Haltom Jeffrey, Trovao Nidia S, Guarnieri Joseph, Vincent Pan, Singh Urminder, Tsoy Sergey, O'Leary Collin A, Bram Yaron, Widjaja Gabrielle A, Cen Zimu, Meller Robert, Baylin Stephen B, Moss Walter N, Nikolau Basil J, Enguita Francisco J, Wallace Douglas C, Beheshti Afshin, Schwartz Robert, Wurtele Eve Syrkin
Department of Genetics Development and Cell Biology, Iowa State University, Ames, IA 50011, USA.
Center for Mitochondrial and Epigenomic Medicine, Division of Human Genetics, The Children's Hospital of Philadelphia, Philadelphia, PA 19104, USA.
medRxiv. 2023 Nov 27:2023.11.27.23298847. doi: 10.1101/2023.11.27.23298847.
The orphan gene of SARS-CoV-2, ORF10, is the least studied gene in the virus responsible for the COVID-19 pandemic. Recent experimentation indicated ORF10 expression moderates innate immunity in vitro. However, whether ORF10 affects COVID-19 in humans remained unknown. We determine that the ORF10 sequence is identical to the Wuhan-Hu-1 ancestral haplotype in 95% of genomes across five variants of concern (VOC). Four ORF10 variants are associated with less virulent clinical outcomes in the human host: three of these affect ORF10 protein structure, one affects ORF10 RNA structural dynamics. RNA-Seq data from 2070 samples from diverse human cells and tissues reveals ORF10 accumulation is conditionally discordant from that of other SARS-CoV-2 transcripts. Expression of ORF10 in A549 and HEK293 cells perturbs immune-related gene expression networks, alters expression of the majority of mitochondrially-encoded genes of oxidative respiration, and leads to large shifts in levels of 14 newly-identified transcripts. We conclude ORF10 contributes to more severe COVID-19 clinical outcomes in the human host.
严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的孤儿基因ORF10,是导致新冠疫情的这种病毒中研究最少的基因。最近的实验表明,ORF10的表达在体外可调节先天免疫。然而,ORF10是否会影响人类的新冠肺炎病情仍不清楚。我们确定,在五种值得关注的变异株(VOC)的95%基因组中,ORF10序列与武汉-1(Wuhan-Hu-1)原始单倍型相同。四种ORF10变异与人类宿主中致病性较低的临床结果相关:其中三种影响ORF10蛋白质结构,一种影响ORF10 RNA结构动态。来自不同人类细胞和组织的2070个样本的RNA测序数据显示,ORF10的积累与其他SARS-CoV-2转录本的积累有条件地不一致。ORF10在A549和HEK293细胞中的表达扰乱了免疫相关基因表达网络,改变了大多数线粒体编码的氧化呼吸基因的表达,并导致14种新鉴定转录本的水平发生大幅变化。我们得出结论,ORF10会导致人类宿主中更严重的新冠肺炎临床结果。