Chen Cancan, Zhong Zhihan, Zhang Wanying, Xia Baijin, Wu Liyang, Liang Liting, Zhang Yiwen, Zhang Hui, Zhang Xu, Pan Ting, Li Linghua, Liu Bingfeng
Institute of Human Virology, Department of Pathogen Biology and Biosecurity, Key Laboratory of Tropical Disease Control of Ministry of Education, Guangdong Engineering Research Center for Antimicrobial Agent and Immunotechnology, Zhongshan School of Medicine, Sun Yat-sen University, Guangzhou, Guangdong, China.
Department of Pathology, The First Affiliated Hospital, Sun Yat-sen University, Guangzhou, Guangdong, China.
J Virol. 2025 Jan 31;99(1):e0117324. doi: 10.1128/jvi.01173-24. Epub 2024 Dec 18.
HIV-1 can integrate viral DNA into host cell chromosomes and establish a long-term stable latent viral reservoir, a major obstacle in curing HIV-1 infection. The reactivation of latent proviruses with latency-reversing agents (LRAs) is a prerequisite for the eradication of viral reservoirs. Previous reports have shown that tannic acid (TA) exerts several biological functions, including antioxidant and antitumor activities. Here, we identified a novel function of TA as a reactivator of HIV-1 latency. TA showed similar features to the HIV-1 transactivator of transcription (Tat) and was able to reactivate a larger number of proviruses from various integration sites. TA also showed a strong synergistic effect with other LRAs acting on different signaling pathways. Further studies revealed that the polycomb repressive complex 1 component, chromobox protein homolog 4 (CBX4), is specifically degraded by TA through ubiquitination. CBX4 is associated with the tri-methylation at lysine 27 of histone H3 (H3K27me3) which was enriched on HIV-1 long terminal repeat regions. The TA-induced CBX4 degradation decreased the H3K27me3 enrichment and subsequently enhanced the transcriptional activity of the integrated proviruses. These results suggest that TA is an efficient LRA aiming to a new target for HIV-1 latency, which could be developed to eradicate latent proviruses.IMPORTANCEHIV-1 remains a global health challenge, with its ability to integrate into the host genome and evade the effects of drugs. To overcome this obstacle, the "shock and kill" strategy was proposed, targeting the reactivation of latent HIV-1 for subsequent eradication through antiretroviral medication and immune system reinforcement. Here, we found a new reactivator for HIV-1 latency, tannic acid (TA), which can reactivate HIV-1 latency widely and deeply. Moreover, we demonstrated that TA could promote the interaction between the polycomb repressive complex 1 component CBX4 and the E3 ubiquitin ligase cullin 4A (CUL4A), resulting in CBX4 degradation through the ubiquitin-proteasome system. These events reduce H3K27me3 enrichment in the HIV-1 long terminal repeat region, thereby promoting HIV-1 transcription and ultimately reactivating HIV-1 latent infection. Our work may facilitate the identification of new latency-reversing agents and provide more theoretical evidence for the molecular mechanism of HIV-1 latency.
人类免疫缺陷病毒1型(HIV-1)可将病毒DNA整合到宿主细胞染色体中,并建立长期稳定的潜伏病毒库,这是治愈HIV-1感染的主要障碍。用潜伏逆转剂(LRA)重新激活潜伏的前病毒是根除病毒库的先决条件。先前的报道表明,鞣酸(TA)具有多种生物学功能,包括抗氧化和抗肿瘤活性。在此,我们确定了TA作为HIV-1潜伏激活剂的新功能。TA表现出与HIV-1转录反式激活因子(Tat)相似的特征,并且能够从各种整合位点重新激活大量前病毒。TA还与作用于不同信号通路的其他LRA表现出强烈的协同效应。进一步的研究表明,多梳抑制复合物1组分,染色盒蛋白同源物4(CBX4),被TA通过泛素化特异性降解。CBX4与组蛋白H3赖氨酸27(H3K27me3)的三甲基化相关,其在HIV-1长末端重复区域富集。TA诱导的CBX4降解降低了H3K27me3富集,随后增强了整合前病毒的转录活性。这些结果表明,TA是一种针对HIV-1潜伏新靶点的有效LRA,可用于开发根除潜伏前病毒的药物。
重要性
HIV-1仍然是一项全球健康挑战,因其能够整合到宿主基因组中并逃避药物的作用。为克服这一障碍,提出了“激活并清除”策略,即针对潜伏HIV-1的重新激活,随后通过抗逆转录病毒药物治疗和增强免疫系统来根除病毒。在此,我们发现了一种用于HIV-1潜伏的新激活剂,鞣酸(TA),它可以广泛而深入地重新激活HIV-1潜伏。此外,我们证明TA可以促进多梳抑制复合物1组分CBX4与E3泛素连接酶cullin 4A(CUL4A)之间的相互作用,导致CBX4通过泛素-蛋白酶体系统降解。这些事件减少了HIV-1长末端重复区域中H3K27me3的富集,从而促进HIV-1转录并最终重新激活HIV-1潜伏感染。我们的工作可能有助于鉴定新的潜伏逆转剂,并为HIV-1潜伏的分子机制提供更多理论证据。