Nuclear Import of Epstein-Barr Virus Nuclear Antig
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病菌学杂志 2006年第4期
Herpesvirus Laboratory, Department of Virology I, National Institute of Infectious Diseases, Tokyo 162-8640, Japan
Environmental Science Division, School of Life Science, Tokyo University of Pharmacy and Life Science, Tokyo 192-0392, Japan
Department of Frontier Biosciences, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan
Genome Dynamics Project, Tokyo Metropolitan Institute of Medical Science, Tokyo 113-8613, Japan
ABSTRACT
Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA-1) is essential for replication of episomal EBV DNAs and maintenance of latency. Multifunctional EBNA-1 is phosphorylated, but the significance of EBNA-1 phosphorylation is not known. Here, we examined the effects on nuclear translocation of Ser phosphorylation of the EBNA-1 nuclear localization signal (NLS) sequence, 379Lys-Arg-Pro-Arg-Ser-Pro-Ser-Ser386. We found that Lys379Ala and Arg380Ala substitutions greatly reduced nuclear transport and steady-state levels of green fluorescent protein (GFP)-EBNA1, whereas Pro381Ala, Arg382Ala, Pro384Ala, and Glu378Ala substitutions did not. Microinjection of modified EBNA-1 NLS peptide-inserted proteins and NLS peptides cross-linked to bovine serum albumin (BSA) showed that Ala substitution for three NLS Ser residues reduced the efficiency of nuclear import. Similar microinjection analyses demonstrated that phosphorylation of Ser385 accelerated the rate of nuclear import, but phosphorylation of Ser383 and Ser386 reduced it. However, transfection analyses of GFP-EBNA1 mutants with the Ser-to-Ala substitution causing reduced nuclear import efficiency did not result in a decrease in the nuclear accumulation level of EBNA-1. The results suggest dynamic nuclear transport control of phosphorylated EBNA-1 proteins, although the nuclear localization level of EBNA-1 that binds to cellular chromosomes and chromatin seems unchanged. The karyopherin NPI-1 (importin 5), a nuclear import adaptor, bound more strongly to Ser385-phosphorylated NLS than to any other phosphorylated or nonphosphorylated forms. Rch1 (importin 1) bound only weakly and Qip1 (importin 3) did not bind to the Ser385-phosphorylated NLS. These findings suggest that the amino-terminal 379Lys-Arg380 is essential for the EBNA-1 NLS and that Ser385 phosphorylation up-regulates nuclear transport efficiency of EBNA-1 by increasing its binding affinity to NPI-1, while phosphorylation of Ser386 and Ser383 down-regulates it.
INTRODUCTION
Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA-1) is essential for the replication of EBV plasmid DNAs in latently infected cells and is also a transcriptional transactivator (4, 41, 45, 46, 54). It has recently been suggested that EBNA-1 enhances B-cell growth and transformation and is critical for the continued survival of EBV-associated Burkitt's lymphoma cells (20, 24, 40). EBNA-1 is the only EBV-encoded protein expressed in all types of latently infected cells (54) and represents one of the most important viral antigens for seroepidemiologic studies and serodiagnostic tests (21, 23, 54, 64). EBNA-1 proteins in the form of homodimers (3, 13, 17) are highly localized in the nucleus (19, 28, 36, 51) and bind in a sequence-specific manner to the EBV DNA oriP region (1, 2, 17, 27, 44, 45), cellular chromosomes/chromatin (29, 48), and cellular replication foci (31). EBNA-1 binding to mitotic cellular chromosomes is widely considered to enable the partition of de novo-synthesized EBV episomal DNAs to daughter cells (29, 48). EBNA-1 proteins are phosphorylated at Ser residues (22) and two phosphorylation domains have been mapped (52). Nonetheless, the effect of phosphorylation on EBNA-1 function is not known.
We have previously reported that EBNA-1 proteins interact with NPI-1 (importin 5), which is a nuclear import adaptor karyopherin (also known as importin ), in addition to Rchl (importin 1), using yeast two-hybrid screening and coimmunoprecipitation analyses of Raji cell lysates (30). Karyopherin (importin ) family proteins recognize various nuclear localization signal (NLS) sequences with or without the aid of adaptor molecules such as karyopherin (7, 11, 63). The EBNA-1 sequence 379Lys-Arg-Pro-Arg-Ser-Pro-Ser-Ser386 targets cross-linked carrier proteins to the nucleus (1), but it is not known whether all eight residues are necessary for NLS function. This 379KRPRSPSS386 sequence is referred to as the EBNA-1 NLS in this report.
Reported NLS amino acid sequences in different nuclear proteins are very diverse (12, 49, 57) and lack a strict consensus sequence, but generally are short and characterized by a high proportion of positively charged residues (7, 12). Monopartite NLSs have a single cluster of basic residues: the prototype sequences are the very basic simian virus 40 large T NLS (PKKKRKV) and the more hydrophobic c-Myc NLS (PAAKRVKLD) (10, 39). Bipartite NLSs have a motif with two interdependent basic domains and a mutation-tolerant spacer: the prototype sequences are the nucleoplasmin NLS (VKRPAATKKAGQAKKKKLD) and N1/N2 NLS (RKKRKTEEESPLKDKDAKKSKQEP) (12, 33, 56).
Many monopartite NLSs are 7 to 9 residues long and contain a helix-disrupting amino-terminal amino acid (proline or glycine) followed by at least three basic amino acids, while other NLSs contain basic amino acids flanking a proline residue (10). The EBNA-1 NLS belongs to the latter type. It has been proposed previously that Lys-x-x-Lys/Arg (where x can be any residue) (57), Lys-Arg/Lys-x-Arg/Lys (5), and several positively charged amino acids (Arg or Lys) associated with a Pro (18) represent consensus sequences of different groups of known monopartite NLSs. The EBNA-1 NLS fits this Lys-Arg/Lys-x-Arg/Lys sequence pattern. The KRPR tetrapeptide is also present in the NLSs of two other viral proteins, 281KRPRP of adenovirus E1A (47) and 189VSRKRPRP196 of polyomavirus large T, although the precise limits of the polyomavirus T NLS have not been defined (53).
The transport of proteins into the nucleus is a key regulatory step in functions of nuclear proteins (63). In the present study we examined whether and how phosphorylation of the Ser residues in the EBNA-1 NLS affects nuclear import and interaction with karyopherin proteins. The EBNA-1 position 380 to 397 phosphorylation region includes almost the entire NLS and adjacent Ser-rich QSSSSGSP (amino acids 387 to 394) sequence (1, 30, 52) (Fig. 1C). We also analyzed which amino acids in the eight-residue EBNA-1 NLS are crucial for nuclear localization.
MATERIALS AND METHODS
Construction of chimeric GST-NLS-GFP proteins. EBNA-1 NLS substitution mutant-inserted GST-NLS-GFP proteins glutathione S-transferase (GST)-GEKRPRSPSS-GFP, GST-GEAAPASPSS-GFP(379AAPA), GST-GEKRPRAPAA-GFP(383APAA), GST-GEKRPRDPDD-GFP(383DPDD), GST-GEKRPRAPSS-GFP (S383A), GST-GEKRPRSPAS-GFP(S385A), GST-GEKRPRSPSA-GFP(S386A), GST-GEKRPRSPAA-GFP(S385A, S386A) and GST-GEKRPRDPSS-GFP(S383D) (Fig. 1A) were constructed by inserting NLS oligonucleotides GATCCGGAGAAAAGAGGCCCAGGAGTCCCAGTAGTCAGC for GST-GEKRPRSPSS-GFP, GATCCGGAGAAGCGGCGCCCGCGAGTCCCAGTAGTCAGC for GST-GEAAPASPSS-GFP(379AAPA), GATCCGGAGAAAAGAGGCCCAGGGCACCCGCAGCACAGC for GST-GEKRPRAPAA-GFP(383APAA), GATCCGGAGAAAAGAGGCCCAGGGACCCCGACGACCAGC for GST-GEKRPRDPDD-GFP(383DPDD), GATCCGGAGAAAAGAGGCCCAGGGCACCCAGTAGTCAGC for GST-GEKRPRAPSS-GFP (S383A), GATCCGGAGAAAAGAGGCCCAGGAGTCCCGCAAGTCAGC for GST-GEKRPRSPAS-GFP(S385A), GATCCGGAGAAAAGAGGCCCAGGAGTCCCAGTGCACAGC for GST-GEKRPRSPSA-GFP(S386A), GATCCGGAGAAAAGAGGCCCAGGAGTCCCGCAGCACAGC for GST-GEKRPRSPAA-GFP(S385A,S386A), and GATCCGGAGAAAAGAGGCCCAGGGACCCCAGTAGTCAGC for GST-GEKRPRDPSS-GFP(S383D), into the BamHI-SmaI site of pGEX2T (Pharmacia)-derived vectors for the previously described GST-NES-GFP (60) (substitutions are indicated in boldface).
Synthetic peptides derived from the EBNA-1 NLS and their conjugation to biotinylated bovine serum albumin. EBNA-1 NLS-derived peptides CYGGEKRPRSPSSQ, CYGGEAAPASPSSQ, CYGGEKRPRAPAAQ, CYGGEKRPRAPSSQ, CYGGEKRPRSPASQ, CYGGEKRPRSPSAQ, CYGGEKRPRDPDDQ, Ser383-phophorylated CYGGEKRPR-pS-PSSQ (pS stands for phosphoserine), Ser385-phosphorylated CYGGEKRPRSP-pS-SQ, Ser386-phosphorylated CYGGEKRPRSPS-pS-Q, CYGGEKRPRDPSSQ, and CYGGEKRPRSPDSQ (Fig. 1B) were synthesized by GenScript (New Jersey). The amino-terminal CYGG sequence was added to facilitate cross-linking of the synthetic peptides to biotinylated bovine serum albumin (bBSA) and the synthetic peptides were chemically conjugated to bBSA as previously described (26). The designations and structures of the peptide-tagged bBSAa are listed in Fig. 1A. Peptide-conjugated bBSA proteins contained 7 to 10 peptides per bBSA molecule, as judged by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE). Rhodamine isothiocyanate-labeled BSA was prepared essentially as described previously (60).
Construction of GFP fusion proteins of the EBNA-1 NLS and flanking sequence mutants. A GFP fusion polypeptide of EBNA-1 that lacks the Gly-Gly-Ala copolymer (65, 66), designated GFP-EBNA1, has been previously described (29, 31). GFP-EBNA1 mutants were constructed by the method of PCR-based site-directed mutagenesis. The GFP fusion protein of the EBNA-1 mutant with 379AAPA382 was designated GFP-EBNA1(379AAPA). The other GFP-EBNA-1 mutants were designated in the same fashion. The structures and names of a series of GFP fusion proteins of EBNA-1 mutants with an amino acid substitution mutation in the NLS, amino acids 379 to 394, and flanking sequences are as follows: GFP-EBNA1(383APAA), GFP-EBNA1(379AAPA), GFP-EBNA1(388AAAAGA), GFP-EBNA1(K379A), GFP-EBNA1(R380A), GFP-EBNA1(P381A), GFP-EBNA1(R382A), GFP-EBNA1(S383A), GFP-EBNA1(P384A), GFP-EBNA1(S385A), GFP-EBNA1(S386A), and GFP-EBNA1(E378A) (Fig. 1C).
The PCR primers used to construct the GFP-EBNA1 mutants are as follows: GACGTGGAGAAGCGGCGCCCGCGAGTCCCAGTAG for GFP-EBNA1(379AAPA), GTGGACGTGGAGAAGCGAGGCCCAGGAGTCCCAG for GFP-EBNA1NL1-1(K379A), GACGTGGAGAAAAGGCGCCCAGGAGTCCCAGTAG for GFP-EBNA1(R380A), GAGAAAAGAGGCCCGCGAGTCCCAGTAGTCAGTC for GFP-EBNA1(R382A), GAGGCCCAGGGCTCCCGCTGCTCAGTCATCATC for GFP-EBNA1(383APAA), GAGGCCCAGGGATCCCGATGATCAGTCATCATC for GFP-EBNA1(383DPDD), AGTAGTCAGGCAGCAGCAGCCGGGGCTCCACCGCGC for GFP-EBNA1(388AAAAGA), GGACGTGGAGCAAAGAGGCCCAGGAGTCCC for GFP-EBNA1(E378A), GGACGTGGAGAAAAGAGGGCCAGGAGTCCC for GFP-EBNA1(P381A), AAGAGGCCCAGGGCTCCCAGTAGTCAG for GFP-EBNA1(S383A), GAGGCCCAGGAGTGCCAGTAGTCAGTCATCATC forGFP-EBNA1(P384A), CCCAGGAGTCCCGCTAGTCAGTCATCA for GFP-EBNA1(S385A), and AGGAGTCCCAGTGCTCAGTCATCATCA for GFP-EBNA1(S386A). They were synthesized by Texas Genomics Japan (Tokyo, Japan). PCR was done using DNA polymerase KOD-Plus-201 (Toyobo, Osaka, Japan). Base sequences of PCR products were determined with an ABI PRISM 3100-Avant genetic analyzer (Applied Biosystems, Foster City, California).
Cell line, transfection, and laser scanning microscopy. The cell line HeLa was obtained from the American Type Culture Collection through the Japanese Cancer Research Resources Bank (Japan) and was cultured in F-12 Ham's medium containing 10% fetal bovine serum. Transfection with plasmids expressing GFP fusion proteins of the EBNA-1 NLS and flanking sequence mutants was done with Lipofectin reagent (Invitrogen, California). Confocal laser scanning microscopy of transfected cells stained with Hoechst dye 33258 was described previously (29, 31). The mean and median values of percentages of nuclear GFP in 20 transfected cells per GFP-EBNA-1 mutant were calculated using Photoshop CS (Adobe Systems, California).
Microinjection assays. Microinjection was carried out as previously described (58, 59). Briefly, GST-NLS-derived 10-amino-acid polypeptides tagged with GFP (3 mg/ml) were microinjected into the cytoplasm of HeLa cells grown on coverslips and incubated at 37°C. HeLa cells were fixed by 3.7% formaldehyde at the indicated times, and fluorescence of GFP was detected. bBSA conjugated with different peptides (3 mg/ml) was injected together with rhodamine isothiocyanate-BSA (50)into the HeLa cytoplasm and the cells were incubated at 37°C. HeLa cells were fixed and permeabilized at the indicated times, and the subcellular localization of conjugated proteins was detected by Alexa 488-labeled streptavidin (Molecular Probes) as described previously (58). The average fraction of GFP intensity present in the nuclei in three or four cells in each microscopic image was calculated using Photoshop CS (Adobe Systems, California).
Solution binding analyses of EBNA-1 NLS-derived peptides with karyopherin proteins. Recombinant karyopherin proteins, Flag-NPI-1, Flag-Rch1, and Flag-Qip1, were described previously (58). bBSA proteins conjugated to EBNA-1 NLS-derived peptides were incubated with karyopherin in the presence of avidin-agarose at 4°C for 2 h as described previously (58). After extensive washing, bound proteins were eluted, analyzed by SDS-PAGE, and stained with Coomassie brilliant blue (58).
Luciferase assays. The effector plasmids pME18-EBNA1, pME18-EBNA1(379AAPA), pME18-EBNA1(383APAA), and pME18-EBNA1(383DPDD) were constructed on expression vector pME18S carrying the SR promoter (constructed by K. Maruyama et al., Tokyo Medical and Dental University) so that they have the same EBNA-1 mutant sequences as those in the above-described GFP-EBNA1(379AAPA), GFP-EBNA1(383APAA), and GFP-EBNA1(383DPDD) plasmids, respectively. Activation of transcription from the oriP-BamHI C-Luc reporter (43), a kind gift from B. Sugden, was measured in HeLa cells; 1.0 μg of oriP-BamHI C-Luc and 1.0 μg of an effector were cotransfected into 1.0 x 105 or 2.0 x 105 cells per plate (60-mm diameter) using Lipofectamine (Invitrogen, Carlsbad, California). Luciferase assays were carried out using Promega's luciferase assay system (Promega, Madison, Wisconsin) according to the manufacturer's instruction.
RESULTS
EBNA-1 Lys379 and Arg380 are both essential for nuclear localization. In order to identify amino acid residues in the EBNA-1 NLS that are essential for its activity, we performed point-mutation analyses. Microinjection experiments showed that a chimeric protein containing a wild-type EBNA-1 NLS, GST-GEKRPRSPSS-GFP, was transported into the nucleus with maximal accumulation within 3 h postinjection (Fig. 2A). In contrast, the nuclear import of a chimeric protein containing an NLS mutant with substitutions of Ala for the basic amino acids GST-GEAAPASPSS-GFP, was greatly reduced (Fig. 2A and Table 1). In addition, bBSA tagged with a synthetic EBNA-1 NLS peptide, bBSA-E1NLS, was transported into the nucleus 1 h postinjection (Fig. 2B). However, the nuclear import of bBSA tagged with the NLS mutant peptide with Ala substituted for the three basic amino acids, bBSA-E1NLS(379AAPA), was also greatly reduced (Fig. 2B; Table 2). In these assays, rhodamine isothiocyanate-BSA was added to the NLS sequence-inserted chimeric proteins or NLS peptide-tagged bBSA immediately before microinjection to serve as an internal injection marker in the same injected cell. The intracellular localization profiles of rhodamine isothiocyanate-BSA are also shown in Fig. 2.
Transfection analyses of GFP-EBNA1 proteins with the basic amino acid-to-Ala substitutions in NLS were performed using confocal microscopy of living HeLa cells to analyze the effects of the mutation on the steady-state level of EBNA-1 in the nucleus. GFP-EBNA1 showed a highly nuclear localization profile (28-30), referred to as a "mostly nuclear localization profile" in this study (Fig. 3A). Nuclear GFP varied in the range of 55% to 100% among the 20 cells transfected with GFP-EBNA1 (mean, 90% ± 4% [standard deviation]; median, 98%) (Fig. 3A; Table 3). GFP-EBNA1(379AAPA) proteins, however, were highly localized in the cytoplasm (Fig. 3Ba) in the majority of cells (>75%) and in both the nucleus and cytoplasm in the remainder (<25%) (Fig. 3Bb) (mean, 21.8 ± 4%; median, 18%). It is to be noted that nuclear localization of GFP-EBNA1(379AAPA) is explained partially by its association with cellular chromosomes (25, 29, 48) during the nuclear envelope-disintegrated mitotic phase, as is the case with wild-type EBNA-1 (data not shown).
The single basic amino acid-substituted mutants GFP-EBNA1(K379A) (Fig. 3C) and GFP-EBNA1(R380A) (Fig. 3D) were found to localize primarily to the cytoplasm of <50% of transfected cells (Fig. 3Ca and Da) and to cytoplasm and nuclei in the remainder (Fig. 3Cb and Db); the mean nuclear GFP intensity in cells transfected with GFP-EBNA1(K379A) was 45 ± 6% (median, 43%). The mean nuclear GFP intensity in cells transfected with GFP-EBNA1(R380A) was similar (40 ± 7%; median, 43%). The other basic amino acid-substituted mutant GFP-EBNA1(R382A) proteins localized to the nucleus, to almost the same degree as wild-type EBNA-1 (Fig. 3F); the mean percentage of nuclear GFP intensity in cells transfected with GFP-EBNA1(R382A) was 84 ± 5% (median, 90%). The Pro381-substituted EBNA-1 NLS mutant, GFP-EBNA1(P381A) (Fig. 3E), and the Pro384-substituted GFP-EBNA1(P384A) mutant (Fig. 3G) also localized to the nucleus, as did wild-type EBNA-1; the mean nuclear GFP intensity in cells transfected with GFP-EBNA1(P381A) was 88 ± 2% (median, 91%) and that with GFP-EBNA1(P384A) was 94 ± 2% (median, 99%). The single amino acid substitution EBNA-1 NLS mutant GFP-EBNA1(E378A) also localized to the nucleus (Fig. 3H), like the wild-type (mean, 93 ± 4%; median, 99%). Localization profiles of GFP-EBNA1 mutants along straight lines arbitrarily drawn in the photomicrographs of transfected cells are included in Fig. 3 to show the relative intensities of GFP and Hoechst dye 33258 in the nucleus and cytoplasm.
These results indicate that the two basic amino acids, Lys379 and Arg380, are essential for nuclear localization, but Arg382, Pro381, Pro384, and Glu378 are not critical.
Microinjection shows that Ser383 and Ser385 residues of the EBNA-1 NLS are crucial for nuclear import of GST-NLS-GFP protein and NLS-tagged BSA. To test the effects of EBNA-1 NLS phosphorylation on nuclear localization, we analyzed nuclear import of NLS peptide-inserted GST-GFP chimeric proteins and bBSA cross-linked to the NLS peptide bBSA-E1NLS in HeLa cells by microinjection. GST-GEKRPRSPSS-GFP synthesized in Escherichia coli was not transported into the nucleus very quickly, but it had accumulated there 3 h after injection, as shown in Fig. 2Aa. bBSA-E1NLS was transported into the nucleus within 60 min (Fig. 5A). In contrast, the Ser-to-Ala substitution protein GST-GEKRPRAPAA-GFP(383APAA) was present in the nucleus only in small amounts 3.0 h postinjection (Fig. 4A; Table 1), and bBSA cross-linked to the Ser-to-Ala substitution NLS peptide, bBSA-E1NLS(383APAA), was also present only in small amounts 1.0 h postinjection (Fig. 5B; Table 2). The results indicate that Ser residues of the EBNA-1 NLS are crucial for efficient nuclear import of GST-NLS-GFP protein and NLS-tagged BSA.
Next, we separately analyzed the requirement for Ser383, Ser385, and Ser386 for nuclear import. GST-GEKRPRAPSS-GFP(S383A) was present in the nucleus only in small amounts 3.0 h postinjection (Fig. 4B; Table 1), suggesting that Ser 383 is crucial for efficient EBNA-1 nuclear import. bBSA cross-linked to the Ser383-to-Ala substitution NLS peptide, bBSA-E1NLS(S383A), was transported into the nucleus slightly more slowly than bBSA-E1NLS (Fig. 5F; Table 2), suggesting that multiples (7 to 10) of the Ser383-to-Ala substitution NLS peptide per bBSA molecule allowed bBSA-E1NLS(S383A) transport into the nucleus. GST-GEKRPRSPAS-GFP(S385A) and GST-GEKRPRSPSA-GFP(S386A) were transported into the nucleus at a slightly reduced rate (Fig. 4C and D; Table 1) and GST-GEKRPRSPAA-GFP(S385A, S386A) was transported at a more reduced rate (Fig. 4E; Table 1). bBSA-E1NLS(S385A) was also transported at a slightly reduced rate (Fig. 5G; Table 2), whereas bBSA-E1NLS(S386A) was transported into the nucleus even faster than bBSA-E1NLS (Fig. 5H; Table 2). Together, these results all suggest that Ser383 and Ser385 are important for nuclear translocation.
Phosphorylation of Ser residues in the EBNA-1 NLS regulates nuclear transport efficiency. To analyze the impact of Ser phosphorylation on nuclear transport, synthetic peptides derived from the EBNA-1 NLS were cross-linked to bBSA, and nuclear import was assessed following microinjection. bBSA cross-linked to the NLS peptide, bBSA-E1NLS, was transported into the nucleus with almost maximal accumulation within 60 min (Fig. 5A).
bBSA tagged with the Ser385-phosphorylated peptide, bBSA-E1NLS(pS385), was more rapidly transported into the nucleus (within 30 min) than bBSA-E1NLS (Fig. 5D; Table 2). bBSA cross-linked to either the Ser383- or the Ser386-phosphorylated NLS peptide, bBSA-E1NLS(pS383) or bBSA-E1NLS(pS386), respectively, migrated more slowly into the nucleus than bBSA-E1NLS (Fig. 5C and E; Table 2). bBSA with the Ser385Asp substitution peptide, bBSA-E1NLS(S385D), was transported into the nucleus almost as rapidly as bBSA-E1NLS(pS385) (FIG. 5J; Table 2). GST-GEKRPRDPSS-GFP(S383D) was less efficiently transported than GST-GEKRPRSPSS-GFP (Fig. 4I), consistent with the slightly reduced nuclear transport rate of bBSA-E1NLS(pS383) (Fig. 5C; Table 2).
bBSA cross-linked to the NLS peptide in which all Ser at 383, 385, and 386 were replaced with Asp [bBSA-E1NLS(383DPDD)] was transported into the nucleus with an efficiency similar to bBSA-E1NLS (Fig. 5K; Table 2). The Ser-to-Asp substitution protein GST-GEKRPRDPDD-GFP, mimicking GST-KRPRpSPpSpS-GFP, was translocated to the nucleus within 3 h, similar to GST-GEKRPRSPSS-GFP (Fig. 4G; Table 1). These results possibly resulted from a balance between the effects of acceleration and deceleration of transport caused by phosphorylation of all three serine residues.
Ser-to-Ala substitution in the EBNA-1 NLS does not significantly affect nuclear accumulation levels of GFP-EBNA-1 in transfected cells. To analyze the effects on nuclear localization of NLS Ser phosphorylation, a set of GFP-EBNA-1 mutants with Ser-to-Ala or Ser-to-Asp substitutions in the 379KRPRSPSS386 sequence was constructed (Fig. 1C). Substitution of three Ser residues with Asp in the NLS [GFP-EBNA1(383DPDD)], mimicking simultaneous Ser phosphorylation, did not affect nuclear localization or accumulation levels (Fig. 6B), in agreement with the result of microinjection analysis of GST-GEKRPRDPDD-GFP(383DPDD) (Fig. 4G); the mean percentage of nuclear GFP in cells transfected with GFP-EBNA1(383DPDD) was 95 ± 3%, and the median was 99%.
Surprisingly, GFP-EBNA1(383APAA), GFP-EBNA1(S383A), and GFP-EBNA1(S385A) also did not reduce nuclear accumulation levels (Fig. 6C to E). The mean percentages of nuclear GFP intensity in cells transfected with GFP-EBNA1(383APAA), GFP-EBNA1(S383A), and GFP-EBNA1(S385A) were 90 ± 5%, 89 ± 3%, and 90 ± 6% (median values, 96, 99, and 97%, respectively). GFP-EBNA1(S386A), which was included here for comparison, did not affect nuclear accumulation levels, as expected (Fig. 6F); mean nuclear GFP intensity in cells transfected with GFP-EBNA1(S386A) was 93 ± 3% (median, 99%). These results indicate that Ser at amino acid 383, 385, or 386 is not essential for nuclear accumulation of EBNA-1 to a high level.
We also asked whether the carboxyl-adjacent Ser-rich 387QSSSSGS393 sequence is involved in regulating the level of EBNA-1 in the nucleus. However, GFP-EBNA1(388AAAAGA) with Ser-to-Ala substitutions at all five Ser residues in the carboxyl-adjacent 387QSSSSGS393 (Fig. 6G) showed a localization profile similar to that of GFP-EBNA1; the mean proportion of nuclear GFP intensity in cells transfected with GFP-EBNA1(388AAAAGA) was 93 ± 9% (median, 96%). This indicates that phosphorylation of Ser residues in the QSSSSGSP sequence is not required for nuclear accumulation of EBNA-1.
Analyses of karyopherin interactions with phosphorylated and nonphosphorylated forms of EBNA-1 NLS. We previously reported that the karyopherin NPI-1 (importin 5) binds to EBNA-1 (30) as well as the karyopherin Rch1 (importin 1) (14, 30, 42). To examine the effects of phosphorylation of and amino acid substitutions in the EBNA-1 NLS, we analyzed interactions of NLS mutant peptides with recombinant NPI-1 (importin 5), Rch1 (importin 1), and Qip1 (importin 3) (61) using the biotin-avidin affinity binding assays.
NPI-1 did not bind to bBSA-E1NLS(379AAPA) (Fig. 7A), consistent with failure of nuclear import of bBSA-E1NLS(379AAPA) (Fig. 2B). NPI-1 bound to bBSA-E1NLS(pS385) much more strongly than to bBSA-E1NLS (Fig. 7A), a finding in agreement with the accelerated nuclear import rate of bBSA-E1NLS(pS385) (Table 2). In contrast, NPI-1 bound to bBSA-E1NLS(pS383) and bBSA-E1NLS(pS386) only weakly (Fig. 7A; Table 2). NPI-1 bound to bBSA-E1NLS(383APAA) more weakly than to bBSA-E1NL (Fig. 7A), in agreement with its greatly reduced nuclear import rate (Table 4). These data agree with our previous findings that EBNA-1 protein synthesized in Escherichia coli interacted with NPI-1 much less efficiently than EBNA-1 synthesized in Raji cells (30) and indicate that phosphorylation of S385, but neither S383 nor S386, is required for the interaction of EBNA-1 with NPI-1. NPI-1 bound to bBSA-E1NLS(S385D) and bBSA-E1NLS(S383D) only weakly, but bound to bBSA-E1NLS(383DPDD) as strongly as bBSA-E1NLS(pS385) (Fig. 7B). NPI-1 bound to bBSA-E1NLS(S383A), bBSA-E1NLS(S385A) and bBSA-E1NLS(S386A) only weakly (Fig. 7B; Table 2).
Interaction of Rch1 with bBSA-E1NLS was minimal (Fig. 7A). Rch1 also bound more strongly to bBSA-E1NLS(pS385) than to bBSA-E1NLS(pS383) and bBSA-E1NLS(pS386) (Fig. 7A). However, Rch1 binding to bBSA-E1NLS(pS385) was much weaker than NPI-1 binding (Fig. 7A). Also, the interaction of Rch1 with bBSA cross-linked to the other EBNA-1 NLS-derived peptides was very weak (Fig. 7A and B). Interactions of Qip1 with any of these EBNA-1 NLS-derived peptides were absent (Fig. 7A and B).
Effects of NLS mutations on the activation of transcription from the BamHI C promoter by EBNA-1 expressed transiently in cotransfection luciferase assays. To test whether the above described regulation of nuclear import efficiency of EBNA-1 is involved in its multifunctional properties, we first performed DNA replication/retention assays by cotransfection of plasmid pME18-EBNA1 with oriP-BamHI C-Luc or oriP-minus (43), which were kind gifts from B. Sugden (University of Wisconsin), and by growing HeLa cells. However, the activity of transiently expressed EBNA-1(GA), the expression of which was confirmed by Western blotting performed as previously described (31), to support oriP-plasmid once per cell cycle replication/retention was too low to detect a de novo-synthesized DpnI-resistant band of linearized oriP-BamHI C-Luc by Southern blotting, the detection sensitivity of which was 2.04 copies per cell (0.01 ng per lane of gel electrophoresis) using a 32P-labeled probe (1.9 x 109 cpm/μg) (data not shown). In parallel analyses, in HeLa S3#8 cells that constitutively express full-length-EBNA-1 (N. Yoshizawa-Sugata and H. Masai, unpublished) a de novo-synthesized oriP-BamHI C-Luc band was detected (data not shown).
To analyze whether the nuclear import regulation of EBNA-1 affects the activation of transcription by EBNA-1, we constructed plasmids pME18-EBNA1, pME18-EBNA1(379AAPA), pME18-EBNA1(383APAA), and pME18-EBNA1(383DDPD) to assess the effects of the NLS mutation in the absence of GFP. Luciferase assays using HeLa cells cotransfected with the oriP-BamHI C-Luc reporter plasmid (43) (kindly provided by B. Sugden) and pME18-EBNA1(379AAPA) showed that the Ala substitution mutation 379AAPA, which greatly reduces nuclear import and localization of EBNA-1, caused a significant reduction in the activation of transcription from the BamHI C-Luc reporter at 48, 72, and 96 h after transfection, compared to pME18-EBNA1 and pME18-EBNA1(383DPDD) (Table 4). However, pME18-EBNA-1(383APAA), which greatly reduces the efficiency of nuclear import of EBNA-1, did not reduce the activation of transcription from the BamHI C-Luc reporter (Table 4). These results are consistent with the finding that the 383APAA Ala substitution mutation did not reduce the nuclear intensity of GFP-EBNA1 (Fig. 6C to E). Further, they indicate that under the present experimental conditions of transient expression of EBNA-1 in cotransfection assays, the Ser-to-383APAA mutation that causes the great reduction in the nuclear transport efficiency of EBNA-1 proteins does not affect the transcriptional activator function of EBNA-1.
DISCUSSION
Regulation of nuclear transport by phosphorylation of sites that are adjacent to NLSs, but not within them, has been reported previously (16, 32-34, 37). The best studied example is that the nuclear import of simian virus 40 T antigen directed by the NLS (126PKKKRKV132) is enhanced by phosphorylation of S112 (34), but is inhibited by phosphorylation of T124 (35, 55, 62). The findings of the present study are summarized in Tables 1 to 3, and the major conclusions are as follows. First, our data suggest that only the amino-terminal 379Lys-Arg380 is essential for both nuclear transport and nuclear accumulation directed by the EBNA-1 NLS and for interaction with the karyopherin NPI-1 protein. This remarkable variability of the N-terminal and C-terminal sequences flanking the EBNA-1 NLS 379KR380 is similar to the simian virus 40 T antigen NLS (amino acids 126 to 132) in which the Lys residue at position 128 is essential for NLS integrity (6, 38). Crystallographic studies of complexes of karyopherin and NLS peptides have shown that the basic residues of the simian virus 40 large T (8, 9) and c-Myc NLSs (8, 15) interact with the binding pockets of the major binding site of the karyopherin molecule. In contrast, no Lys in the downstream cluster of nucleoplasmin (167KKKK170) can be substituted (56). It is not yet clear whether any Lys or Arg residues in the smallest known NLS, KRPRP, can be mutated without loss of function.
Second, the Ser residues of 383SPSS386 in the EBNA-1 NLS are important for efficient nuclear translocation, as shown by microinjection experiments.
Third, Ser383 is crucial for efficient nuclear import, because replacement of Ser383 with either Ala, Asp, or phosphoserine reduced nuclear import. Ser386 is not essential for nuclear transport, but phosphorylation of Ser at position 386 reduces nuclear translocation efficiency, as demonstrated by microinjection analyses.
Fourth, Ser385 is important for nuclear transport and Ser385 phosphorylation accelerates the rate of EBNA-1 nuclear translocation.
Fifth, a reduction of nuclear transport rate does not result in a decrease in the intensity of nuclear GFP-EBNA-1 relative to that of cytoplasmic EBNA-1. The results described in this report suggest that nuclear levels of EBNA-1 are regulated not only by import rate but also by the retention of EBNA-1 in the nucleus due to the association of EBNA-1 with cellular chromosomes and chromatin (29, 48).
Sixth, Ser385 phosphorylation in the EBNA-1 NLS increases the interactions of EBNA-1 with the karyopherin NPI-1 protein. Rch1, on the other hand, bound to EBNA-1 NLS peptides, either phosphorylated or nonphosphorylated, far less strongly than NPI-1, and Qip1 did not bind to any of the EBNA-1 NLS peptides. The very weak binding of NPI-1 to bBSA-E1NLS(S385D) indicates that an effect of phosphorylation of serine at position 385 on the interaction of E1NLS with NPI-1 is highly specific. The finding that NPI-1 bound to bBSA-E1NLS(383DPDD) as strongly as bBSA-E1NLS(pS385) but without resulting in accelerated nuclear transport rates of bBSA-E1NLS(383DPDD) indicates that the strong binding of NPI-1 to the EBNA-1 NLS is not sufficient for accelerated nuclear import. These data need emphasizing because it was previously reported that phosphorylation of Ser112 in the vicinity of the NLS (126PKKKRKV132) of simian virus 40 T antigen enhanced nuclear import but not the affinity of binding between the T-antigen NLS and importin 2 (16). These results indicate that NPI-1 is a major karyopherin member that mediates the nuclear import of EBNA-1 and that phosphorylation of S385 accelerates the nuclear import rate through an increased affinity of NLS for NPI-1.
Lastly, the great decrease in the efficiency of nuclear import of EBNA-1(383APAA) did not reduce activation of transcription from the BamHI C-Luc promoter, in contrast to EBNA-1(379AAPA). However, the high transient expression level of the mutant EBNA-1 proteins may have hindered detection of any possible effects of the reduced nuclear transport efficiency of EBNA-1 on the activation of transcription. Functional effects of the reduced nuclear transport efficiency of EBNA-1 may be complex because of stable colocalization of EBNA-1 with cellular chromosomes and chromatin (29) and may act in concert with other cellular factors, such as cell cycle position or infection with EBV. Furthermore, the regulation of nuclear import efficiency by phosphorylation of the EBNA-1 NLS may be correlated with phosphorylation of other Ser residues of EBNA-1 outside the NLS (22, 52) and required for adequate functional association of EBNA-1 to cellular proteins in EBV-infected cells.
From the present study, we conclude that the amino-terminal 379Lys-Arg380 and Ser383 are the essential elements of the EBNA-1 NLS (amino acids 379 to 386) required for function. It has been found that phosphorylation of Ser385 increases nuclear transport efficiency of EBNA-1 by modulating its affinity to NPI-1, whereas phosphorylation of Ser383 or Ser386 decreases it. This is the first study to suggest any role for Ser phosphorylation in the context of EBNA-1. The results suggest dynamic transport control of phosphorylated EBNA-1 proteins, whereas the steady-state nuclear level of EBNA-1 seems unchanged.
ACKNOWLEDGMENTS
We thank Bill Sugden, University of Wisconsin, for his kind gift of the oriP-BamHI C-Luc (1033) and oriP-minus (1381) plasmids (43).
Financial support for this research was provided by a grant-in-aid from the Ministry of Health, Welfare and Labor.
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Environmental Science Division, School of Life Science, Tokyo University of Pharmacy and Life Science, Tokyo 192-0392, Japan
Department of Frontier Biosciences, Graduate School of Frontier Biosciences, Osaka University, Osaka 565-0871, Japan
Genome Dynamics Project, Tokyo Metropolitan Institute of Medical Science, Tokyo 113-8613, Japan
ABSTRACT
Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA-1) is essential for replication of episomal EBV DNAs and maintenance of latency. Multifunctional EBNA-1 is phosphorylated, but the significance of EBNA-1 phosphorylation is not known. Here, we examined the effects on nuclear translocation of Ser phosphorylation of the EBNA-1 nuclear localization signal (NLS) sequence, 379Lys-Arg-Pro-Arg-Ser-Pro-Ser-Ser386. We found that Lys379Ala and Arg380Ala substitutions greatly reduced nuclear transport and steady-state levels of green fluorescent protein (GFP)-EBNA1, whereas Pro381Ala, Arg382Ala, Pro384Ala, and Glu378Ala substitutions did not. Microinjection of modified EBNA-1 NLS peptide-inserted proteins and NLS peptides cross-linked to bovine serum albumin (BSA) showed that Ala substitution for three NLS Ser residues reduced the efficiency of nuclear import. Similar microinjection analyses demonstrated that phosphorylation of Ser385 accelerated the rate of nuclear import, but phosphorylation of Ser383 and Ser386 reduced it. However, transfection analyses of GFP-EBNA1 mutants with the Ser-to-Ala substitution causing reduced nuclear import efficiency did not result in a decrease in the nuclear accumulation level of EBNA-1. The results suggest dynamic nuclear transport control of phosphorylated EBNA-1 proteins, although the nuclear localization level of EBNA-1 that binds to cellular chromosomes and chromatin seems unchanged. The karyopherin NPI-1 (importin 5), a nuclear import adaptor, bound more strongly to Ser385-phosphorylated NLS than to any other phosphorylated or nonphosphorylated forms. Rch1 (importin 1) bound only weakly and Qip1 (importin 3) did not bind to the Ser385-phosphorylated NLS. These findings suggest that the amino-terminal 379Lys-Arg380 is essential for the EBNA-1 NLS and that Ser385 phosphorylation up-regulates nuclear transport efficiency of EBNA-1 by increasing its binding affinity to NPI-1, while phosphorylation of Ser386 and Ser383 down-regulates it.
INTRODUCTION
Epstein-Barr virus (EBV) nuclear antigen 1 (EBNA-1) is essential for the replication of EBV plasmid DNAs in latently infected cells and is also a transcriptional transactivator (4, 41, 45, 46, 54). It has recently been suggested that EBNA-1 enhances B-cell growth and transformation and is critical for the continued survival of EBV-associated Burkitt's lymphoma cells (20, 24, 40). EBNA-1 is the only EBV-encoded protein expressed in all types of latently infected cells (54) and represents one of the most important viral antigens for seroepidemiologic studies and serodiagnostic tests (21, 23, 54, 64). EBNA-1 proteins in the form of homodimers (3, 13, 17) are highly localized in the nucleus (19, 28, 36, 51) and bind in a sequence-specific manner to the EBV DNA oriP region (1, 2, 17, 27, 44, 45), cellular chromosomes/chromatin (29, 48), and cellular replication foci (31). EBNA-1 binding to mitotic cellular chromosomes is widely considered to enable the partition of de novo-synthesized EBV episomal DNAs to daughter cells (29, 48). EBNA-1 proteins are phosphorylated at Ser residues (22) and two phosphorylation domains have been mapped (52). Nonetheless, the effect of phosphorylation on EBNA-1 function is not known.
We have previously reported that EBNA-1 proteins interact with NPI-1 (importin 5), which is a nuclear import adaptor karyopherin (also known as importin ), in addition to Rchl (importin 1), using yeast two-hybrid screening and coimmunoprecipitation analyses of Raji cell lysates (30). Karyopherin (importin ) family proteins recognize various nuclear localization signal (NLS) sequences with or without the aid of adaptor molecules such as karyopherin (7, 11, 63). The EBNA-1 sequence 379Lys-Arg-Pro-Arg-Ser-Pro-Ser-Ser386 targets cross-linked carrier proteins to the nucleus (1), but it is not known whether all eight residues are necessary for NLS function. This 379KRPRSPSS386 sequence is referred to as the EBNA-1 NLS in this report.
Reported NLS amino acid sequences in different nuclear proteins are very diverse (12, 49, 57) and lack a strict consensus sequence, but generally are short and characterized by a high proportion of positively charged residues (7, 12). Monopartite NLSs have a single cluster of basic residues: the prototype sequences are the very basic simian virus 40 large T NLS (PKKKRKV) and the more hydrophobic c-Myc NLS (PAAKRVKLD) (10, 39). Bipartite NLSs have a motif with two interdependent basic domains and a mutation-tolerant spacer: the prototype sequences are the nucleoplasmin NLS (VKRPAATKKAGQAKKKKLD) and N1/N2 NLS (RKKRKTEEESPLKDKDAKKSKQEP) (12, 33, 56).
Many monopartite NLSs are 7 to 9 residues long and contain a helix-disrupting amino-terminal amino acid (proline or glycine) followed by at least three basic amino acids, while other NLSs contain basic amino acids flanking a proline residue (10). The EBNA-1 NLS belongs to the latter type. It has been proposed previously that Lys-x-x-Lys/Arg (where x can be any residue) (57), Lys-Arg/Lys-x-Arg/Lys (5), and several positively charged amino acids (Arg or Lys) associated with a Pro (18) represent consensus sequences of different groups of known monopartite NLSs. The EBNA-1 NLS fits this Lys-Arg/Lys-x-Arg/Lys sequence pattern. The KRPR tetrapeptide is also present in the NLSs of two other viral proteins, 281KRPRP of adenovirus E1A (47) and 189VSRKRPRP196 of polyomavirus large T, although the precise limits of the polyomavirus T NLS have not been defined (53).
The transport of proteins into the nucleus is a key regulatory step in functions of nuclear proteins (63). In the present study we examined whether and how phosphorylation of the Ser residues in the EBNA-1 NLS affects nuclear import and interaction with karyopherin proteins. The EBNA-1 position 380 to 397 phosphorylation region includes almost the entire NLS and adjacent Ser-rich QSSSSGSP (amino acids 387 to 394) sequence (1, 30, 52) (Fig. 1C). We also analyzed which amino acids in the eight-residue EBNA-1 NLS are crucial for nuclear localization.
MATERIALS AND METHODS
Construction of chimeric GST-NLS-GFP proteins. EBNA-1 NLS substitution mutant-inserted GST-NLS-GFP proteins glutathione S-transferase (GST)-GEKRPRSPSS-GFP, GST-GEAAPASPSS-GFP(379AAPA), GST-GEKRPRAPAA-GFP(383APAA), GST-GEKRPRDPDD-GFP(383DPDD), GST-GEKRPRAPSS-GFP (S383A), GST-GEKRPRSPAS-GFP(S385A), GST-GEKRPRSPSA-GFP(S386A), GST-GEKRPRSPAA-GFP(S385A, S386A) and GST-GEKRPRDPSS-GFP(S383D) (Fig. 1A) were constructed by inserting NLS oligonucleotides GATCCGGAGAAAAGAGGCCCAGGAGTCCCAGTAGTCAGC for GST-GEKRPRSPSS-GFP, GATCCGGAGAAGCGGCGCCCGCGAGTCCCAGTAGTCAGC for GST-GEAAPASPSS-GFP(379AAPA), GATCCGGAGAAAAGAGGCCCAGGGCACCCGCAGCACAGC for GST-GEKRPRAPAA-GFP(383APAA), GATCCGGAGAAAAGAGGCCCAGGGACCCCGACGACCAGC for GST-GEKRPRDPDD-GFP(383DPDD), GATCCGGAGAAAAGAGGCCCAGGGCACCCAGTAGTCAGC for GST-GEKRPRAPSS-GFP (S383A), GATCCGGAGAAAAGAGGCCCAGGAGTCCCGCAAGTCAGC for GST-GEKRPRSPAS-GFP(S385A), GATCCGGAGAAAAGAGGCCCAGGAGTCCCAGTGCACAGC for GST-GEKRPRSPSA-GFP(S386A), GATCCGGAGAAAAGAGGCCCAGGAGTCCCGCAGCACAGC for GST-GEKRPRSPAA-GFP(S385A,S386A), and GATCCGGAGAAAAGAGGCCCAGGGACCCCAGTAGTCAGC for GST-GEKRPRDPSS-GFP(S383D), into the BamHI-SmaI site of pGEX2T (Pharmacia)-derived vectors for the previously described GST-NES-GFP (60) (substitutions are indicated in boldface).
Synthetic peptides derived from the EBNA-1 NLS and their conjugation to biotinylated bovine serum albumin. EBNA-1 NLS-derived peptides CYGGEKRPRSPSSQ, CYGGEAAPASPSSQ, CYGGEKRPRAPAAQ, CYGGEKRPRAPSSQ, CYGGEKRPRSPASQ, CYGGEKRPRSPSAQ, CYGGEKRPRDPDDQ, Ser383-phophorylated CYGGEKRPR-pS-PSSQ (pS stands for phosphoserine), Ser385-phosphorylated CYGGEKRPRSP-pS-SQ, Ser386-phosphorylated CYGGEKRPRSPS-pS-Q, CYGGEKRPRDPSSQ, and CYGGEKRPRSPDSQ (Fig. 1B) were synthesized by GenScript (New Jersey). The amino-terminal CYGG sequence was added to facilitate cross-linking of the synthetic peptides to biotinylated bovine serum albumin (bBSA) and the synthetic peptides were chemically conjugated to bBSA as previously described (26). The designations and structures of the peptide-tagged bBSAa are listed in Fig. 1A. Peptide-conjugated bBSA proteins contained 7 to 10 peptides per bBSA molecule, as judged by sodium dodecyl sulfate (SDS)-polyacrylamide gel electrophoresis (PAGE). Rhodamine isothiocyanate-labeled BSA was prepared essentially as described previously (60).
Construction of GFP fusion proteins of the EBNA-1 NLS and flanking sequence mutants. A GFP fusion polypeptide of EBNA-1 that lacks the Gly-Gly-Ala copolymer (65, 66), designated GFP-EBNA1, has been previously described (29, 31). GFP-EBNA1 mutants were constructed by the method of PCR-based site-directed mutagenesis. The GFP fusion protein of the EBNA-1 mutant with 379AAPA382 was designated GFP-EBNA1(379AAPA). The other GFP-EBNA-1 mutants were designated in the same fashion. The structures and names of a series of GFP fusion proteins of EBNA-1 mutants with an amino acid substitution mutation in the NLS, amino acids 379 to 394, and flanking sequences are as follows: GFP-EBNA1(383APAA), GFP-EBNA1(379AAPA), GFP-EBNA1(388AAAAGA), GFP-EBNA1(K379A), GFP-EBNA1(R380A), GFP-EBNA1(P381A), GFP-EBNA1(R382A), GFP-EBNA1(S383A), GFP-EBNA1(P384A), GFP-EBNA1(S385A), GFP-EBNA1(S386A), and GFP-EBNA1(E378A) (Fig. 1C).
The PCR primers used to construct the GFP-EBNA1 mutants are as follows: GACGTGGAGAAGCGGCGCCCGCGAGTCCCAGTAG for GFP-EBNA1(379AAPA), GTGGACGTGGAGAAGCGAGGCCCAGGAGTCCCAG for GFP-EBNA1NL1-1(K379A), GACGTGGAGAAAAGGCGCCCAGGAGTCCCAGTAG for GFP-EBNA1(R380A), GAGAAAAGAGGCCCGCGAGTCCCAGTAGTCAGTC for GFP-EBNA1(R382A), GAGGCCCAGGGCTCCCGCTGCTCAGTCATCATC for GFP-EBNA1(383APAA), GAGGCCCAGGGATCCCGATGATCAGTCATCATC for GFP-EBNA1(383DPDD), AGTAGTCAGGCAGCAGCAGCCGGGGCTCCACCGCGC for GFP-EBNA1(388AAAAGA), GGACGTGGAGCAAAGAGGCCCAGGAGTCCC for GFP-EBNA1(E378A), GGACGTGGAGAAAAGAGGGCCAGGAGTCCC for GFP-EBNA1(P381A), AAGAGGCCCAGGGCTCCCAGTAGTCAG for GFP-EBNA1(S383A), GAGGCCCAGGAGTGCCAGTAGTCAGTCATCATC forGFP-EBNA1(P384A), CCCAGGAGTCCCGCTAGTCAGTCATCA for GFP-EBNA1(S385A), and AGGAGTCCCAGTGCTCAGTCATCATCA for GFP-EBNA1(S386A). They were synthesized by Texas Genomics Japan (Tokyo, Japan). PCR was done using DNA polymerase KOD-Plus-201 (Toyobo, Osaka, Japan). Base sequences of PCR products were determined with an ABI PRISM 3100-Avant genetic analyzer (Applied Biosystems, Foster City, California).
Cell line, transfection, and laser scanning microscopy. The cell line HeLa was obtained from the American Type Culture Collection through the Japanese Cancer Research Resources Bank (Japan) and was cultured in F-12 Ham's medium containing 10% fetal bovine serum. Transfection with plasmids expressing GFP fusion proteins of the EBNA-1 NLS and flanking sequence mutants was done with Lipofectin reagent (Invitrogen, California). Confocal laser scanning microscopy of transfected cells stained with Hoechst dye 33258 was described previously (29, 31). The mean and median values of percentages of nuclear GFP in 20 transfected cells per GFP-EBNA-1 mutant were calculated using Photoshop CS (Adobe Systems, California).
Microinjection assays. Microinjection was carried out as previously described (58, 59). Briefly, GST-NLS-derived 10-amino-acid polypeptides tagged with GFP (3 mg/ml) were microinjected into the cytoplasm of HeLa cells grown on coverslips and incubated at 37°C. HeLa cells were fixed by 3.7% formaldehyde at the indicated times, and fluorescence of GFP was detected. bBSA conjugated with different peptides (3 mg/ml) was injected together with rhodamine isothiocyanate-BSA (50)into the HeLa cytoplasm and the cells were incubated at 37°C. HeLa cells were fixed and permeabilized at the indicated times, and the subcellular localization of conjugated proteins was detected by Alexa 488-labeled streptavidin (Molecular Probes) as described previously (58). The average fraction of GFP intensity present in the nuclei in three or four cells in each microscopic image was calculated using Photoshop CS (Adobe Systems, California).
Solution binding analyses of EBNA-1 NLS-derived peptides with karyopherin proteins. Recombinant karyopherin proteins, Flag-NPI-1, Flag-Rch1, and Flag-Qip1, were described previously (58). bBSA proteins conjugated to EBNA-1 NLS-derived peptides were incubated with karyopherin in the presence of avidin-agarose at 4°C for 2 h as described previously (58). After extensive washing, bound proteins were eluted, analyzed by SDS-PAGE, and stained with Coomassie brilliant blue (58).
Luciferase assays. The effector plasmids pME18-EBNA1, pME18-EBNA1(379AAPA), pME18-EBNA1(383APAA), and pME18-EBNA1(383DPDD) were constructed on expression vector pME18S carrying the SR promoter (constructed by K. Maruyama et al., Tokyo Medical and Dental University) so that they have the same EBNA-1 mutant sequences as those in the above-described GFP-EBNA1(379AAPA), GFP-EBNA1(383APAA), and GFP-EBNA1(383DPDD) plasmids, respectively. Activation of transcription from the oriP-BamHI C-Luc reporter (43), a kind gift from B. Sugden, was measured in HeLa cells; 1.0 μg of oriP-BamHI C-Luc and 1.0 μg of an effector were cotransfected into 1.0 x 105 or 2.0 x 105 cells per plate (60-mm diameter) using Lipofectamine (Invitrogen, Carlsbad, California). Luciferase assays were carried out using Promega's luciferase assay system (Promega, Madison, Wisconsin) according to the manufacturer's instruction.
RESULTS
EBNA-1 Lys379 and Arg380 are both essential for nuclear localization. In order to identify amino acid residues in the EBNA-1 NLS that are essential for its activity, we performed point-mutation analyses. Microinjection experiments showed that a chimeric protein containing a wild-type EBNA-1 NLS, GST-GEKRPRSPSS-GFP, was transported into the nucleus with maximal accumulation within 3 h postinjection (Fig. 2A). In contrast, the nuclear import of a chimeric protein containing an NLS mutant with substitutions of Ala for the basic amino acids GST-GEAAPASPSS-GFP, was greatly reduced (Fig. 2A and Table 1). In addition, bBSA tagged with a synthetic EBNA-1 NLS peptide, bBSA-E1NLS, was transported into the nucleus 1 h postinjection (Fig. 2B). However, the nuclear import of bBSA tagged with the NLS mutant peptide with Ala substituted for the three basic amino acids, bBSA-E1NLS(379AAPA), was also greatly reduced (Fig. 2B; Table 2). In these assays, rhodamine isothiocyanate-BSA was added to the NLS sequence-inserted chimeric proteins or NLS peptide-tagged bBSA immediately before microinjection to serve as an internal injection marker in the same injected cell. The intracellular localization profiles of rhodamine isothiocyanate-BSA are also shown in Fig. 2.
Transfection analyses of GFP-EBNA1 proteins with the basic amino acid-to-Ala substitutions in NLS were performed using confocal microscopy of living HeLa cells to analyze the effects of the mutation on the steady-state level of EBNA-1 in the nucleus. GFP-EBNA1 showed a highly nuclear localization profile (28-30), referred to as a "mostly nuclear localization profile" in this study (Fig. 3A). Nuclear GFP varied in the range of 55% to 100% among the 20 cells transfected with GFP-EBNA1 (mean, 90% ± 4% [standard deviation]; median, 98%) (Fig. 3A; Table 3). GFP-EBNA1(379AAPA) proteins, however, were highly localized in the cytoplasm (Fig. 3Ba) in the majority of cells (>75%) and in both the nucleus and cytoplasm in the remainder (<25%) (Fig. 3Bb) (mean, 21.8 ± 4%; median, 18%). It is to be noted that nuclear localization of GFP-EBNA1(379AAPA) is explained partially by its association with cellular chromosomes (25, 29, 48) during the nuclear envelope-disintegrated mitotic phase, as is the case with wild-type EBNA-1 (data not shown).
The single basic amino acid-substituted mutants GFP-EBNA1(K379A) (Fig. 3C) and GFP-EBNA1(R380A) (Fig. 3D) were found to localize primarily to the cytoplasm of <50% of transfected cells (Fig. 3Ca and Da) and to cytoplasm and nuclei in the remainder (Fig. 3Cb and Db); the mean nuclear GFP intensity in cells transfected with GFP-EBNA1(K379A) was 45 ± 6% (median, 43%). The mean nuclear GFP intensity in cells transfected with GFP-EBNA1(R380A) was similar (40 ± 7%; median, 43%). The other basic amino acid-substituted mutant GFP-EBNA1(R382A) proteins localized to the nucleus, to almost the same degree as wild-type EBNA-1 (Fig. 3F); the mean percentage of nuclear GFP intensity in cells transfected with GFP-EBNA1(R382A) was 84 ± 5% (median, 90%). The Pro381-substituted EBNA-1 NLS mutant, GFP-EBNA1(P381A) (Fig. 3E), and the Pro384-substituted GFP-EBNA1(P384A) mutant (Fig. 3G) also localized to the nucleus, as did wild-type EBNA-1; the mean nuclear GFP intensity in cells transfected with GFP-EBNA1(P381A) was 88 ± 2% (median, 91%) and that with GFP-EBNA1(P384A) was 94 ± 2% (median, 99%). The single amino acid substitution EBNA-1 NLS mutant GFP-EBNA1(E378A) also localized to the nucleus (Fig. 3H), like the wild-type (mean, 93 ± 4%; median, 99%). Localization profiles of GFP-EBNA1 mutants along straight lines arbitrarily drawn in the photomicrographs of transfected cells are included in Fig. 3 to show the relative intensities of GFP and Hoechst dye 33258 in the nucleus and cytoplasm.
These results indicate that the two basic amino acids, Lys379 and Arg380, are essential for nuclear localization, but Arg382, Pro381, Pro384, and Glu378 are not critical.
Microinjection shows that Ser383 and Ser385 residues of the EBNA-1 NLS are crucial for nuclear import of GST-NLS-GFP protein and NLS-tagged BSA. To test the effects of EBNA-1 NLS phosphorylation on nuclear localization, we analyzed nuclear import of NLS peptide-inserted GST-GFP chimeric proteins and bBSA cross-linked to the NLS peptide bBSA-E1NLS in HeLa cells by microinjection. GST-GEKRPRSPSS-GFP synthesized in Escherichia coli was not transported into the nucleus very quickly, but it had accumulated there 3 h after injection, as shown in Fig. 2Aa. bBSA-E1NLS was transported into the nucleus within 60 min (Fig. 5A). In contrast, the Ser-to-Ala substitution protein GST-GEKRPRAPAA-GFP(383APAA) was present in the nucleus only in small amounts 3.0 h postinjection (Fig. 4A; Table 1), and bBSA cross-linked to the Ser-to-Ala substitution NLS peptide, bBSA-E1NLS(383APAA), was also present only in small amounts 1.0 h postinjection (Fig. 5B; Table 2). The results indicate that Ser residues of the EBNA-1 NLS are crucial for efficient nuclear import of GST-NLS-GFP protein and NLS-tagged BSA.
Next, we separately analyzed the requirement for Ser383, Ser385, and Ser386 for nuclear import. GST-GEKRPRAPSS-GFP(S383A) was present in the nucleus only in small amounts 3.0 h postinjection (Fig. 4B; Table 1), suggesting that Ser 383 is crucial for efficient EBNA-1 nuclear import. bBSA cross-linked to the Ser383-to-Ala substitution NLS peptide, bBSA-E1NLS(S383A), was transported into the nucleus slightly more slowly than bBSA-E1NLS (Fig. 5F; Table 2), suggesting that multiples (7 to 10) of the Ser383-to-Ala substitution NLS peptide per bBSA molecule allowed bBSA-E1NLS(S383A) transport into the nucleus. GST-GEKRPRSPAS-GFP(S385A) and GST-GEKRPRSPSA-GFP(S386A) were transported into the nucleus at a slightly reduced rate (Fig. 4C and D; Table 1) and GST-GEKRPRSPAA-GFP(S385A, S386A) was transported at a more reduced rate (Fig. 4E; Table 1). bBSA-E1NLS(S385A) was also transported at a slightly reduced rate (Fig. 5G; Table 2), whereas bBSA-E1NLS(S386A) was transported into the nucleus even faster than bBSA-E1NLS (Fig. 5H; Table 2). Together, these results all suggest that Ser383 and Ser385 are important for nuclear translocation.
Phosphorylation of Ser residues in the EBNA-1 NLS regulates nuclear transport efficiency. To analyze the impact of Ser phosphorylation on nuclear transport, synthetic peptides derived from the EBNA-1 NLS were cross-linked to bBSA, and nuclear import was assessed following microinjection. bBSA cross-linked to the NLS peptide, bBSA-E1NLS, was transported into the nucleus with almost maximal accumulation within 60 min (Fig. 5A).
bBSA tagged with the Ser385-phosphorylated peptide, bBSA-E1NLS(pS385), was more rapidly transported into the nucleus (within 30 min) than bBSA-E1NLS (Fig. 5D; Table 2). bBSA cross-linked to either the Ser383- or the Ser386-phosphorylated NLS peptide, bBSA-E1NLS(pS383) or bBSA-E1NLS(pS386), respectively, migrated more slowly into the nucleus than bBSA-E1NLS (Fig. 5C and E; Table 2). bBSA with the Ser385Asp substitution peptide, bBSA-E1NLS(S385D), was transported into the nucleus almost as rapidly as bBSA-E1NLS(pS385) (FIG. 5J; Table 2). GST-GEKRPRDPSS-GFP(S383D) was less efficiently transported than GST-GEKRPRSPSS-GFP (Fig. 4I), consistent with the slightly reduced nuclear transport rate of bBSA-E1NLS(pS383) (Fig. 5C; Table 2).
bBSA cross-linked to the NLS peptide in which all Ser at 383, 385, and 386 were replaced with Asp [bBSA-E1NLS(383DPDD)] was transported into the nucleus with an efficiency similar to bBSA-E1NLS (Fig. 5K; Table 2). The Ser-to-Asp substitution protein GST-GEKRPRDPDD-GFP, mimicking GST-KRPRpSPpSpS-GFP, was translocated to the nucleus within 3 h, similar to GST-GEKRPRSPSS-GFP (Fig. 4G; Table 1). These results possibly resulted from a balance between the effects of acceleration and deceleration of transport caused by phosphorylation of all three serine residues.
Ser-to-Ala substitution in the EBNA-1 NLS does not significantly affect nuclear accumulation levels of GFP-EBNA-1 in transfected cells. To analyze the effects on nuclear localization of NLS Ser phosphorylation, a set of GFP-EBNA-1 mutants with Ser-to-Ala or Ser-to-Asp substitutions in the 379KRPRSPSS386 sequence was constructed (Fig. 1C). Substitution of three Ser residues with Asp in the NLS [GFP-EBNA1(383DPDD)], mimicking simultaneous Ser phosphorylation, did not affect nuclear localization or accumulation levels (Fig. 6B), in agreement with the result of microinjection analysis of GST-GEKRPRDPDD-GFP(383DPDD) (Fig. 4G); the mean percentage of nuclear GFP in cells transfected with GFP-EBNA1(383DPDD) was 95 ± 3%, and the median was 99%.
Surprisingly, GFP-EBNA1(383APAA), GFP-EBNA1(S383A), and GFP-EBNA1(S385A) also did not reduce nuclear accumulation levels (Fig. 6C to E). The mean percentages of nuclear GFP intensity in cells transfected with GFP-EBNA1(383APAA), GFP-EBNA1(S383A), and GFP-EBNA1(S385A) were 90 ± 5%, 89 ± 3%, and 90 ± 6% (median values, 96, 99, and 97%, respectively). GFP-EBNA1(S386A), which was included here for comparison, did not affect nuclear accumulation levels, as expected (Fig. 6F); mean nuclear GFP intensity in cells transfected with GFP-EBNA1(S386A) was 93 ± 3% (median, 99%). These results indicate that Ser at amino acid 383, 385, or 386 is not essential for nuclear accumulation of EBNA-1 to a high level.
We also asked whether the carboxyl-adjacent Ser-rich 387QSSSSGS393 sequence is involved in regulating the level of EBNA-1 in the nucleus. However, GFP-EBNA1(388AAAAGA) with Ser-to-Ala substitutions at all five Ser residues in the carboxyl-adjacent 387QSSSSGS393 (Fig. 6G) showed a localization profile similar to that of GFP-EBNA1; the mean proportion of nuclear GFP intensity in cells transfected with GFP-EBNA1(388AAAAGA) was 93 ± 9% (median, 96%). This indicates that phosphorylation of Ser residues in the QSSSSGSP sequence is not required for nuclear accumulation of EBNA-1.
Analyses of karyopherin interactions with phosphorylated and nonphosphorylated forms of EBNA-1 NLS. We previously reported that the karyopherin NPI-1 (importin 5) binds to EBNA-1 (30) as well as the karyopherin Rch1 (importin 1) (14, 30, 42). To examine the effects of phosphorylation of and amino acid substitutions in the EBNA-1 NLS, we analyzed interactions of NLS mutant peptides with recombinant NPI-1 (importin 5), Rch1 (importin 1), and Qip1 (importin 3) (61) using the biotin-avidin affinity binding assays.
NPI-1 did not bind to bBSA-E1NLS(379AAPA) (Fig. 7A), consistent with failure of nuclear import of bBSA-E1NLS(379AAPA) (Fig. 2B). NPI-1 bound to bBSA-E1NLS(pS385) much more strongly than to bBSA-E1NLS (Fig. 7A), a finding in agreement with the accelerated nuclear import rate of bBSA-E1NLS(pS385) (Table 2). In contrast, NPI-1 bound to bBSA-E1NLS(pS383) and bBSA-E1NLS(pS386) only weakly (Fig. 7A; Table 2). NPI-1 bound to bBSA-E1NLS(383APAA) more weakly than to bBSA-E1NL (Fig. 7A), in agreement with its greatly reduced nuclear import rate (Table 4). These data agree with our previous findings that EBNA-1 protein synthesized in Escherichia coli interacted with NPI-1 much less efficiently than EBNA-1 synthesized in Raji cells (30) and indicate that phosphorylation of S385, but neither S383 nor S386, is required for the interaction of EBNA-1 with NPI-1. NPI-1 bound to bBSA-E1NLS(S385D) and bBSA-E1NLS(S383D) only weakly, but bound to bBSA-E1NLS(383DPDD) as strongly as bBSA-E1NLS(pS385) (Fig. 7B). NPI-1 bound to bBSA-E1NLS(S383A), bBSA-E1NLS(S385A) and bBSA-E1NLS(S386A) only weakly (Fig. 7B; Table 2).
Interaction of Rch1 with bBSA-E1NLS was minimal (Fig. 7A). Rch1 also bound more strongly to bBSA-E1NLS(pS385) than to bBSA-E1NLS(pS383) and bBSA-E1NLS(pS386) (Fig. 7A). However, Rch1 binding to bBSA-E1NLS(pS385) was much weaker than NPI-1 binding (Fig. 7A). Also, the interaction of Rch1 with bBSA cross-linked to the other EBNA-1 NLS-derived peptides was very weak (Fig. 7A and B). Interactions of Qip1 with any of these EBNA-1 NLS-derived peptides were absent (Fig. 7A and B).
Effects of NLS mutations on the activation of transcription from the BamHI C promoter by EBNA-1 expressed transiently in cotransfection luciferase assays. To test whether the above described regulation of nuclear import efficiency of EBNA-1 is involved in its multifunctional properties, we first performed DNA replication/retention assays by cotransfection of plasmid pME18-EBNA1 with oriP-BamHI C-Luc or oriP-minus (43), which were kind gifts from B. Sugden (University of Wisconsin), and by growing HeLa cells. However, the activity of transiently expressed EBNA-1(GA), the expression of which was confirmed by Western blotting performed as previously described (31), to support oriP-plasmid once per cell cycle replication/retention was too low to detect a de novo-synthesized DpnI-resistant band of linearized oriP-BamHI C-Luc by Southern blotting, the detection sensitivity of which was 2.04 copies per cell (0.01 ng per lane of gel electrophoresis) using a 32P-labeled probe (1.9 x 109 cpm/μg) (data not shown). In parallel analyses, in HeLa S3#8 cells that constitutively express full-length-EBNA-1 (N. Yoshizawa-Sugata and H. Masai, unpublished) a de novo-synthesized oriP-BamHI C-Luc band was detected (data not shown).
To analyze whether the nuclear import regulation of EBNA-1 affects the activation of transcription by EBNA-1, we constructed plasmids pME18-EBNA1, pME18-EBNA1(379AAPA), pME18-EBNA1(383APAA), and pME18-EBNA1(383DDPD) to assess the effects of the NLS mutation in the absence of GFP. Luciferase assays using HeLa cells cotransfected with the oriP-BamHI C-Luc reporter plasmid (43) (kindly provided by B. Sugden) and pME18-EBNA1(379AAPA) showed that the Ala substitution mutation 379AAPA, which greatly reduces nuclear import and localization of EBNA-1, caused a significant reduction in the activation of transcription from the BamHI C-Luc reporter at 48, 72, and 96 h after transfection, compared to pME18-EBNA1 and pME18-EBNA1(383DPDD) (Table 4). However, pME18-EBNA-1(383APAA), which greatly reduces the efficiency of nuclear import of EBNA-1, did not reduce the activation of transcription from the BamHI C-Luc reporter (Table 4). These results are consistent with the finding that the 383APAA Ala substitution mutation did not reduce the nuclear intensity of GFP-EBNA1 (Fig. 6C to E). Further, they indicate that under the present experimental conditions of transient expression of EBNA-1 in cotransfection assays, the Ser-to-383APAA mutation that causes the great reduction in the nuclear transport efficiency of EBNA-1 proteins does not affect the transcriptional activator function of EBNA-1.
DISCUSSION
Regulation of nuclear transport by phosphorylation of sites that are adjacent to NLSs, but not within them, has been reported previously (16, 32-34, 37). The best studied example is that the nuclear import of simian virus 40 T antigen directed by the NLS (126PKKKRKV132) is enhanced by phosphorylation of S112 (34), but is inhibited by phosphorylation of T124 (35, 55, 62). The findings of the present study are summarized in Tables 1 to 3, and the major conclusions are as follows. First, our data suggest that only the amino-terminal 379Lys-Arg380 is essential for both nuclear transport and nuclear accumulation directed by the EBNA-1 NLS and for interaction with the karyopherin NPI-1 protein. This remarkable variability of the N-terminal and C-terminal sequences flanking the EBNA-1 NLS 379KR380 is similar to the simian virus 40 T antigen NLS (amino acids 126 to 132) in which the Lys residue at position 128 is essential for NLS integrity (6, 38). Crystallographic studies of complexes of karyopherin and NLS peptides have shown that the basic residues of the simian virus 40 large T (8, 9) and c-Myc NLSs (8, 15) interact with the binding pockets of the major binding site of the karyopherin molecule. In contrast, no Lys in the downstream cluster of nucleoplasmin (167KKKK170) can be substituted (56). It is not yet clear whether any Lys or Arg residues in the smallest known NLS, KRPRP, can be mutated without loss of function.
Second, the Ser residues of 383SPSS386 in the EBNA-1 NLS are important for efficient nuclear translocation, as shown by microinjection experiments.
Third, Ser383 is crucial for efficient nuclear import, because replacement of Ser383 with either Ala, Asp, or phosphoserine reduced nuclear import. Ser386 is not essential for nuclear transport, but phosphorylation of Ser at position 386 reduces nuclear translocation efficiency, as demonstrated by microinjection analyses.
Fourth, Ser385 is important for nuclear transport and Ser385 phosphorylation accelerates the rate of EBNA-1 nuclear translocation.
Fifth, a reduction of nuclear transport rate does not result in a decrease in the intensity of nuclear GFP-EBNA-1 relative to that of cytoplasmic EBNA-1. The results described in this report suggest that nuclear levels of EBNA-1 are regulated not only by import rate but also by the retention of EBNA-1 in the nucleus due to the association of EBNA-1 with cellular chromosomes and chromatin (29, 48).
Sixth, Ser385 phosphorylation in the EBNA-1 NLS increases the interactions of EBNA-1 with the karyopherin NPI-1 protein. Rch1, on the other hand, bound to EBNA-1 NLS peptides, either phosphorylated or nonphosphorylated, far less strongly than NPI-1, and Qip1 did not bind to any of the EBNA-1 NLS peptides. The very weak binding of NPI-1 to bBSA-E1NLS(S385D) indicates that an effect of phosphorylation of serine at position 385 on the interaction of E1NLS with NPI-1 is highly specific. The finding that NPI-1 bound to bBSA-E1NLS(383DPDD) as strongly as bBSA-E1NLS(pS385) but without resulting in accelerated nuclear transport rates of bBSA-E1NLS(383DPDD) indicates that the strong binding of NPI-1 to the EBNA-1 NLS is not sufficient for accelerated nuclear import. These data need emphasizing because it was previously reported that phosphorylation of Ser112 in the vicinity of the NLS (126PKKKRKV132) of simian virus 40 T antigen enhanced nuclear import but not the affinity of binding between the T-antigen NLS and importin 2 (16). These results indicate that NPI-1 is a major karyopherin member that mediates the nuclear import of EBNA-1 and that phosphorylation of S385 accelerates the nuclear import rate through an increased affinity of NLS for NPI-1.
Lastly, the great decrease in the efficiency of nuclear import of EBNA-1(383APAA) did not reduce activation of transcription from the BamHI C-Luc promoter, in contrast to EBNA-1(379AAPA). However, the high transient expression level of the mutant EBNA-1 proteins may have hindered detection of any possible effects of the reduced nuclear transport efficiency of EBNA-1 on the activation of transcription. Functional effects of the reduced nuclear transport efficiency of EBNA-1 may be complex because of stable colocalization of EBNA-1 with cellular chromosomes and chromatin (29) and may act in concert with other cellular factors, such as cell cycle position or infection with EBV. Furthermore, the regulation of nuclear import efficiency by phosphorylation of the EBNA-1 NLS may be correlated with phosphorylation of other Ser residues of EBNA-1 outside the NLS (22, 52) and required for adequate functional association of EBNA-1 to cellular proteins in EBV-infected cells.
From the present study, we conclude that the amino-terminal 379Lys-Arg380 and Ser383 are the essential elements of the EBNA-1 NLS (amino acids 379 to 386) required for function. It has been found that phosphorylation of Ser385 increases nuclear transport efficiency of EBNA-1 by modulating its affinity to NPI-1, whereas phosphorylation of Ser383 or Ser386 decreases it. This is the first study to suggest any role for Ser phosphorylation in the context of EBNA-1. The results suggest dynamic transport control of phosphorylated EBNA-1 proteins, whereas the steady-state nuclear level of EBNA-1 seems unchanged.
ACKNOWLEDGMENTS
We thank Bill Sugden, University of Wisconsin, for his kind gift of the oriP-BamHI C-Luc (1033) and oriP-minus (1381) plasmids (43).
Financial support for this research was provided by a grant-in-aid from the Ministry of Health, Welfare and Labor.
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