During animal cell division, the central spindle, an anti-parallel microtubule bundle structure formed between segregating chromosomes during anaphase, cooperates with astral microtubules to position the cleavage furrow. Because the central spindle is the only structure linking the two halves of the mitotic spindle, it is under mechanical tension from dynein-generated cortical pulling forces, which determine spindle positioning and drive chromosome segregation through spindle elongation. The central spindle should be flexible enough for efficient chromosome segregation while maintaining its structural integrity for reliable cytokinesis. How the cell balances these potentially conflicting requirements is poorly understood. Here, we demonstrate that the central spindle in C. elegans embryos has a resilient mechanism for recovery from perturbations by excess tension derived from cortical pulling forces. This mechanism involves the direct interaction of two different types of conserved microtubule bundlers that are crucial for central spindle formation, PRC1 and centralspindlin.
Microtubule bundle structures play crucial roles in animal cell cytokinesis. During anaphase, the central spindle is formed between segregating chromosomes, and, in cooperation with astral microtubules, it determines the position of the cleavage furrow by forming a zone of active Rho GTPase, a master regulator of contractile ring formation1. It also serves as a precursor to the midbody, which recruits factors crucial for the final separation of two daughter cells by membrane abscission2,3. Dynein at the cell cortex generates ‘cortical pulling force’, a mechanical force that pulls astral microtubules towards the cell cortex4,5. As a consequence, the spindle poles are pulled outwards. This force determines spindle positioning and drives chromosome segregation through elongation of the pole-to-pole distance (anaphase B)4,6,7,8,9,10. After anaphase onset, when sister chromatid cohesion has dissolved, the central spindle becomes the only structure that links the two halves of the mitotic spindle. Thus, it is under mechanical tension from the cortical pulling force. How the central spindle maintains its structural integrity under tension while allowing anaphase B pole-to-pole elongation to occur is not well understood.
Molecules important for the formation and function of the central spindle form a protein–protein interaction network that includes two different microtubule-bundling factors, centralspindlin and PRC1 (refs 11, 12). Centralspindlin is a 2:2 heterotetramer of a kinesin-6 subunit MKLP1 (MKLP1/KIF23 in mammals and ZEN-4 in Caenorhabditis elegans) and a non-motor subunit CYK4 containing a GTPase-activating protein (GAP) domain for Rho-family GTPases (MgcRacGAP/RACGAP1 in mammals and CYK-4 in C. elegans)13,14. PRC1 is the metazoan orthologue of yeast Ase1 and plant MAP65 (refs 15, 16). Both centralspindlin and PRC1 show microtubule-bundling activities in vitro and are required for proper formation of the central spindle in vivo. They co-localize to the centre of the central spindle and midbody, where the plus ends of microtubules are bundled in an interdigitating manner17. As important hubs of the protein–protein interaction network, both of these proteins recruit various other factors to the centre of the central spindle and midbody. For example, KIF4 kinesin, a suppressor of microtubule polymerization dynamics, is recruited to the central spindle via interaction with PRC1 and limits the length of the anti-parallel overlap18,19,20,21. ECT2, a major activator of Rho during cytokinesis, accumulates at the spindle midzone through interaction with CYK4 (refs 22, 23, 24, 25, 26, 27) and forms an equatorial zone of active Rho28. Interestingly, a direct interaction between PRC1 and CYK4 has been reported in mammalian cells29. However, the role of the interaction between the two different types of microtubule bundling proteins in central spindle formation remains unclear. Here, we study the response of the central spindle to mechanical perturbation and find that the interaction between centralspindlin and PRC1 plays an important role in the mechanical robustness of this microtubule bundle structure that is critical for cytokinesis.
Resilience of central spindle under mechanical perturbation
To examine the response of the central spindle to increased pulling forces (Fig. 1a), we generated transgenic C. elegans strains expressing mCherry-tagged tubulin and green fluorescent protein (GFP)-tagged CYK-4. During the first mitotic division of control embryos, the bipolar spindle formed promptly following nuclear envelope breakdown (NEBD, time=0). NEBD was monitored by the loss of exclusion of the tubulin signal from pronuclei (Fig. 1b and Supplementary Fig. 1 for grayscale images covering the whole embryos). Approximately 120–150 s following NEBD, the distance between the two spindle poles (Fig. 1c) started to increase, indicating the onset of anaphase, as previously reported30 (Fig. 1d). At the same time, CYK-4 began to accumulate at the spindle midzone (Fig. 1b, control), where the plus ends of the two sets of interpolar microtubules from the two spindle poles form an interdigitating overlap, as confirmed by an accelerated increase in the peak intensity (Fig. 1d, control and Supplementary Fig. 2a for examples of the line profiling of CYK-4::GFP intensity). Within the next 30–60 s, the central spindle was established, with CYK-4 enriching rapidly in the central overlap zone and remaining there for ∼300 s until the cleavage furrow fully ingressed and the central spindle was compacted to form the midbody.
EFA-6 is a negative regulator of the dynein-based cortical pulling force31. In embryos depleted of EFA-6, pole-to-pole elongation was accelerated (from 80 nm s−1 in control embryos to 120 nm s−1; Fig. 1d, efa-6(RNAi)), as expected. In these embryos, CYK-4 accumulated normally until 180 s after NEBD (Fig. 1b,d, efa-6(RNAi)), when the peak corresponding to its accumulation suddenly broadened (Fig. 1b,d, arrowheads). Thereafter, the total amount of CYK-4 detected between the two poles continued to increase, and the tight localization of CYK-4 fluorescence at the midzone was gradually restored (Fig. 1d, black arrows in the ‘CYK-4 peak width’ panels). A similar pattern of CYK-4 accumulation was observed in the embryos depleted of the kinesin-5 BMK-1, which has been reported to function as a brake during spindle elongation in C. elegans embryos32 and other cell types33,34 (Fig. 1b,d, bmk-1(RNAi)). These data indicate that the central spindle has a resilient recovery mechanism that acts against perturbations that cause excessive pole-to-pole separation.
In contrast, in embryos depleted of SPD-1, the C. elegans orthologue of PRC1, the spindle was broken into two halves, and the accumulation of CYK-4 at the midzone dropped drastically (Fig. 1b,d, arrow in spd-1(RNAi) and Supplementary Fig. 2b and c)35. Once it was lost from the spindle midzone, CYK-4 could not re-accumulate there, although much later, it localized to the midbody via the cortical/astral route independent of the central spindle (Fig. 1b,d, double-headed arrows in spd-1(RNAi) panels)35,36. Reciprocally, the dependency of SPD-1 midzone localization on centralspindlin has also been reported35, implying that the cooperative interaction between the two different types of microtubule bundling proteins might be important for the mechanical resilience of the central spindle.
Direct interaction between PRC1 and centralspindlin
A direct interaction between human orthologues of SPD-1 and CYK-4 has been reported29, and a physical interaction between Ase1, a yeast PRC1 homologue, and Klp9, a kinesin that is distantly related to ZEN-4/MKLP1 (although more closely to MKLP2), has also been shown37. We therefore examined whether SPD-1 and CYK-4 physically interact by in vitro pull-down and yeast two-hybrid assays. In vitro translated full-length CYK-4 was pulled down by beads coated with bacterially expressed full-length SPD-1 (Fig. 2a and Supplementary Fig. 3a). Inversely, SPD-1 was bound to beads coated with CYK-4 as well as the CYK-4/ZEN-4 centralspindlin holocomplex (Fig. 2b and Supplementary Fig. 3b). This interaction was also observed in yeast two-hybrid assays between CYK-4 and the N-terminal fragment of SPD-1 and was drastically weakened by deletion of the C-terminal tail of CYK-4 (Fig. 2c,d CYK-4 ΔTail), which is dispensable for both centralspindlin complex assembly and microtubule bundling13,38. In contrast, the CYK-4 C-terminal tail fragment alone showed an interaction with SPD-1 that was enhanced by dimerization by adding back the coiled coil (Fig. 2c and d, CYK-4 Tail and CC+Tail). A similar requirement of the C-terminal tail of CYK-4 was also observed in pull-down assays (Fig. 2e and Supplementary Fig. 4). SPD-1 1–228 was robustly pulled down by CYK-4 fragments containing the C-terminal tail region (FL, 34–681, 121–681 and CC+Tail) but much more weakly by fragments lacking the C-terminal tail (34-618 and CC). These data indicate that the SPD-1–CYK-4 interaction is mediated mainly by the N-terminal region of SPD-1 and the C-terminal tail of CYK-4.
The spd-1 gene was originally isolated in a forward genetic screen for temperature-sensitive cell division defects39. Interestingly, the oj5 allele isolated in this screen as the cause of central spindle defects has been shown to be an R83W mutation35, which lies within the CYK-4-binding region of SPD-1 defined above. We tested whether this mutation affected the SPD-1–CYK-4 interaction and found that it was drastically weakened in both yeast two-hybrid (Fig. 2d) and in vitro pull-down assays (Fig. 2e and Supplementary Fig. 4). Importantly, however, this mutation did not affect other known properties of PRC1, such as dimerization/oligomerization40,41 and microtubule bundling. In yeast two-hybrid assays, the interaction between SPD-1 expressed as bait and SPD-1 as prey was not affected by the R83W mutation (Fig. 2d, bottom row). Consistently, this mutation did not affect the mobility of full-length recombinant SPD-1 in size exclusion chromatography (Fig. 2f). In addition, SPD-1 with the R83W mutation could bind microtubules (Fig. 2g) and bundle microtubules (Fig. 2h) in solution as efficiently as its wild-type counterpart. These data indicate that the R83W mutation specifically affects the interaction between SPD-1 and CYK-4, although we cannot formally exclude possible influences on as-yet-unknown functions of SPD-1/PRC1. These findings strongly suggest that the central spindle defects observed in spd-1(oj5) mutants are caused by the defective binding between PRC1 and centralspindlin, the two major microtubule crosslinking/bundling proteins of the central spindle.
Rupture of central spindle caused by CYK-4 tail mutations
To further assess the physiological importance of the interaction between SPD-1 and CYK-4, we introduced point mutations in CYK-4 that affected its interaction with SPD-1. Sequence comparison of the C-terminal tails of CYK-4 orthologues revealed the presence of two motifs, SILGPVTT and K/R-X-K/R, which have been widely conserved throughout metazoan evolution (Fig. 3a and Supplementary Fig. 5). Mutations in these motifs weakened the SPD-1–CYK-4 interaction, either moderately (IL to NN, IL to AA and SIL to AAA) or more severely (RAR to EAE; Fig. 3b). Similar effects were also observed in an in vitro pull-down assay (Fig. 3c). We generated transgenic animals carrying these mutations (AA and EAE) as well as a deletion of the tail domain (ΔTail) in a cyk-4::gfp transgene and expressed the transgenes in a strain in which endogenous cyk-4 had been deleted. Although the wild-type transgene efficiently suppressed the embryonic lethality caused by the deletion of endogenous cyk-4, embryos expressing the mutant transgenes showed different levels of lethality, according to the severity of the SPD-1-binding defect (Fig. 3d). Although the mild AA mutation caused mild lethality, the more severe EAE mutation caused much higher lethality. The ΔTail mutation resulted in the most severe phenotype (>90% lethality). This close correlation between the in vitro and in vivo phenotypes clearly shows that the SPD-1–CYK-4 interaction plays a crucial role in early C. elegans development.
Next, we examined the influences of the defective SPD-1–CYK-4 interaction on cell division, especially on the robustness of the central spindle. The fluorescence intensities of uniform cytoplasmic CYK-4::GFP during the pre-mitotic stage confirmed that the protein expression level was not affected by the EAE and ΔTail mutations (Supplementary Fig. 6). Consistent with the normal behaviour of CYK-4 in spd-1(RNAi) embryos up to mid-anaphase (NEBD ∼180 s), in the EAE and ΔTail mutant embryos, the bipolar spindle formed normally, and mutant CYK-4 began to accumulate at the spindle midzone at the same time as in wild-type embryos (Fig. 3e,f). However, once it formed, the midzone microtubule bundle was disrupted within 30–60 s. As a consequence, the anaphase spindle was split into two half-spindles, and the poles moved rapidly apart. At the same time, accumulated mutant CYK-4 was lost, detected as a rapid broadening of the peak width and a gradual decrease in the peak intensity (Fig. 3f) of CYK-4::GFP fluorescence, indicating that in some embryos, mutant CYK-4 was retained near the tips of the broken half-spindles for a while (Fig. 3e, arrows). These observations clearly indicate that the SPD-1–CYK-4 interaction is necessary for the robust maintenance of the central spindle after its initial formation.
Suppression of spindle rupture by reduction of tension
Because enhancement of the cortical pulling force by efa-6(RNAi) caused pole separation to accelerate (Fig. 1), we hypothesized that spindle breakage in the absence of the SPD-1–CYK-4 interaction might be suppressed if cortical pulling forces were reduced by the depletion of cortical activators of dynein5,42 (Fig. 4). As previously reported, depletion of the GoLoco domain protein GPR-1/2 or NuMA-related LIN-5 slowed pole-to-pole separation to ∼40–50 nm s−1 (Fig. 4a,b), indicating a reduction in the cortical pulling force43,44,45,46. Under these conditions, an apparently normal central spindle was formed in cyk-4 ΔTail mutant embryos and was maintained thereafter much more stably than in control embryos (Fig. 4a). The peak intensity of CYK-4 ΔTail at late anaphase (240 s after NEBD) was restored to almost 100% of the level of wild-type embryos without RNA interference (RNAi; Fig. 4b). The width of midzone accumulation also became comparable to that of the control, although later, it was slightly broadened (Fig. 4a,b). However, consistent with the role of the G-protein pathway in the regulation of the cortical pulling force in the aster-dependent pathway of cleavage furrow ingression47, cytokinesis failure in cyk-4 ΔTail mutant embryos (13/23) was not suppressed but was rather enhanced by the depletion of GPR-1/2 or LIN-5 (6/6 and 11/11, respectively). Similar restoration of the stability of the central spindle following a reduction in cortical pulling forces was also observed in CYK-4 EAE mutant embryos (Supplementary Fig. 7).
To further examine whether the mechanical fragility of the central spindle in the cyk-4 tail mutants was caused by the lack of SPD-1–CYK-4 interaction or by possible defects in an as-yet-unknown function of the CYK-4 tail, we tested the effect of the reduction of the cortical pulling force in spd-1(oj5) embryos (Fig. 5a,b). As previously reported35, the central spindle was disrupted in spd-1(oj5) embryos, accompanied by the dispersion of transiently accumulated wild-type CYK-4::GFP. In contrast, LIN-5 depletion suppressed the sudden rupture of the central spindle and prolonged the accumulation of CYK-4. These data further indicate that the SPD-1–CYK-4 interaction through the CYK-4 C-terminal tail plays an important role in maintaining the mechanical integrity of the central spindle under tension. This interaction is dispensable for lateral microtubule bundling per se and for the tight localization of CYK-4 to the spindle midzone but becomes crucial when the whole spindle is under mechanical tension equivalent to that experienced during the normal asymmetric first cell division.
Here, we have revealed a molecular mechanism for the mechanical resilience of the central spindle, which is key to reconciling the conflicting requirements for efficient cytokinesis versus spindle positioning and chromosome segregation. Interestingly, this mechanism has been implemented into the core machinery of central spindle formation via the direct interaction of two conserved major microtubule bundlers, PRC1 and centralspindlin. The motifs critical for SPD-1 binding in the C-terminal tail of CYK-4 seem to have been widely conserved throughout metazoan evolution48, with the exception of arthropods and platyhelminthes (Supplementary Fig. 5). Interestingly, arthropods carry out embryonic cleavage using a unique strategy, and the contribution of the cortical pulling force on anaphase B is limited in Drosophila embryos49. Because a direct interaction between centralspindlin and PRC1 has been demonstrated in humans and C. elegans, a pair of distantly related species, it is reasonable to speculate that the binding between them might also be widely conserved. The interaction between centralspindlin and PRC1 in metazoans might be an evolutionary adaptation to the coupled sliding and polymerization mechanism50,51, which originally occurred to drive spindle elongation in eukaryotic ancestors, functioning as an ‘engine brake’ to counteract excess external forces.
External pulling force applied to the central spindle accelerates the anti-parallel sliding of microtubule bundles, which would cause constant ‘leakage’ of microtubule-bundling proteins from the zone of anti-parallel microtubule overlap into the non-bundled part of the microtubules, where binding of the bundling proteins to them would be less stable (Fig. 6a). We speculate that the interaction between different types of microtubule bundlers might compensate for their limitations, such as the inability of PRC1 to carry out active unidirectional transport52,53,54,55 and the low processivity of centralspindlin as a motor, especially when it is not clustered56, potentially helping them return to the anti-parallel microtubule overlap (Fig. 6b). In the absence of the PRC1-centralspindlin interaction, slowing anti-parallel sliding would reduce the leakage of bundling proteins from the overlap zone but not completely prevent it. This notion is consistent with the gradual loss of CYK-4 signals observed at the later time points (Figs 4 and 5, ∼300 s after NEBD). This model also predicts that even when the interaction between PRC1 and centralspindlin is intact, if the cortical pulling force is too strong, the central spindle will still be broken. This situation might have occurred in the case of the midzone rupture reported following KLP-7/CeMCAK depletion4,46. Direct testing of this model would require precise measurement of the distribution of microtubule plus ends and the lengths of anti-parallel overlap as well as the localizations of centralspindlin and PRC1 at higher temporal resolution. In future studies, it will be important to examine how other known protein–protein interactions at the central spindle, such as that between KIF4 chromokinesin and PRC1, which is promoted by Aurora B phosphorylation and suppresses the plus-end dynamics of microtubules18,41,53,57,58, contribute to the mechanical resilience of the central spindle in cooperation with the PRC1–centralspindlin interaction investigated here.
C. elegans strains and culture
The C. elegans strains used in this study are listed in Supplementary Table 1 and were maintained at 20 °C, except for strains containing temperature-sensitive spd-1(oj5) allele, which were maintained at 15 °C. To generate the cyk-4::gfp strains by Mos1-mediated single-copy insertion (MosSCI)59, a 4.5-kb cyk-4 genomic fragment was amplified with a primer pair, 5′-AATCAGGGCCCTCACAAACACAGCACTCGGTC-3′ and 5′-ACTATCCCGGGTACTCACCGGAAACGGAGTC-3′ and cloned into the PspOMI/XmaI site of the pBluescript vector. Following insertion of the gfp sequence between the coding region and the stop codon, the BsiWI/XmaI fragment (from 990 bp upstream of the start codon to 1,072 bp downstream of the stop codon) was subcloned into a MosSCI targeting vector, pCFJ178. The point mutations and deletion were introduced with primer pairs, 5′-GCTCTCTGTGATCGTAGCGCTGCTGGACCAGTTACAACATCACC-3′ and 5′-GGTGATGTTGTAACTGGTCCAGCAGCGCTACGATCACAGAGAGC-3′ (‘AA’), 5′-GTCGGCCAACGCGACTGAAGCAGAAGGTGCTCATCTGC-3′ and 5′-GCAGATGAGCACCTTCTGCTTCAGTCGCGTTGGCCGAC-3′ (‘EAE’), and 5′-TGCAGATGTCCCTAGGAATCGTTGCCAATATAC-3′ and 5′-CATCTGCTGGGGTCGATGTTCCACGAT-3′ (‘ΔTail’). The engineered transgenes were confirmed by sequencing and injected into the EG5003 strain for insertion into chromosome IV. Transgene integration was verified by sequencing. mCherry::tubulin strain (JA1559) was a gift from J. Ahringer (Gurdon Institute, UK).
Embryonic lethality assay
To score the rescue efficiency of cyk-4 null embryonic lethality by the cyk-4::gfp transgenes, the cyk-4::gfp MosSCI strains were crossed into the cyk-4(ok1034) deletion strain (VC859) to obtain worms homozygous for both cyk-4(ok1034) and cyk-4::gfp, which were verified by PCR using a pair of primers, 5′-TTATGGACGGTTGTGT-3′ and 5′-GAGACTGTCACCAGGTTG-3′, and a combination of three primers, 5′-GCCGCACACCTTCTCTTTTGATG-3′, 5′-GCAGTACAGAATAATAAAGTGTG-3′ and 5′-GCACGATTTTTGCCATACTACTG-3′, respectively. In the absence of a cyk-4 transgene, homozygous cyk-4 deletion (ok1034) causes 100% embryonic lethality. The hatching rates of the embryos laid during the first 36 h from late L4 stage by the cyk-4(ok1034); cyk-4::gfp homozygous worms were scored 24 h later.
RNAi depletion was performed by feeding L4 hermaphrodites with HT115(DE3) Escherichia coli clones expressing double-stranded RNA from L4440 plasmid containing a DNA fragment specific for the target gene60. All RNAi clones used in this study (except for that for spd-1, which was made by a primer pair, 5′-GCGGATCCATGGCCCGAAGGCACAG-3′ and 5′-CCCAAGCTTTCACAAAAACTGATTTCGTCTCG-3′) were kindly given by J. Ahringer (Gurdon Institute, UK). Control RNAi was conducted using the HT115(DE3) transformed with the empty L4440 vector. Worms were fed on the RNAi plates for 36 h at 20 °C before imaging. For RNAi in temperature-sensitive strains, L4 hermaphrodites were fed for 72 h at 16 °C before imaging.
Live imaging and quantitative analysis
For live imaging, two or three gravid hermaphrodites were dissected in 2 μl egg salt buffer on a 18 × 18 mm2 coverslip to release embryos, inverted onto 2% (w/v )agarose (in 0.5 × egg salt buffer) pad on a slide glass and sealed with petroleum jelly. The slide was taped onto a modified Linkam PE100-ZAL cooling stage connected to a Linkam sPE94 temperature controller set at 22 °C. Newly fertilized embryos were filmed using an Olympus IX81 inverted microscope, with an UPlanSApo 60 × /1.35 objective and a Yokogawa CSU22 spinning disk scanner unit. Every 30 s, a z-series of 21 planes at 1-μm intervals excited at 491 nm (for CYK-4::GFP), followed by another z-series of 21 planes at 1-μm intervals excited at 561 nm (for mCherry::tubulin), were captured with an iXon EMCCD DV885KCS-VP camera (Andor) at 100 ms exposure with no binning, controlled using Metamorph software (Molecular Devices). For the experiments shown in Fig. 5, the embryos were mounted on an agarose pad on the FCS2 cooling device (Bioptechs) connected to a Nano-Therm System (Bioptechs) set at 18 °C and filmed with a Revolution XD system (Andor) equipped with an iXon Ultra 897 EMCCD camera (Andor).
Time-lapse images were analysed using ImageJ (Rasband, W.S., ImageJ, US National Institutes of Health, Bethesda, MD, USA, http://imagej.nih.gov/ij/, 1997–2011) and R (http://www.r-project.org) software. Equal expression of the wild-type and mutant cyk-4::gfp transgenes was confirmed by measuring the intensities of the GFP signals (Supplementary Fig. 6). For the mCherry::tubulin channel, the z-slice with the best focus of the two spindle poles was identified for each time frame, and using this slice and the three slices above and below it, an average z-projection was produced. For the CYK-4::GFP channel, the z-slice with a peak signal within a minimum oval defined by the two spindle poles was identified, and a z-projection was produced as described above. To remove the variability between embryos, the fluorescence intensities were standardized according to the total signal levels for each embryo during the pre-mitotic stage. Images for presentation were produced by applying the same colour look-up tables to the standardized images. To quantify the accumulation of CYK-4 at the spindle midzone, a line profile along a spline curve that passed these three points (4.4-μm width, 6-μm z-depth) was obtained and the peak height, the peak width at half maximum and the peak area of the line profile were measured.
Protein–protein interaction and other biochemical assays
SPD-1 N-terminally tagged with a chitin-binding domain (CBD) was expressed from pCBD-TEV vector in bacteria and purified with chitin beads (New England Biolabs). CYK-4 N-terminally tagged with glutathione S-transferase was expressed from pGEX-TEV vector in bacteria and purified with glutathione Sepharose 4B (GE Healthcare). The complex of glutathione S-transferase-CYK-4 and CBD-ZEN-4 was expressed from a bicistronic pGEX-6rbs vector in bacteria and purified by sequential binding to chitin beads, elution by TEV protease cleavage of the CBD tag, and binding to glutathione Sepharose 4B. For experiments with radioactive probes, 35S-labelled proteins were produced by TNT T7 Coupled Reticulocyte Lysate System (Promega). A volume of 10 μl of the lysates were mixed with 5 μl of beads with immobilized bacterially expressed proteins in 170 μl cold TGMN butter (20 mM Tris-HCl (pH 8.0), 20% (v/v) glycerol, 5 mM MgCl2, 150 mM NaCl, 0.1% (v/v) NP-40, 1 mM dithiothreitol, 10 μg ml−1 leupeptin, 10 μg ml−1 pepstatin and 0.2 mM phenylmethanesulfonylfluoride). For experiments without radioactive probe, purified SPD-1 1–228 fragments were incubated with amylose beads immobilized with fusion proteins of maltose-binding protein and CYK-4 fragments, and detected by western blotting with an anti-SPD-1 antibody (0.1 μg ml−1), which was produced in rabbit with bacterially expressed full-length recombinant SPD-1 as an immunogen (Eurogentec) and affinity-purified against SPD-1 191-529.
Yeast two-hybrid assay was performed using the ProQuest Two-hybrid System (Invitrogen) according to the manufacturer’s instructions. Size exclusion chromatography of SPD-1 full-length proteins was performed on an Äkta system (GE Healthcare) using a Superdex 200 HR 10/30 column (GE Healthcare) in SD150 buffer (150 mM NaCl, 10 mM HEPES (pH 7.7), 1 mM EGTA, 1 mM MgCl2, 0.2 mM dithiothreitol).
For microtubule binding, 20 μl of the recombinant full-length SPD-1 purified by Superdex chromatography (0.5 mg ml−1 in SD150 buffer) was incubated with 5 μl of taxol-stabilized microtubules (5 mg ml−1) and 25 μl of 2 × BRB80 (160 mM PIPES (pH 6.8), 4 mM MgCl2, 2 mM EGTA, 2 mM GTP, 2 mM dithiothreitol and 40 μM taxol) supplemented with 40% (v/v) glycerol. Microtubules and bound proteins were collected by ultracentrifugation at 131,000g for 20 min using a TLA-100 rotor (Beckman) through a cushion of 1 × BRB80 supplemented with 30% (v/v) glycerol at 25 °C and analysed by SDS–polyacrylamide gel electrophoresis.
Microtubule bundling was assessed by incubating 8 μl of the Superdex-purified SPD-1 (62.5 μg ml−1 in SD150 buffer) with 2 μl of taxol-stabilized microtubules (2.5 mg ml−1) and 10 μl of 2 × BRB80 supplemented with 40% (v/v) glycerol for 10 min at 25 °C. After fixation with 20 μl of 2% (w/v) glutaraldehyde diluted in 1 × BRB80 supplemented with 20% (v/v) glycerol, the microtubules were sedimented onto a coverglass by ultracentrifugation through layers of 5 ml BRB80 and 2 ml of BRB80 supplemented with 10% glycerol using a SW40 rotor (Beckman) at 217,000g for 60 min at 25 °C. The coverglass with sedimented microtubules was fixed with pre-chilled 100% methanol for 10 min at –20 °C and stained for microtubules with DM1a anti-tubulin antibody (Sigma T6199, 1:500 dilution) and Alexa Fluor 488-conjugated anti-mouse secondary antibody (Invitrogen, A11029, 1:2,000 dilution), and observed by an Olympus BX51 microscope equipped with a PlanApo N 60 × /1.42 objective and a CoolSNAP HQ2 CCD camera (Photometrics)38.
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We thank J. Mason, N. Joseph and A. Sossick for their technical assistance; J. Ahringer, E. Miska and their lab members for providing resources and advice on the C. elegans experiments; the Caenorhabditis Genetics Center for providing the C. elegans strains; Y. Kohara for supplying the cDNA clones; N. Burroughs for contributing to the discussion; and R.A. Cross, J.B. Millar and M.E. Douglas for their comments on the manuscript. This work was supported by the Cancer Research UK program grant (C19769/A6356 and A11985) and studentship (C19769/A8024) to M.M. and by core support from CRUK (C6946/A14492) and the Wellcome Trust (092096) to the Gurdon Institute, University of Cambridge. K.-Y.L. received a scholarship from the Cambridge Commonwealth Trust, University of Cambridge.
The authors declare no competing financial interests.
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Lee, KY., Esmaeili, B., Zealley, B. et al. Direct interaction between centralspindlin and PRC1 reinforces mechanical resilience of the central spindle. Nat Commun 6, 7290 (2015). https://doi.org/10.1038/ncomms8290
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