SARS-CoV-2 Orphan Gene ORF10 Contributes to More Severe COVID-19 Disease.

Jeffrey Haltom,Nidia S Trovao, Joseph Guarnieri, Pan Vincent,Urminder Singh, Sergey Tsoy, Collin A O'Leary,Yaron Bram, Gabrielle A Widjaja, Zimu Cen,Robert Meller, Stephen B Baylin,Walter N Moss,Basil J Nikolau,Francisco J Enguita,Douglas C Wallace,Afshin Beheshti,Robert Schwartz,Eve Syrkin Wurtele

medRxiv : the preprint server for health sciences(2023)

引用 0|浏览3
暂无评分
摘要
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.
更多
查看译文
AI 理解论文
溯源树
样例
生成溯源树,研究论文发展脉络
Chat Paper
正在生成论文摘要