能解释了SARS-CoV-2的高致病性。在人类中,对感染初始阶段重要的基因包括 、 、 (编码冠状病毒结合受体); 、 、 、 、 (编码参与冠状病毒进入细胞的蛋白酶); (ATP依赖性RNA解旋酶DDX1基因,促进冠状病毒复制);以及 、 、 和 (编码具有抗病毒作用的干扰素诱导跨膜蛋白)。这些基因在许多组织中表达(包括那些易受SARS-CoV-2影响的组织);其中描述了影响编码蛋白结构及其特性和表达水平的罕见和常见变体。一些具有已证实功能意义的常见基因变体的特征在于世界人群中等位基因频率的变异性,这可以决定COVID-19患病率以及该病理病程临床特征的人群间差异。对SARS-CoV-2易感性形成重要的基因的表达水平受表观遗传修饰、感染时的合并症、用药情况和不良习惯的影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7d0f/8254434/16dfd1939c0c/11177_2021_1458_Fig1_HTML.jpg

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