Institut de Génétique Humaine. Laboratoire de Virologie Moléculaire, CNRS Université de Montpellier. Montpellier. France.
Department of Structural Virology, National Center for Global Health and Medicine, 1-21-1 Toyama, Shinjuku-ku, Tokyo 162-8655, Japan.
Sci Adv. 2023 Nov 3;9(44):eadh3642. doi: 10.1126/sciadv.adh3642.
Unintegrated retroviral DNA is transcriptionally silenced by host chromatin silencing factors. Here, we used the proteomics of isolated chromatin segments method to reveal viral and host factors associated with unintegrated HIV-1DNA involved in its silencing. By gene silencing using siRNAs, 46 factors were identified as potential repressors of unintegrated HIV-1DNA. Knockdown and knockout experiments revealed POLE3 as a transcriptional repressor of unintegrated HIV-1DNA. POLE3 maintains unintegrated HIV-1DNA in a repressive chromatin state, preventing RNAPII recruitment to the viral promoter. POLE3 and the recently identified host factors mediating unintegrated HIV-1 DNA silencing, CAF1 and SMC5/SMC6/SLF2, show specificity toward different forms of unintegrated HIV-1DNA. Loss of POLE3 impaired HIV-1 replication, suggesting that repression of unintegrated HIV-1DNA is important for optimal viral replication. POLE3 depletion reduces the integration efficiency of HIV-1. POLE3, by maintaining a repressive chromatin structure of unintegrated HIV-1DNA, ensures HIV-1 escape from innate immune sensing in primary CD4 T cells.
未整合的逆转录病毒 DNA 被宿主染色质沉默因子转录沉默。在这里,我们使用分离的染色质片段的蛋白质组学方法来揭示与未整合 HIV-1DNA 相关的病毒和宿主因子,这些因子参与其沉默。通过 siRNA 的基因沉默,鉴定出 46 个因子作为未整合 HIV-1DNA 的潜在抑制剂。敲低和敲除实验表明 POLE3 是未整合 HIV-1DNA 的转录抑制剂。POLE3 将未整合的 HIV-1DNA 维持在抑制性染色质状态,防止 RNAPII 募集到病毒启动子。POLE3 和最近发现的介导未整合 HIV-1DNA 沉默的宿主因子 CAF1 和 SMC5/SMC6/SLF2,对不同形式的未整合 HIV-1DNA 表现出特异性。POLE3 的缺失会损害 HIV-1 的复制,表明抑制未整合 HIV-1DNA 对于最佳病毒复制很重要。POLE3 的耗竭降低了 HIV-1 的整合效率。POLE3 通过维持未整合 HIV-1DNA 的抑制性染色质结构,确保 HIV-1 逃避原发性 CD4 T 细胞中的先天免疫感应。