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TPX2 is a Ran-regulated spindle assembly factor that is required for kinetochore fiber formation and activation of the mitotic kinase Aurora A. TPX2 is enriched near spindle poles and is required near kinetochores, suggesting that it undergoes dynamic relocalization throughout mitosis. Using photoactivation, we measured the movement of PA-GFP-TPX2 in the mitotic spindle. TPX2 moves poleward in the half-spindle and is static in the interzone and near spindle poles. Poleward transport of TPX2 is sensitive to inhibition of dynein or Eg5 and to suppression of microtubule flux with nocodazole or antibodies to Kif2a. Poleward transport requires the C terminus of TPX2, a domain that interacts with Eg5. Overexpression of TPX2 lacking this domain induced excessive microtubule formation near kinetochores, defects in spindle assembly and blocked mitotic progression. Our data support a model in which poleward transport of TPX2 down-regulates its microtubule nucleating activity near kinetochores and links microtubules generated at kinetochores to dynein for incorporation into the spindle.
The mitotic spindle self-assembles from microtubules and associated structural and regulatory proteins and is required for chromosome segregation during cell division. Microtubules, the major structural element of the spindle, are dynamically unstable polymers that alternate stochastically between phases of growth and rapid shortening (Mitchison and Kirschner, 1984 ). During spindle assembly in mammalian cells, dynamic microtubules nucleated at each centrosome search for and capture kinetochores on replicated chromosomes (Kirschner and Mitchison, 1986 ). In cells lacking centrosomes, microtubules assemble near chromatin/kinetochores, in a Ran-dependent manner, and are subsequently polarity sorted and organized into a bipolar array (Heald et al., 1996 ; Wilde and Zheng, 1999 ). Recent work has shown that the chromatin-dependent pathway functions in centrosome containing cells as well: spindle formation can proceed after centrosome destruction or elimination and microtubule formation is observed near chromosomes/kinetochores in cells treated and released from nocodazole (Khodjakov et al., 2000 ; Hinchcliffe et al., 2001 ; Tulu et al., 2006 ). In centrosome-containing cells, microtubules formed near chromatin interact with centrosomal microtubules for incorporation into the spindle (Khodjakov et al., 2003 ). In addition to dynamic instability, spindle microtubules exhibit an additional dynamic behavior called flux, which is characterized by the slow, poleward movement of the microtubule lattice (Mitchison, 1989 ). At metaphase, spindle flux, or sliding (Burbank et al., 2007 ), is accompanied by the balanced addition and loss of tubulin subunits from microtubule plus-ends near the spindle equator and minus-ends near spindle poles, respectively (Rogers et al., 2005 ).
Many microtubule-associated proteins and molecular motors regulate the nucleation, turnover, and flux of spindle microtubules, but our understanding of the mechanism(s) by which these factors function is still incomplete. TPX2 is a Ran-regulated microtubule-associated protein (Trieselmann et al., 2003 ) that nucleates, binds, and bundles microtubules in vitro; is required for microtubule formation at kinetochores; and contributes to spindle pole organization (Schatz et al., 2003 ; Brunet et al., 2004 ; Tulu et al., 2006 ). TPX2 localizes to spindle fibers but not polar astral microtubules and is enriched at spindle poles (Garrett et al., 2002 ; Gruss et al., 2002 ). The N terminus of TPX2, which binds and activates Aurora A kinase, is required for microtubule nucleation at chromosomes and to establish spindle length (Bayliss et al., 2003 ; Koffa et al., 2006 ; Bird and Hyman, 2008 ). A large C-terminal domain is required to localize TPX2 to the spindle, and the extreme C terminus interacts with Eg5 (Brunet et al., 2004 ; Eckerdt et al., 2008 ). In Xenopus laevis extracts, TPX2 is part of the hepatoma up-regulated protein (HURP) complex, which is composed of XMAP215, Aurora A, Eg5, TPX2, and HURP and is required for Ran-dependent bipolar spindle formation (Koffa et al., 2006 ).
Localization of the kinesin Xklp2 to spindle poles requires TPX2 and dynein (Wittmann et al., 1998 ). Dynein activity is also required for the poleward transport of the plus-end–directed bipolar kinesin Eg5, which interacts with the p150 subunit of dynactin as well as with TPX2 (Blangy et al., 1997 ; Eckerdt et al., 2008 ; Uteng et al., 2008 ). Based on these observations, we hypothesized that in the half-spindle, TPX2, alone or as part of a larger complex, is transported poleward, leading to its accumulation at microtubule minus-ends. Using photoactivation, we report that TPX2 is transported in the half-spindle and is static on interzonal microtubules. TPX2 transport in the half-spindle is sensitive to inhibition of Eg5 and dynein and to suppression of microtubule flux with nocodazole. The C-terminal 35 amino acids of TPX2, which interact with Eg5, are required for poleward transport.
All materials for cell culture were obtained from Sigma-Aldrich (St. Louis, MO), with the exception of Opti-MEM, which was obtained from Invitrogen (Carlsbad, CA) and fetal bovine serum, which was obtained from Altanta Biologicals (Norcross, GA). Unless otherwise noted, all other chemicals were obtained from Sigma-Aldrich.
Parental LLC-Pk1 cells and LLC-Pk1 cells expressing enhanced green fluorescent protein (EGFP)-α-tubulin (referred to here as LLC-Pk1-α) were grown as described previously (Tulu et al., 2003 ). For immunofluorescence, cells were rinsed twice in warm, calcium- and magnesium-free phosphate-buffered saline (PBS−/−), followed by fixation in ice-cold methanol or 3.2% paraformaldehyde, 0.1% glutaraldehyde, and 0.5% Triton in PBS−/−. Fixed cells were rinsed in PBS−/− containing 0.02% sodium azide and 0.1% Tween 20. The following primary antibodies were used in these experiments: MCAK, gift from Dr. Claire Walczak (Indiana University, Bloomington, IN); Mad2, a gift from Dr. Alexey Khodjakov (Wadsworth Center, Albany, NY); YL½ (Accurate Chemical, Westbury, NY); Hec1, TPX2, and Kif2a (Novus Biologicals, Littleton, CO); and p150 (BD Biosciences, Franklin Lakes, NJ). Incubations with primary antibodies were performed for 1 h at 37°C, using the manufacturer's recommended dilution. Cyanine (Cy)3-labeled (Jackson ImmunoResearch Laboratories, West Grove, PA) or fluorescein isothiocyanate-labeled (Sigma-Aldrich) secondary antibodies were used at the recommended dilution for 60 min at 37°C. Coverslips were mounted in Vectashield containing 4′,6-diamidino-2-phenylindole to visualize DNA (Vector Laboratories, Burlingame, CA) and sealed with nail polish.
To measure the interkinetochore distance, LLC-Pk1 cells expressing green fluorescent protein (GFP)-CenpA were used. For nocodazole treatment, cells were incubated with 3.3 μM nocodazole for 4 h. Cells were transfected with mCherry TPX2 or mCherry TPX2-710 and examined at 48 h after transfection. The number of cells/kinetochore pairs analyzed were as follows: nocodazole-treated cells, 6/45; no transfection, nonaligned, 8/40; no transfection, aligned, 5/43; transfection with mCherry TPX2, aligned, 7/40; transfection with mCherry TPX2-710, aligned, 9/40; and transfection with mCherry TPX2, nonaligned, 6/42. For the experiments with transfected cells, we chose cells that contained similar levels of red fluorescence from the transfected protein.
Photoactivatable (PA)-EGFP and mCherry-tagged TPX2 were generated by subcloning hTPX2 into pCMV-PA-EGFP or pCMV-mCherry (Trieselmann et al., 2003 ; Tulu et al., 2003 ). Nucleofection was performed using an Amaxa nucleofector following the protocol recommended by the manufacturer (Lonza Walkersville, Walkersville, MD). Cell lines expressing EGFP- or PA-EGFP-TPX2 were prepared as described previously (Wadsworth et al., 2005 ). Full-length human Eg5, the kind gift from Dr. Ann Blangley, was tagged with EGFP for transfection into mammalian cells. Proteins tagged with EGFP are referred to as having a GFP tag in this manuscript. The CC1 fragment of p150 was prepared as described previously (Ferenz and Wadsworth, 2007 ).
For glutathione transferase (GST) pull-down experiments, the N-terminal half of TPX2 (TNT, 1-364), the C-terminal half of TPX2 (TCT, 365-745), and TCT lacking the C-terminal 35 amino acids (TCTΔ35) were subcloned into pGEX-4T-1 (GE Healthcare, Little Chalfont, Buckinghamshire, United Kingdom) and purified from bacteria (BL-21). His-tagged Eg5 (amino acids 1-685, corresponding to the head-stalk region) was expressed in bacteria. GST pull-down was performed as described previously (Ma et al., 2009 ). In the experiment shown in Figure 4, 1/70 and one half the volume of supernatants and pellets were applied to the gel, respectively.
Images were acquired using an Eclipse TE300 microscope (Nikon, Tokyo, Japan) equipped with a 100× phase numerical aperture 1.4 objective lens, a spinning disk confocal scan head (PerkinElmer, Wellesley, MA), and an Orca ER cooled charge-coupled device camera (Hamamatsu, Bridgewater, NJ). All images were taken using a dual-wavelength filter cube. Image acquisition was controlled by MetaMorph software (Molecular Devices, Sunnyvale, CA). Photoactivation was performed as described previously (Tulu et al., 2003 ; Ferenz and Wadsworth, 2007 ). Photoactivations that were performed within 3.5 μm of a spindle pole were defined as near the pole; photoactivation >3.5 μm from the nearest pole were defined as far from the pole.
The movement of photoactivated regions was measured as described, with the following modification. The position of the edge of the activated region closest to the chromosomes was tracked; in previous work, measurements were made using the edge of the activated region closest to the pole. Individual photoactivated regions, corresponding to bundles of kinetochore microtubules were used for these and our previous measurements. The values reported here differ from those reported previously because the poleward edge of the photoactivated mark moves faster than the edge nearest to the chromosomes (Ferenz and Wadsworth, 2007 ). In prometaphase and metaphase cells, spindle length remained constant as judged by spindle pole position, which was visible due to dim fluorescence of activated tubulin. Similarly, in anaphase cells, which were photoactivated in the interzonal region, pole-to-pole distance did not change over the time frame of the experiment (typically <3 min). In telophase cells, anaphase B was completed before photoactivation; spindle pole position was not marked in these cells due to the difficulty in precisely locating the spindle pole.
To inhibit microtubule dynamics, cells were incubated with nocodazole at 10 nM for 1 h before imaging. Antibodies to MCAK and Kif2a were used as described previously (Ferenz and Wadsworth, 2007 ). To inhibit dynein, cells were microinjected with p150 CC1 as described previously (Wadsworth, 1999 ). Before microinjection, all solutions were centrifuged at maximal speed in a microcentrifuge at 4°C through a syringe tip filter held in a microcentrifuge tube. siRNA to Eg5 was performed as described previously (Tulu et al., 2006 ) by using the sequence 5′-CUGAAGACCUGAAGACAAU-3′. Monastrol was prepared in dimethyl sulfoxide and used at 200 μM. To assay microtubule assembly near chromosomes and centrosomes, cells were incubated with 3.3 μM nocodazole for ~3 h before washout with drug-free medium (Tulu et al., 2006 ).
To examine the dynamic behavior of TPX2 in live cells, we transfected LLC-Pk1 cells with EGFP- or PA-EGFP–tagged TPX2 and generated cell lines expressing each fusion protein (Wadsworth et al., 2005 ; hereafter LLC-Pk1-GFP-TPX2 and LLC-Pk1-PA-GFP-TPX2). The distribution of the tagged proteins in live cells was indistinguishable from endogenous TPX2 observed in cells fixed and stained with antibodies to TPX2 (Supplemental Figure 1). Time-lapse imaging showed that GFP-TPX2 is nuclear during interphase (Wittmann et al., 2000 ; Gruss et al., 2002 ) and associates with microtubules immediately upon nuclear envelope breakdown. In prometaphase and metaphase cells, TPX2 localizes along spindle microtubules, but not detectably on polar astral microtubules, and is enriched toward the spindle poles. In anaphase and telophase cells, TPX2 localizes to interzonal and midbody microtubules, respectively (Supplemental Figure 1 and Supplemental Movie 1). Because overexpression of TPX2 has been reported previously to result in mitotic cells with aberrant spindle morphology (Garrett et al., 2002 ; Gruss et al., 2002 ), we quantified spindle morphology in both cell lines (Supplemental Figure 1). We found that the percentage of multipolar and monopolar spindles was increased in cells expressing either PA-GFP- or GFP-TPX2 as compared with parental cells. The mitotic index of GFP-TPX2 cells, but not PA-GFP-TPX2 cells, was reduced when compared with control cells. These features were not completely unexpected because the cells express both endogenous TPX2 and the fluorescent construct. In addition, the fluorescent tag, which is located at the N terminus of TPX2, could interfere with the activation of Aurora A kinase (Bayliss et al., 2003 ). The alternative strategy, placing the tag on the C terminus, was not used because the C terminus also mediates important aspects of TPX2 function (see below). However, only cells with morphologically normal mitotic spindles were selected for experiments, and these cells progressed through mitosis without any detectable abnormalities.
We measured the dynamic behavior of TPX2 and microtubules in LLC-Pk1 cells by using photoactivation of fluorescence (see Materials and Methods). TPX2 was photoactivated in the half-spindle of prometaphase and metaphase cells and on interzonal microtubules in anaphase and telophase cells (Figure 1A and Supplemental Movie 2). The average velocity of photoactivated marks was determined from kymographs (Ferenz and Wadsworth, 2007 ), by using the edge of the mark closest to the chromosomes (see Materials and Methods).
The results of these experiments demonstrate that TPX2 moves poleward in the half-spindle, at a rate of ~1.4 μm/min in metaphase and prometaphase cells (Table 1). In contrast, TPX2 on interzonal microtubules was nearly static (~0.3 μm/min) (Figure 1, A–C, and Table 1). Because motion of TPX2 in the half-spindle seemed to decrease near the pole (Figure 1B), we compared TPX2 transport after photoactivation near and far from the pole (see Materials and Methods). The data show that the rate of TPX2 motion was significantly decreased near spindle poles (Figure 1C and Table 1). Together, these results demonstrate that the dynamic behavior of TPX2 is regionally regulated in the mammalian mitotic spindle.
We also measured the rate of microtubule flux using photoactivation of PA-GFP-tubulin (Tulu et al., 2003 ; Ferenz and Wadsworth, 2007 ). In the half-spindle of prometaphase and metaphase cells, microtubule flux occurs at average rates of 0.86 ± 0.3 and 0.96 ± 0.4 μm/min, respectively. These values are lower than reported previously for these cells because we measured the edge of the photoactivated mark near the chromosomes (see Materials and Methods). These values are consistent with rates of flux measured in other tissue culture cells (Cameron et al., 2006 ). The rate of microtubule flux is statistically significantly different from the rate of TPX2 motion (Figure 1D). However, on interzonal microtubules in anaphase and telophase cells, the rate of motion of microtubules and TPX2 were not significantly different (Figure 1D). These results show that the poleward motion of TPX2 in metaphase cells occurs at a rate that is faster than microtubule flux in these cells.
Because TPX2 is a microtubule-binding protein (Schatz et al., 2003 ), poleward flux of microtubules could contribute to motion of TPX2. We treated cells with low concentrations of nocodazole to suppress microtubule dynamics (Vasquez et al., 1996 ) and reduce microtubule flux. Under these conditions, the rate of TPX2 poleward motion was significantly reduced in prometaphase and metaphase cells (Figure 2, A and B). To determine whether the slow motion of TPX2 in nocodazole-treated cells resulted from the slow, residual flux in these cells, we compared the rates of microtubule flux and TPX2 motion in nocodazole-treated cells (Figure 2C). The data show that the rate of microtubule flux is reduced to a greater extent than TPX2 motion, demonstrating that flux alone is not responsible for TPX2 motion under these conditions.
In addition to reducing microtubule flux with nocodazole, we microinjected cells with antibodies directed against human Kif2a, a kinesin-13 that has been shown to be required for poleward flux of microtubules in human cells (Ganem et al., 2005 ) and contribute to flux in LLC-Pk1 cells (Ferenz and Wadsworth, 2007 ). In this experiment, we also coinjected anti-MCAK antibodies, a treatment that prevents monopolar spindle formation after inhibition of Kif2a (Ganem et al., 2005 ; Ferenz and Wadsworth, 2007 ). After microinjection, the rate of TPX2 poleward motion was reduced in both prometaphase and metaphase cells (Figure 2, A and B), further demonstrating that poleward motion of TPX2 in the half-spindle is sensitive to inhibition of microtubule flux.
TPX2 was originally identified as a factor that was required for the dynein-dependent localization of the kinesin Xklp2 to spindle poles (Wittmann et al., 2000 ), suggesting that dynein is required for TPX2 transport. To examine this possibility, cells were microinjected with the CC1 fragment of the p150 subunit of dynactin, a treatment that interferes with the dynein–dynactin interaction and blocks dynein-dependent processes in cells (Quintyne et al., 1999 ; Gaetz and Kapoor, 2004 ; Ferenz and Wadsworth, 2007 ). The results show that the rate of poleward motion of TPX2 in prometaphase and metaphase cells is reduced after microinjection of CC1 (Figure 3, A and B, and Supplemental Movie 3). Furthermore, TPX2 was more uniformly distributed along spindle fibers in CC1 injected compared with control cells (Figure 3C). Inhibition of dynein/dynactin by microinjection of CC1 resulted in accumulation of the p150 subunit of dynactin at kinetochores but did not alter the localization of Kif2a at spindle poles (Supplemental Figure 2, A and B), consistent with previous work (Howell et al., 2001 ; Ferenz and Wadsworth, 2007 ).
A direct interaction between the C-terminal 35 amino acids of TPX2 and Eg5 has been demonstrated using purified X. laevis proteins (Eckerdt et al., 2008 ), and each protein has been reported to accumulate at spindle poles. We examined the distribution of myc-GFP-Eg5 and mCherry-TPX2 in LLC-Pk1 cells throughout mitosis by using spinning disk confocal microscopy. We found that the two proteins colocalized along spindle microtubules from prophase to anaphase and were enriched at spindle poles. In telophase cells, TPX2, but not Eg5, associated with bundles of midbody microtubules (Supplemental Figure 1E).
Next, we examined the contribution of Eg5 to poleward motion of TPX2 in the mammalian spindle. Because poleward transport of TPX2 and Eg5 in the half-spindle are dynein dependent (Uteng et al., 2008 ), we hypothesized that Eg5 could contribute to transport by linking TPX2 to dynein. To test this, we measured poleward motion of TPX2 in cells that were treated with siRNA to deplete, or monastrol to inhibit, Eg5 (Mayer et al., 1999 ). Poleward movement of TPX2 was dramatically reduced on monastrol-induced monopolar spindles, compared with motion in untreated prometaphase cells (Figure 4, A and C). In Eg5 siRNA-treated cells, poleward movement of TPX2 was also statistically significantly reduced, compared with untreated prometaphase cells (Figure 4, A and C, and Supplemental Movie 4). Poleward motion of TPX2 in monastrol-treated and siRNA-depleted cells was not significantly different (p = 0.23).
To determine whether mammalian TPX2 and Eg5 interact, we performed GST pull-down assays using the C- or N-terminal half of TPX2 (TCT and TNT), or TCT lacking the last 35 amino acids (TCTΔ35), each tagged with GST and a human Eg5 head-stalk construct (Eg5HS) (Trieselmann et al., 2003 ; Eckerdt et al., 2008 ). The results showed that Eg5HS interacted with the TCT fragment more strongly than with TNT or TCTΔ35 (Figure 4B). This interaction is likely to be weak or dynamic, because only a fraction of the input protein was recovered. Consistent with this possibility, standard immunoprecipitation failed to show an interaction between Eg5 and TPX2 (data not shown).
To determine whether the C terminus of TPX2 is important for poleward motion, we tagged TPX2 lacking the terminal 35 amino acids (TPX2-710) with PA-GFP and performed photoactivation. For this experiment, we selected cells containing morphologically normal bipolar spindles (see below). After photoactivation in the half-spindle, poleward motion of PA-GFP-TPX2-710 was greatly reduced, compared with control cells, and the photoactivated protein rapidly redistributed throughout the spindle (Figure 4D and Supplemental Movie 5). These data show that TPX2 and Eg5 colocalize in mammalian cells, that the purified mammalian proteins interact in vitro and that the C terminus of TPX2 is required for efficient poleward transport.
To determine whether the TPX2–Eg5 interaction contributes to microtubule organization during spindle formation, we examined live and fixed cells overexpressing mCherry-tagged full-length TPX2 or TPX2-710. Both full-length TPX2 and TPX2-710 associated with microtubules in transfected cells (Figure 5, A and C, and Supplemental Figure 3). In live cells expressing GFP-tubulin, expression of TPX2-710 resulted in a disorganized spindle, characterized by bundles of microtubules near chromosomes, and failure to progress through mitosis (Figure 5A and Supplemental Movie 6). We quantified the spindle phenotype using fixed cells (Figure 5, B and C). Approximately 40% of cells expressing TPX2-710 showed a disorganized spindle, characterized by microtubules extending into the cell periphery and bundles of microtubules near chromosomes, and defects in chromosome alignment. The remainder of the cells had normal bipolar or collapsed monopolar spindles. Mitotic spindles in cells overexpressing full-length TPX2 were either bipoles or monopoles, consistent with previous work showing that overexpression of TPX2 induces spindle shortening (Figure 5, A and C, and Supplemental Figure 3; Eckerdt et al., 2008 ). Less than 10% of cells expressing full-length TPX2 showed a disorganized spindle phenotype. These results show that expression of TPX2-710 results in supernumerary microtubules in the cell periphery and disorganized bundles of microtubules near chromosomes.
To determine whether the microtubule bundles formed near chromosomes corresponded to kinetochore fibers, we fixed and stained cells expressing TPX2-710 to visualize microtubules and kinetochores (Figure 5C). In control cells, and cells expressing full-length TPX2, bundles of microtubules terminated at Hec1-positive kinetochores (Figure 5C, top and middle, insets). In cells expressing TPX2-710, some of the microtubule bundles that form in these cells terminate at Hec1-positive sites, but unattached kinetochores and syntelic attachments, were frequently observed (Figure 5C, bottom, insets).
Next, we examined microtubule stability in TPX2-transfected cells. Bundles of microtubules in cells expressing TPX2 or TPX2-710 were present after incubation at 4°C for 20 min (Yang et al., 2007 ), a treatment that disassembles labile microtubules but not kinetochore fiber microtubules. However, unlike microtubule bundles in control cells or cells expressing full-length TPX2, microtubule bundles in cells expressing TPX2-710 were disorganized (Figure 5D).
Finally, because many chromosomes failed to align at the spindle equator in the cells overexpressing TPX2-710, we measured the interkinetochore distance in control cells and cells expressing TPX2 or TPX2-710 (Figure 5E). The results show that interkinetochore distance was statistically significantly decreased in cells expressing truncated TPX2 compared with control metaphase cells and with cells expressing full-length TPX2. Interkinetochore distance was also reduced in cells expressing full-length TPX2 compared with control cells. These results demonstrate that expression of truncated TPX2 interferes with chromosome alignment and development of interkinetochore tension.
To determine whether the TPX2–Eg5 interaction impacts microtubule formation near chromosomes, we used a nocodazole washout assay (Tulu et al., 2006 ). When control LLC-Pk1 cells expressing GFP-tubulin are released from nocodazole, microtubules assemble near chromosomes and at centrosomes and subsequently coalesce to form a bipolar spindle (Figure 6A and Supplemental Movie 7). In contrast, when cells expressing full-length or TPX2-710 were released from nocodazole, microtubule formation in the chromosome region was greatly enhanced and coalescence of microtubule foci into a bipolar spindle failed (Figure 6A and Supplemental Movies 8 and 9). In some cases, discrete puncta of fluorescence were observed in the chromosome region, probably corresponding to microtubules forming at kinetochores (Figure 6A, bottom, 36 min). Because the level of overexpression of each protein varies in the transfected cells, we could not quantitatively compare the extent of microtubule formation in these experiments. However, although both full-length and truncated TPX2 promoted microtubule formation near chromosomes in this assay, only full-length TPX2 accumulated at the center of microtubule foci, whereas the truncated protein was mostly diffuse (Figure 6A, right), consistent with its behavior after photoactivation.
The results of our experiments demonstrate that TPX2 in the half-spindle is transported toward spindle poles during prometaphase and metaphase of mitosis. TPX2 in the interzone, and near spindle poles, is transported much more slowly. Poleward transport of TPX2 is sensitive to inhibition of dynein, Eg5, and microtubule flux. Transport requires the C-terminal 35 amino acids of TPX2, and overexpression of TPX2 lacking this domain results in defects in kinetochore fiber formation, chromosome attachment, spindle formation and mitotic progression. Our results demonstrate that the dynamics of TPX2 in the spindle is regionally regulated and that an interaction of TPX2 with Eg5 is important for spindle microtubule organization and kinetochore fiber formation.
It is well established that spindle microtubules move poleward in mitotic cells, but our understanding of the dynamic behavior of other spindle components is still incomplete. Recent work shows that the mitotic motor Eg5 is transported toward microtubule minus ends in the half-spindle of Xenopus extract spindles in a dynein-dependent manner and is static in the interzone (Uteng et al., 2008 ). In Drosophila cells, Eg5 rapidly exchanges with spindle microtubules, making short poleward excursions (Cheerambathur et al., 2008 ). We now show that TPX2, like Eg5 in X. laevis spindles, is transported poleward in the half-spindle and is static on interzonal microtubules and near spindle poles (Uteng et al., 2008 ). In LLC-Pk1 cells during anaphase and telophase, spindle elongation overlaps temporally with chromosome-to-pole motion and was typically completed before photoactivation of interzonal microtubules. Thus, the absence of poleward motion of TPX2 in the interzone could result because TPX2 is bound to static, or slowly moving, microtubules and/or static Eg5 in the interzone (Uteng et al., 2008 ).
Our data support the view that motion of TPX2 in the half-spindle results from transport along fluxing microtubules. First, TPX2 motion was faster than microtubule flux in these cells, suggesting that flux alone cannot account for the poleward motion of TPX2. Second, in cells treated to reduce microtubule flux, the motion of TPX2 was faster than the residual microtubule flux. Third, the extent to which TPX2 motion in the half-spindle was reduced after inhibition of dynein or Eg5 was greater than the extent to which these same inhibitors altered microtubule flux (Ferenz and Wadsworth, 2007 ). Finally, the observation that TPX2-710 fails to move poleward but shows diffuse labeling along microtubules after photoactivation, supports the idea that TPX2 motion is dependent on an interaction with Eg5.
Many spindle components are enriched at spindle poles, and in several cases dynein contributes to this accumulation. For example, the microtubule-associated protein NuMA directly interacts with dynein/dynactin for transport to spindle poles, where it contributes to pole focusing (Merdes et al., 2000 ). Poleward motion of spindle assembly checkpoint proteins is also dynein dependent, but how dynein/dynactin mediates this transport is not yet clear (Howell et al., 2001 ). Numerous other proteins accumulate at spindle poles, but the contribution, if any, of dynein has not been determined (i.e., XMAP215). Here, we show that TPX2 moves poleward in a dynein-dependent manner and that this is mediated by an interaction with Eg5.
Understanding how dynein mediates transport of spindle components is complicated by the fact that dynein also contributes to spindle microtubule organization and motion (Gaglio et al., 1997 ; Heald et al., 1997 ; Ferenz and Wadsworth, 2007 ). Although poleward microtubule motion, or flux, has been reported to be insensitive to inhibition of dynein (Sawin and Mitchison, 1991 ; Maiato et al., 2005 ; Cameron et al., 2006 ; Ferenz and Wadsworth, 2007 ), recent studies show that spindle flux has two velocity modes and that the flux rate is reduced near spindle poles (Yang et al., 2008 ). Inhibition of dynein activity shifts the velocity distribution to a single mode and eliminates the regional variation in flux rate, demonstrating that dynein contributes to spindle microtubule flux behavior (Yang et al., 2008 ). We observed that, like microtubule flux, TPX2 transport is greatly reduced near spindle poles. Regional differences in TPX2 behavior could result from differences in microtubule behavior near and far from the spindle pole, association of TPX2 with distinct classes of spindle microtubules, differences in motor behavior in different spindle locations, and/or distance from the chromosome derived Ran-gradient (Kalab et al., 2006 ). Understanding the regulation of spindle microtubule organization and transport is an important goal of future studies.
TPX2 is required for microtubule assembly in the chromatin-dependent spindle assembly pathway and the N-terminal Aurora A interacting domain of TPX2 is essential for this activity (Bird and Hyman, 2008 ). Cells expressing TPX2 lacking the Aurora A interacting region, or with point mutations that block the TPX2-Aurora A interaction, assemble functional bipolar spindles that are very short (Bird and Hyman, 2008 ). The C-terminal half of TPX2 is required for its spindle localization and overexpression of a large C-terminal domain blocks centrosome separation in cultured Xenopus cells (Brunet et al., 2004 ; Eckerdt et al., 2008 ). Microinjection of excess Eg5 rescues this defect, demonstrating that an interaction with TPX2 regulates Eg5 function in vivo (Eckerdt et al., 2008 ). In addition to these activities, we show that overexpression of TPX2-710, but not full-length TPX2, results in the formation of extensive bundles of microtubules near chromosomes in intact cells. Based on this observation, we hypothesize that poleward transport of TPX2 down regulates the microtubule-nucleating activity of TPX2 near kinetochores. In the nocodazole washout assay, both full-length TPX2 and TPX2-710 induced extensive microtubule formation near chromosomes, further emphasizing the need for regulation of TPX2 activity during spindle formation.
Our observations are consistent with a model (Figure 6B) in which Ran in the vicinity of chromosomes activates TPX2 leading to microtubule formation (Figure 6Ba), either directly or by activation of other Ran-dependent proteins (Trieselmann et al., 2003 ; Groen et al., 2009 ). Chromosome-associated microtubules are then organized into mature kinetochore fibers and incorporated into the spindle in an Eg5 and dynein-dependent manner (Figure 6B, b and c) (Maiato et al., 2004 ). Expression of full-length TPX2 can induce spindle shortening, a phenotype that may result from inhibition of Eg5-generated outward forces (Eckerdt et al., 2008 ) (Figure 6Bc, question mark in d) but does not detectably alter kinetochore fiber formation (Figure 6Bd). In contrast, interfering with the Eg5/TPX2 interaction, by expression of TPX2-710, results in excessive microtubule formation near chromosomes (Figure 6Be) and defects in chromosome alignment, kinetochore fiber organization, and mitotic progression. Our results demonstrate that the interaction between TPX2 and Eg5 is important for kinetochore fiber formation and may function to link microtubules formed in the chromosome-dependent pathway to dynein for incorporation into the spindle.
We thank the members of the Lee and Ross laboratories (University of Massachusetts, Amherst, MA) for constructive comments during the course of this work and Dr. L. Collins for reading the manuscript. We thank Drs. Alexey Khodjakov (Wadsworth Center, New York State Department of Health, Albany, NY) and Claire Walczak (Indiana University, Bloomington, IN) for antibodies, Drs. George Patterson and Jennifer Lippincott-Schwartz (National Institutes of Health, Bethesda, MD) for PA-GFP, and Drs. Anne Blangy (Centre de Recherches de Biochimie and Macromoléculaire, Montpellier, France) and Susan Gilbert (Rennselaer Polytechnic Institute, Troy, NY) for Eg5 constructs. We especially thank Dr. John Willoughby (University of Massachusetts) for advice and reagents for the GST pull-down experiments. This work was supported by grant GM 59057 from the National Institutes of Health (to P. W.) and a Canadian Cancer Society grant (to A.W.).
This article was published online ahead of print in MBC in Press (http://www.molbiolcell.org/cgi/doi/10.1091/mbc.E09-07-0601) on January 28, 2010.