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© The Rockefeller University Press,
0021-9525/2001//141 $5.00
The Journal of Cell Biology, Volume 152, Number 1,
, 2001 141-156
Original Article |
Nxt1 Is Necessary for the Terminal Step of Crm1-Mediated Nuclear Export
paschal{at}virginia.edu
Soluble factors are required to mediate nuclear export of protein and RNA through the nuclear pore complex (NPC). These soluble factors include receptors that bind directly to the transport substrate and regulators that determine the assembly state of receptor–substrate complexes. We recently reported the identification of NXT1, an NTF2-related export factor that stimulates nuclear protein export in permeabilized cells and undergoes nucleocytoplasmic shuttling in vivo (Black, B.E., L. Lévesque, J.M. Holaska, T.C. Wood, and B.M. Paschal. 1999. Mol. Cell. Biol. 19:8616–8624). Here, we describe the molecular characterization of NXT1 in the context of the Crm1-dependent export pathway. We find that NXT1 binds directly to Crm1, and that the interaction is sensitive to the presence of Ran-GTP. Moreover, mutations in NXT1 that reduce binding to Crm1 inhibit the activity of NXT1 in nuclear export assays. We show that recombinant Crm1 and Ran are sufficient to reconstitute nuclear translocation of a Rev reporter protein from the nucleolus to an antibody accessible site on the cytoplasmic side of the NPC. Further progress on the export pathway, including the terminal step of Crm1 and Rev reporter protein release, requires NXT1. We propose that NXT1 engages with the export complex in the nucleoplasm, and that it facilitates delivery of the export complex to a site on the cytoplasmic side of NPC where the receptor and substrate are released into the cytoplasm.
Key Words: nuclear transport • NES • Crm1 • Ran • NXT1
© 2001 The Rockefeller University Press
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Introduction |
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125 mD) that spans the double membrane of the NE (Stoffler et al. 1999; Wente 2000). The NPC contains a central channel that mediates facilitated import and export of a large variety of transport substrates. The specificity of transport, that is to say whether a macromolecule undergoes import or export, generally requires a cis-acting nuclear localization signal (NLS) or a nuclear export signal (NES). These signals are recognized by transport receptors, which mediate interactions with the NPC and facilitate translocation of the macromolecule to the appropriate compartment. Most of the receptors for import and export described to date are members of the importin-β (also called karyopherin-β) superfamily of proteins. This includes Crm1, the nuclear export receptor for NES-containing proteins, such as protein kinase inhibitor (PKI) (Wen et al. 1995; Fornerod et al. 1997; Stade et al. 1997). In the nucleus, Ran-GTP stabilizes Crm1 binding to NES-containing proteins, resulting in the formation of a trimeric export complex (Fornerod et al. 1997). The physical basis of export complex translocation through the NPC, including the mechanisms that influence the direction of export complex movement through the NPC, have not been defined. There is also limited data addressing the terminal step of export, which refers to the posttranslocation events that result in disassembly of the export complex, and in the case of Crm1, release of its NES-containing cargo into the cytoplasm. One key component in the terminal step of export is Ran-GTP, which has the capacity to serve as a molecular switch to terminate both NES binding to Crm1, and Crm1 binding to the NPC (Fornerod et al. 1997; Kehlenbach et al. 1999). The terminal step of export could occur when a protein binds Ran-GTP and dissociates it from the export complex. The Ran-binding protein RanBP1, or RanBP1-like domains in the nucleoporin RanBP2, are candidates for promoting the dissociation reaction in this manner (Kehlenbach et al. 1999). Alternatively, RanGAP could activate the Ran GTPase in the context of the export complex, perhaps using RanBP1 as a cofactor, and convert GTP to GDP (Bischoff et al. 1995; Askjaer et al. 1999; Paraskeva et al. 1999). Because of its extremely low affinity for Crm1, Ran-GDP would rapidly dissociate from the complex, resulting in NES release from Crm1. RanGAP could also function in the dissociation-based mechanism by activating the GTPase activity of Ran-GTP that has already dissociated from the export complex. In both cases, RanGAP-dependent conversion of Ran-GTP to Ran-GDP would make export complex reassembly unfavored, making the disassembly reaction essentially irreversible. These models for terminating export are consistent with the electron microscopic immunolocalization of RanGAP and RanBP2 on the cytoplasmic side of the NPC (Matunis et al. 1996; Mahajan et al. 1997), as well as the cytoplasmic distribution of RanBP1 (Richards et al. 1996).
The mechanisms of nuclear import and export are of interest because of their importance to basic cell physiology and their relevance to the life cycles of medically important viruses. Retroviruses, such as HIV-1, require specific interactions with the host cell machinery for both nuclear import and export of viral proteins and nucleic acids (Stevenson 2000). Integration of the viral genome into the DNA of nondividing cells requires translocation of the preintegration complex through the NPC in a mechanism that involves importin-β as the import receptor. Transcription of the viral genome generates an 13-kb RNA, which is exported to the cytoplasm and used as the template for protein synthesis and virion production (Cullen 2000). Nuclear export of HIV-1 RNA depends on a cis-acting signal within the RNA, which is termed the Rev response element (RRE) (Malim et al. 1989). The RRE provides the binding site for Rev, an HIV-1 protein whose leucine-rich NES is, in turn, recognized by the host export machinery (Fischer et al. 1995). This occurs when the export receptor Crm1 binds to the NES of Rev, an interaction that is stabilized by Ran-GTP. Current models suggest that a complex consisting of RRE RNA, Rev, Crm1, and Ran-GTP assembles in the nucleoplasm and undergoes translocation through the NPC (Gorlich and Kutay 1999; Nakielny and Dreyfuss 1999). In the absence of an efficient pathway for nuclear export, HIV-1 RNA is subject to nuclear retention and splicing because it contains introns (Sodroski et al. 1986). Thus, nuclear export of full-length genomic RNA is necessary for viral replication.
In previous work, we identified a protein we named NXT1 for NTF2-related export protein 1 (Black et al. 1999). The evolutionary relatedness of NXT1 and NTF2 (26% identity) suggests these proteins should have related functions in the cell. We found that NTF2 binds Ran-GDP and functions in nuclear import (Moore and Blobel 1994; Paschal and Gerace 1995; Paschal et al. 1996), and that NXT1 binds Ran-GTP and functions in nuclear export (Black et al. 1999). Both NXT1 and NTF2 are nuclear proteins, and NXT1 shuttles between the nucleus and cytoplasm. One striking difference is that the steady-state distribution of NXT1 includes the NPC. The NPC localization of NXT1 persists after digitonin permeabilization of the plasma membrane, a condition that releases many soluble proteins from the cell. Evidence that NXT1 is an export factor was obtained by showing that the recombinant protein stimulates nuclear export of PKI in permeabilized cells (Black et al. 1999). NXT1-dependent export of PKI required the addition of cytosol and could be blocked by the Crm1-specific inhibitor leptomycin B (LMB) (Wolff et al. 1997). These findings, together with more recent data showing that NXT1 can stimulate nuclear export of U1 snRNA in permeabilized cells (Ossareh-Nazari et al. 2000), led us to conclude that NXT1 functions on an export pathway for which Crm1 is the receptor.
NXT1, which has been referred to as p15, has also been described as a cofactor for a viral RNA export pathway for which a protein termed TAP is the receptor (Katahira et al. 1999). TAP can bind directly to the constitutive transport element (CTE) of transcripts encoded by the Mason-Pfizer monkey virus (Hammarskjöld 1997), and it can stimulate nuclear export of the RNA in oocytes (Gruter et al. 1998). Although NXT1 binds directly to TAP (Katahira et al. 1999; Lévesque, L., and B.M. Paschal, unpublished observations), there is no data addressing how this interaction regulates CTE RNA export. The host cell function of the NXT1–TAP interaction may involve nuclear export of mRNA. This prediction is based on the relatedness of TAP to the mRNA export factor Mex67p (23% identity, expectation value 10–11), and the fact that coexpression of NXT1 and TAP can rescue the viability of a mex67 mutant in Saccharomyces cerevisiae (Katahira et al. 1999).
Here, we have characterized the molecular function of NXT1 in Crm1-mediated nuclear export. We have used a cell-based assay and recombinant factors to reconstitute nuclear export of a Rev reporter protein. We find that Crm1 and Ran are sufficient to reconstitute Rev transport from the nucleolus to the cytoplasmic side of the NPC. This likely reflects the accumulation or arrest of the export complex at an intermediate step in the pathway. We demonstrate that NXT1 is required for progression through the terminal step in the nuclear export pathway, resulting in the release of Crm1 and Rev from the cytoplasm side of the NPC. The terminal step also requires RanBP1 as a cofactor, which may reflect RanBP1- and RanGAP-dependent conversion of Ran-GTP to Ran-GDP as part of the release mechanism. We show that NXT1 binds directly to Crm1, and a point mutation in NXT1 that reduces Crm1 binding also reduces its export activity. Our results indicate that NXT1 is a cofactor that facilitates the terminal step in Crm1-dependent export.
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Materials and Methods |
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PKI Export Assay
The PKI export assays were performed in suspension-culture HeLa cells, as described previously (Holaska and Paschal 1998). In brief, nuclear import of FITC–streptavidin (STV)–NLS in digitonin permeabilized cells is mediated by the phenyl-Sepharose–treated cytosol, which is depleted of Crm1, as assayed by immunoblotting (Holaska and Paschal 1998). Biotinylated PKI enters the nucleus via diffusion and binds the FITC–STV–NLS. Export reactions were performed using the indicated export factors, the samples were fixed, and mounted on slides. Nuclear export in this assay is not dependent on the addition of recombinant RanBP1. This is likely due to the fact that the cytosol used to drive the import of FITC–STV–NLS contains RanBP1, and it is not released efficiently during the wash step between the import and export steps of the assay. Nuclear export was quantitated by measuring the reduction of nuclear fluorescence that occurs upon the addition of export factors (Holaska and Paschal 1998). The reduction in nuclear fluorescence in our assay is a result of nuclear export and not degradation of FITC–STV–NLS (Holaska and Paschal 1998; data not shown).
Recombinant Proteins
The export factors used to reconstitute nuclear export were expressed as recombinant proteins in bacteria and stored at –80°C as single-use aliquots. The expression and purification of His-tagged Ran (Gorlich et al. 1994), glutathione-S-transferase (GST)–tagged Ran (Richards et al. 1995), His-tagged Crm1 (Englmeier et al. 1999), GST-tagged RanBP1 (either intact or thrombin-cleaved) (Richards et al. 1995), and biotinylated PKI (Holaska and Paschal 1998) has all been described. Wild-type NXT1 (sequence data available from GenBank/EMBL/DDBJ under accession no. AF156958) expression and purification from the inclusion body fraction has been described previously (Black et al. 1999). Point mutations in the NXT1 open reading frame were generated in the bacterial expression vector using the QuickChange site-directed mutagenesis system (Stratagene). The COOH-terminal truncation was generated in a PCR reaction that amplified the NXT1 open reading frame, with a stop codon engineered to remove the final four codons. The protocol used for expression and purification of the wild-type NXT1 protein was used for the mutant NXT1 proteins.
Protein-binding Assays
Solid-phase Ran-binding assays have been described previously (Black et al. 1999). In brief, recombinant proteins were adsorbed to microtiter wells (5 µg NXT1 added/well, each well with a capacity of 20 ng), which was followed by extensive wash and blocking steps (Black et al. 1999). Ran, preloaded with [
-32P]GTP or [
-32P]GTP, was incubated in wells containing the indicated proteins immobilized in high-binding 96-well plates (Corning). Similarly, [35S]Crm1 (Ossareh-Nazari and Dargemont 1999), expressed in reticulocyte lysate, was incubated in wells containing the indicated immobilized proteins. The radiolabeled proteins that bound to the wells were eluted with SDS and quantitated by scintillation counting. Ran or Crm1 binding to BSA-coated wells was designated background and subtracted from the wells containing the immobilized recombinant proteins in both radiolabel and ELISA detection methods.
Recombinant Crm1 binding in the solid-phase assays was measured by ELISA (Delphin et al. 1997) using an anti-Crm1 antibody. After the binding reaction, wells were washed 3x, and the anti-Crm1 antibody (1:1,000) was incubated in 0.5x transport buffer containing 0.2% Tween 20 and 1% BSA for 2 h at room temperature. Wells were washed 5x and goat anti–rabbit horseradish peroxidase–coupled secondary antibody (Pierce Chemical Co.) was incubated in the same buffer for 1 h at room temperature. Horseradish peroxidase activity was measured, using 2,2' azino-di-(3-ethylbenzthiozoline sulfonic acid) as a colorimetric substrate, on a microplate reader (ELX800; Bio-Tek Instruments, Inc.) to measure the absorbance at 410 nm. NXT1 binding in solid-phase assays was analyzed by immunoblot using a rabbit polyclonal antibody raised against a peptide (CGTVKFEGNKQRDFNQN) that corresponds to an internal sequence in mouse NXT1. All binding assays were performed in duplicate and the values shown represent the mean ± SD.
RNA Export Assays
U1 snRNA, mRNA, and tRNA export assays in permeabilized HeLa cells have been described previously (Ossareh-Nazari et al. 2000). After the export reactions, samples were centrifuged at 210 g for 5 min to separate nuclear and supernatant fractions. Radiolabeled RNA was visualized after separation on an 8% acrylamide gel containing 7 M urea. The level of export was quantitated using the Bioprint acquisition system and Bioprofil software. The values for RNA export correspond to the ratio of RNA in the supernatant fraction to the sum of RNA present in the nuclear and supernatant fractions. Quantitation of U1 snRNA and tRNA export is from three independent experiments. Quantitation for mRNA export is from two independent experiments.
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Results |
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We used a cell line that expresses the NES-containing protein Rev fused to the ligand-binding domain of GR and GFP, which undergoes nuclear import after dexamethasone addition (Love et al. 1998). The Rev–GR–GFP fusion concentrates in nucleoli, and after digitonin permeabilization, undergoes cytosol-dependent nuclear export (Fig. 1; and Love et al. 1998). We observed that Rev–GR–GFP translocation from nucleoli to the NPC, indicated by the accumulation of fluorescence at the NE, requires the addition of Ran and Crm1 (Fig. 1). We found that NXT1 stimulates Ran and Crm1-dependent export, resulting in a marked reduction in both nucleolar- and NE-associated fluorescence. NXT1-stimulated export of Rev–GR–GFP was blocked by LMB (Fig. 1). This is consistent with our previous data showing that NXT1 stimulation of PKI export can be blocked by LMB (Black et al. 1999). A low level of Rev–GR–GFP was detected at the NE in the reaction containing Ran, Crm1, and NXT1, which was absent in the reaction containing cytosol (Fig. 1). This suggests that additional factors, such as RanBP1, may be required for highly efficient release of NES substrate from the NPC in permeabilized cells (see below). In summary, these data indicate that NXT1, Crm1, and Ran-GTP function cooperatively to mediate nuclear export of the NES substrate Rev–GR–GFP.
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-NPC), using the pan-nucleoporin antibody RL1 (Snow et al. 1987). To determine whether Rev–GR–GFP accumulation occurs on the nuclear or cytoplasmic side of the NPC, we used an antibody to GFP (Seedorf et al. 1999) and stained the cells after permeabilization with digitonin. Since the NE remains intact under this condition, the cytoplasmic side of the NPC is accessible to the antibody, whereas the nucleoplasmic side is not. Using the anti-GFP detection assay, we found that Rev–GR–GFP accumulates on the cytoplasmic side of the NPC in the presence of Crm1 and Ran (Fig. 2, NE Intact, -GFP), but not in the absence of these factors (see below). Pretreatment of cells with 1% Triton X-100 resulted in permeabilization of the NE and detection of GFP in both compartments (Fig. 2, NE Permeabilized). Thus, a complex consisting minimally of Crm1, Ran-GTP, and Rev–GR–GFP is delivered to the cytoplasmic side of the NPC in our permeabilized cell assay, and it can be revealed by antibody detection.
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NXT1). This suggests that NXT1 does not stimulate Rev–GR–GFP release through a simple transient interaction with the export complex. It also indicates that NXT1 probably interacts with the export complex in an early step of export, before the arrival of the export complex on the cytoplasmic side of the NPC. However, the activity of NXT1 is manifest in a late step of export, which includes substrate release into the cytoplasm.
Because NXT1 is a Ran-GTP–binding protein that shuttles between the nucleus and cytoplasm, we considered the formal possibility that its nuclear export function involves nuclear export of Ran-GTP. That is, NXT1 could facilitate the delivery of Ran-GTP from the nucleoplasm to the cytoplasm. Hypothetically, Ran-GTP could be used to dissociate export complexes on the cytoplasmic side of the NPC. NTF2 appears to perform what might be considered a reciprocal function, because it facilitates the delivery of Ran-GDP from the cytoplasm to the nucleoplasm, and after nucleotide exchange, Ran-GTP is used to dissociate import complexes on the nucleoplasmic side of the NPC. If the primary function of NXT1 is to deliver Ran-GTP to the cytoplasm, then addition of excess Ran-GTP should promote release of Rev–GR–GFP from the cytoplasmic side of the NPC. However, we found that Ran-GTP addition does not stimulate Rev–GR–GFP release from the NPC (Fig. 4, Ran+Crm1Ran-GTP). Importantly, the Rev–GR–GFP in this assay is not irreversibly arrested on the cytoplasmic side of the NPC, since it can be released by the addition of cytosol (Fig. 4, Ran+Crm1Cytosol). This may reflect the presence of a soluble-release activity that acts directly on the export complex. Alternatively, release of Rev–GR–GFP might occur when export complexes assemble from HeLa cytosol–derived Crm1. Newly assembled export complexes could then promote dissociation of preexisting export complexes by competing for a limited number of binding sites on the cytoplasmic side of the NPC. We addressed this using cytosol pretreated with phenyl-Sepharose to remove Crm1 (Holaska and Paschal 1998). Addition of phenyl-Sepharose–treated cytosol (PS Cytosol) was much less effective than control cytosol in promoting Rev–GR–GFP release (Fig. 4, Ran+Crm1PS Cytosol), and nucleolar fluorescence remained significantly brighter in the phenyl-Sepharose–treated cytosol samples. Whereas these results do not rule out a role for a soluble release activity, they suggest that cytosolic Crm1 and the ongoing assembly and translocation of export complexes may represent part of the release mechanism for preexisting export complexes.
We addressed whether the function of NXT1 in the terminal step of export also involves the release of the receptor Crm1 from the NPC. We performed Rev–GR–GFP export assays, and monitored the level of Crm1 localized to the cytoplasmic face of the NPC by immunofluorescence microscopy. The antibody approach for Crm1 detection in this experiment is similar to that used to detect Rev–GR–GFP (Fig. 2Fig. 3Fig. 4), where the integrity of the NE is maintained. Using a Crm1 antibody (Kehlenbach et al. 1998), we observed a high level of Crm1 accumulation on the cytoplasmic face of the NPC that was dependent upon the addition of recombinant Ran and Crm1 (Fig. 5, +Ran+Crm1). A visible accumulation of Rev–GR–GFP at the NE was only observed in the presence of both Ran and Crm1, suggesting these proteins may be part of an export complex situated on cytoplasmic face of the NPC. Including NXT1 in the reaction caused a substantial reduction in the level of Crm1 on the cytoplasmic face of the NPC (Fig. 5, +Ran+Crm1+NXT1). Therefore, these data indicate that NXT1 stimulation of nuclear export involves release of both the NES receptor (Crm1) and the NES substrate Rev–GR–GFP.
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95 nM (Fig. 6 B), providing an explanation for the RanGAP-insensitive binding of Crm1 to NXT1 (Fig. 6 A). However, Ran did stimulate Crm1 binding to NXT1, which reduced the apparent KD of this interaction to 30 nM (Fig. 6 B). To determine if NXT1 can regulate the interaction of Crm1 with NES substrate, we used an assay to measure direct binding of Crm1 to PKI, performed in the presence of Ran-GTP. Crm1 binding to the immobilized PKI, in this assay, is highly specific, since binding is blocked by LMB and the NES mutant of PKI (L41,44A) shows only background level of binding (Fig. 6 C, MUT). Including NXT1 in the reaction did not affect the level of Crm1 binding to PKI (Fig. 6 C), even when the assay was performed over a 100-fold concentration range of Crm1 (Fig. 6 D). We also examined whether NXT1 affects Ran-GTP binding to Crm1, assayed in the presence of NES substrate. Ran-GTP binding to immobilized Crm1 was saturable and increased only slightly in the presence of NXT1 (Fig. 6 E). Our data demonstrate that whereas NXT1 binds directly to an export complex containing Crm1 and Ran-GTP, it does not to play a primary role in regulating NES recognition or promoting complex assembly. Since we observed a cooperative effect of NXT1 and RanBP1 in the release of Rev–GR–GFP from the NPC (Fig. 3), we examined if these two proteins can directly interact. We immobilized GST-RanBP1, GST-Ran, and GST in microtiter wells, the latter proteins serving as controls for binding specificity. Recombinant NXT1 bound to GST-Ran, but not to immobilized GST-RanBP1, or to GST. These data suggest the action of NXT1 and RanBP1 in the release of export complexes from the NPC is unlikely to involve a direct interaction between these proteins.
NXT1 Mutants Deficient in Crm1-mediated Export
Our mutational analysis of NXT1 was based on a structural model generated using the crystal structure of NTF2 (Bullock et al. 1996; Black et al. 1999). We designed point mutations (N48E, E102N, and R107A) to alter highly conserved residues in solvent-exposed loops that are predicted to be proximal to the Ran-binding domain of NXT1. We also deleted four amino acids from the COOH terminus of NXT1 (
DWAS), since the COOH terminus of NTF2 helps stabilize Ran-GDP binding (Clarkson et al. 1997). Finally, we mutated a phylogenetically conserved lysine (K127A), whose spatial position is predicted to be removed from the Ran-binding surface, in NXT1. We expressed and purified the mutant NXT1 proteins and characterized them using both nuclear export and binding assays, as described below.
We first examined the activity of the mutants using the PKI export assay, which permits quantitative analysis of export activity by measuring nuclear fluorescence at the end of the export reaction (Black et al. 1999). We have described multiple controls to show that the reduction in nuclear fluorescence reflects bona fide nuclear export (Holaska and Paschal 1998). We have also used the PKI assay previously to show that wild-type NXT1 can stimulate nuclear export of PKI in the presence of a subsaturating concentration of HeLa cytosol (Black et al. 1999). We found that the addition of recombinant Ran, Crm1, and NXT1 is sufficient to promote nuclear export of biotinylated PKI complexed with fluorescent STV (Fig. 7A and Fig. B, bPKI/FITC-STV-NLS). We assayed each of the NXT1 mutant proteins in a similar manner, and determined that the R107A and K127A mutants were severely deficient in their ability to promote nuclear export of the PKI substrate (Fig. 7 B). The E102N mutant was also significantly reduced in export activity, whereas the N48E and DWAS mutants showed an intermediate level of export activity.
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DWAS, each of the mutant proteins were able to bind Ran-GTP at levels that were comparable to wild-type NXT1 (Fig. 8 A). We next tested whether these immobilized NXT1 proteins could interact with [35S]Crm1, which was synthesized in reticulocyte lysate. The N48E, E102N, and K127A mutants showed a slight reduction in Crm1 binding. Interestingly, the DWAS mutant that showed a reduction in Ran-GTP binding was deficient for Crm1 binding as well (Fig. 8 B). In contrast, we found that the R107A mutant, which showed a wild-type activity for Ran-GTP binding, was deficient for Crm1 binding. Taken together, our data show that the COOH terminus of NXT1 is important for its export function in permeabilized cells and for its interactions with two components of the export complex, Ran-GTP and Crm1. Arginine 107, which is conserved among all known NXT1 orthologs (Black et al. 1999) and probably located on an exposed loop of the protein, appears to be critical for binding Crm1.
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We examined the effect of the R107A mutation on the export of three different RNA substrates: U1 snRNA, mRNA, and tRNA. NXT1-dependent export of all three RNA substrates is observed when the wild-type protein is assayed in reactions that contain a subsaturating concentration (15% by volume) of Xenopus cytosol. The R107A NXT1 mutant showed a threefold reduction in its ability to promote U1 snRNA export (Fig. 9). In contrast, the R107A mutant promoted nuclear export of mRNA to the same level as wild-type NXT1, and the R107A mutant protein was also active in promoting export of tRNA. These results, together with the reduced activity of the R107A mutant in the PKI export assay (Fig. 7) and the Crm1-binding assay (Fig. 8 B), indicate that the export function of NXT1 is specifically linked to its interaction with Crm1. The reduced activity of the NXT1 mutant R107A in the U1 snRNA export pathway, compared with mRNA and tRNA export pathways, suggests it is possible to uncouple its interactions with different export receptors.
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Discussion |
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In addition to its role in Crm1-mediated export, NXT1 also participates directly in viral RNA export mediated by a protein termed TAP (Katahira et al. 1999). Transcripts encoded by the Mason-Pfizer monkey virus contain a CTE that functions as a cis-acting export signal (Hammarskjöld 1997) that is recognized by TAP in the nucleus (Gruter et al. 1998). A complex of TAP and NXT1 appears to bind CTE-containing RNA and facilitates its export to the cytoplasm. Whether NXT1 performs analogous functions in the Crm1 and TAP export pathways, the latter predicted to involve release of CTE-containing RNA from the cytoplasmic side of the NPC, is an important question for future study.
NXT1 Is a Cofactor for Crm1-dependent Export
The mechanism of NXT1-dependent export is likely to involve its direct interactions with Ran-GTP and Crm1. All three factors are necessary for efficient nuclear export, and NXT1 can bind directly to Ran-GTP (Black et al. 1999) and Crm1 (this study) in vitro. Moreover, the apparent KD of Crm1 for NXT1 (90–100 nM) is reduced three- to fourfold in the presence of Ran-GTP (25–35 nM), indicating that these proteins display cooperative binding. Independent evidence that Ran-GTP can regulate the interaction between Crm1 and NXT1 was obtained in a solid-phase binding assay using Crm1 translated in reticulocyte lysate. We found that treating the lysate with excess RanGAP to convert Ran-GTP to Ran-GDP significantly reduced Crm1 binding to NXT1. These data imply that Ran-GTP bridges the interaction between Crm1 and NXT1, or that Ran-GTP binding alters Crm1 to a conformation that is more favorable for binding NXT1. Our identification of a mutant NXT1 (R107A) that is wild-type for Ran-GTP binding, but deficient for Crm1 binding, suggests that NXT1 has binding sites for both Ran-GTP and Crm1. We also found that Crm1 binding to PKI in the presence of Ran-GMP-PNP, which in our solid phase assay is specific for a wild-type NES and inhibited by LMB, was unaffected by NXT1. We conclude from this result that NXT1 does not stimulate the initial formation of the export complex, however, we cannot rule out the possibility that NXT1 affects export complex stability, or targeting to the nuclear side of the NPC in vivo.
NXT1 Promotes NES Substrate Release from the NPC
Our experiments clearly demonstrate that NXT1 facilitates the release of NES substrate in the terminal step of nuclear export, which appears to be a rate-limiting step in this and probably all export pathways. The first indication that NXT1 might function in this capacity came from our observation that NXT1 reduces the Crm1/Ran-dependent accumulation of Rev–GR–GFP at the NPC. Because this occurs under conditions where the level of Rev–GR–GFP at nucleoli is also reduced, NXT1 does not act as an inhibitor of Ran/Crm1-dependent delivery of Rev–GR–GFP to the NPC. Rather, NXT1 is a positively acting factor for nuclear export.
We used antibody detection of Rev–GR–GFP to demonstrate that Crm1 and Ran are sufficient for delivery of NES substrate to the cytoplasmic side of the NPC. In the absence of the components necessary to release Rev–GR–GFP from the NPC, we observe an accumulation of the NES substrate on the cytoplasmic side of the NPC. We found that addition of recombinant NXT1 was sufficient to promote a substantial level of Rev–GR–GFP release from the NPC, as assayed by fluorescence microscopy. However, quantitative release of Rev–GR–GFP was only observed in reactions containing HeLa cytosol, or in reactions containing Crm1, Ran, NXT1, and RanBP1 (Fig. 3). This result is interesting in light of the recent proposal that RanBP1 plays a role in the terminal step of nuclear export (Askjaer et al. 1999; Kehlenbach et al. 1999). Ran-GTP in the context of an export complex is protected from RanGAP-stimulated hydrolysis, and the addition of RanBP1 overcomes this protection (Askjaer et al. 1999; Paraskeva et al. 1999), thereby acting as a RanGAP cofactor. Based on these properties and the localization of RanGAP on the cytoplasmic side of the NPC (Matunis et al. 1996; Mahajan et al. 1997), conversion of Ran-GTP to Ran-GDP by RanGAP and RanBP1 could trigger the disassembly of the export complex in the terminal step of nuclear export. Using purified proteins, it has been shown that Crm1 prebound to an immobilized NES in the presence of Ran-GTP can be released only if RanGAP and RanBP1 are added (Askjaer et al. 1999). It has also been found that Crm1, arrested at the NPC in the presence of the Ran mutant Q69L, can be dissociated by addition of RanBP1 or a Ran-binding domain from RanBP2 (Kehlenbach et al. 1999), though this probably reflects a displacement rather than a hydrolysis reaction. Our assay system, which detects the release of Rev–GR–GFP from the cytoplasmic side of the intact NPC, displays a dependence on both NXT1 and RanBP1. NXT1 does not function as a coactivator of RanGAP in vitro (Black et al. 1999), which, together with our current findings, indicates the terminal step of export involves more than Ran-GTP hydrolysis stimulated by RanGAP. Including NXT1 in reactions with Crm1, Ran, and RanBP1 also led to the reduction in the level of Crm1 detected on the cytoplasmic face of the NPC (Fig. 5), indicating the entire export complex is released from the NPC. On this note, it will be of interest to determine how release of the export substrate may be coordinated with the release of Crm1 from the NPC, reactions that could occur either simultaneously or sequentially.
Model of NXT1 Function in NES Export
We have created a working model of nuclear export that integrates our molecular characterization of NXT1 with previous studies on Crm1 and other components of the pathway (Fig. 10). Nuclear export is predicted to initiate in the nucleoplasm with a series of protein–protein interactions that ultimately terminate in the cytoplasm with the release of NES substrate. The first step is Crm1 binding to NES substrate, which is stabilized by Ran-GTP. We propose that a second step of export includes the assembly of NXT1 into the complex in the nucleoplasm, which is followed by its targeting to the NPC. The third step of export is translocation of the complex through the central channel of the NPC. The fourth step is the disassembly of the complex, which results in NES substrate release into the cytoplasm.
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The current model of the terminal step of nuclear export, release of NES substrate from the cytoplasmic side of the NPC, relies on Ran-GTP as a key regulatory subunit that dictates the assembly state of the export complex. RanBP1 and related domains in RanBP2 can destabilize, and possibly dissociate, the interaction between Ran-GTP and Crm1 in the export complex. Ran-GTP is essential for high-affinity binding of Crm1 to NES substrate (Fornerod et al. 1997), and RanBP1 addition can stimulate the dissociation of these proteins (Fig. 3) (Kehlenbach et al. 1999). Subsequent RanGAP-stimulated hydrolysis of Ran-GTP to Ran-GDP makes the release reaction irreversible, because Crm1 fails to bind Ran-GDP. Our analysis revealed that RanBP1 was insufficient to stimulate the release reaction, as it had a negligible effect in our assay, unless NXT1 was included as well (Fig. 3). This indicates that NXT1 and RanBP1 perform distinct functions in the release reaction. One possibility is that NXT1 promotes transfer of the export complex from a proximal accumulation site to a more distal site, where RanBP1, RanBP2, and RanGAP can complete the release reaction. In this scenario, NXT1, bound to an export complex, would facilitate its forward progress within the NPC. Determining whether NXT1- and RanBP1-facilitated NES substrate and receptor release occur through a single reaction step or through sequential reaction steps, and mapping the location of these intermolecular events within the substructure of the NPC, should provide significant insight into the mechanism of nuclear export.
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Acknowledgments |
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Financial support by the NIH (GM58639 to B.M. Paschal), the Association de Recherche contre le Cancer and the Fondation pour la Recherche Médicale to C. Dargemont, and the Lucille P. Markey Charitable Trust is gratefully acknowledged.
Submitted: 1 August 2000
Revised: 13 November 2000
Accepted: 14 November 2000
Abbreviations used in this paper: CTE, constitutive transport element; GFP, green fluorescent protein; GR, glucocorticoid receptor; GST, glutathione-S-transferase; LMB, leptomycin B; NE, nuclear envelope; NES, nuclear export signal; NLS, nuclear localization signal; NPC, nuclear pore complex; PKI, protein kinase inhibitor; RRE, Rev response element; STV, streptavidin.
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) or absence (
) of 500 nM Ran. A 20-amino acid peptide containing the NES of PKI (500 nM) was included in the binding reactions. (C and D) NXT1 does not affect the affinity of Crm1 for NES substrate. Reactions were performed in the presence of Ran (200 nM) that had been preloaded with GMP-PNP. In C, either wild-type or the NES mutant (L41,44A) (
