Presence of a functional but dispensable Nuclear Export Signal in the HTLV-2 Tax protein
© Chevalier et al; licensee BioMed Central Ltd. 2005
Received: 14 October 2005
Accepted: 14 November 2005
Published: 14 November 2005
Human T-cell leukemia virus type 1 and type 2 are related human retroviruses. HTLV-1 is the etiological agent of the Adult T-cell Leukemia/Lymphoma and of the Tropical Spastic Paraparesis/HTLV-1 Associated Myelopathy, whereas, HTLV-2 infection has not been formally associated with any T-cell malignancy. HTLV-1 and 2 genomes encode, respectively, the Tax1 and Tax2 proteins whose role is to transactivate the viral promoter. HTLV-1 and HTLV-2 Tax sequences display 28% divergence at the amino acid level. Tax1 is a shuttling protein that possesses both a non canonical nuclear import (NLS) and a nuclear export (NES) signal. We have recently demonstrated that Tax1 and Tax2 display different subcellular localization and that residues 90–100 are critical for this process. We investigate in the present report, whether Tax2 also possesses a functional NES.
We first used a NES prediction method to determine whether the Tax2 protein might contain a NES and the results do suggest the presence of a NES sequence in Tax2. Using Green Fluorescent Protein-NES (GFP-NES) fusion proteins, we demonstrate that the Tax2 sequence encompasses a functional NES (NES2). As shown by microscope imaging, NES2 is able to mediate translocation of GFP from the nucleus, without the context of a full length Tax protein. Furthermore, point mutations or leptomycin B treatment abrogate NES2 function. However, within the context of full length Tax2, similar point mutations in the NES2 leucine rich stretch do not modify Tax2 localization. Finally, we also show that Tax1 NES function is dependent upon the positioning of the nuclear export signal "vis-à-vis" GFP.
HTLV-2 Tax NES is functional but dispensable for the protein localization in vitro.
HTLV-1 and HTLV-2 are closely related retroviruses that infect T-cells in vivo, with a probable preferential tropism for CD4+ and CD8+ cells respectively . HTLV-1 is the etiological agent of the Adult T-cell Leukemia/Lymphoma (ATLL) and of the Tropical Spastic Paraparesis/HTLV-1 Associated Myelopathy (TSP/HAM), while HTLV-2 infection, even if originally described in a patient suffering of atypical hairy T-cell leukemia, has only been linked to infrequent cases of TSP/HAM "like" disease [2–4]. Both HTLV-1 and HTLV-2 genomes encode a viral transactivator (Tax1 and Tax2 respectively). Tax1 has an oncogenic potential and is responsible for cell-transformation in vitro [5, 6]. Tax1 and Tax2 display approximately 75% nucleotide sequence homology. Strikingly however, several reports have now demonstrated that although the critical functional regions of the proteins are well conserved (i.e. NF-κB and CREB/ATF activation domains), the two transactivators exhibit a number of major phenotypical differences [1, 7–18]. Nevertheless, Tax2 is capable of immortalizing human lymphocytes and, although to a lesser extent than Tax1, of transforming rat cells in vitro [10, 19].
Eukaryotic cells are compartmentalized into the cytoplasm and the nucleus by the nuclear envelope [20, 21]. The nuclear envelope contains nuclear pore complexes (NPCs), which mediate the traffic of molecules between the two compartments. The nucleo-cytoplasmic traffic of large molecules is regulated by specific nuclear import and export systems. Proteins that contain classical Nuclear Localization Signals (NLSs) are imported into the nucleus by importin α/β protein heterodimers. So far, six importin α family members and one importin β have been described . Importin α binds to NLS containing proteins, whereupon importin β is responsible for the docking of the importin cargo complex to the cytoplasmic side of the NPC, followed by translocation of the complex through the NPC. A classical monopartite NLS consists of a stretch of basic amino acids such as arginines and lysines. Contrary to this, the Nuclear Export Signal (NES) generally consists of a leucine/isoleucine-rich sequence . The classical NES pattern is L-x(2,3)- [LIVFM]-x(2,3)-L-x- [LI], where L can either be L, I, V, F or M, but many known NES regions do not conform to these limitations . For example, the spacing between the hydrophobic residues is variable and NES regions can also be rich in glutamate, aspartate and serine . The first nuclear export pathway to be discovered involved the chromosome region maintenance 1 (CRM1) receptor, exporting proteins containing a nuclear export signal (NES) . CRM1 binds to a Nuclear Export Signal (NES)-containing protein and to the NPC. Several ways of regulating NES-dependent export have been reported, including masking or unmasking the NES and post-translational modifications of the NES-containing protein .
Cellular fractionation and immunofluorescence experiments performed with HTLV-1 infected and Tax1 transfected cells have demonstrated that Tax1 was present both in the nuclear and cytoplasmic fractions. However, the distribution of the protein between these two compartments is unequal and depends on the cell-line used [27–31]. The Tax1 48 amino terminal sequence contains a non-canonical functional NLS  that allows the protein to enter the nucleus, where Tax1 localizes to discrete nuclear bodies (also called Tax Speckled Structures (TSS) . In addition, Tax1 also contains a "Rev-like" Nuclear Export Signal (NES) spanning from amino acid 189 to 202. This NES is insensitive to leptomycin B within the context of the full-length protein . Both localization signals (NLS and NES) are likely to be involved in the shuttling of Tax1, but this process is still not clearly understood .
We have recently reported that, although Tax2 contains a functional NLS domain, the protein localizes predominantly to the cytoplasm in HTLV-2 immortalized or transformed infected T-cells as well as in Tax2 transfected cells . These results were further confirmed in another laboratory  which also demonstrated that the NLS domain was confined to the 40 first N-terminal amino acids. We also demonstrated that the region spanning amino acids 90 to 100 was critical for Tax2 localization . The recent report of a Tax1 NES sequence prompted us to examine the possible presence of a NES in Tax2. In addition to the 90–100 domain, this sequence could serve as a second domain involved in Tax2 localization. We show in this report that, although HTLV-2 Tax protein contains a NES sequence that is active without the context of a full-length protein, this domain is dispensable for the Tax2 localization.
HTLV-2 Tax protein sequence contains a putative NES domain
We lately demonstrated that the HTLV-2 Tax protein has an intracellular localization that is different from that of Tax1, both in infected and transfected cells (i.e. Tax2 localizes more to the cytoplasm than Tax1) and that, within the Tax sequence, the 90–100 domain was critical for the protein localization . These results were confirmed lately . Another recent article reported that, in addition to the previously characterized NLS, HTLV-1 Tax protein also contains a Nuclear Export Signal (NES) comprising amino acids 189 to 202 (KRIEELLYKISLTT). This sequence contains a string of hydrophobic amino acids (I191, L195, I198 and L200)  and has the ability to redirect the Green Fluorescent Protein (GFP) to the cytoplasm. Within the Tax1 NES sequence, residues L195 (formerly named L194 ) and L200 appear to be critical for the Tax1 NES function. As an example, when Tax1 L200 is mutated to an alanine, the GFP-Tax1 localization is altered .
We set out to investigate whether, despite these differences, the Tax2 putative NES was functional. To this end, we affixed the 189–202 amino-acid domain of Tax2 to the N-terminus of the GFP sequence (NES2-EGFP) using the pEGFP-N1 vector as previously reported . The NES2-EGFP construct was then transiently transfected in 293T (data not shown) and Hela cells, as these cells have frequently been used for Tax localization studies [17, 27]. As a positive control, the NES Tax1 sequence was also fused to the N-terminus of the GFP (NES1-EGFP). In the absence of a Tax NES sequence, the GFP protein is nearly equally distributed between the cytoplasm and the nucleus of the transfected cells ( and data not shown). However, the GFP signal was almost entirely cytoplasmic when the protein was fused to the Tax2 putative NES (Figure 2B panel a and Figure 2C for fractionation). This suggests that this latter sequence mediates an active transport of GFP in vitro. Unexpectedly, and contrary to a previous report , the NES1-EGFP fusion protein was diffused in both the nucleus and the cytoplasm with a nuclear content that was much higher than that of NES2-EGFP (Figure 2B panels a vs. b and Figure 2C). We obtained and sequenced the construct that has been used in Dr Wigdahl's laboratory and the sequence results showed that the Tax1 NES domain had been cloned to the C-terminus part of the GFP rather than to the N-terminus (data not shown). Consequently, a second series of recombinant plasmids was made using the pGFP-C3 vector, allowing for a GFP C-terminal fusion construct. As with the NES2-EGFP construct, GFP-NES2 was mostly cytoplasmic (Figure 2B panel c), while, under these experimental conditions, GFP-NES1 was also, as previously published, preponderant in the cytoplasm (Figure 2B panel d). Interestingly, subcellular fractionation experiments clearly demonstrated that, even in that case, the GFP-NES1 nuclear fraction was more abundant than that of GFP-NES2 (Figure 2C right panel). Altogether, these results suggest that, without the context of a full length protein, Tax2 NES domain is active both when fused to the N- or to the C-terminus part of the GFP, while Tax1 NES functions more efficiently when fused to the C-end of GFP.
Within Tax2 NES sequence, several leucine residues are critical for a CRM-1 dependent function
Evaluating the role of Tax2 leucine 188
The localization of GFP-Tax2 is not altered by mutations in the NES
Both in infected and in transfected cells, Tax1 and Tax2 are found in the nucleus and in the cytoplasm in different proportions: Tax1 being more abundant in the nucleus, while Tax2 is more prone to be found in the cytoplasm [16, 35]. In the nucleus, Tax1 and Tax2 interact with transcription factors and activate the cyclic-AMP response element and activating transcription factor (ATF) binding (CREB/ATF) pathway, while in the cytoplasm the viral transactivators interact with several members of the NF-κB transduction pathway [5, 37]. Tax1/Tax2 activation of CREB/ATF is needed for an efficient viral gene expression, while the permanent activation of NF-κB has been suggested to be critical, at least in HTLV-1 infected cells, for evading apoptosis. In order to activate the CREB/ATF and NF-κB pathways, both Tax1 and Tax2 must therefore shuttle between these two compartments .
A Nuclear Export Signal (amino acid 189 to 202) has recently been described in Tax1 . Amino acids 1 to 58 constitute non canonical Nuclear Localization Signals [16, 32] in both Tax1 and Tax2, but amino acids 90 to 100 are also critical for the localization of the viral transactivators . Using prediction software as well as in vitro assays, we now describe another domain of Tax2. This sequence represents a Nuclear Export Signal (NES), with different functional characteristics from that of NES1. For example, the percentage of the GFP-NES2 protein that is present in the nucleus of the transfected cells is slightly different from that of GFP-NES1 protein. In addition, Tax2 NES is functional, no matter if it is fused to the N-terminal or the C-terminal of GFP, which is not the case of NES1 which is more active when fused to the C-terminus of GFP. We have also determined here that the NES of Tax2 can direct nuclear export via the CRM1 pathway, and that point mutations at positions 195 and 200 abrogate NES mediated translocation. All in all, these results demonstrate that the NES sequences of Tax1 and Tax2 have different functional profiles reflecting their slightly different sequences, and that the divergent amino acids are likely to be critical for the NES activity. The predictor software suggested that, in the Tax2 sequence, leucine 188 might also be part of the NES domain. This leucine is absent from Tax1 and, strikingly, when added to the NES1-EGFP construct, it restores the function of the Tax1 NES.
However, the most important result of this study is that, within the context of the whole Tax2 protein, mutating one or several leucine residues has no or an extremely limited impact on Tax2 localization. This could have been indicative of a secondary NES in the sequence being able to mediate translocation on its own, but this theory is not supported by the NetNES computational analysis. Therefore, this hypothesis is very unlikely. It would also disagree with our report that LMB treatment of Tax2 transfected cells did not abolish protein translocation . Hence, we consider that the very modest increase in the GFP-Tax2 nuclear signal observed with some GFP-Tax2 mutants constructs as compared to GFP-Tax2 is not consistent with a strong use of this NES sequence by Tax2. Altogether, these results imply that the Tax2 protein uses other means of export from the cell nucleus leading to the observed strong cytoplasmic signal. This is consistent with our previous results showing that the 90–100 Tax domain, which does not behave as a NES, is critical for the protein localization . Our results are therefore paradoxical: while Tax1 possesses a NES domain, it localizes predominantly in the nucleus at the equilibrium, whereas Tax-2, whose NES sequence is dispensable, has a predominant cytoplasmic localization.
In conclusion, without the context of the protein, both Tax1 and Tax2 seem to possess working nuclear export signals. If one regards the nuclear localization signal and nuclear export signal as competing forces, the Tax2 NES seems to be a more efficient mediator than that of Tax1 in terms of cytoplasmic versus nuclear abundance of the proteins without the context of a full-length protein. This observation is supported by the computational analysis as well as by our in vitro data. However, Tax2 does not need its NES signal to relocate to the cytoplasm. Rather, it seems to employ a different, hitherto uncharacterized translocation system, as we have previously suggested . The implications of this paradox are that, even though a fully functional nuclear export signal is embedded in the Tax2 sequence, it is not actually necessary for the protein translocation under the conditions tested here. However, its functional conservation suggests that it might have a biological impact on the protein functions. Future in vivo studies will decipher whether the presence of the "NES" sequence in the HTLV-2 Tax protein has any role during the viral cycle.
Cell culture and drug treatment
Hela and 293T cells were grown in Dulbecco's modified Eagle's medium supplemented with 10% fetal bovine serum and antibiotics (penicillin 100 U/ml and streptomycin at 100 μg/ml). Cell lines were maintained at 37°C in 5% CO2. When indicated, cells were incubated with leptomycin B (Sigma) at 40 nM for 3 h.
GFP-NES, NES-EGFP and GFP-Tax protein construction
The GFP-NES and NES-EGFP recombinants plasmids were obtained by cloning double stranded oligonucleotides into GFP-C3 and EGFP-N1 vectors (Clontech), using SacI/EcoRI and XhoI/PstI restriction sites respectively. Single or combined point mutations (at amino acids 188, 191, 194, 195 and 200) were also made in GFP-Tax1 and GFP-Tax2 sequences using the quick change mutagenesis kit (Stratagene) . The nucleotide sequences of all constructs were determined using the DYEnamic ET Terminator Cycle Sequencing Kit (Amersham Biosciences) on an Applied Biosystems 373A DNA sequencer. Of note, during the course of these experiments, we noticed that the amino-acid numbering that has been used in Alefantis article was incorrect . The first lysine of the Tax1 NES sequence is at position 189 and not 188 as reported previously. We have therefore modified the amino acid number accordingly.
For microscopic analyses, Hela cells were seeded in eight-well chamber glass slides, at a concentration of 3 × 104 cells/well and transfected the next day with 0,3 μg of DNA using the Effectene reagent (Qiagen). For immunoblot analyses, 293T cells were seeded on 6-well plates at 6 × 105 cells/well and transfected the next day with 2 μg of DNA using the Polyfect reagent (Qiagen) following the manufacturer's instructions.
Twenty-four hours after transfection, 293T cells were washed twice with PBS, lysed (Tris-HCl pH 7,4 50 mM, NaCl 120 mM, EDTA 5 mM, NP40 0,5%, Na3VO4 0,2 mM, DTT 1 mM, PMSF 1 mM) in the presence of protease inhibitors (Complete, Boehringer) and incubated on ice. Cell debris were pelleted by centrifugation. Protein concentration was determined by Bradford (Biorad). Samples were loaded into 10% Tris/Glycine gels (Invitrogen) subjected to electrophoresis at 130V and transferred onto a nitrocellulose membrane (Immobilon-P, Millipore). Membranes were blocked in a 5% PBS-milk solution, incubated with a specific anti-GFP antibody (JL-8, BD 1:1000) overnight at 4°C. The next day, the membranes were washed and incubated with an anti-mouse horseradish peroxidase-conjugated secondary antibody (Amersham Biosciences 1:40000) and developed using the SuperSignal West Pico Kit (Pierce). To control for the amount of protein loaded per well, membranes were stripped with the Re-blot Plus Kit (Chemicon International), and re-probed with a specific anti β-tubulin antibody (sc9104 Santa Cruz Biotechnology 1:1000).
Green fluorescent protein analyses
Twenty-four hours after transfection, the cells were washed with PBS, fixed with 4% paraformaldehyde (Sigma) and washed with PBS. Nucleic acids were stained with 4'-6'-diamine-2 phenylindole dihydrochloride (DAPI)-containing mounting medium (Vectashield, Vector). Cells were visualized with a Zeiss Axioplan 2 imaging microscope X40 using a Zeiss Axiocam HRc (color) camera and the Zeiss Apotome software. Given the fact that the localization of the GFP-fusion proteins is similar in Hela and in 293T, and because 293T cells are complex to handle in immunofluorescence experiments, we used these cells only for the western-blot analyses.
Nuclear and cytoplasmic extraction
Twenty-four hours after transfection, the cells were washed with PBS. Nuclear and cytoplasmic fractions were then isolated using the sub-cellular proteome extraction kit (Calbiochem) following the manufacturer's instructions. Samples were subjected to immunoblot analyses as described above.
NetNES software analysis
This software predicts leucine-rich nuclear export signals (NES) in eukaryotic proteins using a combination of neural networks (NN) and hidden Markov models (HMM). The prediction server calculates a combined 'NES score' from the NN and HMM scores. If the calculated 'NES score' exceeds the threshold, then that particular residue is expected to participate in a nuclear export signal. This is denoted with a "Yes" in the column "Predicted". Of note, the reason why one gets different scores for the same residues when comparing Tax1 and Tax2 sequences is that the score depends not only on the residue in question, but also on a number of previous residues which, in the case of E193 for example, are not identical between the two sequences.
This work was funded by Institut Pasteur, by grants from l'Association de Recherche sur le Cancer (ARC # 4781) and from ARECA to RM, fellowships from le Ministère de la Recherche to SAC, from CANAM and Pasteur Weizmann fellowships to LM and from Association Virus Cancer Prévention and La Ligue Contre le Cancer to SC. RM is supported by INSERM.
- Feuer G, Green PL: Comparative biology of human T-cell lymphotropic virus type 1 (HTLV-1) and HTLV-2. Oncogene. 2005, 24 (39): 5996-6004. 10.1038/sj.onc.1208971.PubMed CentralView ArticlePubMedGoogle Scholar
- Gessain A, Barin F, Vernant JC, Gout O, Maurs L, Calender A, de The G: Antibodies to human T-lymphotropic virus type-I in patients with tropical spastic paraparesis. Lancet. 1985, 2 (8452): 407-410. 10.1016/S0140-6736(85)92734-5.View ArticlePubMedGoogle Scholar
- Murphy EL, Fridey J, Smith JW, Engstrom J, Sacher RA, Miller K, Gibble J, Stevens J, Thomson R, Hansma D, Kaplan J, Khabbaz R, Nemo G: HTLV-associated myelopathy in a cohort of HTLV-I and HTLV-II-infected blood donors. The REDS investigators. Neurology. 1997, 48 (2): 315-320.View ArticlePubMedGoogle Scholar
- Poiesz BJ, Ruscetti FW, Gazdar AF, Bunn PA, Minna JD, Gallo RC: Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci U S A. 1980, 77 (12): 7415-7419.PubMed CentralView ArticlePubMedGoogle Scholar
- Grassmann R, Aboud M, Jeang KT: Molecular mechanisms of cellular transformation by HTLV-1 Tax. Oncogene. 2005, 24 (39): 5976-5985. 10.1038/sj.onc.1208978.View ArticlePubMedGoogle Scholar
- Jeang KT, Giam CZ, Majone F, Aboud M: Life, death, and tax: role of HTLV-I oncoprotein in genetic instability and cellular transformation. J Biol Chem. 2004, 279 (31): 31991-31994. 10.1074/jbc.R400009200.View ArticlePubMedGoogle Scholar
- Mahieux R, Pise-Masison CA, Lambert PF, Nicot C, De Marchis L, Gessain A, Green P, Hall W, Brady JN: Differences in the ability of human T-cell lymphotropic virus type 1 (HTLV-1) and HTLV-2 tax to inhibit p53 function. J Virol. 2000, 74 (15): 6866-6874. 10.1128/JVI.74.15.6866-6874.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Mahieux R, Pise-Masison CA, Nicot C, Green P, Hall WW, Brady JN: Inactivation of p53 by HTLV type 1 and HTLV type 2 Tax trans-activators. AIDS Res Hum Retroviruses. 2000, 16 (16): 1677-1681. 10.1089/08892220050193137.View ArticlePubMedGoogle Scholar
- Ross TM, Minella AC, Fang ZY, Pettiford SM, Green PL: Mutational analysis of human T-cell leukemia virus type 2 Tax. J Virol. 1997, 71 (11): 8912-8917.PubMed CentralPubMedGoogle Scholar
- Ross TM, Pettiford SM, Green PL: The tax gene of human T-cell leukemia virus type 2 is essential for transformation of human T lymphocytes. J Virol. 1996, 70 (8): 5194-5202.PubMed CentralPubMedGoogle Scholar
- Semmes OJ, Majone F, Cantemir C, Turchetto L, Hjelle B, Jeang KT: HTLV-I and HTLV-II Tax: differences in induction of micronuclei in cells and transcriptional activation of viral LTRs. Virology. 1996, 217 (1): 373-379. 10.1006/viro.1996.0126.View ArticlePubMedGoogle Scholar
- Sieburg M, Tripp A, Ma JW, Feuer G: Human T-cell leukemia virus type 1 (HTLV-1) and HTLV-2 tax oncoproteins modulate cell cycle progression and apoptosis. J Virol. 2004, 78 (19): 10399-10409. 10.1128/JVI.78.19.10399-10409.2004.PubMed CentralView ArticlePubMedGoogle Scholar
- Tanaka Y, Hayashi M, Takagi S, Yoshie O: Differential transactivation of the intercellular adhesion molecule 1 gene promoter by Tax1 and Tax2 of human T-cell leukemia viruses. J Virol. 1996, 70 (12): 8508-8517.PubMed CentralPubMedGoogle Scholar
- Tripp A, Liu Y, Sieburg M, Montalbano J, Wrzesinski S, Feuer G: Human T-cell leukemia virus type 1 tax oncoprotein suppression of multilineage hematopoiesis of CD34+ cells in vitro. J Virol. 2003, 77 (22): 12152-12164. 10.1128/JVI.77.22.12152-12164.2003.PubMed CentralView ArticlePubMedGoogle Scholar
- Tsubata C, Higuchi M, Takahashi M, Oie M, Tanaka Y, Gejyo F, Fujii M: PDZ domain-binding motif of human T-cell leukemia virus type 1 Tax oncoprotein is essential for the interleukin 2 independent growth induction of a T-cell line. Retrovirology. 2005, 2: 46-10.1186/1742-4690-2-46.PubMed CentralView ArticlePubMedGoogle Scholar
- Meertens L, Chevalier S, Weil R, Gessain A, Mahieux R: A 10-amino acid domain within human T-cell leukemia virus type 1 and type 2 tax protein sequences is responsible for their divergent subcellular distribution. J Biol Chem. 2004, 279 (41): 43307-43320. 10.1074/jbc.M400497200.View ArticlePubMedGoogle Scholar
- Meertens L, Pise-Masison C, Quere N, Brady J, Gessain A, Mahieux R: Utilization of the CBP but not the p300 co-activator by human T-lymphotropic virus type-2 Tax for p53 inhibition. Oncogene. 2004, 23 (32): 5447-5458. 10.1038/sj.onc.1207719.View ArticlePubMedGoogle Scholar
- Niinuma A, Higuchi M, Takahashi M, Oie M, Tanaka Y, Gejyo F, Tanaka N, Sugamura K, Xie L, Green PL, Fujii M: Aberrant activation of the interleukin-2 autocrine loop through the nuclear factor of activated T cells by nonleukemogenic human T-cell leukemia virus type 2 but not by leukemogenic type 1 virus. J Virol. 2005, 79 (18): 11925-11934. 10.1128/JVI.79.18.11925-11934.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Endo K, Hirata A, Iwai K, Sakurai M, Fukushi M, Oie M, Higuchi M, Hall WW, Gejyo F, Fujii M: Human T-cell leukemia virus type 2 (HTLV-2) Tax protein transforms a rat fibroblast cell line but less efficiently than HTLV-1 Tax. J Virol. 2002, 76 (6): 2648-2653. 10.1128/JVI.76.6.2648-2653.2002.PubMed CentralView ArticlePubMedGoogle Scholar
- Fahrenkrog B, Koser J, Aebi U: The nuclear pore complex: a jack of all trades?. Trends Biochem Sci. 2004, 29 (4): 175-182. 10.1016/j.tibs.2004.02.006.View ArticlePubMedGoogle Scholar
- Xu L, Massague J: Nucleocytoplasmic shuttling of signal transducers. Nat Rev Mol Cell Biol. 2004, 5 (3): 209-219. 10.1038/nrm1331.View ArticlePubMedGoogle Scholar
- Quensel C, Friedrich B, Sommer T, Hartmann E, Kohler M: In vivo analysis of importin alpha proteins reveals cellular proliferation inhibition and substrate specificity. Mol Cell Biol. 2004, 24 (23): 10246-10255. 10.1128/MCB.24.23.10246-10255.2004.PubMed CentralView ArticlePubMedGoogle Scholar
- la Cour T, Kiemer L, Molgaard A, Gupta R, Skriver K, Brunak S: Analysis and prediction of leucine-rich nuclear export signals. Protein Eng Des Sel. 2004, 17 (6): 527-536. 10.1093/protein/gzh062.View ArticlePubMedGoogle Scholar
- la Cour T, Gupta R, Rapacki K, Skriver K, Poulsen FM, Brunak S: NESbase version 1.0: a database of nuclear export signals. Nucleic Acids Res. 2003, 31 (1): 393-396. 10.1093/nar/gkg101.PubMed CentralView ArticlePubMedGoogle Scholar
- Daelemans D, Costes SV, Lockett S, Pavlakis GN: Kinetic and molecular analysis of nuclear export factor CRM1 association with its cargo in vivo. Mol Cell Biol. 2005, 25 (2): 728-739. 10.1128/MCB.25.2.728-739.2005.PubMed CentralView ArticlePubMedGoogle Scholar
- Yashiroda Y, Yoshida M: Nucleo-cytoplasmic transport of proteins as a target for therapeutic drugs. Curr Med Chem. 2003, 10 (9): 741-748. 10.2174/0929867033457791.View ArticlePubMedGoogle Scholar
- Alefantis T, Barmak K, Harhaj EW, Grant C, Wigdahl B: Characterization of a nuclear export signal within the human T cell leukemia virus type I transactivator protein Tax. J Biol Chem. 2003, 278 (24): 21814-21822. 10.1074/jbc.M211576200.View ArticlePubMedGoogle Scholar
- Felber BK, Paskalis H, Kleinman-Ewing C, Wong-Staal F, Pavlakis GN: The pX protein of HTLV-I is a transcriptional activator of its long terminal repeats. Science. 1985, 229 (4714): 675-679.View ArticlePubMedGoogle Scholar
- Goh WC, Sodroski J, Rosen C, Essex M, Haseltine WA: Subcellular localization of the product of the long open reading frame of human T-cell leukemia virus type I. Science. 1985, 227 (4691): 1227-1228.View ArticlePubMedGoogle Scholar
- Kiyokawa T, Kawaguchi T, Seiki M, Yoshida M: Association of the pX gene product of human T-cell leukemia virus type-I with nucleus. Virology. 1985, 147 (2): 462-465. 10.1016/0042-6822(85)90149-7.View ArticlePubMedGoogle Scholar
- Slamon DJ, Press MF, Souza LM, Murdock DC, Cline MJ, Golde DW, Gasson JC, Chen IS: Studies of the putative transforming protein of the type I human T-cell leukemia virus. Science. 1985, 228 (4706): 1427-1430.View ArticlePubMedGoogle Scholar
- Smith MR, Greene WC: Characterization of a novel nuclear localization signal in the HTLV-I tax transactivator protein. Virology. 1992, 187 (1): 316-320. 10.1016/0042-6822(92)90320-O.View ArticlePubMedGoogle Scholar
- Semmes OJ, Jeang KT: Localization of human T-cell leukemia virus type 1 tax to subnuclear compartments that overlap with interchromatin speckles. J Virol. 1996, 70 (9): 6347-6357.PubMed CentralPubMedGoogle Scholar
- Burton M, Upadhyaya CD, Maier B, Hope TJ, Semmes OJ: Human T-cell leukemia virus type 1 Tax shuttles between functionally discrete subcellular targets. J Virol. 2000, 74 (5): 2351-2364. 10.1128/JVI.74.5.2351-2364.2000.PubMed CentralView ArticlePubMedGoogle Scholar
- Turci M, Romanelli MG, Lorenzi P, Righi P, Bertazzoni U: Localization of HTLV-2 Tax protein is dependent upon a nuclear localization determinant in the N-terminal region. GeneGoogle Scholar
- Fornerod M, Ohno M, Yoshida M, Mattaj IW: CRM1 is an export receptor for leucine-rich nuclear export signals. Cell. 1997, 90 (6): 1051-1060. 10.1016/S0092-8674(00)80371-2.View ArticlePubMedGoogle Scholar
- Sun SC, Yamaoka S: Activation of NF-kappaB by HTLV-I and implications for cell transformation. Oncogene. 2005, 24 (39): 5952-5964. 10.1038/sj.onc.1208969.View ArticlePubMedGoogle Scholar
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