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微小RNA在慢病毒潜伏和持续存在调控中的作用。

Role of micro-RNAs in regulation of lentiviral latency and persistence.

作者信息

Bagasra Omar, Stir Ariana E, Pirisi-Creek Lucia, Creek Kim E, Bagasra Alexander U, Glenn Nancy, Lee Jeremy S

机构信息

Department of Biology, South Carolina Center for Biotechnology, Orangeburg, SC 29115, USA.

出版信息

Appl Immunohistochem Mol Morphol. 2006 Sep;14(3):276-90. doi: 10.1097/00129039-200609000-00005.

Abstract

Small interfering RNAs have been demonstrated to serve as a molecular defence against numerous retroviruses in plants and insects and, more recently, in primates. With the recent findings of micro-RNAs (miRNAs) that seem to play a pivotal role in the survival of the host, we have explored the role of miRNAs in lentiviral (LV) replication. We have previously hypothesized that, at least in the case of lentivirus infection, small interfering RNAs are involved in the inhibition of these types of viruses by the formation of intramolecular triplex formation (triplexes) between the polypurine tracks sequences of LV provirus and miRNAs and blocking the viral replication at the preintegration complex levels, placing these viruses into a suspended latency. Using several latently and chronically infected LV cell lines and human PBMCs from HIV-1-infected individuals, we show that perinuclear triplexes are formed in LV-infected cells. The number of triplexes decreased in cells with productive replication of LVs. Therefore, the degree of replication of HIV-1 and other LVs, both in the HIV-1 or other LV-infected cell lines and the HIV-1 infected PBMCs, inversely correlate with the number of cytoplasmic triplexes present in a particular cell. This correlation was further confirmed by the stimulation of PBMCs and LV-infected cell lines with appropriate mitogens. Treatment with Tagetin, a RNA polymerase III inhibitor, resulted in a significant decrease in triplexes and a dramatic increase in the LV replication. Our data suggest that triplex formation may be an important mechanism of LV latency mediated by endogenous miRNAs.

摘要

小分子干扰RNA已被证明在植物、昆虫以及最近在灵长类动物中可作为对抗多种逆转录病毒的分子防御机制。随着最近发现微小RNA(miRNA)似乎在宿主存活中起关键作用,我们探究了miRNA在慢病毒(LV)复制中的作用。我们之前曾假设,至少在慢病毒感染的情况下,小分子干扰RNA通过在LV前病毒的多聚嘌呤序列与miRNA之间形成分子内三链体(三链复合物)来抑制这类病毒,并在整合前复合物水平阻断病毒复制,使这些病毒进入潜伏状态。使用几种潜伏性和慢性感染LV的细胞系以及来自HIV-1感染者的人外周血单核细胞(PBMC),我们发现LV感染的细胞中形成了核周三链复合物。在LV进行有效复制的细胞中,三链复合物的数量减少。因此,HIV-1和其他LV在HIV-1或其他LV感染的细胞系以及HIV-1感染的PBMC中的复制程度与特定细胞中存在的细胞质三链复合物数量呈负相关。用适当的促细胞分裂剂刺激PBMC和LV感染的细胞系进一步证实了这种相关性。用RNA聚合酶III抑制剂Tagetin处理导致三链复合物显著减少,LV复制急剧增加。我们的数据表明,三链复合物的形成可能是内源性miRNA介导LV潜伏的重要机制。

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