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Spindle assembly and elongation involve poleward and away-from-the-pole forces produced by microtubule dynamics and spindle-associated motors. Here, we show that a bidirectional Drosophila Kinesin-14 motor that moves either to the microtubule plus or minus end in vitro unexpectedly causes only minor spindle defects in vivo. However, spindles of mutant embryos are longer than wild type, consistent with increased plus-end motor activity. Strikingly, suppressing spindle dynamics by depriving embryos of oxygen causes the bidirectional motor to show increased accumulation at distal or plus ends of astral microtubules relative to wild type, an effect not observed for a mutant motor defective in motility. Increased motor accumulation at microtubule plus ends may be due to increased slow plus-end movement of the bidirectional motor under hypoxia, caused by perturbation of microtubule dynamics or inactivation of the only other known Drosophila minus-end spindle motor, cytoplasmic dynein. Negative-stain electron microscopy images are consistent with highly cooperative motor binding to microtubules, and gliding assays show dependence on motor density for motility. Mutant effects of the bidirectional motor on spindle function may be suppressed under normal conditions by motor: motor interactions and minus-end movement induced by spindle dynamics. These forces may also bias wild-type motor movement toward microtubule minus ends in live cells. Our findings link motor : motor interactions to function in vivo by showing that motor density, together with cellular dynamics, may influence motor function in live cells.
Spindles undergo assembly, elongation and disassembly by a dynamic interplay between poleward and away-from-the-pole forces produced by microtubule dynamics and spindle-associated microtubule motors (1,2). Poleward forces contribute to pole formation during spindle assembly (3–5), while away-from-the pole forces are needed for spindle elongation, and opposing poleward and away-from-the pole forces are required to maintain spindles and prevent their collapse (6,7).
Microtubule dynamics includes dynamic instability, the sudden rapid depolymerization or polymerization of microtubules (8), and poleward microtubule flux, slow movement of microtubules toward the poles thought to be driven by microtubule depolymerization at the poles and sliding of microtubules against one another (9–11). Microtubule depolymerization has been shown to produce sufficient force to drive poleward chromosome movement (12–14). Forces produced by microtubule polymerization, together with those produced by microtubule depolymerization and poleward flux, may also be needed to assemble and maintain spindles.
Spindle-associated microtubule motors include cytoplasmic dynein (15,16) and motors of the kinesin family (17–19). Like other cytoskeletal motors, these motors move directionally along their filament, toward either the fast polymerizing/depolymerizing plus ends or the more stable minus ends at the nucleating center. Dynein and kinesin motors could attach spindle fibers to one another and chromosomes to spindle microtubules to assemble and maintain the meiotic or mitotic apparatus. The motors modulate microtubule dynamics and mediate spindle and chromosome dynamics (17,18,20,21). Motors could function by binding to a microtubule or kinetochore by their tail and to another microtubule by their motor domain, and move along the microtubule, sliding spindle fibers past one another or chromosomes along spindle microtubules (17,18).
Roles of specific motors in the spindle have been inferred by analysis of mutants. Early work showed that loss of function in yeast cells of two presumed plus-end Kinesin-5 (formerly BimC) (22) motors, Cin8 and Kip1, causes collapse of mitotic spindles (6) that can be suppressed by mutation of a minus-end Kinesin-14 (formerly C-terminal) motor, Kar3 (7). This has led to the idea that opposing forces are needed to maintain mitotic spindle integrity. Loss-of-function mutants have similarly been used to demonstrate that Ncd, the minus-end Kinesin-14 motor of Drosophila, functions in pole formation in oocyte meiotic spindles (4,5,23,24) and attachment of centrosomes to poles in mitotic spindles (25,26). These roles are consistent with the minus-end directionality of Ncd and presence of microtubule minus ends at spindle poles, implying that directionality of movement is important to Ncd function in the spindle.
Directionality of kinesin motors is thought to be determined by the neck, immediately adjacent to the conserved motor domain (27–29). Studies of chimeric and neck-mutated motors (28,30–34) showed that the neck plays an essential role in directionality. The neck has been proposed to function by mediating a minus-end-directed displacement of the Ncd motor along the microtubule (34,35) or by amplifying plus-end movements of the Kinesin-1 (formerly conventional kinesin) conserved motor domain (33).
Information regarding the mechanism of Ncd neck function has come from analysis of a mutant that causes the motor to move either to the microtubule plus or minus end (34). An altered neck residue in the mutant reduces interactions of the neck with the conserved motor domain. Microtubule gliding assays showed that velocity of the mutant motor was normal, but directionality was defective, resulting in gliding in either direction. Single-motor laser trap assays revealed a conformational or angle change of the motor that occurs upon motor binding to a microtubule. This movement was biased toward the minus end for wild-type Ncd but occurred in either direction for the neck mutant, indicating that the mutated neck residue is required for directional movement of Ncd to the microtubule minus end. The model that has emerged from these studies is that interactions of the neck with the conserved motor domain result in a movement, probably of the stalk/neck, that displaces the Ncd motor toward the minus end (35,36).
The importance of directionality to motor function in the spindle has been demonstrated for only a few motors that include Cin8, Kip1 and Kar3 (6,7). Because cellular dynamics could modulate motor function in ways that are presently not well understood, it is important to study motors in live cells to determine their effects in vivo. Here, we test the effect of altered directionality on Ncd function in the spindle by making germline transformants of the bidirectional neck mutant and analyzing live oocytes and embryos of mutant females. Unexpectedly, our findings can be explained by effects of motor : motor interactions, together with spindle dynamics, on motor directionality and function in vivo.
Ncd, the minus-end Kinesin-14 motor of Drosophila, functions in spindle assembly in oocytes and early embryos. To test the effects of altered directionality on motor function in the spindle, we made germline transformants expressing a mutant of Ncd, NcdNK11, a bidirectional motor that moves either toward the microtubule plus or minus end in vitro (34). The motor was fused to a bright variant of green fluorescent protein, S65T GFP (37), denoted GFP*, regulated by the native ncd promoter. Genetic tests showed that the ncdnk11gfp* transgene rescues the frequent chromosome missegregation of cand, an ncd null mutant deleted for the promoter and 5′ end of both ncd and the closely apposed ca gene (38). Tests of two lines, M25M2 and M25M3#10, are shown in Table 1. The M25M2 mis-segregation frequency did not differ significantly from wild type (χ2 = 1.338, 1 df, p = 0.25). The M25M3#10 missegregation frequency did differ significantly from wild type (χ2 = 5.806, 1 df, p = 0.016), but the difference was small (0.87% cf 0.20%; Table 1). The ncdnk11gfp* M25M3#10 transgene, when tested in ncdnk11gfp* cand/+ females heterozygous for the transgene and cand, showed little or no evidence for dominant effects on meiotic and early mitotic chromosome segregation. One copy of the ncdnk11gfp* M25M2 transgene did not fully rescue cand females, but this was also observed for one copy of a wild-type ncdgfp* transgene, M3M1 (Table 1). Thus, the genetic tests failed to show specific loss-of-function or dominant mutant effects caused by the ncdnk11gfp* transgene.
Ncd is a spindle motor required for spindle assembly in oocytes and centrosome attachment to poles in early embryos (4,5,23,24,26). The effects of the bidirectional motor were examined in oocytes and early embryos of cand females homozygous for the ncdnk11gfp* transgene. Analysis of meiotic spindles in live ncdnk11gfp* M25M3#10 oocytes by laser-scanning confocal microscopy showed normal bipolar spindles (n = 14, total = 21) with some frayed spindles (n = 5) and spindles with split poles (n = 2) (Figure 1). Wild-type ncdgfp* #4121 oocytes (23,26) showed normal bipolar spindles (n = 15, total = 17) with a few spurred or multipolar spindles (n = 2). The analysis indicates that meiotic spindles undergo normal assembly in ncdnk11gfp* oocytes and do not differ significantly in overall appearance from wild-type ncdgfp* oocytes (χ2 = 2.358, 1 df, p = 0.125). Although defective meiotic spindles are observed in ncdnk11gfp* oocytes, they are also observed at low frequency in wild-type ncdgfp* oocytes. Neither ncdnk11gfp* nor wild-type ncdgfp* oocytes showed spindle defects as severe as those of cand or other ncd null mutant oocytes, which frequently exhibit small, widely separated spindles associated with missegregating chromosomes (4,23,39,40).
Analysis of early cleavage spindles and division kinetics in live ncdnk11gfp* embryos showed that both were normal. The time from microtubule nucleation in prometaphase to midbody formation in telophase of cycle 10 was not significantly different (ncdnk11gfp* M25M2, mean ± SEM = 263 ± 7 s, n = 14) or only slightly different (ncdnk11gfp* M25M3#10, 270 ± 8 s, n = 16) from wild-type ncdgfp* #4121 embryos (253 ± 7 s, n = 17) (Table 2). Strikingly, the pole-to-pole length of mitotic spindles at metaphase was greater in the ncdnk11gfp* mutant than wild type, and the difference in length increased at anaphase (Table 2). The increased spindle length is consistent with increased plus-end motor activity in the mutant that elongates the spindles by pushing the poles apart. The anaphase spindles of mutant embryos frequently appeared bent (ncdnk11gfp* M25M2, n = 43, total = 307; ncdnk11gfp* M25M3#10, n = 51, total = 276) compared with those of wild-type ncdgfp* #4121 embryos (n = 25, total = 395) (M25M2, χ2 = 11.163, 1 df, p = 0.0008; M25M3#10, χ2 = 24.568, 1 df, p < 0.0001), possibly due to unequal forces acting on the spindle fibers at anaphase. Discernible effects on mitotic spindles are thus observed in ncdnk11gfp* mutant embryos, but are not as pronounced as in other ncd mutants, which show severe centrosome loss and spindle pole defects (25,26).
The genetic and cytological analyses indicate that the NcdNK11GFP* motor is expressed in ncdnk11gfp* embryos and binds to spindle microtubules, but the bidirectional motor has relatively little effect on spindles in live cells compared with cand and other loss-of-function ncd mutants. One possibility is that the plus-end motility of the bidirectional mutant is suppressed in vivo. To examine this possibility, we deprived embryos of oxygen to block spindle dynamics and reduce motor activity in early cleavage divisions. Under these conditions, we observed striking effects on mitotic spindles of ncdnk11gfp* embryos that differed significantly from those of wild type.
Oxygen deprivation blocks early cleavage spindle dynamics and greatly delays or arrests cell cycle progression (41,42). Hypoxic wild-type ncdgfp* #4121 embryos progressed slowly through the cell cycle or were arrested in interphase or metaphase, as reported previously. Metaphase-arrested spindles contained prominent astral microtubules with centrosomes that showed reduced NcdGFP* fluorescence (Figure 2, arrowheads). Spindles were narrow and tapered, consisting of thick bundles of brightly fluorescent fibers that terminated at the metaphase plate, differing markedly in appearance from the barrel-shaped metaphase spindles of normal embryos (Figure 2A). Antibody staining of fixed hypoxic embryos (not shown) showed the same distribution of tubulin as of the Ncd motor, although some of the motor associated with spindle microtubules is probably lost during the fixation and staining procedures. Analysis of live embryos is thus more likely to show the actual motor distribution. The tapered appearance of the metaphase-arrested spindles of oxygen-derived embryos may be caused by disassembly of the nonkinetochore spindle fibers under hypoxia, leaving the more stable kinetochore fibers and astral microtubules. The metaphase-arrested spindles showed a gap at the metaphase plate (Figure 2, arrows) corresponding to the chromosomes, which were observed in DAPI-stained fixed hypoxic embryos.
Oxygen-deprived ncdnk11gfp* mutant embryos showed delayed or arrested mitotic divisions with prominent astral microtubules and reduced centrosome fluorescence (Figure 2C,D), as observed for hypoxic wild-type embryos. The spindle fibers of hypoxic ncdnk11gfp* embryos comprised thick, brightly fluorescent bundles, like the bundled spindle fibers of hypoxic wild-type ncdgfp* embryos (Figure 2B). Strikingly, the astral microtubules of arrested spindles were brightly fluorescent with the NcdNK11GFP* motor and frequently appeared more brightly fluorescent at the distal or plus ends (Figures 2C,D and 3A,B,C; asterisks). Measurements showed greater motorGFP* fluorescence at the distal ends of astral microtubules of ncdnk11gfp* embryos, compared with the proximal ends (ncdnk11gfp* M25M2, n = 314, total = 654 microtubules from 45 spindles of eight embryos; ncdnk11gfp* M25M3#10, n = 451, total = 779 microtubules from 49 spindles of 17 embryos) (Table 3). The frequency of astral microtubules in ncdnk11gfp* embryos with increased motorGFP* at the plus ends was significantly higher than in wild-type ncdgfp* #4121 embryos (n = 132, total = 578 microtubules from 54 spindles of 11 embryos) (M25M2, χ2 = 83.671, 1 df, p < 0.0001; M25M3#10, χ2 = 165.507, 1 df, p < 0.0001) (Table 3).
We also examined spindles of hypoxic ncdNKgfp* mutant embryos that express an Ncd mutant motor that binds to microtubules but does not move on microtubules in in vitro gliding assays (43). The spindles of hypoxic ncdNKgfp* M5M2 mutant embryos were delayed or arrested in mitosis and exhibited long astral microtubules, like those of hypoxic wild-type ncdgfp* and ncdnk11gfp* mutant embryos. In contrast to hypoxic wild-type and ncdnk11gfp* embryos, however, ncdNKgfp* embryos did not show a break in fluorescence at the metaphase plate (Figure 2E), which may be due to stabilization of the spindle fibers caused by tight binding of the mutant motor to microtubules. The hypoxic ncdNKgfp* embryos also did not show reduced centrosomal fluorescence, and the astral microtubules only infrequently showed increased motorGFP* fluorescence at the distal, compared with the proximal ends (n = 13, total = 214 microtubules from 23 spindles of six embryos) (Table 3). Instead, the spindle asters typically showed fluorescent centrosomes and decreasing fluorescence of astral microtubules from the proximal to the distal end (Figure 3D). These observations indicate that the diminished centrosomal fluorescence and the accumulation of motorGFP* fluorescence at the microtubule distal, or plus ends observed in hypoxic wild-type ncdgfp* embryos, and at significantly higher frequency in hypoxic ncdnk11gfp* embryos, is dependent on Ncd motility.
A possible explanation of the relatively minor mutant effects of the NcdNK11 bidirectional motor under normal conditions in vivo is that plus-end motility is suppressed by motor : motor interactions that bias directionality toward the microtubule minus end. Interactions of NcdNK11 motors with one another could cause the motors to bind cooperatively to spindle fibers and move in the same direction, influenced by spindle dynamics or the other known Drosophila minus-end spindle motor, cytoplasmic dynein. To test whether NcdNK11 shows cooperativity of binding to microtubules in vitro, motors were mixed with microtubules on a grid, negatively stained and examined using electron microscopy (EM). Grids prepared without motor showed microtubules with a pale outline of negative staining (Figure 4A). Grids of wild-type Ncd-decorated microtubules showed microtubules with a continuous dark outline (Figure 4B, top), adjacent to microtubules with a paler outline (Figure 4B, bottom). The dark outline is due to negatively stained motors bound to the surface of the microtubule and is not observed for microtubules negatively stained in the absence of motors (Figure 4A). The continuous dark outline indicates that the microtubule is fully decorated with motors along its length. These fully decorated microtubules lie adjacent to paler microtubules, which appear almost bare of motors. Grids of NcdNK11-decorated microtubules also showed fully decorated microtubules (Figure 4C, top) adjacent to microtubules that were almost bare of motors (Figure 4C, bottom). These results are consistent with cooperative binding of the Ncd and NcdNK11 motors to microtubules during grid preparation. Similar observations have been reported by others (44).
We also assayed wild-type Ncd and NcdNK11 to determine whether the motors showed density-dependent effects on motility in microtubule-gliding assays in vitro. The motors were fused to glutathione S-transferase (GST) to attach the motor to anti-GST antibody-coated glass surfaces. Gliding assays of motors at different densities showed slower velocity with decreasing motor density and a threshold density after which no microtubules were bound to the glass surface (Figure 5). The threshold density is a measure of the lowest motor density required to bind microtubules to the surface. The GST/NcdNK11 motor showed lower mean velocities at motor densities comparable to wild-type GST/Ncd and an approximately 2-fold higher threshold density for binding microtubules to the surface than wild-type GST/Ncd (Figure 5). These results indicate that both the NcdNK11 mutant and wild-type Ncd are dependent on interactions with other motors on the glass surface for motility in gliding assays, but the NcdNK11 motor shows a greater dependence on motor density than wild-type Ncd.
Directional movement of molecular motors is thought to be essential to their cellular function, permitting directed transport of cargo along actin filaments or microtubules. Here, we test the effect of altered directionality of minus-end Ncd on its function in the spindle by examining oocytes and early embryos expressing a bidirectional motor that moves either to the microtubule plus or minus end in vitro (34). Unexpectedly, we find that the mutant motor has little effect on meiotic or early mitotic chromosome segregation when assayed genetically, or on the cytological appearance of oocyte and early embryo spindles. The possibility that the motor is not expressed, or is unstable, is excluded by its expression as a GFP fusion protein and the observation of brightly fluorescent mitotic spindles that assemble and undergo division with kinetics similar to those of wild type. Mutant ncdnk11gfp* oocytes showed some frayed spindles or spindles with split poles, and ncdnk11gfp* embryos showed a higher frequency of bent anaphase spindles than wild-type ncdgfp* embryos, and a small but significant increase in pole-to-pole length at metaphase and anaphase. These relatively minor effects indicate that the mutant motor is expressed and functional, and are consistent with abnormal, or plus-end, activity of the mutant motor. The finding that the mutant motor causes only slight effects in oocytes or embryos that otherwise lack Ncd raises the possibility that plus-end motility of the bidirectional motor is suppressed under normal conditions.
To test the idea that the plus-end motility of the bidirectional motor is suppressed, we blocked spindle dynamics and reduced motor activity by depriving embryos of oxygen. Hypoxic wild-type ncdgfp* embryos were greatly delayed in cell cycle progression or arrested in interphase or metaphase, as reported previously (41,42). Arrested metaphase spindles exhibited prominent astral microtubules and thick bundles of stable microtubules that are probably kinetochore fibers. Non-kinetochore spindle fibers are less stable than kinetochore fibers (45–47) and probably disassemble under hypoxia and do not reassemble. Stabilization of kinetochore fibers could cause metaphase arrest by preventing entry into anaphase and poleward movement of chromosomes. Entry into anaphase is likely to be exquisitely sensitive to changes in microtubule dynamics. Hypoxic ncdnk11gfp* mutant embryos showed effects similar to those of wild type with narrow, tapered metaphase-arrested spindles, thick bundles of brightly fluorescent spindle fibers, prominent astral microtubules and diminished motorGFP* fluorescence at centrosomes. The mutant motor accumulated at the distal or plus ends of astral microtubules at significantly higher frequency than in wild-type embryos, consistent with increased plus-end movement.
The effects of hypoxia on the ncdnk11gfp* mutant embryos thus paralleled those of wild type except for the accumulation of NcdNK11GFP* at distal or plus ends of astral microtubules. Accumulation of the NcdNK11GFP* motor at astral microtubule tips can be explained by the increased ability of the NcdNK11 motor to move slowly to microtubule plus ends under hypoxic conditions in vivo, consistent with its movement toward plus or minus ends in vitro (34). This interpretation is supported by the effects observed for NcdNKGFP*, a motor that binds tightly to microtubules, but is defective in microtubule-stimulated ATPase activity and shows no microtubule motility in vitro (43). Spindles of hypoxic ncdNKgfp* embryos were greatly delayed or arrested in mitosis with prominent astral microtubules, like those of wild-type ncdgfp* and ncdnk11gfp*. However, centrosomes were not depleted of motorGFP* fluorescence, and astral microtubules did not show frequent accumulation of fluorescence at their distal ends.
Not all of the NcdNK11GFP* accumulation observed under hypoxia was at the distal ends of microtubules – accumulation of fluorescence was also observed at astral microtubule proximal or minus ends in both wild-type ncdgfp* and ncdnk11gfp* spindles (Figure 3), consistent with minus-end movement of the wildtype and mutant motors. However, the motorGFP* distribution was shifted toward the microtubule plus ends in ncdnk11gfp*, compared with ncdgfp* spindles (Table 3). Why would hypoxia limit minus-end motor activity more dramatically than plus-end activity? This may be because there are fewer known minus-end spindle motors in Drosophila – only Ncd and cytoplasmic dynein – compared with the relatively large number of plus-end kinesin motors. Slow decrease of both plus- and minus-end motor activities under hypoxia might favor the perdurance of plus-end motor activity and cause NcdNK11 to switch into a plus-end mode due to motor: motor interactions (see below), revealing the plus-end activity of NcdNK11GFP*.
Another possible explanation for the increased accumulation of NcdNK11GFP* at microtubule plus ends is that the motorGFP* is transported under hypoxia to microtubule distal ends by plus-end spindle motors. We do not favor this possibility as it should result in a similar distribution of wild-type NcdGFP* and NcdNKGFP* as for NcdNK11GFP*, and this was not observed.
Our observations support the interpretation that accumulation of the wild-type NcdGFP* and NcdNK11GFP* motors at astral microtubule distal ends is due to the ability of the NcdNK11 mutant motor to move slowly toward the plus ends, as well the minus ends, under hypoxic conditions in vivo. This interpretation should be taken cautiously, as hypoxia can cause complex reactions in cells. Although this presumed plus-end movement was observed both for the wild-type and bidirectional NcdNK11 motors, its frequency was significantly increased for the bidirectional motor. The absence of mutant effects under normal conditions means that plus-end movement in the mitotic spindle may be suppressed under normal conditions for the NcdNK11 bidirectional motor. This is also probably true for wild-type Ncd, whose displacements are not always directed toward the minus end in laser trap assays (34).
We asked whether the NcdNK11 motor shows a dependence on interactions with other motors for binding to microtubules and motility in vitro. Binding of the NcdNK11 motor to microtubules is highly cooperative, as revealed by EM of negatively stained motor-decorated microtubules showing fully decorated microtubules adjacent to nearly bare microtubules. Decoration of microtubules with motors for EM is typically done with excess motor to ensure binding by the motor to available sites on the microtubule. It is therefore unusual to observe fully decorated microtubules next to microtubules that are almost completely bare, as shown in Figure 4B,C. This indicates a high degree of cooperativity for microtubule binding by the NcdNK11 motor, which we also observed for wild-type Ncd.
Tests of Ncd and NcdNK11 dependence on density for motility by serially diluting the motor and performing gliding assays showed density dependence for maximal gliding velocity and a threshold density after which microtubules did not land and glide. These properties are characteristic of nonprocessive motors (48) and are consistent with single-motor laser trap assays demonstrating that Ncd is a nonprocessive motor (34,49). In previously reported coverslip-gliding assays, the NcdNK11 bidirectional motor showed long gliding excursions toward either the microtubule plus or minus end and occasional reversals of direction, rather than frequent switching between plus- and minus-end gliding (34), consistent with interactions between motors on the coverslip that influence directionality. This suggests that motor directionality is subject to motor : motor interactions on the coverslip and that interactions of motors arrayed along spindle fibers might suppress plus-end movement in vivo.
The NcdNK11 motor shows evidence for cooperativity in binding to microtubules and density dependence in translocating microtubules in motility assays in vitro. The directional movement of NcdNK11 in vivo could be influenced by cooperativity of binding by the motors to spindle fibers and interactions of motors with one another after binding. Interactions of adjacent NcdNK11 motors might cause arrays of motors along spindle microtubules to move in the same direction. Spindle dynamics, including poleward flux of microtubules (9–11), and minus-end movement of cytoplasmic dynein, could bias movement of NcdNK11 toward the microtubule minus end under normal conditions, overcoming any tendency of the motor to move toward the plus end. Blocking spindle dynamics and reducing motor activity under hypoxia could cause a switch to plus-end directionality, due to a higher number of plus-end motors still active in the spindle. This would be consistent with predictions from computer modeling of increased directionality switching by lower densities of NcdNK11 motors due to cooperative effects of motors on single microtubules (50). This could explain why the plus-end directionality of NcdNK11 is suppressed under normal conditions, but revealed by hypoxia, although other effects caused by hypoxia could account for the accumulation of motorGFP* fluorescence at microtubule plus ends that we interpret as plus-end movement by the motor.
These observations suggest that spindle dynamics and other motors might also influence directionality of wild-type Ncd, whose displacements are biased toward the minus end in laser trap assays, but are not exclusively minus-end-directed (34). Our findings imply that Ncd directionality in the cell is dependent on motor density and can be influenced by interacting dynamic processes. The increased accumulation of motorGFP* at microtubule plus ends in hypoxic wild-type ncdgfp* and ncdnk11gfp* mutant embryos is consistent with this idea. Thus, minus-end directionality of wild-type Ncd could be rectified in live cells under normal conditions by spindle dynamics and the other known Drosophila minus-end spindle motor, cytoplasmic dynein, rather than being due to motor determinants alone.
Kinesin proteins are referred to throughout using the new family names (22).
A cDNA encoding the bidirectional Ncd mutant motor, NcdNK11 N340K, fused at the C terminus to S65T GFP (37), denoted GFP*, was ligated to pCaSpeR3 (51) and injected into w; Δ2-3 Sb/+ embryos. The ncdnk11gfp* transgene is regulated by the native ncd promoter (38). Transformants were selected by w+ eyecolor rescue, and lines were made homozygous for the cand null mutant of ncd or heterozygous for cand and the TM3 balancer chromosome. Transgenic lines were analyzed by polymerase chain reaction (PCR) and DNA sequencing. Lines selected for further analysis were confirmed by molecular analysis as containing the ncdnk11gfp* transgene with the N340K mutation and no other ncd gene. Homozygous ncdnk11gfp* cand females were tested for rescue of cand, which causes high levels of chromosome nondisjunction and loss, as described (52). Females heterozygous for cand and ncd+ with one copy of the ncdnk11gfp* transgene were tested for dominant effects, and females homozygous for cand with one copy of the transgene were tested for haplo-insufficiency. The wild-type control for the genetic tests was Oregon R.
Transgenic lines expressing a cDNA encoding the Ncd N600K mutant, which is defective for motor movement on microtubules but not binding to microtubules or nucleotide (43), were recovered as fusions to gfp*, as described above. The ncdNKgfp* lines were made into stocks with cand and TM3, and tested by PCR and DNA sequence analysis for the presence of the mutation and absence of other ncd genes. Genetic tests showed failure of ncdNKgfp* to rescue cand (data not shown).
DNA was prepared from one to five flies for molecular analysis of transgenic ncdnk11gfp* and ncdNKgfp* lines. Polymerase chain reaction was performed using primers that flank the ncdnk11 or ncdNK mutations and one of the two introns present in the wild-type ncd gene, producing a 572-bp fragment from the cDNA transgene and a 632-bp fragment from wild-type ncd. The null mutant, cand, contains a deletion of the promoter and 5′ end of ncd that includes the region corresponding to one of the primers, and thus produced no PCR fragment. Polymerase chain reaction-amplified DNA was gel purified for sequence analysis by the Duke University Comprehensive Cancer Center DNA Analysis Facility (Durham, NC, USA).
Spindles were examined in live oocytes and embryos produced by cand females with four copies of wild-type ncdgfp* (line #4121: M3M1; M9F1) (23,26), or two copies of ncdnk11gfp* (M25M2 or M25M3#10). To visualize meiotic spindles, oocytes were dissected from ovaries in Schneider’s Drosophila medium containing 10 or 15% FCS and mounted in medium under a glass coverslip on an oxygen-permeable Teflon membrane supported by a custom metal slide (53). Meiotic spindles were imaged within 25–80 min after starting dissection to exclude changes in spindles caused by oocyte hydration. For analysis of mitosis, embryos were collected at 30-min intervals, aged on collection plates 15 min to 1 h, dechorionated, and mounted as for oocytes, but in halocarbon oil 27 (Sigma Chem. Co., St. Louis, MO, USA) instead of Schneider’s medium. Live oocytes and embryos were imaged using a Bio-Rad MRC600 laser-scanning confocal microscope equipped with a 63X/1.4 NA Plan-Apochromat objective and custom GFP filter block (23,26).
Embryos, including those of ncdNKgfp* (M5M2) cand females, were collected and dechorionated as described above, then crowded closely together and mounted under a coverslip on a glass slide. Slides were aged for 1–1.5 h to allow hypoxia to develop, and embryos were imaged 1–3 h after slide preparation. In some cases the coverslip was sealed to the slide using VALAP (1:1:1 Vaseline : lanolin : paraffin, heated until clear). Fixed hypoxic embryos were stained with anti-Ncd antibodies (25,54) followed by FITC-labeled secondary antibodies and rhodamine-conjugated anti-α-tubulin antibody to label the motor and spindle microtubules, respectively, and the chromosomes were stained with DAPI. Images of the DAPI-stained chromosomes were acquired with a Princeton Instruments Penta-Max-1317-K cooled CCD camera mounted on a Leica Dialux 22 microscope using a 63X/1.4 NA Plan-Apochromat objective and overlaid on confocal images of the motor- or tubulin-labeled spindles. FITC was visualized using the Bio-Rad MRC600 confocal system and GFP filter block described above and rhodamine was visualized using a custom rhodamine filter block (568/10x excitation, Q578LP dichroic and HQ598/40 BP emission filter; Chroma Technology Corp., Rockingham, VT, USA).
Spindle length at metaphase and anaphase was determined by measuring from the center of one centrosome to the other using the line tool of NIH Image and time-lapse images of live, early syncytial blastoderm embryos collected under normal conditions. The distribution of motorGFP* along astral microtubules of metaphase-arrested spindles of hypoxic embryos was quantified from projections of Z-series images made using the brightest point projection method of NIH Image. Astral microtubules were traced with the line tool to measure the pixel values along their length. Measurements were displayed as plots of greyscale value versus length and microtubules were scored as −, 0 or + for less, the same, or greater fluorescence at the distal, relative to the proximal end.
Bacterially expressed, purified dimeric motor protein was mixed with microtubules on a grid in a volume of 5 μL at a concentration of 2–3 μm motor and 1–2.4 μm microtubules (tubulin dimer) in 20 mm HEPES pH 7.2, 1 mm EGTA, 5 mm MgCl2, 1 mm DTT, 11–13 mm NaCl, 20 μm taxol and 1 mm AMP·PNP. Grids were negatively stained with 1% uranyl acetate and examined in a Philips Tecnai F20 electron microscope. Grids prepared with motor and microtubules but without nucleotide (with apyrase) gave similar results as with AMP·PNP, i.e. fully decorated microtubules adjacent to undecorated microtubules.
Microtubule-gliding assays of wild-type Ncd (MC1) (55) and NcdNK11 were performed (56) using serial dilutions of lysates prepared from cells expressing the motors as GST fusions. GST/Ncd and GST/NcdNK11 are identical except for the NK11 N340K mutation. Lysates were quantitated for GST/Ncd or GST/NcdNK11 on Western blots containing known amounts of purified GST/Ncd by cross-reaction with anti-GST antibodies. Velocities were tracked from videotapes using a custom tracking program (a gift of T Salmon and N Gliksman, University of North Carolina, Chapel Hill, NC, USA). Motor concentrations were normalized to correct for the relative amounts of wild-type Ncd and NcdNK11 in lysates used in the gliding assays.
We thank E Dagenbach for staining and analyzing fixed embryos, T Shen for microtubule tracking, and B Sullivan for rhodamine-labeled anti-α-tubulin antibody. This study was supported by grants from the NIH to SAE, Royal Swedish Academy of Sciences to HNS, and HFSP to KH and SAE.