- Open Access
A nucleolar localizing Rev binding element inhibits HIV replication
AIDS Research and Therapyvolume 3, Article number: 13 (2006)
The Rev protein of the human immunodeficiency virus (HIV) facilitates the nuclear export of intron containing viral mRNAs allowing formation of infectious virions. Rev traffics through the nucleolus and shuttles between the nucleus and cytoplasm. Rev multimerization and interaction with the export protein CRM1 takes place in the nucleolus. To test the importance of Rev nucleolar trafficking in the HIV-1 replication cycle, we created a nucleolar localizing Rev Response Element (RRE) decoy and tested this for its anti-HIV activity. The RRE decoy provided marked inhibition of HIV-1 replication in both the CEM T-cell line and in primary CD34+ derived monocytes. These results demonstrate that titration of Rev in the nucleolus impairs HIV-1 replication and supports a functional role for Rev trafficking in this sub-cellular compartment.
HIV-1 gene expression is finely regulated . Transcription from the HIV-1 long terminal repeat (LTR) produces a full length RNA of 9 Kb from which several mRNAs are then generated by splicing (the 4 Kb singly spliced and 2 Kb fully spliced RNAs) . While the fully spliced RNAs are exported to the cytoplasm, where they are translated into the regulatory and accessory proteins, the late structural proteins and reverse transcriptase (RT) are derived from unspliced or singly spliced RNAs which are transported to the cytoplasm only upon binding of Rev to the Rev Responsive Element (RRE), which is contained in the env coding region . Rev is an 18kDa protein that localizes to both the nucleus and nucleolus [2–4]. It contains a nuclear export signal (NES) as well as a nuclear import signal (NLS) that allow nuclear/nucleolus-cytoplasmic shuttling properties [5, 6]. The NES signal of Rev is recognized by the cellular export factor CRM1, which mediates the nuclear-cytoplasmic export of Rev bound RNAs [7, 8]. Expression of Rev in human cells induces re-localization of CRM1 and some nucleoporins (Nup98 and Nup214) into the nucleolus . Recently, by the use of in vivo fluorescence resonance energy transfer (FRET), multimerization of Rev-GFP and BFP fusion proteins has been shown to occur in the nucleoli of HeLa cells . These observations suggest that the nucleolar trafficking of Rev may be critical for Rev mediated export. To test this hypothesis we used a nucleolar localized decoy that contains the Rev binding element (RBE) [11–14] to sequester Rev within this sub-cellular compartment and test its ability to inhibit HIV-1 replication. The well-characterized U16 small nucleolar RNA (snoRNA)  was used to direct nucleolar delivery of the RBE.
In the present study we demonstrate that stable expression of the U16-RBE chimeric RNA in cultured T-cells and primary monocytes confers strong inhibition of viral replication. These data provide strong evidence that the nucleolar localization of Rev is critical for its functional role in HIV-1 replication and identifies a novel mechanism for inhibition of HIV replication.
Materials and methods
The U16RBE DNA was prepared synthetically as previously described . The Rev Binding Element (RBE) was inserted in the U16 snoRNA sequence by replacing the apical loop . The U16RBE sequence was then subcloned within the Sal I and Xba I sites of the pTZU6+1 expression cassette  generating the pTZU16-RBE clone. The Bam HI and Xba I cleaved fragment from the pTZU16-RBE construct was first filled in with the DNA polymerase Klenow fragment and then inserted in the Nhe I site of the pBabe puro retroviral vector (in the U3 region of the 3'LTR, Fig. 1A) giving rise to the pBabe/U16RBE clone (Fig. 1B). The U6 promoter-U16RBE was also cloned into a Stu I site in the U3 region of the MND/eGFP Banshee retroviral vector 3'LTR (Fig. 1C), generating the MND/eGFP U16RBE construct (Fig. 1D).
HEK 293, CEM and the PG13 packaging cells were maintained as previously described . Transient transfections were carried out using a Calcium Phosphate DNA precipitation kit in accordance with the manufacturer's protocol (GIBCO/BRL, Invitrogen). Briefly, 1 × 106 HEK 293 cells were plated one day prior to transfection. The transfection was carried out using 2–10 μg of plasmid DNA.
Packaging cell line
PG13 was used for packaging of the pBabe/U16RBE and MND/EGFP U16RBE constructs .
CD34+ cell isolation and transduction procedures
CD34+ cells were isolated from fresh umbilical cord blood using anti-CD34+ antibody-coupled magnetic beads (Milteny Biotech, Auburn, CA). Sorted CD34+ cells (purity was above 90% as determined by FACS analysis) were cryopreserved until use for transductions by the viral vectors.
One day prior to transduction, CD34+ cells were thawed rapidly at 37°C, washed and plated at a concentration of 2 × 105 onto Retronectin (Takara, Japan) coated 25 cm2 flasks. The Retronectin concentration for coating was 20 μg/cm2. The CD34+ cells were then pre-stimulated in 5 ml of cytokine media: Iscove's Modified Dulbecco's Media (IMDM – Bio Whittaker, Walkersville, MD), with 20% FBS, 100 U/ml Penicillin, 0.1 mg/ml Streptomycin (Sigma, St. Louis), 2 mM Glutamine (Sigma, St. Louis), IL-3 (10 ng/ml), IL-6 (10 ng/ml), and SCF (10 ng/ml) (R&D Systems, Minneapolis, Minnesota). After 24 hours of pre-stimulation, the media was changed and the CD34+ cells were exposed to the retroviral vector supernatants (MND/eGFP, MND/eGFP U16RBE and Mock). 50% percent retroviral vector supernatant and 50% 2 × cytokine media were used in a total volume of 10 ml per 25 cm2 flask. The 2 × cytokine media has the same composition as the cytokine media but the growth factor concentrations are doubled (20 ng/ml for all cytokines). After 24 hours of infection, the cells were centrifuged, the media removed, and the cells exposed to fresh retroviral supernatant and cytokine media in a total volume of 10 ml.
This process was repeated one more time, leading to 3 rounds of transduction.
After 3 rounds of transduction, CD34+ cells were immediately plated into a Colony Forming Units assay (CFU-assay) or Long Term Bone Marrow Cultures (LTBMCs).
Colony Forming Unit assays
1 × 103 and 2 × 103 transduced CD34+ cells from each vector arm were plated into 1 ml semi-solid methylcellulose media (Methocult, Stem Cell Technologies, Vancouver, Canada). After 14 days, colonies were counted and discriminated into Burst Forming Units Erythroid (BFU-E), Granulocyte-Macrophage Colony Forming Units (CFU-GM) and Granulocyte- Erythroid- Macrophage- Megakaryocyte (CFU-GEMM) Colony Forming Units. The colonies for each vector arm were added and the data expressed as a total colony count per group.
Long term bone marrow cultures
Transduced CD34+ cells were plated into 25 cm2 flasks onto a layer of irradiated normal human bone marrow stroma in cytokine media. The cytokine concentrations for SCF, IL-3 and IL-6 were 10 ng/ml each.
Normal human bone marrow was purchased from Bio Whittaker (Cambrex Bio Science Inc. Rockland, MD), 5 ml were plated directly into Dulbecco's Modified Eagle Media (Cambrex Bio Science) with 10% Fetal Bovine Serum (GIBCO) in a 75 cm2 flask. Bone marrow cells were allowed to adhere overnight. Media and floating cells were removed, and fresh media were added. Stromal cells were allowed to expand for about 4 weeks. After expansion, stromal cells were trypsinised and cryopreserved for later use, or irradiated (2000 rads) and plated into 25 cm2 flasks for LTBMCs at a density of 1 × 105 cells per flask.
CD34+ cells were allowed to expand in the stromal culture flasks. Cell samples were taken for eGFP FACS analysis 2 days after plating to assess the transduction frequency.
10 days after plating, cultures were depleted of the floating cell population, which was used for eGFP cell sorting and subsequent HIV-challenge. After depletion, the remaining cell fraction in the stroma flasks regenerated a high number of floating cells within 14 days. After 6 weeks of LTBMC propagation, a final FACS analysis was performed to assess eGFP expression.
eGFP sorting and propagation of sorted CD34+ progenitor derived cell populations
CD34+ derived cells were sorted for eGFP expression in a MoFLO (Cytomation) cell sorter into 6 well plates containing a layer of irradiated normal human stroma and 2 × cytokine media (20 ng/ml all cytokines). Cells were expanded in these 6 well plates for approximately 5 days. After expansion, cells were removed from the wells and divided into 2 fractions: 1 × 105 cells for eGFP FACS analysis (purity check), and 1 × 106 cells for HIV-challenge.
CEM cells (2.5 × 105) derived from stably transduced clones were infected with HIV-1NL4-3 as previously described . For CD34+ derived monocytes, 1 × 106 sorted CD34+ cells were transferred into 12 × 75 tubes, centrifuged, and resuspended in 100 μl of 2 × cytokine media. 100 μl of HIV-1 JRFL with a titer of 1 × 105 /ml was added to each challenge tube, resulting in a multiplicity of infection (m.o.i.) of 0.01. Cells were incubated at 37°C and 5% CO2 for 3 hours and then 200 μl of 2 × cytokine media were added to each tube and the cells were incubated overnight.
On the following day, cells were washed 4 times and plated into 25 cm2 flasks onto a layer of irradiated S17 cells (kindly provided by Kenneth Dorshkind, UCLA), in 1 × cytokine media in a total volume 10 ml. The cultures were propagated for 28 days and samples were taken weekly. Infections were all performed in duplicate or triplicate.
HIV-1 p24 evaluation
The p24 analyses were performed using the HIV-1 p24 antigen capture assay kit (Science Applications International Corp. Frederick) for the experiment in Fig. 3 and a Beckman/Coulter p24 assay kit (Beckman, FL) for the experiments in Fig. 4B.
RNA extraction and Northern Blot analysis
Total RNA was isolated as previously described . Northern Blot analyses were performed by electrophoresing the isolated total RNA either in a 6% polyacrylamide-7M Urea gel or in a 1. % Agarose formaldehyde gel followed by blotting onto a nylon filter. To simultaneously detect the endogenous U16 snoRNA and the U16RBE RNA, a probe complementary to the 3' end of the U16 was used (Fig. 2A). To detect only the U16RBE a probe complementary to the RBE sequence was used (Fig. 2B). As loading controls probes specific for tRNA3 Lys or the β-Actin were used (Fig. 2).
Nucleolar expression of the Rev Binding Element (RBE) was achieved by substitution of the apical loop of the U16 small nucleolar RNA (snoRNA) with the RBE sequence as previously described . The RBE domain is located within the Rev responsive element (RRE) sequence (within stem-loop IIB, which contains a purine rich "bubble"). Rev has a high binding affinity for this element [11–13]. U16 is a member of the C/D box class of snoRNAs that are primarily involved in post-transcriptional modifications (2' O-methylation) of rRNA molecules . In order to achieve expression of U16RBE in human cells, the chimeric gene was cloned downstream the U6 small nuclear RNA Pol III promoter (clone PTZU16-RBE; ). Intracellular expression and nucleolar compartmentalization of the U16RBE RNA in 293 cells has been previously demonstrated .
To test the intracellular efficacy of the U16RBE against HIV-1 replication, the PTZU16-RBE expression cassette was inserted into the U3 region of the pBabe puro retroviral vector (clone pBabe/U16RBE, Fig. 1). The resulting vector pBabe/U16RBE was then used to transduce the human CEM T cell line. The U6-U16RBE gene inserted within the U3 region of the retroviral vector should be duplicated within the 5' LTR following reverse transcription and integration. Single clones stably expressing U16RBE were isolated following Puromycin selection. Northern blot analyses performed using total RNA extracted from the selected clones showed somewhat varying levels of expression of the RNA decoy (Fig. 2A).
Transcription of the U16RBE could originate from the U6 promoter as well as from the 5' LTR and internal SV40 polII promoters (Fig. 1B). In order to discern the origins of the major transcripts, a Northern blot analysis was performed on RNA separated in a 1.2% Agarose-Formaldeheyde gel to resolve both long and short transcripts. As shown in Fig. 2B, more than 95% of the U16RBE RNA was of a size corresponding to a U6 promoter-driven transcript. Upon longer exposure (data not presented) transcripts of a size originating from the LTR and SV40 promoters can be seen. These results suggest that the majority of the U16RBE RNAs were derived from the Pol III promoters, with minor amounts originating from the LTR or SV40 internal promoters. In addition, transcripts originating from the Pol II promoters that read through the U16RBE structure may be subject to processing by the snoRNA processing machinery. It is not possible to determine how much, if any processing such as this takes place.
We next tested the anti-HIV-1 activity of the U16RBE decoy by challenging several of the stably transduced CEM clones expressing the U16RBE RNA with the HIV-1 NL4-3 strain using a multiplicity of infection of 0.001. As positive and negative controls for this experiment we also challenged CEM clones expressing either a nucleolar localizing anti-HIV-1 wild type ribozyme (wt) or its disabled mutant version (clones U16Rz wt and mutant; ).
At days 1, 10 and 17 post-infection the cell culture supernatants were collected and assayed for the release of the viral p24Gag protein. As shown in Fig. 3, the controls (parental CEM cells and a CEM clonal line expressing the mutant U16Rz) were highly permissive to replication during the 17 days of analysis. In contrast, all the clonal lines expressing U16RBE and the one expressing U16Rz wt were highly resistant to the HIV-1 challenge.
To test the anti-HIV-1 activity of U16RBE in more clinically relevant cells, the PTZU16-RBE cassette was inserted within the U3 region of the 3'LTR of the MND/eGFP retroviral vector (Fig. 1C). This vector allows use of eGFP expression to monitor transduction. The recombinant vector was transduced into human CD34+ progenitor cells purified from umbilical cord blood. Cells were propagated under cell culture conditions that allow differentiation into CD4+ monocytes. Cell counts after pre-stimulation and transduction were similar for both mock and recombinant vectors, with cell viability greater than 90% and cell expansion about two-fold in all cases (data not presented). To assess potential toxicities of the vectors, colony assays were carried out using the transduced CD34+ cells. Although some differences in colony forming numbers were observed between the three samples (Table 1A), in our hands these small differences are not significant, suggesting no overt toxicity of the U16RBE expression.
The transduction efficiency (TD) was assessed by FACS analyses (monitoring eGFP expression) of the cells at days 1 and 45 post transduction (Table 1B). The TD was between 3 and 6 % of the gated population on day 1 post-transduction as determined by measuring eGFP expression. After 45 days, expression of eGFP dropped to less than 1%. The relatively low level of transduction efficiency is a consequence of the vector preparation and can vary significantly from experiment to experiment. The drop in eGFP expression is due to epigenetic silencing of the LTR driving EGFP in this vector. The Pol III promoter expression does not diminish during this time (H.Li, D. Castanotto and J. Rossi-unpublished observations).
Ten days after transduction the cells were sorted for eGFP expression. The sort purity was checked 5 days later with no significant differences among the various vector transduced cells (data not shown). Northern Blot analyses, carried out on total RNAs isolated from the eGFP sorted CD34+ derived cells, showed readily detectable levels of the U16RBE RNA, which were comparable to the levels of the endogenous U16 snoRNA (Fig. 4A).
The sorted cells were next challenged on the day of FACS analysis with the M-tropic HIV-1 JRFL isolate at a multiplicity of infection of 0.01. On days 1, 7, 14, 21 and 28 post-infection, the supernatants were collected and tested for p24Gag protein accumulation.
As shown in figure 4B, while the mock and the eGFP sorted CD34+ cells transduced with the parental MND/EGFP vector were highly permissive to viral replication, cells expressing the MND/eGFP U16RBE resulted in over 4 logs of inhibition out to 28 days post infection.
We previously exploited the use of the U16 snoRNA as a vector for the nucleolar delivery of therapeutic anti-HIV ribozyme and TAR decoy RNAs [17, 18]. It was previously demonstrated that substitution of the apical loop of U16 with the RBE sequence gave rise to an RNA decoy that localized in the nucleoli of 293 cells and was able to interact with Rev in X. laevis oocytes . In these studies the interaction of the U16RBE decoy with Rev induced the re-localization of the decoy from the nucleus to the cytoplasm. Although we were not able to follow this trafficking in the present experiments, we assume this re-localization also took place in the T- cells and monocytes used in the present studies.
Our primary interest in the present studies was whether or not the U16RBE would sequester Rev sufficiently to inhibit HIV-1 replication in human CEM T-cells and in primary monocytes derived from hematopoietic progenitor CD34+ cells.
To test this possibility we inserted the U6 expression cassette containing the U16RBE sequence within the U3 region of the 3'LTR of two different retroviral vectors, pBabe puro and MND/eGFP (giving rise to pBabe/U16RBE and MND/eGFP U16RBE constructs, Fig. 1). Using the pBabe/U16RBE plasmid we first transduced the CEM T cell line and selected Puromycin resistant clones stably expressing the U16RBE (Fig. 2). We challenged some of these clones with HIV-1 NL4-3 and demonstrated that over a period of 17 days the decoy conferred near complete inhibition of viral replication (Fig. 3). To further test the U16RBE RNA as a possible candidate for hematopoietic stem cell gene therapy for HIV-1, the anti-HIV-1 activity of the U16RBE decoy was tested in human umbilical cord blood CD34+ derived monocytes. The CD34+ cells were transduced with either the MND/eGFP or MND/eGFP U16RBE constructs and allowed to differentiate into monocytes in culture. FACS sorted, transduced monocytes were challenged with HIV-1 JRFL at a multiplicity of infection of 0.01 and the infection was monitored for a period of 28 days (Fig. 4B). While the controls (mock and MND/eGFP transduced CD34+ cells) readily supported viral replication resulting in secretion of μg quantities of p24Gag, the CD34+ derived cells expressing the U16RBE showed four logs of p24 inhibition even after 28 days post infectious challenge (Fig. 4B).
In conclusion, we have demonstrated that the nucleolar localizing U16RBE decoy is a potent inhibitor of the HIV-1 replication. These results suggest that this inhibitor could be a candidate for anti-HIV gene therapy. The decoy could be used alone or in combination with other potent therapeutic RNAs, such as anti-HIV short hairpin RNAs . Rev is essential for HIV-1 structural gene expression and full length viral RNA packaging and consequently sequestering of this protein via the decoy resulted in strong anti-HIV activity. It is highly likely that the decoy-Rev complex traffics to the cytoplasm as was observed in the Xenopus oocytes  since Crm1 is the transport carrier in both organisms. Targeting Rev in the nucleolus allows capturing of this protein prior to its interaction with the viral RRE. Furthermore, this strategy is unlikely to result in emergence of viral Rev mutants that can no longer bind the decoy since these would also be defective in binding to the viral RBE. In such a dual component system, mutants in Rev would have to co-evolve with altered forms of the RBE to escape the inhibitory activity of the decoy. Since the U16RBE is encoded in a small gene, it should be easy to combine this with other antiviral RNAs such as shRNAs. A combinatorial approach, which includes the U16RBE, should increase the overall antiviral potency  and further minimize the occurrence of viral escape mutants. Although the nucleolar localization of some HIV proteins , and perhaps of some classes of HIV RNAs , has been demonstrated, the functional role of this cellular localization is poorly understood. Concerning Rev, it has been suggested that the nucleoli could be a "storage site" for the protein  and in some cases it has been reported that Rev can function without nucleolar localization [25, 26]. At the same time, it is noteworthy to mention that when Rev is expressed ectopically it localizes primarily within the nucleoli of human cells [2–4] where it multimerizes  and relocates CRM1 and some nucleoporins . Rev multimerization is a critical event for the nucleocytoplasmic transport of incompletely spliced and unspliced HIV RNAs, and the association with CRM1 and nucleoporins is probably critical for its own nuclear export. These latter observations underline a crucial role of the nucleolus in Rev function and therefore in the HIV-1 replicative cycle. One possibility is that use of the Crm1 export pathway provides a mechanism for unspliced HIV RNAs to escape the nonsense mediated decay mechanism, although this is only a hypothetical explanation at this time. The importance of nucleolar trafficking of Rev and HIV is strengthened by the data reported here and by previously published data wherein we demonstrated that a nucleolar localizing TAR decoy  as well as a nucleolar localizing anti-HIV-1 hammerhead ribozyme  are both potent inhibitors of HIV-1 replication.
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This work was supported by a MURST (PRIN and "Centro di eccellenza BEMM") and ISS (Programma Nazionale di ricerca sull'AIDS- progetto n. 40D.17) grants to IB and NIH NIAID 42552 and 29329 to JJR. The authors would like to acknowledge the contributions of L. Cagnon and J. Kim for assisting with the HIV assays.