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能够复制的表达基因组内 microRNA 的 HIV-1 病毒揭示了影响病毒复制的离散 RNA 干扰机制。

Replication competent HIV-1 viruses that express intragenomic microRNA reveal discrete RNA-interference mechanisms that affect viral replication.

机构信息

Molecular Virology Section, Laboratory of Molecular Microbiology, National Institute of Allergy and Infectious Diseases, Bethesda MD, 20892, USA.

出版信息

Cell Biosci. 2011 Nov 23;1(1):38. doi: 10.1186/2045-3701-1-38.

Abstract

BACKGROUND

It remains unclear whether retroviruses can encode and express an intragenomic microRNA (miRNA). Some have suggested that processing by the Drosha and Dicer enzymes might preclude the viability of a replicating retroviral RNA genome that contains a cis-embedded miRNA. To date, while many studies have shown that lentiviral vectors containing miRNAs can transduce mammalian cells and express the inserted miRNA efficiently, no study has examined the impact on the replication of a lentivirus such as HIV-1 after the deliberate intragenomic insertion of a bona fide miRNA.

RESULTS

We have constructed several HIV-1 molecular clones, each containing a discrete cellular miRNA positioned in Nef. These retroviral genomes express the inserted miRNA and are generally replication competent in T-cells. The inserted intragenomic miRNA was observed to elicit two different consequences for HIV-1 replication. First, the expression of miRNAs with predicted target sequences in the HIV-1 genome was found to reduce viral replication. Second, in one case, where an inserted miRNA was unusually well-processed by Drosha, this processing event inhibited viral replication.

CONCLUSION

This is the first study to examine in detail the replication competence of HIV-1 genomes that express cis-embedded miRNAs. The results indicate that a replication competent retroviral genome is not precluded from encoding and expressing a viral miRNA.

摘要

背景

逆转录病毒能否编码和表达内源性 microRNA(miRNA)尚不清楚。有人认为,Drosha 和 Dicer 酶的加工可能会使包含顺式嵌入 miRNA 的复制性逆转录病毒 RNA 基因组失去活力。迄今为止,虽然许多研究表明,含有 miRNA 的慢病毒载体可以有效地转导哺乳动物细胞并表达插入的 miRNA,但尚无研究检查在故意内源性插入 bona fide miRNA 后,对 HIV-1 等慢病毒的复制的影响。

结果

我们构建了几种 HIV-1 分子克隆,每个克隆都包含一个位于 Nef 中的离散细胞 miRNA。这些逆转录病毒基因组表达插入的 miRNA,并且在 T 细胞中通常具有复制能力。插入的内源性 miRNA 对 HIV-1 复制表现出两种不同的后果。首先,发现 HIV-1 基因组中具有预测靶序列的 miRNAs 的表达降低了病毒复制。其次,在一种情况下,插入的 miRNA 被 Drosha 异常有效地加工,这种加工事件抑制了病毒复制。

结论

这是第一项详细研究表达顺式嵌入 miRNA 的 HIV-1 基因组复制能力的研究。结果表明,具有复制能力的逆转录病毒基因组不会被排除在外,不能编码和表达病毒 miRNA。

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