SARS-CoV-2 ORF8基因CAA=TAA和AAA=TAA终止密码子突变多见于B.1.1.7变异与流行的L84S点突变无关

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引用次数: 0

摘要

SARS-CoV-2的5种挥发性有机化合物主要在全球造成100万人死亡,分别为B.1.1.7(英国)、B.1.351(南非)、P.1(巴西)、B.1.617.2(印度)和B.1.1.529(非洲)。在HIV介导的发病机制中,小反式激活蛋白(TAT, NEF, REV)调节细胞基因的转录。同样,初步报告表明,冠状病毒ORF8蛋白作为组蛋白模拟物,具有许多表观遗传变化和免疫调节功能,破坏了染色质结构。ORF8蛋白与免疫球蛋白结构域也有一些相似之处,可以抑制HMC-1和ifn - β的功能。在进化过程中,冠状病毒基因组ORF8区域的382个核苷酸缺失(∆382)导致病毒载量和致病性较弱(accession no.MT374101)。通过BLAST搜索缺失边界,筛选出少量ORF8蛋白截断突变体。C>T碱基在27972nt的变化和A>T碱基在28095nt的变化产生了两个终止密码子(CAA=TAA和AAA=TAA),产生26AA和67AA长ORF8截断蛋白。在突变边界选择寡核苷酸进行类似的Blast-N搜索,得到许多ORF8突变体具有不同的S24L、V32L、P38S、R52I、A65V、Y73C、L84S、K92E和V100L突变,有或没有TAA终止突变。主要突变发生在B.1.1.7系,该系发生69HV和145Y突变,ORF1ab多蛋白3675KSF缺失。然而,一个ORF8突变体(加入号:OW221449)属于24LPP刺缺失的Omicron BA.2变体,其他属于24LPP刺缺失和69HV刺缺失的Omicron BA.5变体(accession no . OP733645和OP671680)。1个终止密码子突变体(加入号:OP711842)也有63nt ORF7a/b的删除。突变没有改变ORF8基因的发夹结构,ORF8蛋白形成稳定的二聚体球形三维结构,与多种宿主蛋白相互作用。显然,如此丰富的B.1.1.7谱系ORF8蛋白截断突变体的产生可能是2021年冠状病毒α变异体灭绝的原因之一。ORF8突变体作为宿主蛋白调节剂的作用是根据冠状病毒基因组中的其他缺失和突变来解释的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
SARS-CoV-2 ORF8 gene CAA=TAA and AAA=TAA Termination Codon Mutations found mostly in B.1.1.7 Variants was Independent of Popular L84S Point Mutations
Five VOCs of SARS-CoV-2 mainly caused million deaths worldwide and named as B.1.1.7 (U.K.), B.1.351 (South Africa), P.1 (Brazil), B.1.617.2 (India), and B.1.1.529 (Africa). In HIV mediated pathogenesis, small trans activator proteins (TAT, NEF, REV) modulate transcription of cellular genes. Similarly, preliminary reports indicated that corona virus ORF8 protein acts as histone mimics disrupting chromatic structure with many epigenetic changes and immune modulator functions. ORF8 protein had also some similarities to immunoglobulin domains and inhibited HMC-1 and IFN-beta functions. During evolution a 382-nucleotide deletion (∆382) in the ORF8 region of the corona virus genome leads to weak virus load and weak pathogenicity (accession no.MT374101). We BLAST searched deletion boundary and was selected few ORF8 protein truncated mutants. The C>T base change at 27972nt and another A>T base change at 28095nt created two termination codons (CAA=TAA and AAA=TAA) to produce 26AA and 67AA long ORF8 truncated proteins. Similar Blast-N search with oligonucleotides selected at the mutation boundaries gave many ORF8 mutants with distinct S24L, V32L, P38S, R52I, A65V, Y73C, L84S, K92E and V100L mutations with or without TAA termination mutations. Major mutations found in B.1.1.7 lineage which had spike 69HV and 145Y mutations and ORF1ab polyprotein 3675KSF deletion. However, one ORF8 mutant (accession no. OW221449) belongs to Omicron BA.2 variant with 24LPP spike deletion and others to Omicron BA.5 variants (accession nos. OP733645 and OP671680) with 24LPP and 69HV deletion in the spike protein. One termination codon mutant (accession no. OP711842) has also 63nt ORF7a/b deletions. Mutation did not change the hairpin structure in the ORF8 gene and ORF8 protein formed dimeric stable globular 3-D structure to interact with many host proteins. Clearly, generation of such abundant B.1.1.7 lineage ORF8 protein truncated mutants may be one of the causes for the extinction of Alpha variant of corona virus in 2021. Roles of ORF8 mutants as host proteins modulator were explained in light of other deletions and mutations in corona virus genome.
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