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初始新冠病毒可靠的交互式DNA甲基化标记及其生物学意义。

The Initial COVID-19 Reliable Interactive DNA Methylation Markers and Biological Implications.

作者信息

Zhang Zhengjun

机构信息

School of Computer, Data and Information Sciences, University of Wisconsin, Madison, WI 53706, USA.

出版信息

Biology (Basel). 2024 Apr 7;13(4):245. doi: 10.3390/biology13040245.

Abstract

Earlier research has established the existence of reliable interactive genomic biomarkers. However, reliable DNA methylation biomarkers, not to mention interactivity, have yet to be identified at the epigenetic level. This study, drawing from 865,859 methylation sites, discovered two miniature sets of Infinium MethylationEPIC sites, each having eight CpG sites (genes) to interact with each other and disease subtypes. They led to the nearly perfect (96.87-100% accuracy) prediction of COVID-19 patients from patients with other diseases or healthy controls. These CpG sites can jointly explain some post-COVID-19-related conditions. These CpG sites and the optimally performing genomic biomarkers reported in the literature become potential druggable targets. Among these CpG sites, cg16785077 (gene ), cg25932713 (gene ), and cg22930808 (gene ) at DNA methylation levels indicate that the initial SARS-CoV-2 virus may be better treated as a transcribed viral DNA into RNA virus, i.e., not as an RNA virus that has concerned scientists in the field. Such a discovery can significantly change the scientific thinking and knowledge of viruses.

摘要

早期研究已证实存在可靠的交互式基因组生物标志物。然而,在表观遗传水平上,可靠的DNA甲基化生物标志物,更不用说其交互性,尚未被确定。本研究从865,859个甲基化位点中发现了两组微型的Infinium MethylationEPIC位点,每组有八个CpG位点(基因),它们相互之间以及与疾病亚型存在交互作用。这些位点能够对新冠患者与其他疾病患者或健康对照进行近乎完美(准确率96.87 - 100%)的区分。这些CpG位点可以共同解释一些新冠后相关病症。这些CpG位点以及文献中报道的表现最优的基因组生物标志物成为了潜在的可成药靶点。在这些CpG位点中,DNA甲基化水平上的cg16785077(基因)、cg25932713(基因)和cg22930808(基因)表明,最初的严重急性呼吸综合征冠状病毒2(SARS-CoV-2)病毒或许最好被视作转录为RNA病毒的病毒DNA,而非该领域科学家所关注的RNA病毒。这样的发现能够显著改变对病毒的科学认知和思维。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/943c/11048280/49ceb896106d/biology-13-00245-g001.jpg

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