Gutierrez Denisse A, Valdes Luis, Serguera Che, Llano Manuel
Department of Biological Sciences, University of Texas at El Paso, 500 West University Ave., El Paso, TX 79968, USA.
INSERM MIRCen LMB, Fontenay-aux-Roses, France.
J Gen Virol. 2016 Jul;97(7):1686-1692. doi: 10.1099/jgv.0.000466. Epub 2016 Mar 30.
PARP-1 silences retrotransposons in Drosophila, through heterochromatin maintenance, and integrated retroviruses in chicken. Here, we determined the role of viral DNA integration and cellular heterochromatin in PARP-1-mediated retroviral silencing using HIV-1-derived lentiviral vectors and Rous-associated virus type 1 (RAV-1) as models. Analysis of the infection of PARP-1 knockout and control cells with HIV-1 harbouring WT integrase, in the presence or absence of an integrase inhibitor, or catalytic-dead mutant integrase indicated that silencing does not require viral DNA integration. The mechanism involves the catalytic activity of histone deacetylases but not that of PARP-1. In contrast to Drosophila, lack of PARP-1 in avian cells did not affect chromatin compaction globally or at the RAV-1 provirus, or the cellular levels of histone H3 N-terminal acetylated or Lys27 trimethylated, as indicated by micrococcal nuclease accessibility and immunoblot assays. Therefore, PARP-1 represses retroviruses prior to viral DNA integration by mechanisms involving histone deacetylases but not heterochromatin formation.
PARP-1通过维持异染色质沉默果蝇中的逆转座子,并沉默鸡中的整合逆转录病毒。在此,我们使用HIV-1衍生的慢病毒载体和1型劳斯相关病毒(RAV-1)作为模型,确定了病毒DNA整合和细胞异染色质在PARP-1介导的逆转录病毒沉默中的作用。对PARP-1基因敲除细胞和对照细胞用携带野生型整合酶的HIV-1进行感染分析,在存在或不存在整合酶抑制剂或催化失活突变型整合酶的情况下,结果表明沉默不需要病毒DNA整合。其机制涉及组蛋白脱乙酰酶的催化活性,而不涉及PARP-1的催化活性。与果蝇不同,禽类细胞中PARP-1的缺失并未影响整体染色质的紧实程度或RAV-1前病毒处的染色质紧实程度,也未影响组蛋白H3 N端乙酰化或赖氨酸27三甲基化的细胞水平,这通过微球菌核酸酶可及性和免疫印迹分析得以表明。因此,PARP-1在病毒DNA整合之前通过涉及组蛋白脱乙酰酶而非异染色质形成的机制抑制逆转录病毒。