microRNA机制是HIV-1感染中药物诱导的转录抑制的一个组成部分。

Lawrence Carpio, Zachary Klase, William Coley, Irene Guendel, Sarah Choi, Rachel Van Duyne, Aarthi Narayanan, Kylene Kehn-Hall, Laurent Meijer, Fatah Kashanchi
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引用次数: 0

摘要

RNA干扰在操纵细胞和病毒机制以维持HIV-1感染期间的潜伏期中起着重要作用。HIV-1产生几个microrna,包括一个来自TAR元件的microrna,它改变宿主对感染的反应。由于细胞周期蛋白/cdk复合物对病毒转录很重要,这些研究集中在可能抑制病毒转录的cdk抑制剂上,而不影响正常的细胞机制。罗斯科维汀和黄吡醇是研究充分的cdk抑制剂,在低IC50下有效抑制其靶cdks。这些cdk抑制剂以及未来可能出现的药物都受到microRNA机制的影响。根据我们的研究,我们开发了第三代衍生产品,称为CR8#13。在缺乏Dicer的细胞中,有较高水平的基础病毒ltr报告转录。当添加药物,特别是黄酮吡醇和CR8#13时,在缺乏Dicer的细胞中,LTR的转录抑制作用较弱。此外,在HIV-1克隆(pNL4.3)转染后,与Dicer缺陷系(单核细胞)相比,在含有Dicer的细胞系(t细胞)中,CR8和CR8#13衍生物被证明是更有效的病毒转录抑制剂。接下来,我们询问添加CR8或CR8#13是否可能增加含有HIV-1 LTR细胞中TAR microRNA的水平。我们发现,在药物治疗后,3'TAR microRNA产生量增加,导致microRNA募集到LTR, microRNA募集导致染色质改变、Pol II磷酸化改变和病毒转录抑制。总之,我们的研究结果表明,病毒microRNA,特别是由HIV-1 LTR产生的TAR microRNA,通过操纵宿主细胞机制来限制病毒LTR启动子的转录,负责维持潜伏感染。随着microRNA机制的存在,cdk抑制剂能够显著增加TAR microRNA的数量,导致病毒LTR转录的下调。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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microRNA machinery is an integral component of drug-induced transcription inhibition in HIV-1 infection.

RNA interference plays a significant role in manipulating cellular and viral mechanisms to maintain latency during HIV-1 infection. HIV-1 produces several microRNAs including one from the TAR element which alter the host's response to infection. Since cyclin/cdk complexes are important for viral transcription, these studies focus on the possible cdk inhibitors that inhibit viral transcription, without affecting normal cellular mechanisms. Roscovitine and Flavopiridol are well-studied cdk inhibitors that are effective at suppressing their target cdks at a low IC50. These cdk inhibitors and possibly future generations of drugs are affected by microRNA mechanisms. From our studies, we developed a third generation derivative called CR8#13. In cells that lack Dicer there was a higher level of basal viral LTR-reporter transcription. When drugs, specifically Flavopiridol and CR8#13 were added, the transcriptional inhibition of the LTR was less potent in cells that lacked Dicer. Also, after transfection with HIV-1 clone (pNL4.3), CR8 and CR8#13 derivatives were shown to be more effective viral transcription inhibitors in cell lines that contained Dicer (T-cells) as compared to Dicer deficient lines (monocytes). We next asked whether the addition of CR8 or CR8#13 could possibly increase levels of TAR microRNA in HIV-1 LTR containing cells. We demonstrate that the 3'TAR microRNA is produced in higher amounts after drug treatment, resulting in microRNA recruitment to the LTR. MicroRNA recruitment results in chromatin alteration, changes in Pol II phosphorylation and viral transcription inhibition. In conclusion, our results indicate that viral microRNA, specifically the TAR microRNA produced from the HIV-1 LTR is responsible for maintaining latent infections by manipulating host cell mechanisms to limit transcription from the viral LTR promoter. With the microRNA machinery present, cdk inhibitors are able to significantly increase the amount of TAR microRNA, leading to downregulation of viral LTR transcription.

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Properties and kinetics of microRNA regulation through canonical seed sites. Aptamer-mediated selective delivery of short RNA therapeutics in cancer cells. Enzyme-triggered PEGylated siRNA-nanoparticles for controlled release of siRNA. RNAi2013: RNAi at Oxford. Sub-cellular temporal and spatial distribution of electrotransferred LNA/DNA oligomer.
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