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Vol. 18, Issue 1, 282-294, January 2007

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The Interplay of the N- and C-Terminal Domains of MCAK Control Microtubule Depolymerization Activity and Spindle Assembly

Stephanie C. Ems-McClung^*, Kathleen M. Hertzer^*, Xin Zhang, Mill W. Miller, and Claire E. Walczak^*

*Medical Science Program and Department of Biology, Indiana University, Bloomington, IN 47405; and Department of Biological Sciences, Wright State University, Dayton, OH 45435

Submitted August 17, 2006; Revised September 27, 2006; Accepted October 30, 2006
Monitoring Editor: Stephen Doxsey

	ABSTRACT

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Spindle assembly and accurate chromosome segregation require the proper regulation of microtubule dynamics. MCAK, a Kinesin-13, catalytically depolymerizes microtubules, regulates physiological microtubule dynamics, and is the major catastrophe factor in egg extracts. Purified GFP-tagged MCAK domain mutants were assayed to address how the different MCAK domains contribute to in vitro microtubule depolymerization activity and physiological spindle assembly activity in egg extracts. Our biochemical results demonstrate that both the neck and the C-terminal domain are necessary for robust in vitro microtubule depolymerization activity. In particular, the neck is essential for microtubule end binding, and the C-terminal domain is essential for tight microtubule binding in the presence of excess tubulin heterodimer. Our physiological results illustrate that the N-terminal domain is essential for regulating microtubule dynamics, stimulating spindle bipolarity, and kinetochore targeting; whereas the C-terminal domain is necessary for robust microtubule depolymerization activity, limiting spindle bipolarity, and enhancing kinetochore targeting. Unexpectedly, robust MCAK microtubule (MT) depolymerization activity is not needed for sperm-induced spindle assembly. However, high activity is necessary for proper physiological MT dynamics as assayed by Ran-induced aster assembly. We propose that MCAK activity is spatially controlled by an interplay between the N- and C-terminal domains during spindle assembly.

	INTRODUCTION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Bipolar spindle assembly is essential for the faithful segregation of chromosomes into two daughter nuclei. Defects in this process are often associated with aneuploidy, which can lead to cancer or birth defects. The bipolar spindle is composed of a dynamic array of microtubules (MTs) and their associated proteins, including various MT-associated proteins and motor proteins, which are essential for proper spindle assembly (Gadde and Heald, 2004; Mogilner et al., 2006). Proper MT dynamics are highly regulated during the transition between interphase and mitosis, and many regulators of MT dynamics are critical for proper spindle assembly both in cells and in Xenopus laevis egg extracts (Kline-Smith and Walczak, 2004). In egg extracts, spindle assembly is dominated by chromatin-mediated MT nucleation and organization (Sawin and Mitchison, 1991). During chromatin-mediated spindle assembly, randomly nucleated MTs around chromatin become organized into an astral array that leads to the formation of a bipolar spindle due to the generation of anti-parallel overlapping MTs that are extended and focused into poles by molecular motors and MT-associated proteins (Walczak et al., 1997, 1998; Sharp et al., 2000; Gaetz and Kapoor, 2004; Mitchison et al., 2004, 2005; Goshima et al., 2005; Koffa et al., 2006). In addition to relying on molecular motors to organize and slide MTs, bipolarity also depends on the regulation of proper physiological MT dynamics by depolymerizing proteins that include depolymerizing kinesins and Op18/stathmin (Andersen et al., 1997; Ganem and Compton, 2004; Rogers et al., 2004; Sharp et al., 2005). One major signal chromatin uses to promote spindle assembly is the activation of the small GTPase Ran via its chromatin-linked exchange factor, RCC1 (Bilbao-Cortes et al., 2002; Moore et al., 2002; Li et al., 2003). Addition of Ran-GTP, the activated form of Ran, to egg extracts results in bipolar spindle formation from the proper regulation of MT nucleation, MT dynamics, and molecular motor activities (Wilde and Zheng, 1999; Carazo-Salas et al., 2001; Wilde et al., 2001). Although Ran-induced spindle activities are dependent on chromatin, it is unclear how many chromatin-induced activities are independent of Ran. One such activity is the stabilization of MTs around chromatin by the chromosome passenger complex through the regulation of the depolymerizing kinesin MCAK and Op18/stathmin (Sampath et al., 2004; Gadea and Ruderman, 2006).

Kinesins are molecular motors that convert the chemical energy of ATP into mechanical work specifically on MTs. The majority of kinesins are homodimeric proteins that walk along MTs carrying various cargos such as vesicles, proteins, and chromosomes (Hirokawa and Takemura, 2004; Wozniak et al., 2004; Miki et al., 2005). Many kinesins are important for mitosis and spindle assembly such that upon depletion by RNAi in cells or by immunodepletion in extracts, defects occur that either inhibit mitosis or impair spindle assembly (Walczak et al., 1998; Goshima and Vale, 2005; Zhu et al., 2005). Kinesins are categorized into 14 families (Lawrence et al., 2004; Miki et al., 2005) and are composed of four different domains: a conserved catalytic MT-stimulated ATPase domain; a class-specific neck domain that is essential for motility (Vale and Goldstein, 1990; Case et al., 1997; Endow and Waligora, 1998); a "stalk" domain that often functions to dimerize the protein; and the "tail" domain that binds to cargo and/or regulates activity (Hirokawa and Takemura, 2004). The location of these domains within the polypeptide is dependent on the specific family of kinesins, but the neck domain is always adjacent to the catalytic domain (Vale et al., 2000). Although most kinesins walk along MTs, members of the Kinesin-13 family catalytically induce MT depolymerization at both ends of a MT and are necessary to regulate MT dynamics (Desai et al., 1999a, 1999b; Hunter et al., 2003; Helenius et al., 2006).

Structurally, the Kinesin-13s have a central catalytic domain with the neck domain amino-terminal to the catalytic core. The neck and catalytic core are sufficient for MT depolymerization activity in vitro and in vivo (Maney et al., 2001; Newton et al., 2004; Ogawa et al., 2004; Hertzer et al., 2006), with the positively charged neck domain being particularly important for depolymerization activity (Ovechkina et al., 2002). The N-terminal domain of MCAK is necessary (Maney et al., 1998; Wordeman et al., 1999) and perhaps sufficient (Walczak et al., 2002) to target MCAK to kinetochores. The C-terminal domain is responsible for dimerization and plays a role in regulating the ATPase activity of MCAK (Maney et al., 2001; Moore and Wordeman, 2004; Hertzer et al., 2006). Biochemically, MCAK specifically binds to the ends of MTs where it either stabilizes an already bent conformation or induces a curvature at the MT end (Desai et al., 1999b; Moore and Wordeman, 2004; Ogawa et al., 2004; Helenius et al., 2006; Hertzer et al., 2006). In dynamic MTs, this curved protofilament within the MT is unstable and is thought to cause the MT polymer to depolymerize (Desai and Mitchison, 1997; Nogales, 2000). For in vitro–stabilized MTs, it is unclear whether MCAK depolymerizes MTs by removing individual tubulin dimers or tubulin oligomers (Desai et al., 1999b; Hunter et al., 2003; Moores et al., 2006; Tan et al., 2006), but it is thought that the ultimate end product from MCAK-induced MT depolymerization is tubulin heterodimer (Desai et al., 1999b). MCAK may processively depolymerize MTs by a mechanism that involves one-dimensional (1-D) diffusion of MCAK along the MT lattice or by the accumulation of tubulin-MCAK rings at the MT end (Hunter et al., 2003; Helenius et al., 2006; Tan et al., 2006), but it remains unclear how these mechanisms are utilized during depolymerization of dynamic MTs and how the different domains of MCAK contribute to this depolymerization activity.

MCAK predominantly localizes to three regions during mitosis: the spindle poles, the cytoplasm, and the centomeres/kinetochores (Wordeman and Mitchison, 1995; Walczak et al., 1996; Maney et al., 1998). It is unclear what function MCAK plays at the spindle poles, but more is known about the functions of MCAK in the cytoplasm and at the kinetochore (Kinoshita et al., 2006). MCAK was originally identified in cells as a kinesin that associates with mitotic centromeres (Wordeman and Mitchison, 1995) and is now known to regulate cytoplasmic MT dynamics in interphase and mitosis (Maney et al., 2001; Kline-Smith and Walczak, 2002). In extracts, MCAK is the major catastrophe regulator, and depletion perturbs MT dynamics, resulting in large asters with increased amounts of MT polymer that are unable to assemble into a bipolar spindle (Walczak et al., 1996; Tournebize et al., 2000). Antibody inhibition or RNAi of MCAK in cells causes excess polymer formation and/or monopolar spindles that interfere with normal bipolar spindle assembly (Walczak et al., 1996; Kline-Smith and Walczak, 2002; Cassimeris and Morabito, 2004; Ganem and Compton, 2004; Stout et al., 2006). The working model for MCAK inhibition is that the excess MT polymer formation and monopolar spindles are due to suppressed cytoplasmic MT dynamics, which prevent the appropriate capture of MTs by kinetochores and/or the appropriate sorting by molecular motors around chromatin.

MCAK localizes to the inner kinetochore via its N-terminal kinetochore targeting domain and regulates proper kinetochore-MT attachments by depolymerizing MTs that attach incorrectly (Maney et al., 1998; Wordeman et al., 1999; Walczak et al., 2002; Kline-Smith et al., 2004). Overexpression or injection of a dominant negative construct in cells or extracts that replaces endogenous MCAK at the centromere results in normal bipolar spindle assembly, but chromosome alignment and segregation are disrupted (Maney et al., 1998; Walczak et al., 2002; Kline-Smith et al., 2004). Other members of the Kinesin-13 family are also implicated in driving chromosome segregation in anaphase by depolymerizing MTs from both ends (Ganem and Compton, 2004; Rogers et al., 2004; Ganem et al., 2005; Sharp et al., 2005). MCAK and the related Kinesin-13, Klp10A, also associate with the +TIP-tracking proteins APC and EB1, and the interactions may be critical for their ability to +TIP-track on MTs (Banks and Heald, 2004; Mennella et al., 2005; Moore et al., 2005). It is still unknown how or if +TIP tracking is required for spindle assembly or for regulation of MT dynamics in extracts or in cells. MCAK kinetochore targeting, depolymerization activity, tip-tracking, corrections of mal-attached kinetochore MTs, and spindle assembly are all regulated by phosphorylation (Andrews et al., 2004; Lan et al., 2004; Ohi et al., 2004; Holmfeldt et al., 2005; Moore et al., 2005; Knowlton et al., 2006), but the detailed molecular mechanisms of these complex regulated processes remain unknown. Despite the progress that has been made in identifying the mechanism of MCAK-induced MT depolymerization and understanding its physiological functions, many questions remain unanswered. Here we present the first comprehensive domain analysis of MCAK that correlates the roles of different domains both biochemically with purified proteins and physiologically in egg extracts. We show that there is an interplay between the N- and C-terminal domains that is necessary for physiological MT dynamics in extracts and that the N-terminal domain is necessary for efficient spindle assembly even though it is not required for in vitro MT depolymerization activity, MT and tubulin binding, or MT end binding. Additionally, we identify MCAK as an important regulator of spindle bipolarity, which is controlled by the N- and C-terminal domains of MCAK.

	MATERIALS AND METHODS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
Protein Expression and Purification
Green fluorescent protein (GFP) tagged expression constructs used in this work were created by subcloning the MCAK coding sequence from pEGFPC1 deletion constructs (Hertzer et al., 2006) into pFastBac1-GFP using SacI and KpnI restriction sites. Point mutations within the catalytic domain were created using the QuikChange Site-Directed Mutagenesis System (Stratagene, La Jolla, CA). All clones were verified by sequencing. The GFP-tagged proteins were then expressed using the Bac-to-Bac baculovirus expression system (Invitrogen, Carlsbad, CA) in HighFive insect cells. GFP-MCAK (GMCAK) and GMCAK mutants were purified to near homogeneity by conventional chromatography using ion exchange and gel filtration as previously described (Desai et al., 1999b). Modifications of GMCAK are designated as GM for GFP-MCAK followed by the amino acid numbers in parentheses. Protein concentrations are expressed in terms of monomer concentration and were quantified from Colloidal Coomassie Blue G-250–stained SDS polyacrylamide gels and densitometry using BSA as a standard. Densitometry was done using ImageJ software (NIH). At least two individual preparations of proteins were used in the described experiments. His-RanL43E was expressed, purified, and loaded with GTP as previously described (Ems-McClung et al., 2004). 6His-GFP was expressed in BL21(DE3) bacterial cells at 16°C for 24 h and was purified using NiNTA agarose as previously described (Ems-McClung et al., 2004).

Microtubule Preparation
Microtubules were polymerized using either guanylyl-(a,b)-methylene-diphosphonate (GMPCPP; Jena Scientific, Jena, Germany) alone or GMPCPP and paclitaxel to create stable tubulin polymer (Desai and Walczak, 2001; Hertzer et al., 2006). Briefly, recycled tubulin was clarified at 45,000 rpm for 5 min at 2°C in a TLA100 rotor (Beckman, Fullerton, CA). The tubulin concentration was determined by absorbance at 280 nm using 115,000 M^–1 cm^–1 as the extinction coefficient. Clarified tubulin was diluted to 10 µM for depolymerization and end binding assays or 40 µM for tubulin binding assays in BRB80 (80 mM PIPES, pH 6.8, 1 mM MgCl₂, 1 mM EGTA, 1 mM DTT) and polymerized with 0.5 mM GMPCPP at 37°C for 30 min. For GMPCPP/paclitaxel stabilized MTs, 10 µM paclitaxel was added 20 min into the polymerization of the MTs, and the MTs were then allowed to polymerize an additional 10 min. All MT substrates were sedimented at 45,000 rpm at 35°C in a TLA100 (5 min) or TLA100.3 (11 min) rotor. For GMPCPP stabilized MTs, the MT pellet was either resuspend in BRB80 or BRB49 (49 mM PIPES, pH 6.8, 0.61 mM MgCl₂, 0.61 mM EGTA, 1 mM DTT). For GMPCPP/paclitaxel stabilized MTs, the MT pellet was resuspended in BRB80 containing 10 µM paclitaxel.

MT EC₅₀ Assays
MT EC₅₀ assays were done essentially as previously described (Hertzer et al., 2006), except that the reactions were performed at a total ionic strength of 100 mM and included 0.2 µg/µl casein. GMPCPP-stabilized MTs were used at 1 µM, and enzyme concentrations ranged from 0 to 1 µM. MTs and enzyme were incubated at room temperature for 30 min and then sedimented at 45,000 rpm at 22°C in a TLA100 rotor for 5 min. The supernatant was removed and mixed with an equal volume of 2x sample buffer (125 mM Tris-HCl, pH 6.8, 4% SDS, 20% glycerol, 4% -mercaptoethanol). The pellet was resuspended in one reaction volume of 2x sample buffer, added to an equal volume of BRB80, and then the samples were boiled. An equal volume of the supernatant and pellet fractions were electrophoresed on 10% SDS-PAGE gels according to the method of Laemmli (1970) and stained with Colloidal Coomassie Blue. Stained gels were scanned, and the percentage of soluble tubulin heterodimer was determined using ImageJ software. The percentage of soluble tubulin was determined for each reaction condition in Excel (Microsoft, Redmond, WA) and plotted against the log of the enzyme concentration using Prism 4 software (GraphPad, San Diego, CA). For each enzyme, the percentage of soluble tubulin was normalized to the lowest point for the no-enzyme condition and to 100% depolymerization for the maximum response. The best fit curve for the four parameter logistic equation or dose response curve was determined with Prism using the following equation:

where Response is the percentage of tubulin in the supernatant at a particular enzyme concentration; A_min is the percentage of tubulin in the supernatant in the absence of enzyme; A_max is the highest percentage of tubulin in the supernatant attained by the enzyme; logEC₅₀ is the logarithm of the enzyme concentration that causes a response halfway between A_min and A_max; X is the logarithm of the enzyme concentration at a particular concentration; and H is the Hill slope of the curve. The best fit EC₅₀ curve was plotted against the enzyme concentration on a log scale with the mean response for each enzyme concentration and its corresponding standard error of the mean (SEM). Statistical significance between the EC₅₀ and maximum percent soluble tubulin concentrations was determined with an F-test. The F-test compared a model that constrained both curves to have identical EC₅₀ or A_max concentrations to a model that did not have constrained concentrations. Significant differences were considered if p < 0.05. Four or more experiments were performed per enzyme.

Immunofluorescence MT End Binding
MT end binding assays were performed as described previously (Desai and Walczak, 2001) except that reactions were performed at 100 mM total ionic strength, with 1 µM GMPCPP-stabilized MTs, 0.2 µg/µl casein, 2 mM MgATP, and 22.5 nM enzyme. 6His-GFP was used as a control for background staining. Reactions were allowed to proceed for 3 min at room temperature, fixed in 1% gluteraldehyde for 2 min, and then sedimented onto poly-L-lysine–coated coverslips through a 10% glycerol, BRB80 cushion at 12,000 rpm for 45 min in a Beckman JS13.1 rotor at 20°C. The coverslips were then fixed in –20°C methanol for 5 min, rehydrated in TBSTx (20 mM Tris, pH 7.5, 150 mM NaCl, 0.1% Triton X-100), washed, and then processed for immunofluorescence as follows. Coverslips were blocked in AbDil-Tx (2% bovine serum albumin, 20 mM Tris, pH 7.5, 150 mM NaCl, 0.1% Triton X-100, 0.1% sodium azide) for 30 min. To detect the GFP-tagged proteins, the coverslips were probed with 2 µg/ml rabbit anti-GFP antibody (Hertzer et al., 2006) in AbDil-Tx, washed with TBSTx, and then probed with 1:50 dilution donkey anti-rabbit Alexa488 secondary antibody (Invitrogen). The MTs were visualized by probing the coverslips with 1:250 dilution of mouse DM1 anti-tubulin antibody (Sigma-Aldrich, St. Louis, MO), washing with TBSTx, and probing with 1:50 dilution goat anti-mouse Alexa594 secondary antibody (Invitrogen). The coverslips were then mounted onto slides with anti-fade (0.5% p-phenylenediamine, 20 mM Tris-Cl, pH 8.8, 90% glycerol) and sealed with clear nail polish.

Analysis of the extent of MT binding by the different mutants was determined from five pictures taken blindly from each coverslip in four independent experiments. More than 300 microtubules were scored per condition per experiment. Images were taken with a Nikon 90i microscope equipped with a 100x/1.3 NA Plan Fluor oil objective (Nikon, Melville, NY). Digital images were collected at equivalent exposures with a Photometrics Coolsnap HQ cooled CCD camera (Roper Scientific, Trenton, NJ). The camera and shutter were controlled by MetaMorph software (Molecular Devices, Sunnyvale, CA). Per experiment, images were scaled equally to optimize GMCAK binding, and then the remaining images were scaled identically. Each image was quantified for the percentage of MTs that had either end binding events, lattice binding events, or no binding. The mean percentage of binding was plotted with the SEM, and the significant difference from GMCAK was determined using a Student's t test in Excel. All images were processed equivalently in Photoshop (Adobe, San Jose, CA) and assembled in Illustrator (Adobe).

Tubulin Competition Binding Assays
Tubulin competition binding assays were performed similarly to Hertzer et al. (2006). In this experiment, 200 nM of the GFP-tagged MCAK proteins were incubated in BRB27, 88 mM KCl (total ionic strength of 140 mM), with 1.2 µM doubly stabilized (GMPCPP and paclitaxel) MTs, in the presence or absence of 4.7 µM soluble GDP tubulin heterodimer for 15 min at room temperature. Reactions were sedimented at 45,000 rpm in a Beckman TLA100 rotor for 5 min at 22°C. After centrifugation, the supernatant and pellet of each reaction were adjusted to equal volumes and electrophoresed on 10% SDS polyacrylamide gels. Colloidal Coomassie–stained gels from three independent experiments representing multiple protein preparations were scanned, and then the percentage of MCAK partitioning to either the supernatant or the pellet was quantified using ImageJ software. The mean percentage of enzyme bound to MTs or tubulin are graphed with the SEM. Statistically significant differences from GMCAK were determined using a Student's t test in Excel.

Cytostatic Factor Extract Preparation and MCAK Immunodepletion
Cytostatic factor (CSF)-arrested extracts were prepared as previously described (Desai et al., 1999a) from X. laevis laid eggs. Extracts were supplemented with rhodamine-labeled tubulin for visualization of spindle structures. Extracts were immunodepleted of endogenous MCAK by incubation with 4 µg anti-MCAK-NT or nonimmune IgG per 10 µl protein G Dynabeads (Invitrogen) per 40 µl extract for 90 min on ice. Beads were isolated on a magnet for 30 min, and the extract was removed. Depleted extracts were then cycled into interphase with the addition of CaCl₂ and X. laevis sperm for 90 min and recombined on ice for 20 min. An equal volume of CSF-depleted extract was then added to the interphase extract to send it into mitosis. For each add-back reaction, 20 µl of extract was used with add-back of a final concentration of 100 nM 6His-GFP or GFP-tagged enzyme. The spindle assembly reactions were allowed to proceed for 90 min, fixed with 2% formaldehyde, 30% glycerol, BRB80, 0.5% TX-100, 2.5 mM MgCl₂ for 10 min, and then sedimented onto coverslips through a 40% glycerol, BRB80 cushion at 6000 rpm for 20 min at 18°C in a Beckman JS7.5 rotor. Coverslips were postfixed in –20°C methanol for 5 min, rehydrated in TBSTx, stained with 2 µg/ml Hoechst No. 33258 (Sigma-Aldrich) for 5 min, mounted onto slides with anti-fade, and sealed with clear nail polish.

Sperm containing structures were counted on each coverslip as either being part of a spindle, large aster, or monopolar structure. A sperm containing structure was classified as a spindle if it contained two (bipolar spindle) or more (multipolar spindle) focused poles with the majority of the chromatin arranged between the poles. Asters were classified as large when the diameter of the aster exceeded the width of a normal spindle. These large asters typically contained qualitatively more tubulin polymer than small asters and were typical of MCAK depletion (Walczak et al., 1996). Because bipolar spindle formation progresses through intermediate structures, which include half-spindles and small asters, we grouped these in intermediate structures into one category and called it monopolar structures. Sperm containing structures were classified as a small aster when the diameter of the aster was equal to or less than the diameter of a normal bipolar spindle. Chromatin within the small asters were either located close to the aster pole or arranged around the periphery of the astral microtubules. Four separate experiments were analyzed from three different extract preparations with 100 structures counted per reaction. The mean percentages of each structure category are graphed with the SEM. Digital images were acquired with a 60 x 1.4 NA Plan Apo oil objective mounted on a Nikon 90i microscope. Images were processed in Photoshop and assembled in Illustrator (Adobe).

Kinetochore Targeting
Kinetochore targeting experiments were performed similarly to those previously described (Walczak et al., 2002). Briefly, 10 µg/ml nocodazole was added to MCAK-immunodepleted extracts that were then mixed with X. laevis sperm and 100 or 500 nM of the various GFP-tagged MCAK proteins on ice. Reactions were started by transferring the reaction to room temperature and were incubated for 45 min. Reactions were fixed and processed for immunofluorescence as described above except that they were immunostained with 1:430 dilution of rabbit anti-xCENP-A (a kind gift from Aaron Straight) and 1:20,000 donkey anti-rabbit Alexa594 (Invitrogen).

Z-stepped images were taken with a Nikon 90i microscope equipped with a 100x/1.3 NA Plan Fluor oil objective. Three-dimensional maximal projection images were scaled to best represent GMCAK localization, and then the remaining images were scaled identically. All images were processed in Photoshop and assembled in Illustrator (Adobe).

Ran Aster Analysis
Fresh CSF extract supplemented with X-Rhodamine-tubulin was immunodepleted of MCAK or nonimmune IgG as described above. His-RanL43E was added to the extract to a final concentration of 25 µM and GFP, and GFP-tagged MCAK proteins were added back to a final concentration of 100 or 200 nM. Protein addition did not exceed one-tenth the volume of the extract. Reactions were incubated at room temperature for 45 min, fixed, and processed as described above for sperm-assembled spindles. Approximately 300 MT structures were counted per condition per experiment from three separate experiments from two independent extracts and were classified as spindles, small asters, large asters, or MT aggregates. Similar results were seen in two additional independent extracts.

An aster was classified as a small aster if it did not exceed the diameter of the majority of asters observed in the control IgG depletion reaction, which were typical of Ran-induced asters (Kalab et al., 1999; Ohba et al., 1999; Wilde and Zheng, 1999; Carazo-Salas et al., 2001; Gruss et al., 2001). When an aster exceeded the size of a typical Ran-induced aster (small aster), which was typical of MCAK-depleted extract, the aster was categorized as a large aster. MT aggregates formed in MCAK-depleted extracts and were typified by a size that grossly exceeded the size of large asters in the MCAK-depleted extract. These MT aggregates did not have a focused pole, and the MTs were often arranged parallel to one another. In Figure 4B, spindles and small asters were grouped into the category called "Small Asters and Spindles" to represent structures that were rescued in comparison to large asters, which were nonrescued structures typical of the MCAK-depleted phenotype. In Figure 4C, small asters and large asters were grouped into an "Aster" category to exemplify the increased spindle formation that was observed with GM(2-592). The data are graphed as either the mean percentage of small asters and spindles or large asters from the total number of asters and spindles for each construct (Figure 4B) or as the mean percentage of asters, spindles, or MT aggregates from the total number of structures for each construct (Figure 4C). The mean percentages were determined from three independent experiments and graphed with the SEM using Excel (Microsoft). Statistical significance was determined with a Student's t test performed in Excel and was considered significant if p < 0.05. Images were taken with a 40x 1.0 NA Plan Fluor oil objective on a Nikon 90i microscope and processed equivalently in Photoshop and assembled in Illustrator (Adobe).

	RESULTS

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

 
The C-terminal Domain and Neck Are Required for Robust MT Depolymerization Activity
To study MCAK domain function biochemically with purified proteins and physiologically in egg extracts, five deletion constructs with N-terminally tagged GFP were expressed in insect cells and purified to near homogeneity using conventional chromatography (Desai et al., 1999b; Supplementary Figure 1). The modifications removed the N-terminal domain, the neck, and/or the C-terminal domain (Figure 1A). All constructs contained the catalytic domain. For simplicity, GFP-MCAK is referred to as GMCAK, and the GMCAK modified proteins are referenced as GM followed by the amino acids included in the protein. From hydrodynamic analysis, GMCAK has a native molecular weight of 262 kDa, which is slightly larger than its predicted dimeric molecular weight of 220 kDa, suggesting an extended conformation (Hertzer et al., 2006). In contrast, GM(187-592) has a native molecular weight of 74 kDa, which is almost identical to its predicted monomeric molecular weight of 75 kDa (Hertzer et al., 2006). Consistent with the C-terminal domain being responsible for dimerization and being extended, GM(187-731) and GM(263-731) also migrated on gel-filtration with molecular weights that were larger than that predicted for dimers (our unpublished data). GM(263-592), which lacked both the N- and C-terminal domains, eluted as a monomeric protein by gel filtration chromatography (our unpublished data). GM(2-592) migrated on gel filtration and sucrose gradients with a molecular weight that was larger than a monomer but smaller than a dimer. The N-terminal domain alone was not sufficient for dimerization in either two-hybrid or hydrodynamic assays (our unpublished data); therefore we conclude that GM(2-592) is most likely a monomeric protein, although we cannot rule out the possibility that it forms a weak dimer (Maney et al., 2001). Together, these data suggest that the N- and C-terminal domains may exist in an extended state, whereas the neck and catalytic domain in combination or the catalytic domain alone may be more globular.

View larger version (22K): [in this window] [in a new window]   Figure 1. The C-terminal domain and neck of MCAK are necessary for efficient MT depolymerization activity. (A) Schematic diagram of expressed and purified MCAK proteins. The GFP tag is located on the N-terminus but was omitted from the diagrams for simplicity. (B and C) GMPCPP stabilized MTs (1 µM) were incubated with increasing concentrations of enzyme (0–1 µM) for 30 min in saturating MgATP at room temperature. MTs were sedimented, and the soluble tubulin heterodimer removed. Equal volumes of soluble tubulin and MT pellets were electrophoresed on 10% SDS polyacrylamide gels, and the gels were stained with Colloidal Coomassie Blue. The percentage of soluble tubulin was quantified from the stained gels and plotted against the log of the enzyme concentration. The four-parameter logistic equation was used to determine the EC50 concentrations of each enzyme from four or more individual experiments. The curves represent the best fit curve to the data with each point represented by the mean ± SEM.

Under physiological buffer conditions, 1.45 nM GMCAK depolymerized 50% of 1 µM MTs in 30 min (Figure 1B; Supplementary Table 1). Similar to previous work, MT end binding assays illustrated that full-length GMCAK bound MTs well and bound MT ends with high specificity (Supplementary Figure 2; Moore and Wordeman, 2004; Hertzer et al., 2006). Similarly, tubulin competition assays demonstrated that GMCAK only marginally released from MTs in the presence of excess tubulin heterodimer (Supplementary Figure 3), which was consistent with previous results (Moore et al., 2005; Hertzer et al., 2006). Deletion of the N-terminal domain in GM(187-731) resulted in an EC₅₀ of 1.44 nM, which was not significantly different from GMCAK. This indicated that GM(187-731) is also a potent MT depolymerase. MT end binding and tubulin competition assays confirmed that GM(187-731) is a potent MT depolymerase because it bound MTs and released from MTs in the presence of excess tubulin in a manner essentially indistinguishable from GMCAK (Supplementary Figures 2 and 3). In sharp contrast, further truncation of the N-terminus, which deleted the neck in GM(263-731), resulted in a 150-fold reduction in the EC₅₀ for MT depolymerization (213 nM; p < 0.0001; Figure 1B; Supplementary Table 1). MT end binding experiments indicated that GM(263-731) did not depolymerize MTs well because it bound MTs poorly and with reduced MT end specificity (Supplementary Figure 2). Interestingly, in the tubulin competition assays only twofold more GM(263-731) released from MTs in the presence of excess tubulin over that which did not bind MTs, suggesting that GM(263-731) has a low tubulin affinity similar to GMCAK (Supplementary Figure 3). These results are in agreement with previous results showing that the neck domain is very important for robust MT depolymerization activity (Maney et al., 2001; Ovechkina et al., 2002; Hertzer et al., 2006).

Removal of the C-terminal domain in GM(2-592) resulted in a modest decrease (2-fold) in the EC₅₀ for MT depolymerization (2.63 nM) that was statistically different in comparison to GMCAK (p < 0.001; Figure 1C; Supplementary Table 1). The MT end binding results suggest that in comparison to GMCAK, GM(2-592) had a very small but statistically significant reduction in MT end binding (p < 0.01; Supplementary Figure 2). In the tubulin competition assays, there was a slightly reduced ability to bind MTs (p < 0.01), but a nearly fourfold increase in the amount of GM(2-592) that released from MTs in the presence of excess tubulin (p < 0.0001; Supplementary Figure 3). Given the magnitude of the differences between GM(2-592) and GMCAK tubulin binding, we favor the idea that GM(2-592) is likely defective in its ability to release tubulin dimer at the end of its catalytic cycle, similar to what has been observed previously for another monomeric MCAK construct (Hertzer et al., 2006). However, we cannot exclude the possibility that this result is due to a decreased ability of GM(2-592) to diffuse along the MT lattice. Together our in vitro results so far support the ideas that the C-terminal domain is necessary and that the N-terminal domain is dispensable for efficient MT depolymerization (summarized in Figure 5).

Similar to our previous report (Hertzer et al., 2006), GM(187-592) had a fourfold reduction in the EC₅₀ for MT depolymerization (5.46 nM) in relation to GMCAK (p < 0.0001; Figure 1C; Supplementary Table 1). Overall, GM(187-592) bound MT ends with slightly lower specificity (p < 0.001), bound MTs with a slightly lower affinity (p < 0.05), and bound tubulin dimer fivefold more robustly (p < 0.01) than GMCAK (Supplementary Figures 2 and 3). This indicates that perhaps GM(187-592) is less adept at targeting specifically to MT ends or diffusing along the MT lattice as well as releasing from tubulin dimer in the final step of MT depolymerization, which is consistent with our previous results (Hertzer et al., 2006). Because removal of the N-terminal domain severely affected the depolymerization activity of GM(187-592) relative to GM(2-592), these results suggest that the N-terminal domain of MCAK may play a small role in regulating the in vitro MT depolymerization activity, especially when the C-terminal domain is absent. From our previous work with minimal domain MCAK, it is likely that GM(2-592) and GM(187-592) both get stuck at tubulin release, whereas GM(187-592) also gets stuck on the MT lattice, thereby further reducing its MT depolymerization potency (Hertzer et al., 2006). These results indicate that GM(2-592) and GM(187-592) likely have similar biochemical mechanisms, which in part is due to them being monomeric.

Interestingly, removal of the neck domain from GM(187-592) to create GM(263-592) resulted in a protein with a 13-fold higher MT depolymerization activity (16 nM) than GM(263-731; p < 0.0001) and an 11-fold lower MT depolymerization activity than GMCAK (p < 0.0001; Figure 1C; Supplementary Table 1). MT end binding and tubulin competition assays indicate that GM(263-592) was able to bind MTs better than GM(263-731) but bound to MT ends less well than GMCAK, consistent with their differences in MT depolymerization activities (Supplementary Figures 2 and 3). In addition, GM(263-592) released from MTs in the presence of excess tubulin more robustly than GMCAK and GM(263-731; Supplementary Figure 3). These results support the idea that the neck is minimally required for 1-D diffusion (Ovechkina et al., 2002; Helenius et al., 2006), because all proteins except the neckless mutants targeted to MT ends effectively.

Overall, our data support previous work showing that the neck domain is critical and that dimerization is important to MCAK-induced in vitro MT depolymerization activity (Maney et al., 2001; Ovechkina et al., 2002; Hertzer et al., 2006). However, our results extend previous analyses to indicate that the C-terminal domain positively influences MCAK MT depolymerization activity when the neck domain is present, but becomes inhibitory when the neck domain is absent, suggesting a mechanistic interplay between the C-terminal domain and neck that is necessary for efficient MT depolymerization activity.

The N-Terminal Domain Is Required for Efficient Spindle Assembly in MCAK-depleted Extracts
Although our in vitro work gave us new insights into the biochemical mechanism of MCAK, we were interested in understanding how it related to the physiological function of MCAK. Thus, Xenopus CSF extracts were depleted of endogenous MCAK, reconstituted with GMCAK or the various domain mutants (Supplementary Figure 4), and assayed for spindle assembly. The extracts were cycled into interphase in the absence of MCAK, and GMCAK add-back was done at the time of the second CSF addition to ensure that the rescue would show only the effects of the mutants on spindle assembly and not any defects in the intervening interphase. MCAK immunodepletion resulted in 80–90% depletion of endogenous MCAK as determined by Western blot (Supplementary Figure 4A). Cycled spindle assembly of control IgG depleted extract with the add-back of recombinant GFP (IgG + GFP) resulted in a large proportion of spindles (56 ± 10%), a small percentage of large asters (20 ± 5%), and a small percentage of intermediary monopolar structures (23 ± 8%) that consisted of small asters and half spindles (Figure 2; Supplementary Table 2). The spindles in the control IgG depleted extract were of normal morphology, with the majority having normal MT polymer levels and aligned chromosomes, indicating normal physiological MT dynamics (our unpublished observations). We considered this control IgG depletion phenotype as an example of efficient spindle assembly. In contrast, MCAK depletion and add-back of recombinant GFP (M + GFP) resulted in the complete failure to undergo efficient spindle assembly due to suppressed MT dynamics. This was exemplified by very few spindles (4.0 ± 2%, p < 0.05) and the formation of mainly large asters (61 ± 9%, p < 0.01), in comparison to control IgG depleted extract (Figure 2; Supplementary Table 2). The few spindles that formed had excess MT polymer and unaligned chromosomes, indicating suppressed physiological MT dynamics (our unpublished results). This MCAK depletion phenotype is similar to previously reported results (Walczak et al., 1996). In comparison to the MCAK depleted extract, add-back of GMCAK (M + GMCAK) completely rescued spindle assembly as the percentage of spindles, large asters, and monopolar structures were statistically identical to control IgG depletion (Figure 2; Supplementary Table 2). The majority of the spindles had normal MT polymer levels and aligned chromosomes, indicating normal physiological MT dynamics.

Surprisingly, add-back of GM(187-731) [M + GM(187-731)], which lacked the N-terminal domain and had full in vitro MT depolymerization activity, only partially rescued the MCAK depletion phenotype in comparison to GMCAK. This was exemplified by a twofold decrease in spindle formation (27 ± 8%, p < 0.05; Figure 2; Supplementary Table 2). Of the spindles in the GM(187-731) add-back, many of them often had excess MT polymer and poor chromosome alignment in comparison to control IgG or GMCAK add-back, indicating suppressed MT dynamics (our unpublished results). This result was very surprising based on the MT depolymerization and MT binding abilities of GM(187-731). Further truncation of the N-terminus to remove the neck in GM(263-731) and add-back to MCAK depleted extracts resulted in GM(263-731) being unable to rescue spindle assembly in comparison to GMCAK (Figure 2). Specifically, GM(263-731) add-back resulted in an approximate threefold decrease in spindle formation (20 ± 8%, p < 0.05) and a threefold increase in large asters (54 ± 10%, p < 0.05; Figure 2; Supplementary Table 2). The few spindles that formed in the GM(263-731) add-back were characterized by excess MT polymer and unaligned chromosomes. These results strongly imply that the N-terminal domain is important and that the neck is essential for spindle assembly and normal physiological MT dynamics. Surprisingly, these results indicate that competent in vitro depolymerization activity of GM(187-731) did not predict its efficient spindle assembly in extracts. In addition, these results imply that the N-terminal domain of MCAK is critical for efficient spindle assembly.

View larger version (71K): [in this window] [in a new window]   Figure 2. The N-terminal domain of MCAK is required for efficient spindle assembly. CSF extracts were depleted of endogenous MCAK (M) or mock-depleted with IgG (IgG), cycled into interphase with CaCl2, and cycled back into mitosis with additional depleted CSF extract. GFP-tagged proteins were added back to 100 nM final concentration with the second addition of CSF extract. Spindles were assembled for 90 min, fixed, and sedimented onto coverslips, and the chromatin was stained with Hoechst and mounted with anti-fade. (A) Images of representative structures from the add-back experiments are shown with MTs in magenta and chromatin in green. Scale bar, 20 µm. (B) Quantification of the spindles, large asters, and monopolar structures observed in the extracts that are represented in A. The data are graphed as the mean percentage plus the SEM from four independent extracts. An asterisk indicates a significant difference relative to GMCAK add-back.

To further test the theory that the N-terminal domain is necessary for efficient spindle assembly, we added back GM(187-592), which is missing both the N-terminal and C-terminal domains, to MCAK depleted extracts. Similar to GM(187-731), add-back of GM(187-592) only partially rescued spindle assembly. In comparison to GMCAK add-back, add-back of GM(187-592) resulted an approximate twofold decrease in spindle formation (30 ± 7%; p < 0.05), which was identical to what we found for GM(187-731) (Figure 2; Supplementary Table 2). This result is interesting because GM(187-731) and GM(187-592) differed in their in vitro MT depolymerization, MT end binding, and tubulin binding assays. These results suggest that the C-terminal domain of MCAK may not play a major role in spindle assembly, despite its importance in regulating MT depolymerization activity in vitro or that a twofold reduction in depolymerization activity is sufficient for efficient spindle assembly. Finally, add-back of GM(263-592) to MCAK-depleted extracts rescued spindle assembly poorly and was essentially identical to GM(263-731) phenotypically and morphologically (Figure 2). In comparison to GMCAK add-back, GM(263-592) add-back resulted in a threefold decrease in spindle formation (17 ± 5%; p < 0.01) and a threefold increase in large asters (59 ± 8; p < 0.01; Figure 2; Supplementary Table 2). Overall, these add-back experiments show that for efficient spindle assembly in egg extracts, the N-terminal domain is required and the C-terminal domain is not essential (summarized in Figure 5).

High MCAK MT Depolymerization Activity Is Not Necessary for Efficient Sperm-induced Spindle Assembly
We were surprised that GM(187-731), which had full in vitro MT depolymerization activity, did not effectively rescue spindle assembly and that GM(2-592) fully rescued spindle assembly despite its decreased in vitro MT depolymerization activity. These results suggest that high MT depolymerization activity is not critical for spindle assembly. Because this finding was unexpected, we next asked if three different catalytic domain mutations in full-length MCAK that interfere with catalytic activity to varying degrees would promote spindle assembly in MCAK-depleted extracts. The first mutation was an arginine-to-alanine modification at residue 522 (R522A) within helix 4 that is analogous to conventional kinesin K256, which reduces MT binding without affecting catalysis or MT gliding (Woehlke et al., 1997). In our in vitro depolymerization assay, GM(R522A) MT depolymerization activity was reduced by about twofold (3.15 nM; p < 0.001) in comparison to GMCAK (1.45 nM), which was similar to the decrease caused by removal of the C-terminal domain in GM(2-592) (Figure 3A; Supplementary Table 1). In comparison to GMCAK add-back, add-back of GM(R522A) to MCAK depleted extracts resulted in similar spindle assembly efficiency (Figure 3B). Specifically, add-back of GM(R522A) to MCAK depleted extracts resulted in only a 1.4-fold lower percentage of spindles (40 ± 4%) and a twofold higher percentage of large asters (36 ± 11%) in comparison to GMCAK add-back (Figure 3B; Supplementary Table 2). Despite rescuing spindle assembly, the spindles in the GM(R522A) add-back displayed increased MT polymer and unaligned chromosomes, suggesting reduced physiological MT dynamics (our unpublished data).

View larger version (30K): [in this window] [in a new window]   Figure 3. High MT depolymerization activity is not necessary for efficient sperm-induced spindle assembly. (A) The three catalytic domain mutants, GM(R522A), GM(E529A), and GM(296-308), were assayed for MT depolymerization activity, quantified, and graphed as described in Figure 1, B and C. (B) The catalytic domain mutants were added back to cycled MCAK-depleted extracts (M), and assayed for their ability to rescue spindle assembly as described for Figure 2. Quantification of the observed structures is graphed as the mean percentage plus the SEM from three independent experiments. An asterisk denotes a significant difference relative to add-back of GMCAK.

The third mutation we analyzed was the deletion of the KVD finger (amino acids 296-308) that is critical for the ability of MCAK to depolymerize MTs in cells (Ogawa et al., 2004; Shipley et al., 2004). The MT depolymerization activity of GM(296-308) was 11-fold decreased (15.7 nM; p < 0.0001) in comparison to GMCAK (1.45 nM) and was similar to the depolymerization activity of GM(263-592), a very poor depolymerase (Figure 3A; Supplementary Table 1). GM(296-308) add-back partially rescued spindle assembly in MCAK-depleted extracts, suggesting that GM(296-308) was less efficient at promoting spindle assembly (Figure 3B). In comparison to GMCAK, GM(296-308) add-back resulted in spindle formation that was reduced by only 1.7-fold (31 ± 12%), large asters were increased threefold (56 ± 14%; p < 0.05), and monopolar structures were twofold reduced (14 ± 2%; Figure 3B; Supplementary Table 2). Essentially all the spindles that formed in the GM(296-308) reactions had excess MT polymer and unaligned chromosomes, indicating suppressed MT dynamics (our unpublished results). Overall, this data suggests that robust in vitro MT depolymerization activity is not necessary for efficient sperm-induced spindle assembly such that up to a 4.5-fold reduction in depolymerization activity is sufficient (summarized in Figure 5).

Because the N-terminus is necessary for MCAK kinetochore-targeting (Maney et al., 1998; Walczak et al., 2002), one possible explanation for the differences seen in spindle assembly assays relative to the in vitro depolymerization assays could be that the GMCAK mutants targeted differently to kinetochores. To test this idea, we analyzed the localization of each GMCAK mutant to kinetochores using MCAK-depleted extracts in which the microtubule polymerization was inhibited with nocodazole to enrich for kinetochore proteins. GMCAK localized prominently to kinetochores in these targeting assays as seen previously (Supplementary Figure 5B; Walczak et al., 2002). In contrast, GM(187-731) did not target to kinetochores (Supplementary Figure 5C). Unexpectedly, GM(2-592) also did not target to kinetochores when added back to endogenous levels (100 nM; Supplementary Figure 5D). However, when GM(2-592) was added back to five times the endogenous level (500 nM), it targeted to kinetochores nicely (Supplementary Figure 5D'), whereas add-back of GM(187-731) did not target to kinetochores at this level (Supplementary Figure 5C'). These results indicate that GM(2-592) targeted to kinetochores 5- to 10-fold less efficiently than GMCAK and that the C-terminal domain positively regulates the degree of kinetochore targeting, similar to that demonstrated in mammalian cells (Maney et al., 1998). In addition, the three catalytic domain mutant proteins targeted robustly to kinetochores in the targeting assay when added back to 100 nM (Supplementary Figure 5, E–G). Together, these results support the idea that robust kinetochore targeting of MCAK is not necessary for sperm-induced spindle assembly, but is likely important for proper chromosome alignment as reported previously (Walczak et al., 2002; Kline-Smith et al., 2004).

The N-Terminal Domain Regulates Physiological MT Dynamics, and the C-Terminal Domain Regulates Spindle Bipolarity
One complication of our analysis of spindle assembly reactions is that MTs are nucleated from both centrosomes and chromatin in the extracts, and therefore it was impossible to dissect whether these two sources of MTs were differentially affected by MCAK loss. We wanted to identify a physiological assay by which we could evaluate MT dynamics without any contribution from chromatin. Because mostly small asters and a small percentage of bipolar spindles form with the addition of activated Ran (Kalab et al., 1999; Ohba et al., 1999; Wilde and Zheng, 1999; Carazo-Salas et al., 2001; Gruss et al., 2001), this system may provide a means to directly test the ability of MCAK to regulate physiological MT dynamics independent of its role in chromatin-mediated spindle formation. We depleted MCAK and added back GMCAK to Ran-induced aster assembly reactions (Figure 4). Depletion of MCAK and induction of aster assembly by addition of His-RanL43E resulted in the formation of a very small percentage of spindles and small asters (15 ± 1%) with the majority of the structures being large asters (85 ± 1%) and large MT aggregates (28 ± 3%; Figure 4; Supplementary Table 3). This phenotype indicates that the physiological MT dynamics in the extract are severely suppressed in response to MCAK depletion, and is similar to the sperm-induced phenotype of MCAK depletion. Add-back of physiological levels of GMCAK (100 nM), as we did in the chromatin-induced spindle assembly assay, resulted in mostly small asters and a small percentage of spindles with a substantial percentage of large MT aggregates (our unpublished data). Instead, add-back of GMCAK to twice the physiological level (200 nM) was needed to reduce the large MT aggregates to near control IgG levels (6 ± 2%) while maintaining high percentages of small asters and spindles (86 ± 5%; Figure 4, B and C; Supplementary Table 3). Thus, the Ran system allowed us to study the contributions of the GMCAK mutants to the regulation of physiological MT dynamics.

View larger version (39K): [in this window] [in a new window]   Figure 4. The N-terminal domain regulates physiological MT dynamics and the C-terminal domain regulates spindle bipolarity. Asters and spindles were induced by the addition of 25 µM RanL43E to control or MCAK-depleted extracts to which 200 nM GFP, GMCAK, GM(187-731), GM(2-592), GM(187-582), GM(R522A), GM(E529A), and GM(296-308) were added. Reactions were incubated for 45 min at room temperature, fixed, sedimented onto coverslips, and mounted with anti-fade. (A) Representative images are shown and were scaled identically. Scale bar, 10 µm. (B) Quantification of the structure type is graphed as the mean percentage of the total structures plus the SEM from three independent experiments. (C) Quantification of the aster types is graphed as the mean percentage from the aster and spindle total plus the SEM from three independent experiments. Small asters and spindles, which represent rescued structures, were combined and are compared with large asters. An asterisk indicates significant difference relative to GMCAK add-back.

If the hypothesis is true that the proper regulation of MCAK depolymerization activity via the N-terminal domain is necessary for spindle assembly, then we would expect GM(2-592) to rescue the MCAK-depletion phenotype in the Ran system. Indeed, add-back of GM(2-592) fully rescued the MCAK depletion phenotype (Figure 4), indicating that the N-terminal domain is necessary for regulating physiological MT dynamics. Specifically, add-back of GM(2-592) resulted in 85 ± 3% small asters and spindles and only 15 ± 3% large asters, which were statistically equivalent to add-back of GMCAK (Figure 4B; Supplementary Table 3). Surprisingly, GM(2-592) add-back to MCAK-depleted extracts dramatically increased the number of spindles that formed (52 ± 8%) to levels higher than control IgG depleted extract (10 ± 1%; p < 0.05; Figure 4, A and C; Supplementary Table 3). This increase in spindle assembly over control IgG depletion was also seen with add-back of 100 nM GM(2-592), but was not observed when GM(2-592) was added to non-MCAK depleted extracts (our unpublished results). Increased spindle assembly with GM(2-592) add-back was completely unexpected and suggests that MCAK may have an undefined role in promoting spindle bipolarity that is likely promoted by the N-terminal domain and inhibited by the C-terminal domain. To fully assess the importance of the N-terminal domain in MT depolymerization activity in the absence of the C-terminal domain, GM(187-592) was added back to the extract. Similar to the sperm induced add-back assay, GM(187-592) did not fully rescue the MCAK depletion phenotype in the Ran-induced assembly assay (Figure 4, A and B; Supplementary Table 3). Specifically, add-back of GM(187-592) resulted in a twofold decrease in small aster and spindle formation (41 ± 6%, p < 0.01), a fourfold increase in large aster formation (59 ± 6%, p < 0.01), and a threefold increase in MT aggregates (18 ± 3%, p < 0.05) in comparison to GMCAK add-back (Figure 4; Supplementary Table 3). These results support the idea that the N-terminal domain of MCAK is essential for the proper regulation of physiological MT dynamics in extracts.

Our sperm-induced spindle assembly assays with the catalytic domain mutants suggested that robust MT depolymerization activity is not critical for spindle assembly, but it was unclear how their decreased activity would affect physiological MT dynamics in the absence of chromatin. GM(R522A) add-back rescued the MCAK depletion phenotype similar to GMCAK, indicating that GM(R522A) has wild-type physiological MT depolymerization activity (Figure 4). In particular, GM(R522A) add-back resulted in a high percentage of small asters and spindles (73 ± 10%), a relatively low percentage of large asters (27 ± 10%), and a small percentage of MT aggregates (4 ± 1%), which were statistically identical to GMCAK add-back (Figure 4, B and C; Supplementary Table 3). In contrast, add-back of GM (E529A) poorly rescued the MCAK-depleted Ran aster phenotype and was similar to GM(187-731) and GM(187-592) add-back (Figure 4, A and B). Add-back of GM(E529A) resulted in a 2.5-fold decrease in small asters and spindles (35 ± 9%, p < 0.01) and an approximate fivefold increase in large asters (65 ± 9%, p < 0.01) in comparison to GMCAK add-back, suggesting that GM(E529A) had a reduced ability to regulate physiological MT dynamics (Figure 4B; Supplementary Table 3). Add-back of GM(296-308) failed to rescue the MCAK-depleted phenotype entirely and had an approximate sixfold decrease in small asters and spindles (15 ± 5%; p < 0.001), a sixfold increase in large asters (85 ± 5%; p < 0.001), and a fivefold increase in MT aggregates (30 ± 8%; p < 0.05) in comparison to GMCAK add-back (Figure 4; Supplementary Table 3). The GM(296-308) phenotype was essentially identical to the MCAK-depleted phenotype in which physiological MT dynamics are drastically suppressed (Figure 4; Supplementary Table 3). These results are different from the sperm-induced spindle assembly assay in which GM(E592A) and GM(296-308) were able to rescue the MCAK depletion phenotype to some degree.

Together the results from the sperm-induced and Ran-induced spindle assembly assays indicate that in the presence of chromatin, robust MCAK MT depolymerization activity is not important for spindle assembly, but becomes critical in the absence of chromatin. We believe that it is likely that chromatin exerts an additional level of control over the regulation of MT dynamics, which may aid in spindle assembly when MCAK activity is less robust. Overall, our results indicate that high MCAK MT depolymerization activity in vitro (EC₅₀ 1.45–3.15 nM) is sufficient for the proper regulation of physiological MT dynamics, that physiological MCAK MT depolymerization activity is regulated through the N-terminal domain, and that MCAK promotes bipolar spindle assembly through an interplay between the N- and C-terminal domains (summarized in Figure 5).

View larger version (17K): [in this window] [in a new window]   Figure 5. Summary of the in vitro and extract activities of GMCAK and its various mutants. The data from each experiment are summarized with plus signs to delineate the extent of activity. Four consecutive plus signs indicate the highest activity (+ + + +) and a minus sign indicates no activity (–). ND indicates activity was not determined for that assay. Each GMCAK mutant is represented schematically based on the domain(s) deleted or mutated. The domains are as depicted in Figure 1. The catalytic domain mutants are full-length GMCAK proteins with either a point mutation (R522A or E529A) or a 13-amino acid deletion (296-308) within the catalytic domain.

	DISCUSSION

TOP ABSTRACT INTRODUCTION MATERIALS AND METHODS RESULTS DISCUSSION REFERENCES

Robust MT Depolymerization Activity Is Not Necessary for Sperm-induced Spindle Assembly
We were surprised by our finding that full MCAK depolymerization activity was not necessary to get efficient sperm-induced spindle assembly. One explanation could be that the maximum depolymerization activity at physiological ratios of MCAK to tubulin is most important. In our in vitro MT depolymerization assays, the EC₅₀ of GMCAK is 1.5 nM using 1 µM MTs (or a ratio of 1 MCAK to 1000 tubulin dimers). In contrast, the physiological ratio of MCAK to tubulin is 1–100. Perhaps, if the EC₅₀ value is <10 nM, any differences are insignificant. Alternatively, it may be more appropriate to ask how much of the MTs can be fully depolymerized in the in vitro assays when the concentration of enzyme is 10 nM. Using this analysis, GMCAK and GM(2-592)