The ongoing pandemic that resulted from coronavirus disease (COVID-19), which is caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2), had been spiraling out of control with no known antiviral drugs or vaccines. Due to the extremely serious nature of the disease, it has claimed many lives, with a mortality rate of 3.4% declared by the World Health Organization (WHO) on March 3, 2020. The aim of this study is to gain an understanding of the regulatory nature of the proteins involved in COVID-19 and to explore the possibility that microRNA (miRNA) could become a major component in the decoding of the virus. In the study, we were able to correlate the host protein gene BCL2L1 with miRNA miR-23b via network analysis. MiRNAs have previously been associated with the antiviral properties of various viral diseases, such as enterovirus 71 and hepatitis. They have been reported to act as antiviral regulators, since they are an integral component in the direct regulation of viral genes. MiRNAs are also capable of enabling the virus to avoid the host immune response by suppressing the IFN-α/β signaling pathway or increasing the production of IFN-α/β and as a result, inhibiting the viral infection. Here, we explain and shed light on the various correlations in the miRNA-gene-disease association that are seen in the host proteins of COVID-19.
【저자키워드】 COVID-19, miRNA, SARS-CoV-2, Severe acute respiratory syndrome coronavirus 2, Gene regulation, HCoV, human coronavirus, IFN, interferon, WHO, World Health Organization, DNA, Deoxyribonucleic acid, COVID-19, coronavirus disease, TF, Transcription factor, PPI analysis, miRNA-gene regulation, MiRNA, MicroRNA, CDC, Control and Prevention, ncRNA, Non-coding RNA, PPI, Protein-Protein Interaction, TRRUST, Transcriptional regulatory relationships unraveled by sentence-based text-mining, SFN, Steiner Forest Network,