Human cellular microRNA hsa-miR-29a interferes with viral nef protein expression and HIV-1 replication
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Cellular miRNAs play an important role in the regulation of gene expression in eukaryotes. Recently, miRNAs have also been shown to be able to target and inhibit viral gene expression. Computational predictions revealed earlier that the HIV-1 genome includes regions that may be potentially targeted by human miRNAs. Here we report the functionality of predicted miR-29a target site in the HIV-1 nef gene.
We find that the human miRNAs hsa-miR-29a and 29b are expressed in human peripheral blood mononuclear cells. Expression of a luciferase reporter bearing the nef miR-29a target site was decreased compared to the luciferase construct without the target site. Locked nucleic acid modified anti-miRNAs targeted against hsa-miR-29a and 29b specifically reversed the inhibitory effect mediated by cellular miRNAs on the target site. Ectopic expression of the miRNA results in repression of the target Nef protein and reduction of virus levels.
Our results show that the cellular miRNA hsa-miR29a downregulates the expression of Nef protein and interferes with HIV-1 replication.
KeywordsLong Terminal Repeat Jurkat Cell HEK293T Cell Lock Nucleic Acid Human miRNAs
MicroRNAs (miRNAs) are naturally occurring small RNA molecules that modulate gene expression by binding to partially complementary target sites usually located in the 3'UTR of protein coding transcripts. They have been implicated in biological functions like tissue differentiation, establishment of cell fate during development, apoptosis and oncogenesis [2, 3, 4, 5]. The cellular miRNA, hsa-miR-32 has been shown to directly interfere with the replication of primate foamy virus in HeLa cells and to reduce viral RNA levels. Another cellular miRNA, miR-122a, involved in cellular stress response and modulated by interferon beta, can also influence the susceptibility to Hepatitis C virus [7, 8, 9]. Earlier, we had predicted sites in the HIV-1 genome that can be potentially targeted by human encoded miRNAs using consensus target prediction, and we had proposed the possibility that the cellular levels of these miRNAs may determine disease progression following HIV-1 infection. Here we experimentally confirmed our computational predictions by demonstrating that the expression of specific cellular miRNAs can reduce target protein expression and HIV-1 replication in cultured human cells.
Results and discussion
To address whether the appropriate miRNAs are expressed in cells susceptible to HIV-1 infection, we first tested for the presence of hsa-miR-29a and 29b in PBMCs isolated from healthy volunteers. We also probed for hsa-miR-29c, as this novel sequence-related miRNA has been added to the hsa-miR-29 family since our original prediction (Fig. 1B). Hwang et al. have earlier reported that miR-29c could not be detected in HeLa cells. However, we detected mature hsa-miR-29a, b and c in PBMCs, using primer extension of species specific probes against 29a, b and c (Fig. 1C, upper panel). To identify cells suitable for overexpression of these miRNAs or their depletion using anti-miRNA molecules, we determined the endogenous levels of hsa-miR-29a, b and c in a variety of cell lines. The epithelial derived HeLa cell line has been used widely for reporter assays. We found that HeLa cells expressed 29 a, b and c miRNAs (Fig. 1C, middle panel) at levels comparable to PBMCs. HEK293T cells used extensively for HIV-1 single cycle replication studies, on the other hand, did not show detectable levels of miRNA (Fig. 1C, lower panel). However, in later experiments we could observe expression of hsa-miR-29a, b in HEK293T cells using miRNA specific qRT-PCR Taqman assays. HEK293T cells, therefore, appeared to be appropriate for artificially expressing the miRNAs and for studying anti-HIV-1 potential in single cycle replication experiments. In addition, cell line specific miRNA expression profiling studies have reported that 29 a, b and c are expressed in Jurkat cells .
Locked nucleic acid (LNA)-modified anti-miRNA molecules interfere with miRNA function in a highly specific manner. We used LNA-modified anti-miRNA oligonucleotides against hsa-miR-29a and 29b (Fig. 2C) to "knock-down" the cellular miRNAs. Such knock-down should restore reporter activity from the luc-nef fusion construct. Indeed, co-transfection of the luc-nef reporter construct with LNA-modified anti-miR29a and b partially restored the reporter activity in HeLa cells (Fig. 2D and 2E). LNA-modified anti-miR29a was the more effective of the two, restoring reporter activity to 2.5 times that of untreated controls. LNA-modified anti-miR29a and b had no effect on the luciferase vector without the fused nef target sequence, supporting the specificity of the LNA-miRNA interactions (Fig. 2D and 2E).
Although Nef was initially reported to be a negative factor for HIV-1, later results from several laboratories including ours [24, 25] have found that Nef enhances HIV replication. Interfering with Nef expression is expected to decrease viral replication. Thus, the findings that the inhibition of Nef by ectopic over expression of miR29a and 29b reduced viral replication and that the suppression of endogenous miR29a by anti-miR29a LNA increased viral replication are wholly consistent.
Accumulating evidence indicates that miRNAs of both viral and host origin may influence host-virus interaction in a variety of ways: as direct modulators of viral replication, as factors affecting viral susceptibility, and as indirect modulators of cellular genes that influence viral propagation [26, 27, 28, 29]. In this regard, artificial inhibition of the miRNA processing machinery using siRNAs against Dicer and Drosha has been shown to result in faster replication of HIV-1 in PBMCs. Dicer was also shown to be important in cellular resistance to infection by Vesicular Stomatitis Virus and influenza A virus since cells with Dicer defective alleles or cells with knockdown of Dicer exhibited hypersusceptibility to infection by these viruses [31, 32, 33]. A recent report posited that different stages of HIV-1 progression starting with infection followed by the transition from latency to activated replication appears to be associated with discrete expression profiles of cellular miRNAs. That study demonstrated a region common to the 3'UTRs of all HIV-1 transcripts, except nef, which is targeted by a cluster of five cellular miRNAs. These miRNAs were suggested to collectively aid in the establishment of viral latency. Based on those observations, one could reason that a panel of miRNA inhibitors might activate latent HIV-1 infection . Compatible with such reasoning, Wang et al. have indeed recently demonstrated that the suppression of anti-HIV-1 miRNAs in monocytes facilitates HIV-1 infectivity, while the increase in macrophages of miRNAs that target HIV-1 inhibited viral replication. Our current results are consistent with the emerging concept that augmenting the expression of cellular anti-viral miRNAs can be a useful strategy in developing anti-HIV-1 therapeutics. In addition expression levels of natural anti-HIV miRNAs may also be useful in studying susceptibility to infection.
miRNAs are nodal molecules in an intricate network of host-virus interactions that form a chain of strategies and counter strategies developed by the virus and the host. Taken together, the range of interactions between the HIV-1 and host cells suggests that miRNAs may be involved in fine tuning the transition from latency to activation, the clearance of latent HIV-1 reservoirs, and the reduction of virion production. Cellular miRNAs with anti-viral roles may have additional roles in host cellular functions. Anti-HIV-1 therapeutics based on the regulation of miRNA levels will have to address how these changes perturb normal cellular homeostasis.
pEGFP-N3 (Clontech), pMIR-REPORT™ Luciferase (Ambion) and pMIR-REPORT™ β-gal control plasmid (Ambion) were commercially procured. pEGFP-N3-miR-29a and -29b expressing constructs were prepared as follows: first, PCR amplification of fragments containing pre-miRNA 29a (407 bp) and 29b (417 bp) was carried out using the following primer pairs: 5'-ACAGGATATCGCATTGTTGG-3' and 5'-TATACCACATGCAATTCAG-3' (for 29a) and 5'-CCCAGGCATGCTCTCCCATC-3' and 5'-CATTTGTGATATATGCCACC-3' (for 29b). Next, pEGFP-N3 vector was linearized using restriction enzyme SmaI. Blunt-ends generated were modified by Taq polymerase mediated addition of T overhangs and ligated to the PCR fragments. Luc-nef was constructed as follows: 100 bp sequence containing the nef target region was PCR amplified from the HIV-1 genome using primers (restriction site underlined), 5'-CCGACTAGTTTGGCAGAACTACACACC-3' and 5'-CCCAAGCTTGGCCTCTTCTACCTTATC-3', restriction digested with SpeI and HindIII, and cloned into corresponding sites in pMIR-REPORT. All clones were confirmed by sequencing.
DNA oligonucleotides and LNA modified anti-miRNA
DNA oligonulceotides used for PCR amplification of pre-miRNA and flanking regions, and primer extension based detection of miRNAs were commercially procured (The Centre for Genomic Application, India). Locked nucleic acid-modified oligonucleotides were procured from Proligo.
Total RNA was isolated from PBMC, HeLa and HEK293T cells using Trizol method (Invitrogen). 5 μg total RNA from each sample was annealed to 10 pmol oligonucleotide designed to capture hsa-miR-29a, -b and -c, respectively followed by extension using radiolabeled P32-dCTP and M-MuLV Reverse Transcriptase at 37°C for 30 mins. RNA was denatured and samples resolved on 18% Urea-PAGE. Radioactive bands were detected on Fujifilm FLA2000 phosphorimager. Sequence of the oligonucleotides used is given in Fig 1B, lower panel.
10 μg of total RNA from luc and luc-nef tranfected HeLa cells were resolved on 1.5% agarose gel and transferred onto nylon membrane, followed by overnight hybridization with radioactive probe of luciferase prepared as follows: 1.6 kb fragment generated by restriction digestion of pMIR-REPORT™ Luciferase (Ambion) using BamHI and XhoI and radiolabeled using NEBlot™ kit (NEB). β-actin was used as a loading control. Radioactive bands were detected using Typhoon TRIO imager, GE Healthcare.
Real time PCR
Real time quantification of miRNA expression was performed using TaqMan probes specific for hsa-mir-29a and 29b employing the TaqMan microRNA assays kit (Applied Biosystems) according to manufacturer's protocol. hsa-mir-92 was used as an internal control.
HeLa, HEK293T and Jurkat cells were propagated in MEM, DMEM and RPMI (Gibco) respectively, supplemented with 10% FBS (Gibco), 1mM sodium pyruvate, 2 mM L-glutamine and 1× Antibiotic (Sigma; broad-spectrum) in 5% CO2 and humidified 37°C.
Transfection and Reporter assay
HeLa cells were co-transfected with pMIR-REPORT (luc or luc-nef), pMIR-REPORT β-gal and varying concentrations of LNA-modified anti-miR-29a or -29b using siPORT NeoFX transfection agent (Ambion), according to the manufacturer's protocol. 24 hrs after transfection, cells were lysed in 1× RLB and assayed for luciferase and β-gal activity using luciferase and β-gal assay system (Promega) respectively, according to manufacturer's directions. HEK293T cells were co-transfected with pcDNA-HA-Nef and miRNA clones (pEGFP-N3-miR-29a or -29b) or control vector (pEGFP-N3) using calcium phosphate precipitation. Cells were lysed 36 hrs post-transfection to proceed with immunoblot experiment using Nef antibody.
Single cycle replication studies
HEK293T were co-transfected with miRNA clones or control vector along with HIV-1 molecular clone pNL4.3 using Lipofectamine 2000. After 48 hrs of transfection, culture supernatant was collected for p24 antigen ELISA (Perkin Elmer Life Science, USA) and cells were lysed for immunoblot experiment using Nef antibody. Similar transfection and assay was also carried out in human CD4+ Jurkat T cells using Amaxa nucleofection system.
The authors wish to acknowledge Souvik Maiti for assistance in designing Locked Nucleic acid probes and Sridhar Sivasubbu and Ashok Patowary for supporting experiments. The HIV-1 molecular clone pNL4.3 was obtained from the NIH AIDS Reagent program, USA and the HA-Nef expression vector was a kind gift of Prof. Warner Greene, USA. This work was supported by funding from Council for Scientific and Industrial Research. MH was supported by a fellowship from Council for Scientific and Industrial Research. The authors thank Director, NCCS for his encouragement and support.
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