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发表于 2009-4-25 09:34 |只看该作者 |倒序浏览 |打印

1 Laboratory of Molecular Biology, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 208924 g7 e, K# [5 ~* v3 m
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2 Center for Cancer Biology and Nutrition, Alkek Institute of Biosciences and Technology, Texas A&M University System Health Science Center, Houston, TX 77030
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Abstract5 [% b. H$ _' N  g

Nucleostemin (NS) was identified as a stem cell– and cancer cell–enriched nucleolar protein that controls the proliferation of these cells. Here, we report the mechanism that regulates its dynamic shuttling between the nucleolus and nucleoplasm. The nucleolar residence of nucleostemin involves a transient and a long-term binding by the basic and GTP-binding domains, and a dissociation mechanism mediated by the COOH-terminal region. This cycle is propelled by the GTP binding state of nucleostemin. We propose that a rapid nucleostemin cycle is designed to translate extra- and intra-cellular signals into the amount of nucleostemin in the nucleolus in a bidirectional and fast manner.
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Abbreviations used in this paper: Act-D, actinomycin D; iFRAP, inverse FRAP; MPA, mycophenolic acid; NS, nucleostemin.7 Y2 N- M: W  ?
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Introduction
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Stem cells are the building blocks during organogenesis. In adults, they are responsible for replacing natural cell loss and may promote recovery after injury. To maintain tissue homeostasis and avoid tumor formation, it is critical to adjust the stem cell division rate based on the supply of nutrients and mitogens, as well as the factors that signal the size of the tissue (Bullough, 1965). However the molecular program regulating the transition of stem cells between the actively dividing and quiescent states remains unclear.9 V6 x5 @. I$ s0 [7 o2 R7 \
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As a step in this direction, we have identified a novel gene nucleostemin (NS) (Tsai and McKay, 2002) that is preferentially expressed in the nucleoli of neural stem cells, embryonic stem cells, and several cancer cell lines. NS is required for stem cells and cancer cells to remain in the cell cycle, suggesting that the rate of proliferation in these cells can be modulated by the activity of NS. Given that NS is localized primarily in the nucleolus where key features of cell growth including ribosome biogenesis occur, partitioning the amount of NS between the nucleolar and nucleoplasmic compartments could provide a way to regulate its activity. This idea is supported by previous reports demonstrating a positive correlation between the size of the nucleolus, the nucleolar activity, and the cell growth rate (Derenzini et al., 1998, 2000). To date, little is known about the molecular machinery that allows the cells to adjust their nucleolar size dynamically and reversibly.4 M! v1 o& H9 \: H* C" J

The structure of the nucleolus is complex, and the analysis of nucleolar functions is further complicated by the fact that many of the nucleolar proteins are found both in the nucleolus and the nucleoplasm (Chen and Huang, 2001; Dundr and Misteli, 2002; Fox et al., 2002). In this manuscript, we investigate the mechanism that controls the NS distribution. Our findings suggest a GTP-driven cycling mechanism that modulates the amount of NS in the nucleolus in a fast and bidirectional manner.
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Results and discussion

NS shuttles between the nucleolus and the nucleoplasm  T7 ~1 N: p6 x. a# I: Q

In addition to its predominant nucleolar distribution, NS is also present at low levels in the nucleoplasm (Tsai and McKay, 2002). To determine the mechanism controlling the NS localization, we first examined if there is a dynamic exchange of NS between these two compartments using the FRAP and inverse FRAP (iFRAP) approaches. Photobleaching experiments were conducted on GFP-tagged NS protein (NS-GFP) in living cells using time-lapse confocal microscopy (Phair and Misteli, 2000). U2 OS cells or CHO cells were chosen because of their large, flat-shaped nucleoli, resistance to phototoxicity, and their high levels of endogenous NS expression. In addition to strongly labeled nucleoli, the expressed NS-GFP also gave weak, diffuse signals in the nucleoplasm, similar to the endogenous NS (Fig. 1 A1, NS vs. NS-GFP). After actinomycin D (Act-D) treatment, an RNA polymerase inhibitor that blocks transcription by intercalating between nucleotide base pairs and induces nucleolar reorganization (Recher et al., 1971a,b), both the endogenous NS and NS-GFP were redistributed from the nucleolus to the nucleoplasm, with the strongest signals surrounding the nucleolar region (Fig. 1 A2). The total amount of NS-GFP protein appears higher than the endogenous NS in the Act-D–treated cells, which may be due to the different promoters that drive their expression (cytomegalovirus vs. the endogenous NS promoter). Based on the basal distribution and the parallel changes in localization after Act-D treatment of wild-type NS-GFP, as well as the growth arrest effect seen with the mutated NS-GFP (Tsai and McKay, 2002), we used NS-GFP as a living tracer to track the dynamic distribution of endogenous NS.

In the first study, cells with two nucleoli of comparable size and intensity were photobleached in only one of their nucleoli by a short laser pulse that irreversibly quenched the GFP signal. The recovery of fluorescence in the bleached nucleolar area (Fig. 1, B and C; label 1) reached 95% (y axis: 0.758) of the plateau level (y axis: 0.783) within 39 s, reflecting the unbleached nucleoplasmic NS-GFP moving into the nucleolus. The dissociation rate of NS from the nucleolus was measured by recording the signal loss in the nonbleached nucleolus of the same cells (iFRAP). 95% (y axis: 0.822) of the lost signals (y axis: from 1 to 0.813) (Fig. 1 B and C; label 2) were reached within 46 s after photobleaching. Together, these results show that NS moves bidirectionally between the nucleolus and the nucleoplasm. The coordinated changes of fluorescence signals in the bleached and nonbleached nucleoli and the fast kinetics of this process supports that these findings are not caused by protein synthesis or by protein degradation as a result of photobleaching. Finally, the fluorescent recovery rate of NS-GFP relative to the plateau recovery intensity remains constant regardless of the cell types used to express it (Fig. S1, available at http://www.jcb.org/cgi/content/full/jcb.200409053/DC1). These data reveal a bidirectional shuttling of NS between the nucleolus and nucleoplasm at a rate that is fast and cell type independent.

GTP binding regulates the nucleolar targeting of NS

The structure of NS consists of an NH2-terminal basic (B) domain, followed by a coiled-coil (C) domain, two GTP-binding motifs (G4: KXDL; G1: GXXXXGK[S/T]), a COOH-terminal acidic domain (A), and an intermediate (I) region between the G1 motif and the A-domain (Fig. 2 A, top). The GTP-binding motifs of NS allow us to investigate how the GTP-binding state of NS directly influences its nucleolar distribution. To this end, we generated single amino acid mutation on the conserved residues in the G4 or G1 motif (Fig. 2 A, bottom). G256 and G261 are conserved among NS and the Ras family. The N176I mutation mimics the constitutive negative Ras mutant N116I (Huang and Chuang, 2000). GTP-binding assays demonstrated a specific retention of NS by the GTP-conjugated agarose, and this interaction was blocked by preincubating NS with 10 mM free GTP (Fig. 2 B) (Iismaa et al., 1997). This GTP-binding capacity of NS depends on the G1 motif, as single amino acid substitution of the conserved G256 residue (Fig. 2 C, G256V) decreased its GTP-binding ability to the control level (CT, the COOH-terminal 188 aa polypeptide of NS lacking the G4 and G1 motifs). These findings demonstrate a role of the G1 motif in the GTP binding of NS. Just as the NH2-terminal B-domain was required for the nucleolar distribution of NS (Fig. 2 D, NS-dB), mutations in the G1 motif (G256V or G261V) also blocked the nucleolar localization of NS, and created a diffuse distribution in the nucleus. Mutation on the N176 residue, which is not conserved in the small GTPase family, exhibited a partial blocking effect on the nucleolar localization of NS. Cells expressing the N176I mutant, while maintaining a nucleolus-predominant distribution, displayed higher nucleoplasmic intensity than the wild-type NS, with a slight variation from cells to cells (N176I-a, b). Based on these observations, we concluded that N176 is not as critical in mediating the GTP binding as the conserved G256 or G261, and used G256V as the prototypical non-GTP-binding mutant for NS in the following experiments. By contrast, deletions in the C-domain (NS-dC), I-domain (NS-dI), or A-domain (NS-dA) did not affect the static distribution of NS in the nucleolus. These results show that both the B-domain and the wild-type GTP-binding domain are required for the nucleolar targeting of NS.

Notably, despite the requirement of the GTP-binding motifs for the nucleolar localization of NS, B-domain alone was sufficient to target the GFP protein to the nucleolus (Fig. 2 D, Bas). This finding suggests an inhibitory mechanism that gates the nucleolus-targeting activity of the full-length NS, and that it is regulated by the GTP-binding state of NS. To map this region, deletions of the B-, C-, I-, or A-domain were created in the G256V background. Although dB(G256V) (Fig. 2 E1), dC(G256V) (Fig. 2 E2), and dA(G256V) (Fig. 2 E4) remained diffuse in the nucleoplasm, a deletion of the I-domain was able to restore the nucleolar phenotype of the G256V mutant (Fig. 2 E3), indicating that the I-domain acts as the gating mechanism that prevents the non-GTP-bound NS from moving into the nucleolus. These results demonstrate that NS uses its GTP-binding property as a molecular switch to control the transition between the nucleolus- and the nucleoplasm-localized states, and this process involves the interaction between the B-, GTP-binding, and I-domains.; f3 D5 Y9 B: ]

Mechanisms controlling the nucleolar residence of NS, x* T9 d2 I2 w

Both the B-domain and the GTP-binding domain contribute to the nucleolar localization of NS, as evidenced by the nucleolus-exclusive distribution of the dB(G256V) double mutant (Fig. 2 E1) and the nucleolus-inclusive diffuse distribution of individual mutation (NS-dB and G256V, Fig. 2 D). To investigate how the B-domain and the full-length NS protein differ in their distribution, we compared the nucleolar residence time of the B-domain alone and the full-length protein using a FRAP paradigm where a 1.5-μm-diameter circle within the nucleolus was bleached. Despite its apparent wild-type static distribution, the B-domain alone has a much faster recovery kinetic than the wild-type protein (Fig. 3, A, D, and E; Bas vs. NS-Wt). 2.5 s after photobleaching, the fluorescent recovery of Bas has reached 87.6% of the prebleach level, compared with the 75.5% recovery of the full-length protein (P

To dissect the structural requirement for the high affinity binding of NS in the nucleolus, FRAP experiments were conducted on mutants that were deleted of the C-, I-, and A-domains. A deletion in the domain required for the high affinity binding would decrease the retention time, whereas a deletion in the domain necessary for the dissociation from the high affinity binding site would increase the retention time. Our data showed that deletions of the I- and A-domains prolonged the retention time of NS-GFP in the nucleoli. With the NS-dA mutant, only 64.0% recovery of the prebleach intensity was reached at 2.5 s after photobleaching (Fig. 3, B, D, and E; NS-dA, P
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The data presented so far demonstrate that GTP binding is required to release the I-domain from blocking the nucleolar targeting of the B-domain, and is involved in the long-term nucleolar engagement of NS. To address the relationship between the dissociation of guanine nucleotides in NS and the dissociation of NS from its high affinity binding site in the nucleolus, we compared the nucleolar retention time of dI(G256V) with that of NS-dI (Fig. 3 C). dI(G256V) harbors the G256V mutation that abolishes the GTP-binding ability of NS and is deleted of the I-domain that would have prevented the nucleolar targeting of the G256V mutant. Lacking the I-domain required for the dissociation step, the FRAP recovery time for both NS-dI and dI(G256V) was delayed compared with the wild-type NS. By comparison, dI(G256V) mutant showed faster recovery than the NS-dI mutant. At 30 s after photobleaching, dI(G256V) recovered 81.4% of the prebleached intensity, whereas the NS-dI mutant recovered 75% (Fig. 3 D, E, right table; P 9 a' ]4 O4 z" }

Lowering intracellular GTP level decreases the nucleolar retention of NS

To further support the notion that guanine nucleotide dissociation correlates with the nucleolar exit of NS, we investigated if changing the intracellular GTP level would affect the shuttling kinetics of NS. To lower the intracellular GTP level, mycophenolic acid (MPA), which inhibits the rate-limiting enzyme inositide 5'-monophosphate dehydrogenase (IMPDH) of de novo guanine nucleotide biosynthesis (Majumdar et al., 1995; Olah et al., 1988), was applied to U2 OS cells transfected with NS-GFP. Photobleaching experiments were conducted in which 3-μm-diameter nucleoli were bleached and recorded for signal recovery over a 67-s period. The FRAP results revealed shortened nucleolar residence time of NS in cells treated with 40 μM MPA. At 10 s after photobleaching, the fluorescent signal recovered 80% of the prebleach level in the 40-μM MPA-treated cells, whereas control cells reached only 72% (Fig. 4, A and C; P
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The FRAP rate of NS is distinctly different from a non-GTP-binding nucleolar protein, B23
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Previous work has shown that lowering the GTP level could alter the distribution of a non-GTP-binding nucleolar protein, B23, which also displayed a dynamic property to shuttle between the nucleolus and nucleoplasm (Finch et al., 1993; Chen and Huang, 2001). In the next experiment, we investigate the difference in the cycling kinetics between NS and B23. FRAP results demonstrated that the exchange rate for B23 was distinctively slower than that of NS (Fig. 5 A). At 2.5 and 5 s after photobleaching, B23 reached only 53.0% (± 1.8; mean ± SEM) and 63.6% (± 1.8) of its prebleach level, whereas the wild-type NS returned to 63.0% (± 1.1) and 72.2% (± 0.9) of the prebleach intensity at the same time points (P $ H/ l/ R$ Q" v& i
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In this manuscript, we show that NS shuttles between four different states in the nucleus (Fig. 5 B). In the nucleoplasm, the non-GTP-bound state of NS is prevented from being localized to the nucleolus by the I-domain, and this inhibitory mechanism is released upon GTP binding. The nucleolus-bound NS exhibits a fast FRAP rate when mediated by the B-domain and a slow FRAP rate when mediated by the GTP-binding domain. It is unclear if these two nucleolus-engaged states take place sequentially or cooperatively. Finally, the dissociation of the nucleolus-engaged NS is mediated by the I- and A-domains, and may be triggered by the dissociation of guanine nucleotide. The transition of NS between these four different molecular states in the nucleus constitutes a cycling machinery that operates in a rapid and dynamic manner. With the identification of several putative GTPases in the nucleolus (Racevskis et al., 1996; Jensen et al., 2003; Kallstrom et al., 2003) and the GTP effect on the non-GTP-binding B23 (Finch et al., 1993), this proposed GTP-driven mechanism provides a molecular framework that may explain how some nucleolar proteins move between the nucleolar and nucleoplasmic compartments dynamically.: t" ^: |$ n4 U
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Such a dynamic system also generates a bidirectional, fast, and sensitive measurement to control the amount of NS engaged in the nucleolus. By monitoring the targeting probability and dissociation kinetics, this mechanism can be used to translate the intra- and extra-cellular growth signals into the amount of NS in the nucleolus as a way to dynamically control cell proliferation (Fig. S2, available at http://www.jcb.org/cgi/content/full/jcb.200409053/DC1). In addition, it also allows nucleolar proteins, such as Werner's syndrome protein, DNA topoisomerase, and NS (Blander et al., 1999; Gobert et al., 1999; Tsai and McKay, 2002; Horn and Vousden, 2004), the opportunity to interact with nucleoplasmic proteins such as p53 under physiological conditions. Our findings that the FRAP kinetics of NS remains the same in both p53-wild-type and p53-null cell lines (Fig. S1) indicate that the dynamic distribution of NS is not controlled by p53, but suggest a possibility that it may be involved in controlling the amount of p53 in the active transcriptional sites within the nucleolus (Rubbi and Milner, 2000). Further understanding of the NS machinery and the signaling pathways that control its activity will help elucidate the molecular mechanism that gates the transition of stem cells between the mitotically active and quiescent states in a fast and reversible way.! o" ?& c" P4 t. R. d% N* m) Q
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Materials and methods

Deletion and point mutation of NS-GFP fusion constructs
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Deletions and point mutations were introduced by stitching PCR reactions. Both strands of mutagenic primers were synthesized using NS-GFP as the template and paired with respective flanking primers for PCR reactions. The resulting PCR fragments were used as the template for the next round of PCR with only the flanking primers. The final products were restricted, subcloned into expression vector (pCIS), and confirmed by sequencing.9 i2 k1 z# M. [+ a4 z, F/ k. d# J3 k

FRAP and iFRAP

Cells grown in LabTek II chamber slides (Nalgene) were transfected with 0.6 μg plasmid DNA complexed with 3 μl LipofectAMINE 2000 reagent in 1.2 ml Opti-MEM 1 d before the measurement. The photobleaching experiments were performed on a confocal microscope (model 510; Carl Zeiss MicroImaging, Inc.) with a 63x plan-apochromat oil objective (Phair and Misteli, 2000). The GFP signal was excited with the 488-nm argon laser and emission was monitored above 505 nm. Cells were maintained at 35°C with a heat blower. The whole nucleolar region or a small area of the nucleolus was bleached using a short laser pulse administered at 95% of the power for three iterations, with all experiments ensured to achieve 70–80% bleaching of the original intensity. The recovery of signal in the bleached area (FRAP) was monitored. The relative fluorescence intensity was normalized to the nonbleached signal after subtraction of the background signal. Values are averages of at least 20 cells from three independent experiments. The iFRAP paradigm was designed where cells with two nucleoli of comparable size and intensity were chosen and one nucleolus was bleached. The loss of fluorescence from the unbleached nucleoli was determined as described for the FRAP paradigms.$ C) f9 e, H3 T; e( a& ^: G

GTP-binding assay% w% e  F2 x* [( z9 e& J$ H( D, _
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The GTP-binding assays were conducted as described in Iismaa et al. (1997) with 1 μg purified proteins and 80 μl GTP-agarose (2.2 μmol/ml). After extensive wash procedure, the amount of bound protein was detected by Western blot.
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Online supplemental material
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Acknowledgments4 [' p7 x, G: {! I& k$ Z
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We thank Carolyn Smith and Cem Elbi for their helpful advice in the photobleaching experiments, and Dave Owens for his critical comments on this manuscript.

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