Human chromosomes are captured along microtubule walls (lateral attachment) and then tethered to microtubule-ends (end-on attachment) through a multi-step end-on conversion process. Upstream regulators that orchestrate this remarkable change in the plane of kinetochore-microtubule attachment in human cells are not known. By tracking kinetochore movements and using kinetochore markers specific to attachment status, we reveal a spatially defined role for Aurora-B kinase in retarding the end-on conversion process. To understand how Aurora-B activity is counteracted, we compare the roles of two outer-kinetochore bound phosphatases and find that BubR1-associated PP2A, unlike KNL1-associated PP1, plays a significant role in end-on conversion. Finally, we uncover a novel role for Aurora-B regulated Astrin-SKAP complex in ensuring the correct plane of kinetochore-microtubule attachment. Thus, we identify Aurora-B as a key upstream regulator of end-on conversion in human cells and establish a late role for Astrin-SKAP complex in the end-on conversion process.
During cell division, accurate segregation of DNA requires the proper attachment of chromosomes to microtubules. Chromosome-microtubule attachment relies on a macromolecular structure—the kinetochore—that assembles on the centromeric region of chromosomes. We and others showed that kinetochores are predominantly captured along the walls of microtubules (termed lateral kinetochores) and then tethered onto the ends of microtubules (termed end-on kinetochores)1,2,3,4. This dramatic change in the geometry of kinetochore-microtubule (KT-MT) interaction is achieved through a multi-step end-on conversion process. End-on conversion is an indispensable process for lateral kinetochores: only when the ends of microtubules are tethered to the kinetochore, the growth and shrinkage of microtubule-ends (K-fibres) can impart pushing or pulling forces on the chromosome5,6,7. Lesions in the end-on conversion process lead to defective chromosome segregation, as seen in cells lacking the loop region of the kinetochore protein HEC1/Ndc804, 8,9,10,11,12,13, highlighting the importance of understanding how a lateral kinetochore is converted into an end-on kinetochore.
Several evolutionarily conserved kinetochore proteins are known to be important for forming mature attachments capable of load-bearing and end-on pulling events2,3,4, 8, 14,15,16. Using deconvolution microscopy, we recently reported two markers to distinguish the plane of KT-MT attachment in human cells: (i) Mature end-on kinetochores, but not lateral kinetochores, recruit the Astrin-SKAP complex (ii) Mature end-on kinetochores, but not lateral kinetochores, are capable of converting the changes in K-fibre length into kinetochore movements4. However, upstream signaling pathways that control the end-on conversion process have not been established so far in human cells. In yeasts, Aurora-B (Ipl1) kinase was shown to be an important upstream regulator of the end-on conversion process17. Whether Aurora-B plays a similar role in regulating the end-on conversion process in human cells is not known.
Distinct from the end-on conversion process that ensures the correct plane of KT-MT attachment, the error correction process ensures the correct orientation of attachment (referred as biorientation; reviewed in ref. 9). Biorientation defects are resolved by Aurora-B kinase enriched at centromeres through feedback loops18,19,20; it phosphorylates outer-kinetochore substrates causing the detachment of non-bioriented KT-MT attachments (e.g., syntelic end-on attachments)16, 21,22,23,24,25,26,27. In addition, active Aurora-B has been reported in human kinetochores during early mitosis28 and specifically on kinetochores that are laterally attached29. Whether Aurora-B at the outer-kinetochore would destabilise immature lateral attachments is however not known.
Aurora-B and its counteracting phosphatases, PP1 and PP2A, are important for regulating outer-kinetochore assembly, KT-MT attachment stability, chromosome alignment and checkpoint function29,30,31,32,33,34,35,36,37,38. Several Aurora-B counteracting phosphatases are recruited to the centromere and kinetochore in a temporally and spatially restricted manner (reviewed in refs 39, 40). Whether Aurora-B counteracting phosphatases play a role in controlling the plane of KT-MT attachment remains unclear.
Here, we examine the role of Aurora-B kinase and its counteracting phosphatases in the end-on conversion process. We report that Aurora-B kinase impacts the end-on conversion process differently dependent on its sub-cellular localization—outer kinetochore vs. centromere. While Aurora-B targeted to the outer-kinetochore detaches lateral kinetochores prior to end-on conversion, Aurora-B targeted to the centromere stabilizes lateral kinetochores and retards end-on conversion. We find that lateral KT-MT attachments are relatively ‘immune’ to Aurora-B. Next, of the two Aurora-B-counteracting phosphatases, we find that BubR1-associated PP2A, but not KNL1-associated PP1, is the most potent regulator of the end-on conversion process. Finally, we identify the Astrin-SKAP complex as a late player in the end-on conversion process. Thus, we report a novel spatially controlled role for Aurora-B in the end-on conversion process, establish BubR1-associated PP2A as a key phosphatase that counteracts Aurora-B activity during end-on conversion and finally, demonstrate a late role for Aurora-B regulated Astrin-SKAP complex in the end-on conversion process. This study provides the first insight into how Aurora-B mediated signaling controls the plane of kinetochore-microtubule attachments in human cells.
Aurora-B activity is high on immature lateral kinetochores
We first quantified and confirmed the presence of active Aurora-B on lateral kinetochores. For this purpose, HeLa cells were exposed to Monastrol to generate monopolar spindles, which mimic an early mitotic spindle configuration and allow clear distinction between lateral kinetochores and end-on kinetochores4. Immunostaining with antibodies against activating phosphorylation of Aurora-B (pThr232) (Supplementary Fig. 1A) showed that activated Aurora-B is abundant on lateral kinetochores (n KTs > 30; n cells = 10; Fig. 1a). Consistent with this finding, immunostaining with phospho-specific antibodies against Aurora-B substrate sites of the outer KT protein HEC1, Ser44 and Ser5528, showed higher HEC1 phosphorylation on lateral compared to end-on kinetochores (n KTs > 20; n cells = 10; Fig. 1a,b). Thus, Aurora-B activity is high on lateral kinetochores.
Aurora-B at outer-kinetochore facilitate lateral kinetochores
To determine the contribution of outer-kinetochore associated Aurora-B activity in early mitosis, we locally increased Aurora-B activity at the outer-kinetochore by expressing the Mis12-INCENP-GFP fusion protein, wherein a fragment of INCENP that lacks the centromere targeting domain but retains the Aurora-B docking domain is fused to the outer-kinetochore protein Mis1226. As expected, but not reported so far, Mis12-INCENP-GFP expressing HeLa cells showed high levels of HEC1pSer44 phosphorylation at all kinetochores (Supplementary Fig. 1B), confirming the fusion protein’s ability to retain Aurora-B activity at the outer kinetochore. Hence, this approach allowed us to quantify the effect of a localised increase in Aurora-B activity.
To study KT-MT attachment status (end-on vs. lateral) during early mitosis when end-on conversion events occur, we immunostained Monastrol-treated Mis12-INCENP-GFP expressing cells with antibodies against GFP, Tubulin and SKAP, a microtubule-end binding protein41, 42 specifically enriched on end-on but not lateral kinetochores4 (Fig. 1c). In monopolar spindles of control cells, less than 25% of kinetochores were laterally attached and they lacked SKAP4. However, in Mis12-INCENP-GFP expressing cells, more than 95% of kinetochores were laterally attached (Fig. 1d,e) and they lacked SKAP (n cells = 26/31) (Fig. 1d and Supplementary Fig. 1C). The striking defect in the plane of KT-MT attachment observed in Mis12-INCENP-GFP expressing cells was completely reversed following Aurora-B inhibition using ZM447439, as almost all kinetochores were attached to MT-ends and enriched for SKAP (n cells = 20/20) (Fig. 1d,e and Supplementary Fig. 1C). Thus, retaining Aurora-B activity at the outer-kinetochore promotes the incidence of lateral kinetochores, suggesting a failure in the end-on conversion process. The inhibitor studies confirm that this failure is not due to non-specific interference by Mis12-INCENP-GFP fusion protein, but is caused by Aurora-B activity. We conclude that outer-kinetochore associated Aurora-B activity increases the incidence of lateral kinetochores in monopolar spindles that mimic an early mitotic spindle configuration.
Congression resolves Aurora-B induced lateral attachments
We tested if constitutive Aurora-B activity would increase the incidence of lateral kinetochores in bipolar spindles that allow biorientation and inter-kinetochore tension. To study bipolar spindles, we treated cells with MG132, a proteasome inhibitor. MG132 treated cells expressing Mis12-INCENP-GFP displayed a mixture of both congressed and uncongressed kinetochores (Supplementary Fig. 2A–C), as previously reported26. In cells with congressed KTs, we observed KT-MT attachments that were properly bioriented (Supplementary Fig. 2A, insets) and predominantly end-on attached, with a small but statistically significant fraction displaying lateral attachments (Supplementary Fig. 2D). Thus, bipolar spindles partially rescue the end-on conversion defect induced by constitutive Aurora-B activity. We confirmed this finding by quantifying Astrin-SKAP recruitment at kinetochores: although the intensity of KT-associated SKAP was reduced by ~2.5-fold in Mis12-INCENP-GFP expressing cells compared to non-expressing cells, in agreement with previous report43 (Supplementary Fig. 2E and F), SKAP was clearly enriched on congressed and bioriented kinetochore pairs. Thus, bipolar spindles, which allow chromosome congression and biorientation of KT-MT attachments, are able to overcome the end-on conversion defect induced by Aurora-B at the outer-kinetochore.
Aurora-B at outer-kinetochore abrogates end-on conversion
To understand the precise reason for the accumulation of lateral attachments in Mis12-INCENP-GFP expressing cells, we investigated three possibilities: (i) whether lateral kinetochores are due to excessive error-correction (i.e., detachment of end-on kinetochores promoting their recapture onto microtubule walls), (ii) abrogation of the process of converting lateral attachments into end-on attachments or (iii) excessive stabilization of lateral KT-MT interactions. To distinguish between all three mechanisms, we performed time-lapse microscopy of monopolar spindles of cells co-expressing mKate2-Tubulin and Mis12-INCENP-GFP. We tracked the fate of lateral and end-on kinetochores and analysed changes in the plane of KT-MT interaction and KT movements. A Mis12-INCENP(TAA)-GFP mutant with compromised Aurora-B activity26, 44,45,46 was used as a negative control. In control cells expressing Mis12-INCENP(TAA)-GFP, lateral kinetochores bound to microtubule walls were converted into end-on kinetochores as expected (Fig. 2a). Quantitative analysis of the fate of kinetochores in these control cells showed that the vast majority of lateral kinetochores became end-tethered within 50 s (Fig. 2b), following which they underwent forward and regressing movements, which were synchronous with changes in K-fibre length (Fig. 2a (left panels) and c (lower panel)). Such synchronous movement between the kinetochore and MT-end demonstrates the establishment of a productive and mature KT-MT attachment that are capable of converting the change in K-fibre length into kinetochore movement. In stark contrast, in cells expressing Mis12-INCENP-GFP, majority of lateral kinetochores failed to convert into end-on kinetochores (Fig. 2b). In these cells, kinetochore movements were not synchronous with changes in K-fibre length (Fig. 2a (right panels) and c (upper panel)), demonstrating an immature KT-MT attachment state. A significant proportion of lateral kinetochores in Mis12-INCENP-GFP expressing cells underwent detachment (Fig. 2a (right panels) and Fig. 2b (left panel)) and reattached onto microtubule walls (Fig. 2a (right panels)). However, the lifetime of lateral kinetochores was not significantly different in Mis12-INCENP-GFP and Mis12-INCENP(TAA)-GFP expressing cells (Fig. 2d). This unaltered life-time of lateral kinetochores shows that Aurora-B at the outer-kinetochore does not prohibit the capture or the maintenance of lateral kinetochores. Based on our data on KT-MT attachment status, KT movements and KT life-time in live-cells, we conclude that Aurora-B activity allows kinetochore capture and maintenance along microtubule walls but it specifically disrupts the end-on conversion process.
Finally, as KT fate analysis showed that end-on (monotelic) kinetochores remained tethered to MT-ends and did not detach in Mis12-INCENP-GFP expressing cells (Fig. 2b, right panel), we are able to rule out excessive error-correction (detachment of end-on kinetochores) as an indirect cause for increase in lateral kinetochores. In summary, we reveal a novel role for Aurora-B in selectively abrogating the end-on conversion process, without disrupting the establishment or maintenance of lateral attachments (Fig. 2e). We conclude that this novel role of Aurora-B in influencing the plane of KT-MT attachment in human cells is independent of the kinase’s established role in the error-correction process.
Distinct Aurora-B pools disrupt end-on conversion differently
Because active Aurora-B is lost from outer-kinetochore and retained only at the inner centromeric region during metaphase28, we tested whether centromere localized Aurora-B influences the end-on conversion process similarly to outer-kinetochore localized Aurora-B. For this purpose, we performed fixed and live-cell microscopy studies using CenpB-INCENP-GFP, wherein the Aurora-B docking domain is fused to a centromeric protein, CenpB26. As expected CenpB-INCENP-GFP signals were predominantly centromeric and did not extent beyond inner kinetochore region (Supplementary Fig. 5B). In monopolar spindles of CenpB-INCENP-GFP expressing cells, nearly 60% of kinetochores were laterally attached and they lacked SKAP of the Astrin-SKAP complex (Fig. 3a,b), suggesting an end-on conversion defect. This lateral attachment phenotype and lack of Astrin-SKAP complex was rescued under two conditions: in monopolar spindles treated with Aurora-B inhibitor (Fig. 3a,b) and in bipolar spindles with congressed chromosomes (Supplementary Fig. 3A and B). We conclude that a local increase in Aurora-B, restricted to centromere and inner kinetochore region, increases the incidence of lateral kinetochores in monopolar spindles and this altered plane of KT-MT interaction is rescued in congressed kinetochores of bipolar spindles.
To determine the impact of centromere bound Aurora-B on lateral kinetochores, we tracked the fate of kinetochores in cells co-expressing mKate2-Tubulin along with either CenpB-INCENP-GFP or CenpB-INCENP(TAA)-GFP (negative control26). In control cells expressing CenpB-INCENP(TAA)-GFP, the majority of kinetochores were attached to microtubule-ends and stably tethered without detachment episodes (Supplementary Fig. 4A and B). As expected, lateral kinetochores that matured into end-on kinetochores underwent forward and regressing movements, synchronous with changes in the K-fibre length (Supplementary Fig. 4C). In stark contrast, cells expressing CenpB-INCENP-GFP displayed a low incidence of lateral to end-on conversion events (Fig. 3c,d). Detachment episodes of lateral or end-on kinetochores were not high (Fig. 3c,d; while 4/4 syntelic KTs detached, only 3/21 monotelic KTs detached within 10 s). Quantitative analysis of kinetochore movements in CenpB-INCENP-GFP expressing cells showed that lateral kinetochores remained laterally attached and failed to sustain synchronous movements with the MT-ends of the K-fibre (Fig. 3d and Supplementary Fig. 4D), revealing a role for centromere bound Aurora-B in retarding the end-on conversion event.
While both centromeric and outer-kinetochore pools of Aurora-B disrupt end-on conversion, there were two key differences: (i) the lifetime of lateral kinetochores was significantly increased in cells expressing CenpB-INCENP-GFP compared to Mis12-INCENP-GFP (Fig. 3e) and (ii) the number of lateral kinetochores that formed non-productive end-on attachments (end-on attachments lasting less than 30 s) was at least twofolds more in cells expressing CenpB-INCENP-GFP (n KT = 13/34) compared to Mis12-INCENP-GFP (n KT = 6/37).
In summary, we conclude that a local increase of Aurora-B at the outer-kinetochore detaches lateral attachments prior to end-on conversion, whereas Aurora-B at the centromere retains lateral attachments and prevents stable end-on conversion (Fig. 3f). This difference could not be simply explained by gross differences in the extent of fusion protein expression at the kinetochore (Supplementary Fig. 5A) or extent of HEC1 phosphorylation (Supplementary Fig. 5B and C). We propose that the two different spatial pools of Aurora-B may influence downstream targets differently or to different extent leading to distinct impacts upon the end-on conversion process.
BubR1-PP2A but not KNL1-PP1 controls end-on conversion
We hypothesized that Aurora-B counteracting phosphatases at the outer-kinetochore should be essential for end-on conversion, as Aurora-B activity is high at the outer-kinetochore during early prometaphase47. At the outer-kinetochore, two major phosphatases (KNL1 associated PP1 and BubR1 associated PP2A) counteract Aurora-B activity and are needed for the spindle assembly checkpoint or maintaining cold-stable KT-MT attachments30,31,32,33,34,35,36. The extent to which the two phosphatases control the end-on conversion process has not been studied so far. To address this, we first quantified KT-MT attachment status (end-on vs. lateral) in cells conditionally expressing a Venus (YFP) tagged BubR1 mutant that can not interact with PP2A-B56 (BubR1 Δ660–685)31 (Fig. 4a). Consistent with previous reports31, 32, 48, our immunostaining studies showed that in cells depleted of endogenous BubR1, the expression of the BubR1 mutant lacking the PP2A docking domain interfered with both PP2A recruitment and chromosome alignment (Supplementary Fig. 6A, C and E and Fig. 4b). We next assessed the enrichment of Astrin-SKAP complex (a marker of mature end-on attachments) at congressed kinetochores in cells treated with MG132. Cells expressing the BubR1 Δ660–685 mutant failed to recruit Astrin normally in the vast majority of congressed kinetochores, and the kinetochores that displayed Astrin showed a steep fivefold reduction compared to controls (Fig. 4c). Analysis of KT-MT attachment status in MG132-treated BubR1 Δ660–685 mutant expressing cells demonstrated a highly significant increase in laterally attached kinetochores (Fig. 4d,e) in both congressed and uncongressed kinetochores (Supplementary Fig. 7A). Lateral KT-MT attachment status in BubR1 Δ660–685 mutant expressing cells was further confirmed using super-resolution microscopy (Supplementary Fig. 7B). These data indicate an impairment of the end-on conversion process in cells lacking BubR1 associated PP2A, despite chromosome congression. Based on the status of KT-MT attachment and Astrin recruitment, we conclude that (i) laterally attached kinetochores predominate in cells lacking BubR1 associated PP2A and (ii) chromosome congression is insufficient to rescue the end-on conversion defect in cells lacking BubR1 associated PP2A-B56.
We next tested if KNL1 associated PP1 phosphatase is required for end-on conversion by comparing KT-MT attachment changes induced by two LAP-tagged KNL1 mutants: (i) KNL1-2A where Aurora-B mediated phosphorylation sites at the PP1 docking motif are mutated to allow constitutive recruitment of PP1 and (ii) KNL1-4A where the PP1 docking RVSF motif is mutated to abrogate PP1 recruitment30, 37. We first confirmed that PP1 levels are reduced in KNL1 depleted cells expressing LAP-tagged KNL1-4A compared to LAP-tagged KNL1-WT or LAP-tagged KNL1-2A (Supplementary Fig. 6B and D), as reported37. Following MG132 treatment, KNL1 depleted cells expressing either LAP-tagged KNL1-2A or KNL1-WT displayed kinetochores that were congressed and normally end-tethered; whereas, cells expressing LAP-tagged KNL1-4A mutant displayed a mild congression defect (Fig. 4f,g and Supplementary Fig. 6F). A slight increase in lateral kinetochores and reduction in Astrin intensity were observed in cells expressing LAP tagged KNL1-4A mutant, compared to cells expressing either KNL1-2A mutant or KNL1-WT fusion proteins (Fig. 4g and Supplementary Fig. 6G). However, the percentage of lateral kinetochores and extent of Astrin reduction were much lesser in cells expressing the PP1 docking mutant (KNL1-4A) compared to PP2A docking mutant (BubR1 Δ660–685) (Compare Fig. 4e,g; Fig. 4c and Supplementary Fig. 6G). These studies provide first insight into the extent to which the two phosphatases control the plane of KT-MT interaction and highlight the essential role of BubR1 associated PP2A in controlling the maturation of KT-MT attachments.
Astrin-SKAP is a target of Aurora-B during end-on conversion
Because Aurora-B negatively regulates Astrin-SKAP levels at kinetochores43, Astrin-SKAP complex is a potential downstream target of Aurora-B in the end-on conversion process. We quantified KT-MT attachment status in monopolar spindles of Aurora-B inhibited cells depleted of either Astrin or SKAP (Fig. 5a). As expected, in control siRNA treated cells, kinetochores were tethered to MT-ends and were uniformly distant from the spindle poles (Fig. 5b). In contrast, in SKAP siRNA treated cells, kinetochores were dispersed along MT-walls and a reduced proportion of the kinetochores were attached to MT-ends (Fig. 5b and Supplementary Fig. 8A), showing a defect in tethering kinetochores to microtubule-ends despite Aurora-B inhibition. A similar phenotype of increased lateral kinetochores was observed in cells treated with Astrin siRNA despite Aurora-B inhibition (Fig. 5b and Supplementary Fig. 8A). We confirmed that SKAP was absent on the kinetochores of Astrin or SKAP siRNA treated cells (Fig. 5b). We conclude that the Astrin-SKAP complex plays a crucial role in ensuring the correct plane of KT-MT interaction.
KT attachments to MT-ends but not MT-walls rely on SKAP
To determine why end-tethering of kinetochores is compromised in SKAP depleted cells, we tracked the fate of lateral kinetochores in time-lapse movies of cells co-expressing CenpB-DsRed and YFP-Tubulin (Fig. 5c). Analysing the fate of kinetochores showed that in control cells, lateral kinetochores converted into end-on kinetochores normally (Fig. 5d). However, in SKAP depleted cells, lateral kinetochores either remained attached to microtubule walls or detached from microtubule walls and failed to convert into end-on kinetochores (Fig. 5d), showing a failure in the end-on conversion process. The lifetime of lateral kinetochores was comparable in control and SKAP depleted cells (Fig. 5e,f), indicating a dispensable role for SKAP in capturing and maintaining kinetochores along microtubule walls. Although the conversion of a lateral kinetochore into an end-on kinetochore was relatively infrequent in SKAP depleted cells compared to control depleted cells (Fig. 5d), end-tethered kinetochores could be observed in SKAP depleted cells (Supplementary Fig. 8A). Tracking the fate of these end-tethered kinetochores in SKAP depleted cells showed that they rarely remained end-tethered for longer than 30 s, and instead they either became laterally attached or detached (n cells = 4; n KTs = 12). Thus, SKAP facilitates the end-on conversion event and is essential for the stable maintenance of kinetochores at MT-ends but not MT-walls, demonstrating a late role for SKAP in the end-on conversion process.
To confirm that the defect in the plane of KT-MT attachment observed following SKAP depletion is not an siRNA off-target effect, we used a cell line that conditionally expresses an siRNA resistant form of SKAP fused to GFP (GFP-SKAPsiRes)4, 41. Following SKAP siRNA treatment, monopolar spindles of GFP-SKAPsiRes expressing cells exposed to ZM447439 and MG132 (Supplementary Fig. 8B) displayed end-on attached kinetochores, demonstrating a successful rescue of the SKAP depletion induced lateral attachment phenotype (Supplementary Fig. 8C). Thus, we show the first evidence for SKAP’s role in the end-on conversion process, and demonstrate that Aurora-B acts through Astrin-SKAP complex to ultimately define the plane of KT-MT attachment (Fig. 5h).
Because chromosome congression partly rescued the end-tethering defect caused by constitutive Aurora-B activity, we tested if congression can rescue SKAP depletion induced end-tethering defect. Analyzing KT-MT attachments in bipolar spindles following MG132 and ZM447439 treatment showed significantly more lateral kinetochores in SKAP depleted cells, compared to control depleted cells (Fig. 5g and Supplementary Fig. 8D). These data show that SKAP is essential for defining the plane of KT-MT interaction in both bipolar and monopolar spindles.
First, we report a novel role for Aurora-B pathway in controlling the plane of KT-MT attachment in human cells. This role for Aurora-B in the maturation of kinetochore-microtubule attachments is distinct from it’s well established role in detaching erroneous KT-MT attachments (syntelic or merotelic)23, 25, 49. Second, we show that increasing Aurora-B at the centromere or outer-kinetochore promotes the incidence of lateral attachments by influencing different steps of the end-on conversion process. We find that lateral KT-MT attachments are ‘immune’ to Aurora-B regulation. Third, of the two Aurora-B counteracting phosphatases we tested, BubR1 associated PP2A is more important than KNL1 associated PP1 for defining the plane of KT-MT attachment, revealing functional differences between these two outer-kinetochore associated phosphatases. Finally, we uncover a role for the Astrin-SKAP complex in ensuring the lateral to end-on conversion of attachments and maintenance of end-tethered kinetochores. By comparing kinetochores in bipolar and monopolar spindles, we distinguish distinct sequential regulators of the end-on conversion process. Thus, we provide first insight into how the Aurora-B pathway controls the end-on conversion process in human cells.
Our live-cell imaging studies shed light on a physiologically significant puzzle about how human cells protect immature lateral attachments from being destabilized by the error-correction enzyme Aurora-B50. We find that increasing centromeric Aurora-B detaches erroneous syntelic (end-on) attachments but spares immature lateral attachments. These data from monopolar spindles show that immature lateral attachments are neither susceptible to Aurora-B’s error correction activity nor reliant on biorientation, explaining how early-on attachments could form despite a lack of inter-kinetochore tension. Similar protection of immature lateral attachments against destabilization by Aurora-B/Ipl1 is reported in budding yeast17.
In monopolar spindles, which closely mimic early mitotic spindle configuration, we show that Aurora-B activity at the outer-kinetochore allows lateral attachments but blocks end-on conversion. Aurora-B activity at the outer kinetochore is potentially counteracted through BubR1-PP2A that is high on early mitotic kinetochores. Loss of outer-kinetochore associated Aurora-B is likely to tip the balance towards BubR1-associated PP2A phosphatase allowing end-on conversion. Concomitantly, selective enrichment of the Astrin-SKAP complex on MT-end tethered kinetochores4, along with the physical separation of centromeric Aurora-B from outer-kinetochore substrates by end-on attachment mediated kinetochore pulling, could jointly facilitate the maintenance of a mature end-on attachment (Fig. 6).
Previous studies showed that Astrin is not recruited to uncongressed kinetochores lacking BubR1 associated PP2A48. Whether this failure to recruit Astrin is simply due to the lack of congression or directly due to the loss of PP2A was not known. We demonstrate that both Astrin recruitment and end-on attachment status are compromised on congressed kinetochores lacking BubR1 associated PP2A. Thus, BubR1 associated PP2A is required for proper KT-MT attachment even on congressed chromosomes, indicating a new role for BubR1 that is present on metaphase kinetochores51. Whether the lack of BubR1-PP2A mediated end-on conversion event(s) is an important reason for higher sensitivity to loss of BubR1 in Brain Tumour Initiating Cells compared to normal cells52 would be interesting to explore in the future.
How does the Astrin-SKAP complex mediate end-on conversion? Electron microscopy studies indicate that SKAP159–316: Astrin482–850 complex form elongated structures53, and Astrin dimers show a ‘lollypop’ like structure of 80 nm in length with a flexible hinge54. We and others previously showed that a similar hinge region in Ndc80 (loop domain) is required for tethering kinetochores onto microtubule-ends4, 11,12,13. Unlike Ndc80, which is a core kinetochore protein, the Astrin-SKAP complex is recruited to kinetochores at later stages of mitosis55,56,57 and found predominantly on end-tethered kinetochores in human cells4. Future structure studies on Astrin’s hinge domain and the kinetochore receptor(s) of Astrin-SKAP complex are likely to reveal crucial insights into how human cells overcome physical barriers in converting the plane of kinetochore-microtubule attachment. Although Astrin-SKAP complex is essential for normal chromosome segregation in human cells41, 55,56,57,58, a truncation mutation in exon-3 of SKAP did not cause somatic defects in mice59, suggesting that redundant players may support the loss of SKAP in mice.
In summary, our findings uncover Aurora-B kinase as an upstream regulator of the end-on conversion process. Unlike spindle checkpoint mechanisms that rely on the two phosphatases KNL1-associated PP1 and BubR1-associated PP2A-B56, the end-on conversion process relies significantly on BubR1-associated PP2A-B56. Finally, we identify a role for Astrin-SKAP in a late event of the end-on conversion process. Thus, we report one of the key molecular pathways that control the plane of kinetochore-microtubule interaction in human cells.
Cell culture and synchronization
HeLa cells (ATCC) cultured in Dulbecco’s Modified Eagle’s Media supplemented with 10% FCS and antibiotics (Penicillin and Streptomycin) were plated onto glass-bottomed dishes (LabTek) or 13 mm round coverslips. For inhibition studies, cells were treated with 10 µM Monastrol (1305, TOCRIS), 10 µM ZM447439 (2458, TOCRIS) or 10 µM MG132 (1748, TOCRIS). Inducible expression of GFP-SKAPsiRes was achieved by generating HeLa (GFP-SKAP) as clones obtained from transfecting HeLa FRT/TO cells with pCDNA5-FRT/TO-GFP-SKAPsiRes plasmid vector41.
Plasmid and siRNA transfections
siRNA transfection was performed using Oligofectamine according to manufacturers instructions. Briefly, siRNA oligos were incubated in OptiMEM (Invitrogen; 11058-021) and washed 24–36 h prior to analysis. siRNA oligos to deplete Astrin (UCCCGACAACUCACAGAGAAAUU), SKAP (GAAAGAGUCCGAUUCCUAGUU), BubR1 (GAUGGUGAAUUGUGGAAUA) and KNL1 (GCAUGUAUCUCUUAAGGAAUU) were from Dharmacon. Negative control siRNA (12,935–300) was from Invitrogen. HeLaYFP-Tub; CENPB-Red was generated by transiently transfecting pDsRed-CENPB (Clonetech) into HeLaYFP-Tub used extensively for cell division studies60, 61. In four well LabTek dishes, 500 ng of plasmid vectors encoding mKate2-αTubulin (Evrogen) along with plasmid vector encoding Mis12-INCENP-GFP (VSV-Mis12-ΔCen INCENP-GFP), Mis12-INCENP(TAA)-GFP (VSV-Mis12-ΔCen INCENP(TAA)-GFP), CenpB-INCENP-GFP (VSV-CenpB-ΔCen INCENP-GFP) or CenpB-INCENP(TAA)-GFP (VSV-CenpB-ΔCen INCENP(TAA)-GFP)26 were co-transfected into HeLa using Turbofect (R0531, Thermo Scientific) and filmed within 30 h. LAP-tagged KNL1 expression vectors4, 37 were transiently transfected prior to Doxycycline induction. Following transient transfection of plasmids, cells were assessed after 24 h, except in the case of KNL1 expression plasmids where cells were assessed after 30 h. For SKAP siRNA rescue, Tetracycline (Tet) inducible GFP-SKAP HeLa cells were transfected with SKAP siRNA43, 48 h later treated with tetracycline for 1 and 24 h later used for studies. siRNA resistant version of GFP-SKAP expression vector (pCDNA5-FRT/TO-GFP-SKAPsiRes) was generated by wobbling nucleotides using point mutagenesis primer GTAAAGCTGGAGATGAAAGAGGAGCGTGTTAGGT TTTTGGAACAGCAAACCTTATG. Plasmid vectors maps are available on request.
Live-cell time-lapse imaging
Cells were transfected with siRNA oligos or plasmid vectors 72 or 24 h, respectively, prior to imaging (unless stated otherwise in experimental regime) and transferred to Leibovitz’s L15 medium (Invitrogen; 11415064) for imaging at 37 °C. For imaging KT and MT-end dynamics, exposures of 0.04 s and at least 6 Z-planes, 0.1 μm apart, were acquired every 10 s for 5 min using a 100X NA 1.40 oil immersion objective on an Applied Precision DeltaVision Core microscope equipped with a Cascade2 camera under EM mode. Exposure conditions were optimized through long-term high-speed imaging of mKate2-EB3 expressing HeLa cell line62, 63.
Kinetochore-microtubule attachment status determination
To define KT-MT attachment states, we used the following methodology. First, 360° rotation of image stacks (3D volume images) generated using Softworx was used to determine the plane of the K-fibre and KT. Second, end-tethered and lateral kinetochores were confirmed on the basis of their synchronous and asynchronous movement, respectively, between the K-fibre tip and the KT. Change in KT and MT-end (MT) positions through time was measured using Softworx distance measurement tool. Values less than 0.25 μm, sustained for at least 30 s, were marked as synchronous movement of the KT and MT-end. All other values were marked as asynchronous movement of the KT and MT-end. To ensure that the attachment transition measurements are reliable, we only considered end-on kinetochores that remained in end-on state at least for 30 s, lateral kinetochores that remained lateral for greater than 30 s and detached kinetochores that remained detached for at least 20 s. (In Mis12-INCENP-GFP and mKate2-Tubulin coexpressing cells, we expect a signal overlap since Mis12 resides in the KT outer plate where MT-ends reach64. However, in CenpB-DsRed and YFP-Tubulin coexpressing cells, signal overlap is rarely seen). In fixed-cells to set a threshold for high-quality images for quantitative analysis, we excluded cells if greater than 20% of its kinetochores could not be confidently assigned any KT-MT attachment status. Lateral, end-on or detached kinetochores were scored4 and their relative percentages calculated using MS Excel and plotted using Prism Software.
Immunofluorescence, immunoblotting and image analysis
For immunofluorescence, antibodies against HEC1Ndc80 protein65 (1:1000), tubulin (Abcam; ab6160; 1:800), pThr232 Aurora-B (Rockland Inc; 600-401-677; 1:500), total Aurora-B (Abcam; ab3635; 1:800), GFP (Roche; 1181446001; 1:800), mCherry (Thermo Scientific; M11217; 1:2000), SKAP (Atlas; HPA042027; 1:1000), HEC1pSer44 and HEC1pSer5528 (1:500), Astrin (Novus; NB100-74638; 1:1000), B56 (BD Transduction Laboratories; 610615; 1:500) and CREST antisera (Europa; FZ90C-CS1058; 1:2000) were used. DAPI (Sigma) was used to co-stain DNA. Images of immunostained cells were acquired using 100X NA 1.4 objective on a DeltaVision Core microscope equipped with CoolSnap HQ Camera (Photometrics). Volume rendering (SoftWorx) was performed for 3D analysis of KT-MT attachment status. Deconvolution of live and fixed-cell images and 3D volume rendering were performed using SoftWorx. Quantitative immunoblotting was performed on proteins separated on 12% SDS-PAGE gels by transferring them overnight onto Nitrocellulose membrane. Membranes were incubated in primary antibodies against Aurora-B pThr232 (Rockland Inc; 600-401-677; 1:1000), SKAP (Atlas; HPA042027; 1:1000) and γ-Tubulin (Sigma; T6557; 1:800) for an hour and probed using secondary antibodies labeled with infrared fluorescent dyes, which were imaged using an Odyssey imager (Supplementary Fig. 9).
To confirm that sampling is sufficient, we used two statistical tests: First, we performed a proportion test or unpaired Student’s t-test to confirm using P-values that we have sampled sufficient number of cells or kinetochores for concluding on differences we report. Second, we measured standard error over mean (SEM) across experimental repeats or across cells and confirmed that the differences we report are not only based on differences in mean values, but also the spread of the mean values between experiments, cells or kinetochores. SD values were obtained across experiments or cells as indicated in the figure legend.
Super-resolution microscopy experiments
For STORM imaging experiments, HeLa cells were transiently transfected with plasmids encoding Venus-BubR1 ∆660–685 and 24 h later cells were exposed to MG132 for 1 h. Cells were then pre-fixed with 4% PFA in PBS for 20 s, permeabilised with 0.5% Triton X-100 in PBS for 4 min and the fixation step was repeated again for 20 min before quenching with 25 mM glycine for 20 min. One percent BSA in PBS with 0.1% Tween was used for blocking and all washes were performed using 0.1% tween in PBS. Cells were immunostained with primary antibodies against α-Tubulin (clone B-5-1-2, Sigma-Aldrich; T6074; 1:300) and CREST antisera (Europa; FZ90C-CS1058; 1:2000). For secondary antibody, goat anti-mouse AlexaFluor 647 (Molecular Probes; A21236; 1:800) and donkey anti-human CF680 (Biotium; 20278–1; 1:1000) were used.
Samples were mounted and imaged in a custom-made microscope66 and covered with 300 µl of imaging buffer (150 mM Tris-HCl pH 8, 10% (v/w) glucose, 35 mM cysteamine (MEA), 0.5 mg/ml glucose oxidase (Sigma; G7141), and 40 mg/ml catalase (Sigma; C3556)). Typically, 200,000–500,000 frames were recorded. Analysis was performed using custom software written in MATLAB. We acquired two spectral channels simultaneously by splitting the emission with a dichroic (Chroma, T680LPXXR) and assigned the colour based on the relative intensities of the single-molecule localizations in both channels with a cross-talk rate below 0.2%67. Localizations with uncertainties above 25 nm or a fitted size of the PSF above 170 nm were discarded. The data were corrected for sample drift using a custom redundant cross-correlation based algorithm. Images were rendered using a Gaussian with a width proportional to the localization precision.
The data that support the findings of this study are available from the corresponding author upon reasonable request.
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We thank J. DeLuca for phospho-specific HEC1 antibodies, S. Lens for Mis12-INCENP-GFP and CenpB-INCENP-GFP expression vectors, A. Saurin for KNL1 expression vectors and J. Nilsson for BubR1-expressing cell lines. We thank the Draviam group members and in particular Madeleine Hart for comments on the manuscript. We also thank S. Court, P. Ungerer, U. Matti and A. Sossick for technical and infrastructural support. D.C. is supported through an MRC studentship award (MR/K50127X/1; RG70550) and Cambridge Commonwealth, European and International Trust. This work was supported by research funding from Cancer Research UK Career (C28598/A9787), MRC (MR/K50127X/1; RG70550), Royal Society (JP100104) and QMUL laboratory startup grant.
The authors declare no competing financial interests.
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Shrestha, R.L., Conti, D., Tamura, N. et al. Aurora-B kinase pathway controls the lateral to end-on conversion of kinetochore-microtubule attachments in human cells. Nat Commun 8, 150 (2017) doi:10.1038/s41467-017-00209-z
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