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转录组分析揭示了重症COVID-19患者中调节自噬的关键基因。

Transcriptome Analysis Reveals Hub Genes Regulating Autophagy in Patients With Severe COVID-19.

作者信息

Huang Jinfeng, Wang Yimeng, Zha Yawen, Zeng Xin, Li Wenxing, Zhou Meijuan

机构信息

Department of Radiation Medicine, Guangdong Provincial Key Laboratory of Tropical Disease Research, School of Public Health, Southern Medical University, Guangzhou, China.

Jiangmen Central Hospital, Affiliated Jiangmen Hospital of Sun Yat-sen University, Jiangmen, China.

出版信息

Front Genet. 2022 Jul 18;13:908826. doi: 10.3389/fgene.2022.908826. eCollection 2022.

Abstract

The COVID-19 pandemic has currently developed into a worldwide threat to humankind. Importantly, patients with severe COVID-19 are believed to have a higher mortality risk than those with mild conditions. However, despite the urgent need to develop novel therapeutic strategies, the biological features and pathogenic mechanisms of severe COVID-19 are poorly understood. Here, peripheral blood mononuclear cells (PBMCs) from four patients with severe COVID-19, four patients with mild COVID-19, and four healthy controls were examined by RNA sequencing (RNA-Seq). We conducted gene expression analysis and Venn diagrams to detect specific differentially expressed genes (DEGs) in patients with severe disease compared with those with mild conditions. Gene Ontology (GO) enrichment analysis was performed to identify the significant biological processes, and protein-protein interaction networks were constructed to extract hub genes. These hub genes were then subjected to regulatory signatures and protein-chemical interaction analysis for certain regulatory checkpoints and identification of potent chemical agents. Finally, to demonstrate the cell type-specific expression of these genes, we performed single-cell RNA-Seq analyses using an online platform. A total of 144 DEGs were specifically expressed in severe COVID-19, and GO enrichment analysis revealed a significant association of these specific DEGs with autophagy. Hub genes such as , , , and were then found to be most significantly involved in the biological processes of autophagy at the transcriptome level. In addition, six transcription factors, including SRF, YY1, CREB1, PPARG, NFIC, and GATA2, as well as miRNAs, namely, hsa-mir-1-3p, and potent chemical agents such as copper sulfate and cobalt chloride, may cooperate in regulating the autophagy hub genes. Furthermore, classical monocytes may play a central role in severe COVID-19. We suggest that autophagy plays a crucial role in severe COVID-19. This study might facilitate a more profound knowledge of the biological characteristics and progression of COVID-19 and the development of novel therapeutic approaches to achieve a breakthrough in the current COVID-19 pandemic.

摘要

新冠疫情目前已发展成为对人类的全球性威胁。重要的是,与轻症新冠患者相比,重症新冠患者被认为具有更高的死亡风险。然而,尽管迫切需要开发新的治疗策略,但重症新冠的生物学特征和致病机制仍知之甚少。在此,我们通过RNA测序(RNA-Seq)检测了4例重症新冠患者、4例轻症新冠患者和4例健康对照者的外周血单个核细胞(PBMC)。我们进行了基因表达分析和维恩图分析,以检测重症患者与轻症患者相比的特异性差异表达基因(DEG)。进行基因本体(GO)富集分析以确定显著的生物学过程,并构建蛋白质-蛋白质相互作用网络以提取枢纽基因。然后对这些枢纽基因进行调控特征分析和蛋白质-化学相互作用分析,以确定某些调控检查点并识别有效的化学试剂。最后,为了证明这些基因的细胞类型特异性表达,我们使用在线平台进行了单细胞RNA-Seq分析。共有144个DEG在重症新冠中特异性表达,GO富集分析显示这些特异性DEG与自噬显著相关。然后发现 、 、 和 等枢纽基因在转录组水平上最显著地参与自噬的生物学过程。此外,包括SRF、YY1、CREB1、PPARG、NFIC和GATA2在内的6种转录因子以及miRNA,即hsa-mir-1-3p,以及硫酸铜和氯化钴等有效化学试剂,可能协同调节自噬枢纽基因。此外,经典单核细胞可能在重症新冠中起核心作用。我们认为自噬在重症新冠中起关键作用。这项研究可能有助于更深入地了解新冠的生物学特征和进展,以及开发新的治疗方法,从而在当前的新冠疫情中取得突破。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7208/9340158/5798f240c2d6/fgene-13-908826-g001.jpg

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