2019年冠状病毒病(COVID-19)
信使核糖核酸
病毒学
严重急性呼吸综合征冠状病毒2型(SARS-CoV-2)
2019-20冠状病毒爆发
计算生物学
生物
医学
遗传学
基因
传染病(医学专业)
爆发
内科学
疾病
作者
Kyusik Q. Kim,Bhagyashri D. Burgute,Shin‐Cheng Tzeng,Crystal Jing,Courtney F. Jungers,Junya Zhang,Liewei L. Yan,Richard D. Vierstra,Sergej Djuranović,Bradley S. Evans,Hani Zaher
出处
期刊:Cell Reports
[Cell Press]
日期:2022-08-01
卷期号:40 (9): 111300-111300
被引量:37
标识
DOI:10.1016/j.celrep.2022.111300
摘要
Synthetic mRNA technology is a promising avenue for treating and preventing disease. Key to the technology is the incorporation of modified nucleotides such as N1-methylpseudouridine (m1Ψ) to decrease immunogenicity of the RNA. However, relatively few studies have addressed the effects of modified nucleotides on the decoding process. Here, we investigate the effect of m1Ψ and the related modification pseudouridine (Ψ) on translation. In a reconstituted system, we find that m1Ψ does not significantly alter decoding accuracy. More importantly, we do not detect an increase in miscoded peptides when mRNA containing m1Ψ is translated in cell culture, compared with unmodified mRNA. We also find that m1Ψ does not stabilize mismatched RNA-duplex formation and only marginally promotes errors during reverse transcription. Overall, our results suggest that m1Ψ does not significantly impact translational fidelity, a welcome sign for future RNA therapeutics.
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