Chen Liujun, Chen Lang, Zuo Luoshiyuan, Gao Ziang, Shi Yingying, Yuan Peipei, Han Song, Yin Jun, Peng Biwen, He Xiaohua, Liu Wanhong
1 Hubei Province Key Laboratory of Allergy and Immunology, School of Basic Medical Sciences, Wuhan University , Wuhan, China .
2 School of Health Sciences, Wuhan University , Wuhan, China .
AIDS Res Hum Retroviruses. 2018 Jun;34(6):544-549. doi: 10.1089/AID.2017.0177. Epub 2018 May 10.
HIV is the causative pathogen of AIDS, which has generated worldwide concern. Long noncoding RNAs (lncRNAs) are a rising star in virus-host cross-talk pathways; they are differentially expressed during many viral infections and are involved in multiple biological processes. Currently, lncRNA growth arrest-specific transcript 5 (GAS5) is known to be downregulated during HIV-1 infection. However, the functions and mechanisms of GAS5 in HIV-1 infection remain largely unknown. In this report, it was found for the first time that GAS5 could inhibit HIV-1 replication. Interestingly, using bioinformatics analyses (with Genomica and starBase.v2.0), GAS5 was found to potentially interact with miR-873. It was further verified that GAS5 could suppress miR-873. Moreover, miR-873 could promote HIV-1 replication. Together, these results not only suggest that GAS5 may inhibit HIV-1 replication through interaction with miR-873 but the results may also provide novel biomarkers for antiviral drugs or potential targets for future therapeutics for HIV/AIDS.
人类免疫缺陷病毒(HIV)是获得性免疫缺陷综合征(AIDS,艾滋病)的致病病原体,已引起全球关注。长链非编码RNA(lncRNA)是病毒-宿主相互作用通路中的一颗新星;它们在许多病毒感染过程中差异表达,并参与多种生物学过程。目前已知,在HIV-1感染期间,lncRNA生长停滞特异性转录本5(GAS5)表达下调。然而,GAS5在HIV-1感染中的功能和机制仍不清楚。在本报告中,首次发现GAS5可抑制HIV-1复制。有趣的是,通过生物信息学分析(使用Genomica和starBase.v2.0)发现,GAS5可能与miR-873相互作用。进一步证实,GAS5可抑制miR-873。此外,miR-873可促进HIV-1复制。总之,这些结果不仅表明GAS5可能通过与miR-873相互作用来抑制HIV-1复制,而且还可能为抗艾滋病病毒药物提供新的生物标志物或为未来艾滋病治疗提供潜在靶点。