BUB-1 promotes amphitelic chromosome biorientation via multiple activities at the kinetochore

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Version of Record updated: March 8, 2019 (This version)
Version of Record published: December 21, 2018 (Go to version)
Accepted Manuscript published: December 14, 2018 (Go to version)
Accepted: December 13, 2018
Received: August 1, 2018

1. Of interest
Glucagon-like peptide-1 receptor activation stimulates PKA-mediated phosphorylation of Raptor and this contributes to the weight loss effect of liraglutide

Thao DV Le, Dianxin Liu ... Julio E Ayala

Research Article Dec 1, 2023
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Abstract

Accurate chromosome segregation relies on bioriented amphitelic attachments of chromosomes to microtubules of the mitotic spindle, in which sister chromatids are connected to opposite spindle poles. BUB-1 is a protein of the Spindle Assembly Checkpoint (SAC) that coordinates chromosome attachment with anaphase onset. BUB-1 is also required for accurate sister chromatid segregation independently of its SAC function, but the underlying mechanism remains unclear. Here we show that, in Caenorhabditis elegans embryos, BUB-1 accelerates the establishment of non-merotelic end-on kinetochore-microtubule attachments by recruiting the RZZ complex and its downstream partner dynein-dynactin at the kinetochore. In parallel, BUB-1 limits attachment maturation by the SKA complex. This activity opposes kinetochore-microtubule attachment stabilisation promoted by CLS-2^CLASP-dependent kinetochore-microtubule assembly. BUB-1 is therefore a SAC component that coordinates the function of multiple downstream kinetochore-associated proteins to ensure accurate chromosome segregation.

https://doi.org/10.7554/eLife.40690.001

Introduction

During mitosis, the microtubule-based spindle segregates sister chromatids by attaching to the macromolecular kinetochores assembled on centromeres. Accurate segregation of chromosomes requires their biorientation by amphitelic attachments connecting each sister chromatid to microtubules emanating from opposite spindle poles. In metazoans, two main kinetochore microtubule-binding modules ensure efficient interaction with spindle microtubules: the NDC80 complex and the Rod-Zw10-Zwilch (RZZ)-Spindly kinetochore module that recruits dynein-dynactin motors to kinetochores (Gassmann et al., 2008a; Griffis et al., 2007; Scaërou et al., 1999; Starr et al., 1998; Williams et al., 2003). The NDC80 complex interacts with microtubule plus-ends to establish load-bearing end-coupled connections between kinetochores and the mitotic spindle (Cheeseman et al., 2006; DeLuca et al., 2005; McCleland et al., 2003; Wigge and Kilmartin, 2001). Kinetochore-localized dynein mediates initial lateral capture of microtubules to ensure correct kinetochore orientation (Gassmann et al., 2008a). This initial kinetochore orientation limits merotelic connections, where individual kinetochores are attached to both spindle poles, and accelerates formation of NDC80-mediated end-coupled attachments (Rieder and Alexander, 1990; Rieder and Salmon, 1998; Varma et al., 2008). The transition from initial lateral to load-bearing end-coupled attachments is coordinated by the RZZ complex itself, which inhibits NDC80 binding to microtubules until dynein has properly oriented kinetochores (Cheerambathur et al., 2013). Once properly established, load-bearing connections are subsequently reinforced by the SKA complex, which interacts with NDC80 and kinetochore microtubules (Auckland et al., 2017; Cheerambathur et al., 2017; Gaitanos et al., 2009; Helgeson et al., 2018; Janczyk et al., 2017; Schmidt et al., 2012; Theis et al., 2009). During chromosome alignment, several mechanisms promote amphitelic load-bearing attachments (reviewed in (Auckland and McAinsh, 2015; Maiato et al., 2017). Chromosome biorientation through amphitelic attachment is selectively self-stabilised by the tension generated on kinetochores. This tension prevents Aurora B kinase-dependent destabilisation of attachments (reviewed in Lampson and Grishchuk, 2017), and/or promotes TOG (Tumour Over-expressed Gene) domain protein-dependent stabilisation of attachments (Miller et al., 2016). Merotely is also limited by initially high kinetochore microtubule dynamics, which maintain a high turnover of kinetochore-microtubule attachments until biorientation is achieved (Bakhoum et al., 2009a; Bakhoum et al., 2009b; Lampson and Grishchuk, 2017).

An additional key player in the process of chromosome alignment is the kinetochore BUB1 kinase that was originally identified as a component of the Spindle Assembly Checkpoint (SAC), a mechanism that delays anaphase onset until all kinetochores are properly connected to the spindle (reviewed in Joglekar, 2016). BUB1 is also directly involved in establishing proper chromosome attachments to the mitotic spindle. Indeed, independently of the SAC, BUB1 was shown to be essential to preserve ploidy throughout mitosis in budding and fission yeasts (Bernard et al., 1998; Vanoosthuyse et al., 2004; Warren et al., 2002), to promote chromosome alignment and accurate segregation essential for embryonic development in C. elegans oocytes and embryos (Essex et al., 2009; Laband et al., 2017), and to ensure efficient chromosome congression and segregation and prevent aneuploidy in human tissue cultured cells (Johnson et al., 2004; Klebig et al., 2009; Meraldi and Sorger, 2005). However, the molecular mechanism(s) behind these non-SAC functions of BUB1, and how BUB1 influences chromosome attachments to the mitotic spindle remain unclear.

BUB1 mediates the recruitment of several downstream proteins involved in accurate chromosome segregation. BUB1 phosphorylation of histone H2A (Kawashima et al., 2010; Ricke et al., 2012) and subsequent recruitment of the centromeric protein Shugoshin (Fernius and Hardwick, 2007) target protein phosphatase 2A (PP2A) and Aurora B kinase to the inner centromere (Kawashima et al., 2010; Yamagishi et al., 2010). In parallel, BUB1 interacts with BUBR1, which leads to kinetochore recruitment of PP2A (Zhang et al., 2016). Aurora B and PP2A are in turn thought to promote accurate chromosome segregation via their kinetochore regulatory functions (reviewed in Saurin, 2018). However, several studies suggest that BUB1 can regulate kinetochore-microtubule attachment independently of this pathway (Johnson et al., 2004; Meraldi and Sorger, 2005; Perera and Taylor, 2010; Raaijmakers et al., 2018; Windecker et al., 2009). A second function of BUB1 that could account for its role in regulating kinetochore-microtubule attachments is the recruitment of the kinetochore protein CENP-F, via its kinase domain but independently of kinase activity (Berto et al., 2018; Ciossani et al., 2018; Encalada et al., 2005; Johnson et al., 2004). However, the role of CENP-F during chromosome segregation remains controversial (Bomont et al., 2005; Cheeseman et al., 2005; Holt et al., 2005; McKinley and Cheeseman, 2017; Pfaltzgraff et al., 2016). Alternatively, as BUB1 contributes to recruiting the RZZ complex to kinetochores in human cells (Caldas et al., 2015; Zhang et al., 2015), kinetochore-localized dynein-dynactin may be required downstream of BUB1 for establishing amphitelic attachments. Yet, the loss of BUB1-dependent kinetochore targeting of the RZZ complex is not sufficient to account for the lethality of SAC-deficient haploid (HAP1) cells upon BUB1 depletion (Raaijmakers et al., 2018). Altogether, these observations suggest that BUB1 contributes to chromosome biorientation and alignment through one or several additional downstream activities that remain to be identified.

Here, by analysing BUB-1 during mitosis in the C. elegans one-cell embryo or zygotes, we show that it has multiple functions essential for proper chromosome biorientation. Coordination of these activities by BUB-1 is required to prevent merotely and embryonic lethality. We therefore propose that BUB-1 is a key regulator of kinetochore-microtubule interactions that ensures accurate chromosome biorientation and segregation.

Results

BUB-1 inhibits chromosome biorientation

To study BUB-1 function in kinetochore-microtubule attachments, we performed live imaging of control or BUB-1-depleted C. elegans one-cell embryos. To monitor chromosome segregation, we used a strain expressing KNL-1::mCherry to label kinetochores and GFP::γ-Tubulin to track spindle poles (Figure 1A; Video 1). Kymographs allowed visualising the behaviour of kinetochores and spindle poles over time (Figure 1B). Kinetochores are holocentric in the C. elegans nematode and form along the length of sister chromatids (Dernburg, 2001), thus chromosome congression, alignment and segregation were quantified by measuring the space occupied by kinetochores in the spindle pole axis (chromosome span) over time (Figure 1A,C). In C. elegans zygotes, spindle pole separation is primarily driven by cortical pulling forces transmitted through astral microtubules (Grill et al., 2001). Cortical forces are then opposed by load-bearing connections between bioriented chromosomes and the two poles of the mitotic spindle. We therefore also measured spindle elongation (pole to pole distance) over time as an indirect read-out of these connections (Figure 1A,C) (Desai et al., 2003).

Figure 1 with 2 supplements see all

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BUB-1 inhibits chromosome biorientation.

(A) Assay for kinetochore-microtubule attachment formation and chromosome congression. GFP::γ-Tub is used to measure the pole to pole distance, and KNL-1::mCherry is used to measure the chromosome span in the spindle pole axis. (B) Kymographs generated from embryos expressing GFP::γ-Tub and KNL-1::mCherry, for the different indicated conditions. Horizontal scale bar, 5 μm; Vertical scale bar, 20 s. (C) Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions. Top right corner: Arrowhead, spindle pole bump following BUB-1 depletion. (D) Schematics of BUB-1 at kinetochores recruiting its downstream partners HCP-1/2^CENP-F and CLS-2^CLASP. (E) Top: Representative images from time-lapse movies showing BUB-1 dependent localisations of GFP::HCP-1^CENP-F, GFP::HCP-2^CENP-F and CLS-2^CLASP::GFP on chromosomes (H2B::mCherry), at metaphase. Bottom: Quantification of the GFP signal on chromosomes at metaphase. Mann Whitney tests were used to determine significance (GFP::HCP-1 p < 0.0001, GFP::HCP-2 p = 0.0003, CLS-2::GFP p < 0.0001). Scale bar, 5 μm. (F) Immunofluorescent staining of kinetochores (KNL-1) and microtubules (DM1α) in *Δhcp-2* zygotes at metaphase in the indicated conditions. Scale bar, 5 μm. Magnifications of the kinetochore region (highlighted by a dashed rectangle) are shown on the right of each panel. Arrows point to bent merotelic kinetochores in the BUB-1-depleted zygote. Arrowheads show a mono-oriented chromosome in the HCP-1^CENP-F-depleted zygote. Scale bar, 1 μm. (G) Representative images of kinetochores (KNL-1::mCherry, green) and spindle poles (GFP::γ-Tub, magenta), at different times from the onset of chromosome segregation, for the indicated conditions. White arrows point towards sister kinetochores. White asterisks indicate the presence of kinetochore stretches. Scale bar, 5 μm. (H) Quantification of the percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments, in the indicated conditions. Error bars represent the SEM.

https://doi.org/10.7554/eLife.40690.002

Figure 1—source data 1 Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions.: https://doi.org/10.7554/eLife.40690.008
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Figure 1—source data 2 GFP::HCP-1, GFP::HCP-2, and CLS-2::GFP signals on chromosomes at metaphase.: https://doi.org/10.7554/eLife.40690.009
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Figure 1—source data 3 Percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments, in the indicated conditions.: https://doi.org/10.7554/eLife.40690.010
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Video 1

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posterframe for video — One-cell *C. elegans* embryos in the indicated conditions.

10 s per frame. Magenta, γ-Tubulin::GFP (spindle poles); Green, KNL-1::mCherry (kinetochores).

https://doi.org/10.7554/eLife.40690.011

In control zygotes, progressive chromosome congression led to the formation of a tight metaphase plate (Figure 1B,C; Video 1). This correlated with slow spindle pole separation from 80 s after nuclear envelope breakdown (NEBD) until anaphase onset (140 s after NEBD), and was followed by sister chromatid segregation concomitant with fast spindle pole separation (Figure 1B,C). In BUB-1-depleted zygotes, anaphase onset was delayed compared to controls (around 200 s after NEBD, Figure 1B,C), in agreement with BUB-1 promoting anaphase onset through Cdc20 activation (Kim et al., 2017; Kim et al., 2015; Yang et al., 2015). In these embryos, a chromosome congression pause was visible in the kymographs, as evidenced by a constant chromosome span that coincided with a previously described ‘bump’ in the pole separation profile (Kim et al., 2015). This spindle pole bump has been shown to reflect delayed load-bearing attachments (Kim et al., 2015), which are eventually established to allow metaphase plate formation (Figure 1B,C; Video 1). Sister chromatids were connected to opposite spindle poles, but these attachments were not amphitelic. Instead, bent kinetochores during metaphase and kinetochore stretches during anaphase were visible in BUB-1-depleted zygotes, which in holocentric embryos indicate merotelic connections of individual kinetochores to both spindle poles (Figure 1F–H) (Essex et al., 2009; Maton et al., 2015). BUB-1 depletion therefore delays load-bearing attachments, leading to a lag in chromosome congression, followed by the establishment of merotelic attachments to both spindle poles.

We next sought to test which proteins downstream of BUB-1 also affect chromosome attachment or segregation. BUB-1 is required for kinetochore recruitment of the two redundant CENP-F orthologs HCP-1 and 2, which in turn recruit CLS-2^CLASP (Figure 1D) (Cheeseman et al., 2005; Maton et al., 2015). CLASP-family proteins are key regulators of kinetochore microtubule dynamics, which promote kinetochore microtubule growth while limiting their stability (Cheeseman et al., 2005; Lacroix et al., 2018; Maffini et al., 2009; Maiato et al., 2005; Maiato et al., 2003a; Pereira et al., 2006). We imaged C. elegans zygotes expressing endogenous GFP-tagged HCP-1^CENP-F or HCP-2^CENP-F, or a GFP-tagged CLS-2^CLASP transgene, and confirmed their absence from kinetochores upon BUB-1 depletion (Figure 1E; Figure 1—figure supplement 1A,B). In line with previous observations, following depletion of HCP-1/2^CENP-F or CLS-2^CLASP, chromosomes did not congress, and chromosomes and spindle poles separated prematurely 40 s after NEBD concomitant with sister chromatid co-segregation towards the same spindle pole (Figure 1B–H; Video 1) (Cheeseman et al., 2005). This early pole and chromosome separation was not caused by premature anaphase onset, as the fluorescent signal of a Separase activation sensor remained on chromosomes well after they completed separation in absence of HCP-1/2^CENP-F or CLS-2^CLASP (Figure 1—figure supplement 1C–E) (Kim et al., 2015). Instead, a vast majority of chromosomes remained mono-oriented in HCP-1/2^CENP-F- or CLS-2^CLASP-depleted zygotes (Figure 1F–H) (Cheeseman et al., 2005). This indicates that the sister chromatid co-segregation phenotype resulting from depletion of HCP-1/2^CENP-F or CLS-2^CLASP is due to improperly mono-oriented chromosomes rather than premature mitotic exit. Therefore, while being epistatically related at the kinetochore, the depletion of BUB1 and its downstream partners, HCP-1/2^CENP-F or CLS-2^CLASP, have very different effects on chromosome segregation: BUB-1 depletion results in delayed chromosome congression and bioriented yet merotelic attachments, while HCP-1/2^CENP-F or CLS-2^CLASP depletion induces mono-orientation and sister chromatid co-segregation.

We next considered two non-exclusive hypotheses to account for this apparent discrepancy. First, HCP-1/2^CENP-F and CLS-2^CLASP could play an essential function outside of the kinetochore and independently of BUB-1. Second, BUB-1 could be causing the phenotype observed upon HCP-1/2^CENP-F or CLS-2^CLASP depletion. To test the latter hypothesis, chromosome segregation was analysed in zygotes simultaneously depleted of BUB-1 and CLS-2^CLASP. Strikingly BUB-1 depletion restored biorientation and rescued the sister chromatid segregation failure typical of CLS-2^CLASP depletion (Figure 1B,C; Video 1). We also observed similar sister chromatid segregation rescue by co-depleting BUB-1 and HCP-1^CENP-F or HCP-2^CENP-F, in CRIPSR-cas9 generated hcp-2 (Δhcp-2) (Figure 1B,C; Figure 1—figure supplement 2A–C) and hcp-1 (Δhcp-1; Figure 1—figure supplement 2D–E) deletion mutants respectively. BUB-1 and HCP-1^CENP-F (or HCP-2^CENP-F) co-depleted embryos displayed a ‘BUB-1-like’ phenotype with delayed congression (Figure 1B,C) and merotelic attachments to both spindle poles evidenced by bent kinetochores during metaphase and kinetochore stretches during anaphase (Figure 1F–H). We confirmed by immunofluorescence the absence of BUB-1 and HCP-1^CENP-F after RNAi-treatment in the Δhcp-2 strain (Figure 1—figure supplement 2F). Together, these results suggest that BUB-1 prevents chromosome biorientation, and that this activity is revealed in absence of HCP-1/2^CENP-F or CLS-2^CLASP.

Biorientation inhibition requires BUB-1 localisation at the kinetochore

We next tested whether BUB-1 needs to be localised at the kinetochore to exert its inhibitory effects in absence of HCP-1/2^CENP-F and/or CLS-2^CLASP. BUB-1 recruitment to kinetochores depends on phosphorylated MELT repeats located in the N-terminal part of the kinetochore scaffolding protein KNL-1 (Vleugel et al., 2013). To abolish BUB-1 recruitment to kinetochores, we used a C. elegans strain expressing a truncation mutant of KNL-1 (KNL-1^Δ85-505), which lacks all MELT repeats (Figure 2A; Figure 2—figure supplement 1A) (Moyle et al., 2014). We then introduced KNL-1^WT and KNL-1^Δ85-505 RNAi-resistant transgenes in the Δhcp-2 mutant background. As expected, depleting HCP-1^CENP-F along with endogenous KNL-1 in absence of HCP-2 but in presence of the RNAi-resistant KNL-1^WT transgene led to the same phenotype as in absence of HCP-1/2^CENP-F only, characterised by sister chromatid mono-orientation followed by co-segregation (Figure 2B–D; Figure 2—figure supplement 1B; Video 2). In contrast, in the presence of KNL-1^Δ85-505, and therefore in the absence of BUB-1 at kinetochores (Figure 2—figure supplement 1A), co-depleted zygotes displayed a ‘BUB-1-like’ phenotype with delayed congression and bioriented merotelic attachments (Figure 2B–D; Figure 2—figure supplement 1B; Video 2). Together, these results show that BUB-1 inhibitory activity on biorientation depends on its kinetochore localisation.

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Biorientation inhibition requires BUB-1 localisation at the kinetochore.

(A) Schematics of WT KNL-1 and of the ∆85–505 mutant that leads to loss of BUB-1 from kinetochores. (B) Kymographs generated from embryos expressing GFP::γ-Tub and KNL-1::mCherry, for the indicated conditions. (C) Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions. (D) Quantification of the percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments in the indicated conditions. Error bars represent the SEM. Horizontal scale bar, 5 μm; Vertical scale bar, 20 s.

https://doi.org/10.7554/eLife.40690.012

Figure 2—source data 1 Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions.: https://doi.org/10.7554/eLife.40690.015
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Figure 2—source data 2 Percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments, in the indicated conditions.: https://doi.org/10.7554/eLife.40690.016
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BUB-1 kinase domain inhibits biorientation independently of its kinase activity

To determine if BUB-1 kinase activity is required for inhibiting chromosome biorientation, we used three different RNAi-resistant mutant transgenes that affect the kinase domain and/or kinase activity of BUB-1 (Figure 3A): (1) a full truncation of the kinase domain (BUB-1^ΔKD), (2) a dual point mutant that destabilizes the kinase domain and prevents its interaction with the SAC component MDF-1^Mad1 (BUB-1^{K718R ;D847N}), and (3) a point mutant with defective kinase activity by mutation of the catalytic aspartate in the ‘HxD”motif (BUB-1^D814N) (Kang et al., 2008; Moyle et al., 2014). In line with previous findings on BUB-1 function in the regulation of anaphase onset, BUB-1^ΔKD and BUB-1^{K718R ;D847N}, but not BUB-1^D814N, led to delayed anaphase onset (Figure 3—figure supplement 1A,B) (Kim et al., 2015; Yang et al., 2015). Importantly, all of these mCherry-tagged mutants localised to kinetochores in absence of endogenous BUB-1, allowing us to test their influence on kinetochore-microtubule attachments (Figure 3—figure supplement 1C). In absence of endogenous BUB-1, all three mutant transgenes induced only mild variations in the chromosome span and pole separation profiles compared to control embryos, indicating that congression and load-bearing attachment are not drastically altered when BUB-1 kinase activity is impaired (Figure 3—figure supplement 1A,B; Video 3). Additionally, sister kinetochore alignment and segregation was similar to in control embryos, with only occasional merotelic attachments in the BUB-1^ΔKD mutant evidenced by anaphase kinetochore stretches (Figure 3—figure supplement 1D,E). Interestingly, BUB-1^ΔKD prevented HCP-1^CENP-F kinetochore localization (Figure 3—figure supplement 1C) suggesting that BUB1 recruitment of CENP-F via its kinase domain is conserved from humans to C. elegans (Ciossani et al., 2018; Raaijmakers et al., 2018). Furthermore, the presence of mainly bioriented chromosomes with amphitelic attachments in this mutant that lacks kinetochore HCP-1/2^CENP-F, suggests that BUB-1’s inhibitory role during biorientation is dependent on the kinase domain.

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BUB-1 kinase domain inhibits biorientation independently of its kinase activity.

(A) Schematics of wild-type (WT) BUB-1 and of the different BUB-1 mutants. (B) Kymographs generated from embryos expressing GFP::γ-Tub and KNL-1::mCherry, for different indicated conditions. (C) Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions. (D) Quantification of the percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments in the indicated conditions. Error bars represent the SEM. Horizontal scale bar, 5 μm; Vertical scale bar, 20 s.

https://doi.org/10.7554/eLife.40690.018

Figure 3—source data 1 Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions.: https://doi.org/10.7554/eLife.40690.023
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Figure 3—source data 2 Percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments, in the indicated conditions.: https://doi.org/10.7554/eLife.40690.024
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Video 3

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To confirm the kinase domain is essential, we analysed BUB-1 mutants in absence of endogenous BUB-1 and HCP-1/2^CENP-F (Figure 3B,C). BUB-1^WT led to premature pole and chromosome separation (Figure 3B,C) and the establishment of mono-oriented attachments (Figure 3D; Figure 3—figure supplement 1E), as expected in absence of HCP-1/2^CENP-F. In contrast, the phenotype was attenuated with BUB-1^ΔKD and BUB-1^{K718R ;D847N}: chromosome congression was delayed but occurred successfully (Figure 3B,C; Video 3), and chromosome biorientation with merotelic attachments was established (Figure 3D; Figure 3—figure supplement 1E). The appearance of a large proportion of merotelic attachments only after depletion of HCP-1/2^CENP-F in BUB-1^ΔKD (which normally lacks kinetochore-associated HCP-1/2^CENP-F) suggests that HCP-1/2^CENP-F promote non-merotelic attachments independently of its kinetochore localization (Figure 3D and Figure 3—figure supplement 1D). Furthermore, these results confirm that the integrity of the kinase domain is required for BUB-1 inhibition of chromosome congression and biorientation. In contrast, the HCP-1/2^CENP-F loss-of-function phenotype was not rescued by BUB-1^D814N, which specifically disrupts the kinase activity (Figure 3B–D; Figure 3—figure supplement 1E) (Moyle et al., 2014). Altogether, these results demonstrate that BUB-1’s inhibitory role on biorientation depends on its kinase domain, but not its kinase activity.

BUB-1 accelerates non-merotelic end-on attachments via dynein, independently of the inhibitory effect on biorientation

We next sought to identify the mechanism by which kinetochore-localized BUB-1 prevents the establishment of chromosome biorientation in absence of HCP-1/2^CENP-F or CLS-2^CLASP. In mammals, BUB1 contributes to recruiting the RZZ complex, and thus probably also dynein-dynactin, to kinetochores (Caldas et al., 2015; Zhang et al., 2015). Kinetochore-localized RZZ and dynein-dynactin could prevent chromosome congression by accelerating end-on attachments to short non-dynamic microtubules induced by the absence of HCP-1/2^CENP-F or CLS-2^CLASP (Figure 4A). This would promote mono-oriented connections and sister chromatid co-segregation. In contrast, in absence of BUB-1, and thus without kinetochore-localized RZZ and dynein-dynactin, kinetochores are not properly oriented toward spindle poles (Gassmann et al., 2008a). In absence of HCP-1/2^CENP-F or CLS-2^CLASP, this would result in largely merotelic connections to short non-dynamic microtubules, and could provide resistance to cortical traction forces thus restoring chromosome biorientation (Figure 4A).

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BUB-1 accelerates non-merotelic end-on attachments via dynein, independently of the inhibitory effect on biorientation.

(A) Schematics of the potential mechanism for chromosome biorientation inhibition by BUB-1 in absence of HCP-1/2^CENP-F. By orienting kinetochores relative to spindle poles, BUB-1 downstream partners RZZ and dynein-dynactin connect chromosomes in a mono-oriented conformation to short non-dynamic microtubules, leading to premature chromosome segregation. In absence of BUB-1, kinetochore mis-orientation enables the establishment of bioriented merotelic connections capable of resisting cortical traction forces. (B) Left: Representative images from time-lapse movies showing localisations of ZWL-1^Zwilch::GFP and DNC-2::GFP on chromosomes (H2B::mCherry) in the indicated conditions, 100 s after NEBD. Right: Quantifications of the GFP signal on chromosomes 100 s after NEBD. Kruskall Wallis tests with Dunn’s correction for multiplicity were used to assess significance (ZWL-1::GFP bub-1(RNAi) p = 0,0276, ZWL-1::GFP hcp-1/2(RNAi) p = 0,0341, DNC-2::GFP bub-1(RNAi) p = 0,0015, DNC-2::GFP hcp-1(RNAi) p = 0,0671). (C) Kymographs generated from embryos expressing GFP::γ-Tub and KNL-1::mCherry for the indicated conditions. (D) Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions. (E) Quantification of the percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments in the indicated conditions. Error bars represent the SEM. Horizontal scale bars, 5 μm; Vertical scale bar, 20 s.

https://doi.org/10.7554/eLife.40690.026

Figure 4—source data 1 ZWL-1Zwilch::GFP and DNC-2::GFP signals on chromosomes100safter NEBD.: https://doi.org/10.7554/eLife.40690.031
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Figure 4—source data 2 Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions.: https://doi.org/10.7554/eLife.40690.032
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Figure 4—source data 3 Percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments, in the indicated conditions.: https://doi.org/10.7554/eLife.40690.033
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To test this hypothesis, we first analysed the recruitment of RZZ and dynein-dynactin to kinetochores in BUB-1-depleted zygotes. Consistent with previous results in human cells, BUB-1 depletion led to a drastic reduction of the GFP-tagged RZZ complex component ZWL-1^Zwilch at kinetochores (Figure 4B; Figure 4—figure supplement 1A,B). This result is also in line with the significant reduction in kinetochore-localized GFP::CZW-1^ZW10 that was previously observed in the KNL-1^Δ85-505 mutant, which lacks kinetochore-localized BUB-1 (Maton et al., 2015). Reduction in RZZ kinetochore targeting coincided with the complete loss of the GFP-tagged dynactin subunit DNC-2^p50 from kinetochores, which instead localized diffusely on chromosomes and in the spindle region (Figure 4B; Figure 4—figure supplement 1C,D). Therefore BUB-1 is required for dynein-dynactin recruitment to kinetochores in C. elegans zygotes, and the residual pool of RZZ complex that localises to kinetochores independently of BUB-1 does not contribute to dynein-dynactin recruitment. Importantly, both ZWL-1^Zwilch and DNC-2^p50 were present at kinetochores in absence of HCP-1/2 ^CENP-F (Figure 4B; Figure 4—figure supplement 1A–D).

Next, we tested if RZZ and dynein-dynactin participate in the BUB-1-dependent inhibition of chromosome biorientation in absence of HCP-1/2^CENP-F. For this, we co-depleted ZWL-1^Zwilch with HCP-1^CENP-F in the Δhcp-2 strain. This led to a slight improvement in chromosome congression, and chromosome segregation occurred later and more slowly than in absence of HCP-1/2^CENP-F alone (Figure 4C,D; Video 4). This result suggests that RZZ and dynein promote rapid end-on attachments and early co-segregation of sister chromatids in absence of HCP-1/2^CENP-F. However, chromosome biorientation was not restored and sister chromatid still co-segregated in this condition (Figure 4C–E; Figure 4—figure supplement 1E; Video 4). Further evidence confirming the independence of BUB-1 activities in inhibiting chromosome biorientation and in recruiting RZZ and dynein-dynactin came from our analysis of the BUB-1^ΔKD mutant, which could support the normal recruitment of DNC-2^p50 (Figure 4—figure supplement 1F) but did not inhibit chromosome biorientation in absence of HCP-1/2^CENP-F (Figure 3B–D). Therefore, kinetochore recruitment of RZZ and dynein-dynactin by BUB-1 is important for initial end-on attachments, but does not explain BUB-1 inhibition of chromosome biorientation.

Video 4

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However, in contrast to the full BUB-1 depletion, the BUB-1^ΔKD mutant also led to a decreased frequency of merotelic attachments (Figures 3D and 4E) and reduced kinetochore stretches in absence of HCP-1/2^CENP-F (Figure 4—figure supplement 1G). This suggests that the high degree of merotely observed upon BUB-1 codepletion with HCP-1/2^CENP-F is largely caused by the loss of dynein from kinetochores, and that BUB-1 favours amphitelic attachments by recruiting dynein to kinetochores. Furthermore, the spindle pole elongation profile observed in presence of BUB-1^ΔKD (and also in presence of BUB-1^{K718R ;D847N} or BUB-1^D814N) did not display the typical bump indicative of delayed load-bearing attachments, normally observed in absence of BUB-1 (Figure 3—figure supplement 1B) (Kim et al., 2015). Altogether, these results suggest that recruiting the RZZ complex and dynein-dynactin at the kinetochore is a critical function of BUB-1 to promote amphitelic end-on attachments (Gassmann et al., 2008a). However, this activity is not sufficient to account for BUB-1 inhibitory effect on chromosome biorientation in absence of HCP-1/2^CENP-F.

BUB-1 inhibits biorientation in absence of HCP-1/2^CENP-F by preventing SKA complex recruitment

Another hypothesis to explain how BUB-1 inhibits chromosome biorientation could be through the limitation of attachment stability or strength, which would prevent chromosomes from stably engaging in load-bearing connections to both spindle poles. An obvious candidate that destabilises attachments is Aurora B (Figure 5—figure supplement 1A), which is recruited to centromeres downstream of BUB1 in human tissue cultured cells (Ricke et al., 2012). However, previous studies in human cells have ruled out a role for Aurora B in BUB1 function during chromosome alignment (Logarinho et al., 2008; Meraldi and Sorger, 2005; Raaijmakers et al., 2018). We confirmed these results in C. elegans embryos by using a fast-acting temperature-sensitive (ts) AIR-2^{Aurora B} mutant (air-2(or207ts), hereafter air-2(ts)) and by upshifting embryos to the restrictive temperature (26°C) as pronuclei finished migrating (Davies et al., 2017; Severson et al., 2000). Upon upshift of HCP-1/2^CENP-F-depleted air-2(ts) mutant embryos to the restrictive temperature, sister chromatids still co-segregated prematurely (100 s after NEBD). Therefore BUB-1 inhibits chromosome congression and biorientation independently of AIR-2^{Aurora B} activity (Figure 5—figure supplement 1B,C).

If BUB-1 does not promote attachment destabilization, it could instead counteract a stabilizing mechanism. In human cells, BUB1 localization to kinetochores is anti-correlated with SKA1 localization, a member of the SKA complex that strengthens attachment and subsequent congression of chromosomes (Auckland et al., 2017; Schmidt et al., 2012). BUB-1 might therefore inhibit biorientation by limiting the recruitment of the SKA complex to kinetochores (Figure 5A). Accordingly, we found that GFP-tagged SKA-1 was undetectable at kinetochores in absence of HCP-1/2^CENP-F (Figure 5B; Figure 5—figure supplement 2A,B). However, as SKA-1 kinetochore localization depends on the tension exerted at kinetochores by end-on attachments (Cheerambathur et al., 2017), the low tension generated at mono-oriented chromosomes could explain the lack of SKA-1 kinetochore localization in this condition. To exclude this possibility, we generated monopolar spindles in two-cell stage embryos by depleting ZYG-1^Plk4, which is essential for centrosome duplication and subsequent bipolar spindle assembly (Essex et al., 2009; O'Connell et al., 2001). In this condition, SKA-1::GFP accumulated on the chromosome side that faces the spindle monopole, demonstrating that mono-oriented attachments in ZYG-1^Plk4-depleted 2 cell stage embryos provide sufficient tension for SKA complex kinetochore localization (Figure 5B; Figure 5—figure supplement 2A,C). Together, these results suggest that SKA-1 kinetochore recruitment is inhibited in absence of HCP-1/2^CENP-F, but that the mono-oriented attachment configuration is not sufficient to account for the lack of kinetochore SKA-1. Most importantly, SKA-1::GFP kinetochore recruitment was rescued by depleting BUB-1 in absence of HCP-1/2^CENP-F (Figure 5B; Figure 5—figure supplement 2A,B), suggesting that BUB-1 prevents SKA-1 recruitment to kinetochores when HCP-1/2^CENP-F is absent.

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BUB-1 inhibits biorientation in absence of HCP-1/2^CENP-F by preventing SKA complex recruitment.

(A) Schematics of the potential mechanism for chromosome biorientation inhibition by BUB-1 in absence of HCP-1/2^CENP-F. BUB-1 limits attachment maturation by the SKA complex, leading to the incapacity for chromosomes to birorient when microtubules are short and non-dynamic. Co-depleting BUB-1 restores SKA complex recruitment, allowing the strengthening of attachments and therefore the establishment of biorientation even when microtubules are short and non-dynamic. (B) Left: Representative images from time-lapse movies showing the localization of SKA-1::GFP on chromosomes (H2B::mCherry) in the indicated conditions at metaphase. Right: Quantification of the GFP signal on chromosomes at metaphase. Kruskall Wallis tests with Dunn’s correction for multiplicity were used to assess significance (hcp-1(RNAi) p = 0,0006, hcp-1 +bub-1(RNAi) p > 0.9999, zyg-1(RNAi) p > 0,9999). (C) Kymographs generated from embryos expressing GFP::γ-Tub and KNL-1::mCherry for the indicated conditions. (D) Quantification of the percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments in the indicated conditions. (E) Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions. Error bars represent the SEM. Horizontal scale bars, 5 μm; Vertical scale bar, 20 s.

https://doi.org/10.7554/eLife.40690.035

Figure 5—source data 1 SKA-1::GFP signal on chromosomes at metaphase.: https://doi.org/10.7554/eLife.40690.044
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Figure 5—source data 2 Percentage of embryos with chromosomes engaged in amphitelic, merotelic and mono-oriented attachments, in the indicated conditions.: https://doi.org/10.7554/eLife.40690.045
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Figure 5—source data 3 Chromosome span and pole to pole distance as functions of time after NEBD for the indicated conditions.: https://doi.org/10.7554/eLife.40690.046
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We next wanted to test if this novel activity of BUB-1 could account for its inhibitory effect on chromosome biorientation. If BUB-1 inhibition of SKA complex kinetochore recruitment prevents chromosome biorientation in absence of HCP-1/2^CENP-F, two predictions can be made: 1) BUB-1 mutants incapable of inhibiting chromosome biorientation should not prevent SKA complex kinetochore recruitment, and 2) the absence of the SKA complex should abrogate chromosome biorientation in these mutants. To test these predictions, we focused on the BUB-1^ΔKD and BUB-1^{K718R ;D847N} mutants, which are incapable of inhibiting chromosome biorientation, while promoting proper initial end-on attachment through kinetochore recruitment of RZZ and dynein-dynactin. In agreement with our first prediction, both mutants allowed kinetochore recruitment of SKA-1::GFP (Figure 5—figure supplement 2F). Next, to test if this kinetochore localization of the SKA complex is required for chromosome biorientation in the absence of HCP-1/2^CENP-F in these BUB-1 mutants, we used a ska-1 deletion allele (Δska-1). Although required for timely chromosome congression, SKA-1 is a non-essential gene in C. elegans (Figure 5—figure supplement 2D,E) (Cheerambathur et al., 2017). Strikingly in the simultaneous absence of endogenous BUB-1, HCP-1/2^CENP-F and SKA-1, both BUB-1 mutants (BUB-1^ΔKD and BUB-1^{K718R ;D847N}) led to complete failure of chromosome congression and biorientation, along with sister chromatid co-segregation, similar to what is observed after HCP-1/2^CENP-F depletion alone (Figure 5C–E; Figure 5—figure supplement 2G; Video 5). Thus BUB-1^ΔKD and BUB-1^{K718R ;D847N} are capable of sustaining chromosome biorientation in absence of HCP-1/2^CENP-F only when the SKA complex is present. This result suggests that in these two BUB-1 mutants the kinetochore-localized SKA complex is responsible for the observed rescue of chromosome biorientation in absence of HCP-1/2^CENP-F. Altogether, our results suggest that, in absence of HCP-1/2^CENP-F or CLS-2^CLASP, BUB-1 inhibits stable biorientation of chromosomes by preventing SKA complex recruitment to kinetochores (Figure 5A).

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BUB-1 limits merotely by balancing kinetochore microtubule assembly and kinetochore attachment maturation

We next wanted to test the role of BUB-1 downstream activities for accurate chromosome segregation and organismal viability. Upon loss of CLS-2^CLASP -a protein involved in promoting kinetochore microtubule polymerization- C. elegans zygotes present a unique phenotype of premature sister chromatid co-segregation (Cheeseman et al., 2005). We found that this phenotype can be rescued by alleviating BUB-1-mediated inhibition of SKA-1 at the kinetochores, preventing SKA-mediated attachment maturation. These observations suggest that the capacity for chromosomes to engage in stable connections to both spindle poles can be provided either by efficient kinetochore microtubule polymerization or by kinetochore-microtubule attachment maturation. Thus, BUB-1 provides two opposing activities in the establishment of bioriented amphitelic connections: (1) promoting biorientation by recruiting CLS-2^CLASP to kinetochores, and (2) restricting biorientation by limiting SKA-mediated attachment maturation. To probe the functional significance of these opposing BUB-1 activities for accurate chromosome segregation and overall organismal viability, we used the BUB-1 mutants that separate these opposing activities. We used the BUB-1^ΔKD mutant that does not recruit HCP-1/2^CENP-F and CLS-2^CLASP to kinetochores, but nevertheless allows chromosome biorientation due to its incapacity to limit SKA-mediated attachment maturation, to probe the importance of BUB-1 activity in promoting kinetochore microtubule assembly through CLS-2^CLASP kinetochore recruitment. Embryos expressing BUB-1^ΔKD only presented slight merotely at 24°C, but lowering the temperature down to 15°C, and therefore lowering overall microtubule growth (Srayko et al., 2005), raised this rate of merotely by three-fold (Figure 6A). We observed a similar temperature dependency for embryonic lethality in this mutant (Figure 6B). These results suggest that promoting kinetochore microtubule assembly via BUB-1-mediated recruitment of CLS-2^CLASP is required to avoid merotely and embryonic lethality. This is consistent with previous work in human cancer cells with chromosomal instability (Bakhoum et al., 2009a).

Figure 6

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BUB-1 limits merotely by balancing kinetochore microtubule assembly and kinetochore attachment maturation.

(A) Quantification of the percentage of embryos with chromosomes engaged in amphitelic and merotelic attachments in the indicated conditions. Representative images of merotelic and non merotelic segregations are shown based on the KNL-1::mCherry signal 20 s after anaphase onset. White arrowheads point toward kinetochore stretches. (B) Embryonic lethality in the indicated conditions. Kruskall Wallis tests with Dunn’s correction for multiplicity were used to assess significance (WT 15°C (n = 252 embryos) vs 20°C (n = 1934) p > 0,9999, WT 20°C vs 24°C (n = 2107) p > 0,9999, ∆KD 15°C (n = 352) vs 20°C (n = 1104) p = 0,0012, ∆KD 20°C vs 24°C (n = 751) p = 0,4722). (C) Embryonic lethality in the indicated conditions. Kruskall Wallis tests with Dunn’s correction for multiplicity were used to assess significance (WT (n = 2107 embryos) vs K718R;D847N (n = 2663) p < 0,0001, D814N (n = 2181) vs K718R;D847N p < 0,0001, K718R;D847N vs *mdf-1(RNAi)* (n = 3410) p < 0,0001). (D) Quantifications of the integrated signals measured on chromosomes for different GFP-tagged proteins as function of time from NEBD. (E) (I) In prometaphase, BUB-1 localises to kinetochores and favours amphitely via two independent mechanisms. Downstream of BUB-1, the RZZ complex, Spindly and dynein-dynactin orient kinetochores and regulate NDC-80 activity, leading to the acceleration of end-on attachment in a non-merotelic conformation. (II) BUB-1 further contributes to establishing amphitelic attachments by promoting kinetochore microtubule assembly via HCP-1/2^CENP-F and CLS-2^CLASP recruitment, while limiting attachment maturation via the SKA complex. (III) In metaphase, BUB-1 leaves kinetochores allowing attachment maturation by the SKA complex. Scale bar, 5 μm.

https://doi.org/10.7554/eLife.40690.048

Figure 6—source data 1 Percentage of embryos with chromosomes engaged in amphitelic and merotelic attachments in the indicated conditions.: https://doi.org/10.7554/eLife.40690.049
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Figure 6—source data 2 Percentage of embryonic lethality in the indicated conditions.: https://doi.org/10.7554/eLife.40690.050
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Figure 6—source data 3 Percentage of embryonic lethality in the indicated conditions.: https://doi.org/10.7554/eLife.40690.051
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Figure 6—source data 4 Integrated signals measured on chromosomes for the indicated GFP-tagged proteins as function of time.: https://doi.org/10.7554/eLife.40690.052
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We finally addressed the importance of limiting SKA-dependent attachment maturation in the context of dynamic kinetochore microtubules (when HCP-1/2^CENP-F and CLS-2^CLASP are present at the kinetochore). The BUB-1^{K718R ;D847N} mutant does not limit SKA-mediated attachment maturation but still recruits HCP-1/2^CENP-F and CLS-2^CLASP to kinetochores. In contrast to control BUB-1^WT-expressing embryos, we found that BUB-1^{K718R ;D847N} mutant-expressing embryos displayed up to 21% embryonic lethality when raised at 24°C. Embryos depleted of the SAC protein MDF-1^Mad1 did not show the same temperature-dependent lethality (8%), nor did the BUB-1^D814N mutant (3.4%). The BUB-1^{K718R ;D847N} mutant phenotype is therefore not caused by a defective SAC or a lack of BUB-1 kinase activity, but rather by the enhanced microtubule growth at high temperature (Figure 6C). In other words, when load-bearing connections are favoured by high microtubule dynamics, limiting SKA-mediated attachment maturation becomes essential. Together, our data suggest that BUB-1 displays opposing activities at the kinetochore to promote properly bioriented kinetochore-microtubule attachments and to prevent embryonic lethality.

Discussion

The conserved kinase BUB1 is a SAC protein that is also involved in kinetochore-microtubule attachments and proper chromosome segregation in diverse species. However, the molecular mechanisms of this non-SAC role for BUB1 remain elusive. Here, we identify two previously uncharacterized functions of the C. elegans BUB-1 kinase in (1) accelerating end-on kinetochore-microtubule attachments by recruiting the dynein-dynactin complex to kinetochores, and (2) limiting attachment maturation by the SKA complex (Figure 6E). We show this latter activity relies on the BUB-1 kinase domain but is independent of kinase activity. Previously, C. elegans BUB-1 was shown to target the two redundant CENP-F orthologs HCP-1/2^CENP-F to kinetochores, which in turn recruit the CLASP protein CLS-2^CLASP (Cheeseman et al., 2005; Encalada et al., 2005). CLASP at kinetochores promotes microtubule assembly and increases microtubule dynamics, favouring amphitelic attachments (Maffini et al., 2009; Maiato et al., 2003a; Maiato et al., 2005). Therefore, our results show that BUB-1 both promotes amphitely through the RZZ-dynein-dynactin complex and CLS-2^CLASP, while limiting maturation of chromosome biorientation by the SKA complex. Our data also suggest that the coordination of these different activities by BUB-1 is required to avoid merotely and embryonic lethality. These results therefore define a central role for BUB-1 in promoting accurate chromosome biorientation essential to maintain genetic integrity during cell division.

BUB-1-mediated kinetochore recruitment of RZZ and dynein-dynactin

BUB1 contributes to RZZ recruitment in human cells (Caldas et al., 2015; Zhang et al., 2015), however previously this function has not been linked to the role of BUB1 in chromosome alignment and segregation. Here, we show that in C. elegans, BUB-1 also contributes to kinetochore recruitment of the RZZ complex and that this is essential to avoid merotely. In human cells, some RZZ remains at kinetochores following BUB1 depletion, which suggests an additional kinetochore-binding site must exist. The kinetochore protein Zwint, which interacts with the KNL1 C-terminal half, was originally proposed to be the primary kinetochore-docking partner of RZZ in human cells (Kops et al., 2005; Petrovic et al., 2010; Starr et al., 2000; Wang et al., 2004). However, some RZZ remains at kinetochores in human cells even in absence of KNL1 (and thus also in absence of kinetochore-localized Zwint) and BUB1. Consistently, the distant Zwint ortholog KBP-5 is dispensable for RZZ kinetochore recruitment in C. elegans (Varma et al., 2013). A Zwint-, KNL1- and BUB1-independent pathway has therefore been hypothesized to participate in RZZ localization at human kinetochores (Caldas et al., 2015; Silió et al., 2015; Zhang et al., 2015). Although the molecular details of this alternative contact site between RZZ and the kinetochore are still unclear, our results are consistent with this hypothesis, as BUB-1 depletion does not fully abrogate kinetochore RZZ localization (Figure 4B, Figure 4—figure supplement 1A,B).

In contrast, we found that BUB-1 is absolutely required for dynein-dynactin recruitment to kinetochores. One potential explanation for the apparent discrepancy between this complete lack of dynein-dynactin at kinetochores despite partial recruitment of the RZZ complex may stem from BUB-1 downstream partners HCP-1/2^CENP-F, which recruit NUD-2^NudE/el to stabilise dynein-dynactin at kinetochores (Simões et al., 2018). BUB-1 would therefore both recruit dynein-dynactin via the RZZ complex, and stabilise it at kinetochores via HCP-1/2^CENP-F and NUD-2^NudE/el.

Our functional analysis comparing BUB-1-depleted embryos in the presence or absence of the BUB-1^ΔKD mutant, which recruits DNC-2^p50 normally to kinetochores (Figure 4—figure supplement 1F), shows that both BUB-1-mediated RZZ and dynein-dynactin recruitments contribute to accelerating the establishment of end-on attachments and to the prevention of merotely (Figure 4—figure supplement 1G). RZZ and dynein-dynactin therefore constitute a kinetochore module, recruited downstream of BUB-1, that contributes to rapidly and accurately establishing biorientation in early mitosis.

BUB-1 control of microtubule dynamics and attachment maturation

In C. elegans zygotes, BUB-1 targets HCP-1/2^CENP-F to kinetochores, which in turn recruits CLS-2^CLASP (Cheeseman et al., 2005; Encalada et al., 2005). Kinetochore-localized CLS-2^CLASP is thought to promote microtubule polymerization essential for proper chromosome biorientation. Our work stresses the importance of BUB-1 in antagonizing CLS-2^CLASP-dependent kinetochore microtubule assembly by limiting their attachment to kinetochores. We indeed found that upon HCP-1/2^CENP-F or CLS-2^CLASP depletion, chromosomes become bioriented only when kinetochore-localized BUB-1 is absent. Our results further suggest that BUB-1 limits kinetochore-microtubule attachment maturation by preventing SKA complex kinetochore recruitment.

How BUB-1 limits the maturation of kinetochore microtubule attachments by the SKA complex remains unclear. We envision several non-exclusive possibilities. First, BUB-1 could inhibit SKA complex kinetochore recruitment through a direct physical interaction, although we currently do not have evidence for this premise. Second, BUB-1 could indirectly regulate the interaction between the SKA complex and its kinetochore docking partner NDC-80, by recruiting Aurora A at the kinetochore. Indeed, although Aurora B-dependent phosphorylation of the NDC-80 tail prevents enrichment of the SKA complex at kinetochores in C. elegans (Cheerambathur et al., 2017), we rule out here a role for Aurora B as a mediator of BUB-1 inhibition of biorientation (Figure 5—figure supplement 1). In contrast, in human cells, BUB1 was recently shown to recruit Aurora A at the centromere (Eot-Houllier et al., 2018), where it phosphorylates the NDC80 tail (DeLuca et al., 2018). Whether BUB-1-dependent recruitment of Aurora A also restricts SKA complex kinetochore localization remains to be investigated. Finally, BUB-1 could directly or indirectly decrease tension at kinetochores. In C. elegans, kinetochore tension has been proposed to promote SKA complex recruitment (Cheerambathur et al., 2017). We showed that monopolar spindles, in which kinetochore tension is likely low, are compatible with normal level of SKA complex at kinetochores. However, mono-oriented chromosomes, as visible in absence of HCP-1/2^CENP-F or CLS-2^CLASP, could potentially display even lower kinetochore tension, which would abrogate SKA complex kinetochore localization. By increasing tension at kinetochores through an unknown mechanism, BUB-1 could restore SKA complex kinetochore enrichment and chromosome biorientation.

Regardless of the exact mechanism by which BUB-1 regulates the SKA complex, we surprisingly did not observe hyper-recruitment of SKA-1 to kinetochores in the absence of BUB-1 (Figure 5—figure supplement 2A,B), nor in the presence of BUB-1 mutants that do not inhibit chromosome biorientation in absence of HCP-1/2^CENP-F (Figure 5—figure supplement 2F). However, upon depletion of HCP-1/2^CENP-F (proteins dependent upon BUB-1 for kinetochore localisation, Figure 1E), when SKA complex kinetochore recruitment is inhibited, BUB-1 is hyper-recruited to kinetochores (Figure 5—figure supplement 2H,I). Although the reason for this hyper-recruitment is unclear, it suggests that a threshold level of BUB-1 could be required to prevent SKA complex localization at kinetochores. In this context, depleting HCP-1/2^CENP-F or CLS-2^CLASP would therefore amplify the BUB-1-mediated inhibition of SKA complex kinetochore localization, which in the C. elegans embryo is otherwise not apparent and probably extremely transient during prometaphase when biorientation is established. Nevertheless, the embryonic lethality observed in the BUB-1^K718R,D847N mutant incapable of restricting biorientation (but which recruits HCP-1/2^CENP-F and CLS-2^CLASP at kinetochores) at high temperature (21% at 24°C) demonstrates the essential and physiological role of this pathway (Figure 6A–C).

Temporal coordination of antagonistic activities at the kinetochore

Our study provides mechanistic insights into the non-SAC role for BUB-1 in chromosome segregation, suggesting it is a key regulator of the kinetochore-microtubule interface that facilitates amphitelic kinetochore-microtubule attachments and shields chromosomes from merotely. Based on these multiple BUB-1 functions and on the dynamic kinetochore localization of downstream components, we propose a temporal and functional framework for chromosome biorientation (Figure 6D,E). In this model, BUB-1 dependent recruitment of the RZZ complex and of dynein-dynactin favours initial end-on kinetochore-microtubule attachments in bioriented conformations. BUB-1 then controls the stability of these attachments through two opposing activities. First, BUB-1 favours NDC-80-mediated load-bearing attachments via recruitment of HCP-1/2^CENP-F and CLS-2^CLASP, which promote kinetochore microtubule assembly. Second BUB-1 limits attachment maturation by preventing SKA complex kinetochore targeting. Together these activities help establishing amphitelic attachments and preventing errors in chromosome segregation. BUB-1 then progressively leaves from kinetochores in metaphase (Figure 6D; Figure 5—figure supplement 2H,I), allowing SKA complex accumulation and kinetochore microtubule attachment maturation. The high frequency of embryonic lethality observed in C. elegans zygotes in the presence of BUB-1 mutants that uncouple these two functions (BUB-1^ΔKD or BUB-1^{K718R ;D847N}), stresses the importance of coordinating temporally kinetochore microtubule initial attachments and their maturation.

In conclusion, using the C. elegans model, we reveal a non-SAC role for BUB-1 in limiting SKA-mediated attachment maturation, when HCP-1/2^CENP-F or CLS-2^CLASP is deficient. We suspect that this is a conserved and general role of BUB1. Indeed, we found that BUB-1-mediated inhibition of chromosome biorientation is linked to its kinase domain, but not to the kinase activity. This is also the case for the yet unidentified BUB1-dependent activity that prevents lethality of SAC-deficient haploid HAP1 human cells (Raaijmakers et al., 2018). In future work, it will be important to determine whether there is a functional link between BUB-1-mediated regulation of the SKA complex -that we identified here- and the role for BUB-1 in preventing lethality of SAC-deficient haploid human cells. The conservation of all the key molecular players suggests this non-SAC role for BUB-1 in regulating kinetochore-microtubule attachments could be a general and conserved function of BUB1 in metazoans.

Materials and methods

C. elegans strain maintenance

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Supplementary file 1A lists the strains used throughout this study. Strains were maintained on nematode growth medium plates seeded with OP50 bacteria. They were incubated at 23°C, with the exception of the air-2(or207ts) mutant that was maintained at the permissive temperature of 16°C. Most strains were generated by crossing previously existing C. elegans lines. The transgenes generated for the purpose of this study were engineered using CRISPR-Cas9 for the Δhcp-1 and Δhcp-2 strains (see below) and the GFP-tagged endogenous HCP-1 and HCP-2 strains (purchased from SunyBiotech), and using MosSCI for the BUB-1^ΔKD mutant (Katic et al., 2015).

RNA-mediated interference

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Supplementary file 1B lists the dsRNAs used in this study, which were synthesized using the indicated primers and templates. After DNA amplification by PCR, reactions were cleaned (PCR purification kit, Qiagen), and used as templates for T3 and T7 transcription reactions (MEGAscript, Invitrogen) for 5 hr at 37°C. These reactions were cleaned (MEGAclear, Invitrogen), then combined for annealing at 68°C for 10 min and 37°C for 30 min. L4 larvae were injected at the indicated concentrations in the pseudo-coelum, and incubated for 48 hr at 20°C, or 16°C for the air-2(or207ts) mutant.

CRISPR-Cas9 mutant generation

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The mutations in the hcp-1 and hcp-2 loci were generated by using a CRISPR-Cas9 approach previously described (Katic et al., 2015). This strategy aims at generating a deletion between two double-strand breaks surrounding the start codon, and at inserting a screening cassette by Non-Homologous End-Joining. sgRNAs were designed using the http://crispr.mit.edu/ design tool, and cloned in the pIK198 vector under the control of the C. elegans U6 promoter (Injected at 50 ng/μL). Supplementary file 1C lists the sgRNA targets, and their positions relative to the hcp-1 and hcp-2 loci. The cas-9 protease was provided as a cDNA under the eft-3 promoter in the pDD122 vector (50 ng/μL). To help screening for mutations, unc-119(ed3) mutant worms were injected, and the injection mix provided a vector containing an unc-119 rescue cassette (50 ng/μL). In order to linearize this vector, the sequence and PAM targeted by the sgRNA downstream of the ATG were inserted in the vector. In addition, fluorescence markers encoded in vectors pCFJ90 (Pmyo-2::mCherry, 2.5 ng/μL), pCFJ104 (Pmyo-3::mCherry, 5 ng/μL) and pGH8 (Prab-3::mCherry, 5 ng/μL), were also injected. Worms were injected on day 0, cloned, and left to starve. Plates with moving worms were selected and chunked at day 14. Worms expressing the fluorescent co-injection markers were negatively selected on day 15 as worms containing extra-chromosomal arrays. Remaining worms were then cloned, and their progeny was screened by PCR.

Western blotting

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HCP-1 and HCP-2 expression in the Δhcp-1 and Δhcp-2 strains was assessed by immunoblotting. For each well, 50 worms were washed in M9 (22 mM KH₂PO₄, 42 mM Na₂HPO₄, 86 mM NaCl, and 1 mM MgSO₄•7H₂O) supplemented with 0.1% Triton X-100. Worms were then resuspended in 20 μL sample buffer (40% glycerol, 240 mM Tris-HCl, pH 6.8, 8% SDS, 0.04% bromophenol blue, and 5% β-mercaptoethanol) before being boiled for 15 min at 95°C, vortexed for 15 min, and boiled again for 15 min at 95°C. Extracts were then loaded on a NuPAGE 3–8% TrisAcetate Gel (Invitrogen), transferred to nitro-cellulose, and incubated with 1 μg/mL antibodies targeting either HCP-1 C-Terminal domain, HCP-2 N-Terminal or C-Terminal domains. A mouse anti-α-tubulin antibody (DM1α, Abcam) was used as a loading control.

Live imaging and image analysis

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Worms were dissected to free embryos, which were then mounted and imaged as described in (Laband et al., 2018). Acquisitions were made on a spinning disk confocal microscope (Roper Scientific), using a CFI APO LBDA S × 60/NA1.4 oil objective and a CoolSNAP HQ2 CCD camera (Photometrics Scientific). All movies were acquired with a 2 × 2 binning. Metamorph seven software (Molecular devices) was used for control of acquisition parameters. Unless specified otherwise, all movies were acquired at temperatures varying between 22°C and 24°C. The CherryTemp temperature controller system (CherryBiotech) was used to perform imaging experiments at the specific temperatures of 15°C, 24°C and 26°C. Image analysis was performed using Fiji (Schindelin et al., 2012) and the Python scikit-image library (van der Walt et al., 2014).

Pole to pole distance and chromosome span measurements

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Embryos expressing γ-Tubulin::GFP and KNL-1::mCherry were imaged at 10 s intervals, with 3 z slices spaced 2 μm apart for the fluorescence channels, and a single slice per time point for the DIC frame. Measurements were carried out on maximal z-projections of the fluorescence channels. Pole to pole distance was measured using a Python script to segment poles in the GFP channel, and measure distances between their centroids. Chromosome span was measured manually by tracing the shortest line in the spindle pole axis comprising the totality of the KNL-1::mCherry kinetochore signal. Measurements were then aligned with reference to NEBD detected in the DIC channel.

Fluorescence intensity measurements

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Fluorescently tagged protein quantifications (GFP::HCP-1, GFP::HCP-2, CLS-2::GFP, HCP-3HFD::CPAR-1Ntail::GFP, ZWL-1::GFP, DNC-2::GFP, SKA-1::GFP, and BUB-1::GFP) were generated by imaging embryos at 10 s intervals, with 4 z slices spaced 2 μm apart for the fluorescence channels, and a single slice per time point in DIC. This z sampling doesn’t allow the measurement of the integrated signal throughout the spindle, but ensures the spindle, which moves within the embryo, is always in focus in at least one of the slices. Measurements were therefore carried out on maximal z-projections of the GFP channel. A Python script was used to segment chromosomes in the mCherry channel, and allowed access to the integrated GFP signal on chromosomes over time. For each time-point, the average background signal per pixel was measured in the embryo cytoplasm, multiplied by the number of pixels in the segmented chromosomes, and this integrated background signal was then subtracted from the GFP signal on chromosomes. These values were then normalized at every timepoint by the average background value. Measurements were then aligned in time relative to NEBD detected in the DIC channel. For the HCP-3HFD::CPAR-1Ntail::GFP, the background signal was measured around the chromosomes in order to correct the measured signal for unspecific GFP localized in the nucleus prior to NEBD.

Kinetochore localizations of mCherry tagged BUB-1 mutants, mCherry tagged KNL-1 mutants, and of other proteins in these genetic backgrounds, were quantified at specific timepoints by proceeding to 10-pixel wide linescans in the spindle pole axis, and extracting the average of the signal extending 0.85 μm either side of the average chromosome position. This value was then normalized by the average background measured in the cytoplasm.

Chromosome stretch quantification

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Chromosome stretch quantification was carried out manually on the same movies as used for chromosome span quantification. Measurements were made on the maximal projection of the GFP channel, 20 s after anaphase onset detected as the time at which the chromosome span is seen starting to increase. Measurements were obtained from the average signal of a 3-pixel wide line, traced perpendicular to the spindle axis, between the segregating chromosome masses. This signal was normalized by the average signal obtained from an equivalent line measured between poles and chromosomes.

Immunofluorescence and imaging

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A Nikon CFI PLAN APO LBDA 100x/NA1.45 oil objective and a CoolSNAP HQ2 CCD camera (Photometrics Scientific) were used to aquire images of stained embryos with a z-step of 0.1 or 0.2 μm. Embryos were prepared following the protocol described in (Gigant et al., 2017). Custom-made antibodies against BUB-1, HCP-1, HCP-2 and KNL-1 were coupled to either dylight550 or dylight650 (Thermo Scientific) and were used each at a concentration of 1 µg/mL. An anti-α-tubulin diluted 1:100 (DM1α, Abcam) was used to stain microtubules, and chromosomes were stained with Hoechst at 2 µg/mL. Images were deconvolved using the Huygens software (Scientific Volume Imaging). Maximum projections of informative z-plan are presented.

Embryonic lethality assays

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Embryonic lethality was assayed after injecting L4 larvae with dsRNA, leaving them at 20°C during 48 hr for protein depletion, singling them out to lay embryos on plates placed at the specific temperatures of 15°C, 20°C or 24°C during 12 hr, before removing the parent worm and leaving the progeny to develop for 24 hr. Embryonic lethality was then scored as the percentage of dead embryos found within the progeny.

Graphs and statistical analysis

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GraphPad Prism 6 (GraphPad Software) was used to generate graphs and proceed to statistical analysis. The tests used are mentioned in the figure legends.

Data availability

All data generated or analysed during this study are included in the manuscript and supporting files.

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Decision letter

Jon Pines

Reviewing Editor; Institute of Cancer Research Research, United Kingdom
Anna Akhmanova

Senior Editor; Utrecht University, Netherlands

In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.

Thank you for submitting your article "BUB-1 promotes chromosome biorientation by coordinating antagonistic activities at the kinetochore" for consideration by eLife. Your article has been reviewed by four peer reviewers, including Jon Pines as the Reviewing Editor and Reviewer #1, and the evaluation has been overseen by a Reviewing Editor and Anna Akhmanova as the Senior Editor. The following individuals involved in review of your submission have agreed to reveal their identity: Jakob Nilsson (Reviewer #3).

The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.

Summary:

In this study the authors have investigated the role of BUB1 in chromosome segregation using the C. Elegant system. The find that BUB1 has opposing roles in microtubule attachment through interacting with the CENP-F/CLASP proteins and the RZZ/dynein-dynactin pathway. They provide evidence that BUB1 acts to co-ordinate these pathways by promoting microtubule attachment to kinetochores but preventing maturation of attachments by the SKA complex.

This is a careful study in which the authors have exploited the RNAi, imaging and genetic strengths of the C. elegans system to the full. The authors have tested a number of hypotheses to explain the function of BUB1 and present convincing evidence that the BUB1 does interact with two pathways influencing kinetochore-microtubule attachments (CENP-F/CLASP and RZZ/Dunedin/dynactin/SKA).

Essential revisions:

1) The study is very complicated for non-geneticists and very hard to follow. To make this study accessible to a large audience, the authors will need to re-write it and present the models/hypothesis on which their experiments are built up in a much clearer manner. For example: is it really appropriate to call BUB-1's functions "antagonistic" with regards to chromosome biorientation? Similarly, what is the basis for the statement that the BUB-1^ΔKD deletion mutant "is capable of limiting attachment maturation"? The BUB-1^ΔKD deletion is shown to suppresses sister chromatid co-segregation in the absence of HCP-1/2, so wouldn't this mutant therefore be predicted to be INCAPABLE of limiting attachment maturation, similar to the BUB-1^{K718R; D847N} mutant or BUB-1 depletion? The BUB-1^ΔKD deletion is informative for the analysis in Figure 6 because it delocalizes CLS-2 from kinetochores without causing the severe sister co-segregation phenotype associated with CLS-2 depletion. Is that what the authors mean?

2) The authors use only a few embryos (sometimes less than 10), and they re-use the same dataset several times. (For example: the four conditions used in Figure 1F are exactly the same cells used in Figure 4E, and 3 conditions are used again in Figure 5E.) The authors should state the number of independent experiments indicated and explain how they made sure that results are not due to day to day variability (due e.g. to small variations in temperature). When analyzing double mutants, the authors should analyse at least 3 single mutant embryos to make sure that the phenotype is robust. The authors should also point out when the data shown in different figures is the same dataset.

3) The authors should directly demonstrate one of the central assumptions of the study – that depletion of Bub1 leads to a large number of merotelic attachments – by staining for merotelic attachments. The images shown in Figure 1E do not allow one to distinguish between merotely and other type of segregation errors. The kymographs of kinetochores and centrosome markers may be an over-simplification as different errors of attachment could give similar kymographs.

4) Another central conclusion is that the presence of BUB1 at kinetochores antagonizes the binding of the SKA complex to kinetochores. However, only at the very end of the discussion do the authors point out that this role appears only in mutants lacking CLASP or CENP-F. Under physiological conditions, the presence or absence of BUB1 does not seem to influence SKA1 localization. In fact, the authors think that BUB1 only affects SKA1 because it is present at non-physiological levels in embryos lacking CLASP or CENP-F. It is therefore difficult to conclude that the physiological role of Bub1 is to antagonize the SKA complex. Under physiological conditions, this appears not to be the case, which strongly reduces the significance of their conclusions.

5) The authors should discuss the discrepancy between their conclusion in this study that BUB1 is required for the recruitment of the RZZ complex and the conclusions of Essex et al., 2009, that the RZZ complex is recruited to kinetochores independently of Bub1, and their own paper (Maton et al., 2015) that considers BUB1 and RZZ as part of separate branches.

6) The authors should address the apparent discrepancy that they assume that all the functions of CLASP and HCP1/2 originate from their role at kinetochores via BUB1, but in BUB-1 RNAi + BUB1^ΔKD embryos, HCP1/2/CENP-F are not present at kinetochores and chromosome segregation is normal (Figure 3—figure supplement 1). Nevertheless, when HCP1/2 are depleted, merotelic chromosomes appear. This would suggest that HCP1/2 do not require to be brought to kinetochores by BUB1 to prevent merotelic attachments.

https://doi.org/10.7554/eLife.40690.056

Author response

Summary:

In this study the authors have investigated the role of BUB1 in chromosome segregation using the C. Elegant system. The find that BUB1 has opposing roles in microtubule attachment through interacting with the CENP-F/CLASP proteins and the RZZ/dynein-dynactin pathway. They provide evidence that BUB1 acts to co-ordinate these pathways by promoting microtubule attachment to kinetochores but preventing maturation of attachments by the SKA complex.

This is a careful study in which the authors have exploited the RNAi, imaging and genetic strengths of the C. elegans system to the full. The authors have tested a number of hypotheses to explain the function of BUB1 and present convincing evidence that the BUB1 does interact with two pathways influencing kinetochore-microtubule attachments (CENP-F/CLASP and RZZ/Dunedin/dynactin/SKA).

We are pleased the reviewers and editors were enthusiastic about our paper. We have performed additional experiments and made substantial changes to the text and figures to address all suggested revisions.

Essential revisions:

1) The study is very complicated for non-geneticists and very hard to follow. To make this study accessible to a large audience, the authors will need to re-write it and present the models/hypothesis on which their experiments are built up in a much clearer manner. For example: is it really appropriate to call BUB-1's functions "antagonistic" with regards to chromosome biorientation?

We apologize for not being clearer in our original manuscript. Our revised manuscript has been drastically edited and re-written to enhance clarity of our main message. We have also removed some results (HIM-10 experiment on original Figure 4 and BUB-1 full depletion in the Δska-1 strain on original Figure 5), which were not essential for understanding the main message of our study and were introducing unnecessary complexity. We hope this will help the large audience of eLife, including non-geneticists, to follow our study.

We also agree that the use of the term ‘antagonistic’ to describe the various functions of BUB-1 was not appropriate. This term was in fact referring to the opposing effects of BUB-1 on chromosome biorientation: (1) HCP-1/2^CENP-F and CLS2^CLASP-mediated promotion of biorientation and (2) prevention of biorientation through inhibition of SKA complex kinetochore recruitment. As this was potentially misleading, we edited our manuscript to better reflect BUB-1 key role in chromosome biorientation and segregation. We have for example edited the title of our manuscript to: “BUB-1 promotes amphitelic chromosome biorientation via multiple activities at the kinetochore”.

Similarly, what is the basis for the statement that the BUB-1^ΔKD deletion mutant "is capable of limiting attachment maturation"? The BUB-1^ΔKD deletion is shown to suppresses sister chromatid co-segregation in the absence of HCP-1/2, so wouldn't this mutant therefore be predicted to be INCAPABLE of limiting attachment maturation, similar to the BUB-1^{K718R; D84} mutant or BUB-1 depletion?

We thank the reviewers and editors for pointing this mistake to our attention and we apologize for this writing error. It should of course have been “is incapable of limiting attachment maturation”. This mistake has been edited in the revised version of our manuscript.

The BUB-1^ΔKD deletion is informative for the analysis in Figure 6 because it delocalizes CLS-2 from kinetochores without causing the severe sister co-segregation phenotype associated with CLS-2 depletion. Is that what the authors mean?

The reviewers and editors are absolutely right. This is exactly what we mean and the reason why we used this mutant in Figure 6. We have made this clearer in our revised manuscript.

2) The authors use only a few embryos (sometimes less than 10), and they re-use the same dataset several times. (For example: the four conditions used in Figure 1F are exactly the same cells used in Figure 4E, and 3 conditions are used again in Figure 5E.) The authors should state the number of independent experiments indicated and explain how they made sure that results are not due to day to day variability (due e.g. to small variations in temperature). When analyzing double mutants, the authors should analyse at least 3 single mutant embryos to make sure that the phenotype is robust. The authors should also point out when the data shown in different figures is the same dataset.

The high reproducibility of events in the C. elegans zygote does not require a particularly high number of individual embryos to be analyzed. However, for each experiment presented in this study, the sample size is equal or higher to sample size observed in most published studies on C. elegans. Since worms are treated (RNAi, Filming, staining, etc.) individually, each embryo could in theory be considered as an individual biological replicate. The same datasets are presented on several panels (Figure 1F and Figure 4E, Figure 3D and Figure 5E) for clarity only, and used as reference points for analyzing new data. We could in theory remove the already presented conditions from these panels, but this would complicate analysis of new data, as it would require the reader to scan through different figures. For clarity and transparency, we have now included Supplementary file 4, which displays images and datasets presented in different figures and panels. Importantly, kymographs were generated from different representative embryos when the same condition is presented in different panels. Furthermore, the same embryo was only and purposely used in cases when, for a same condition, one panel represents a single timepoint, and another panel represents a temporal series.

3) The authors should directly demonstrate one of the central assumptions of the study – that depletion of Bub1 leads to a large number of merotelic attachments – by staining for merotelic attachments. The images shown in Figure 1E do not allow one to distinguish between merotely and other type of segregation errors. The kymographs of kinetochores and centrosome markers may be an over-simplification as different errors of attachment could give similar kymographs.

Kinetochores are holocentric in the C. elegans nematode and form along the entire length of sister chromatids. Microtubules therefore attach all along the length of these extended kinetochores and do not form kinetochore fibers, as typically observed in monocentric species. For this reason, cold-treatments that specifically lead to spindle but not kinetochore microtubule depolymerization, and which are commonly used to analyze the type of attachment in monocentric cells, are inefficient in C. elegans. Instead, we have now performed immunofluorescence staining of spindle microtubules and kinetochores to clarify the attachment status in various conditions, including in BUB-1-depleted C. elegans zygotes. Importantly, these results allowed the detection of bent kinetochores during metaphase in absence of BUB-1, unambiguously demonstrating the presence of a majority of merotelic attachments in this condition. These new results have been included in a revised Figure 1 (panel F).

4) Another central conclusion is that the presence of BUB1 at kinetochores antagonizes the binding of the SKA complex to kinetochores. However, only at the very end of the discussion do the authors point out that this role appears only in mutants lacking CLASP or CENP-F. Under physiological conditions, the presence or absence of BUB-1 does not seem to influence SKA1 localization. In fact, the authors think that BUB-1 only affects SKA1 because it is present at non-physiological levels in embryos lacking CLASP or CENP-F. It is therefore difficult to conclude that the physiological role of BUB-1 is to antagonize the SKA complex. Under physiological conditions, this appears not to be the case, which strongly reduces the significance of their conclusions.

We respectfully disagree with that assertion. We instead argue that HCP-1/2^CENP-F or CLS-2^CLASP depletions allow to ‘amplify’ and thus to highlight a physiological process that is otherwise less apparent and probably extremely transient at the beginning of mitosis. The embryonic lethality associated with a high degree of merotely observed in the BUB-1 mutants incapable of restricting biorientation further demonstrates the essential and physiological role of this pathway (Figure 6A-C). In the same way that outer kinetochore expansion (which physiologically occurs transiently during prometaphase in tissue cultured cells, when kinetochores are not yet attached to microtubules) is primarily observed and studied in response to drug-mediated depolymerization of microtubules, this novel physiological function of BUB-1 is highlighted in conditions that decrease kinetochore microtubule dynamics. We have now added this notion to our revised discussion for clarity.

5) The authors should discuss the discrepancy between their conclusion in this study that BUB1 is required for the recruitment of the RZZ complex and the conclusions of Essex et al., 2009, that the RZZ complex is recruited to kinetochores independently of BUB1, and their own paper (Maton et al., 2015) that considers BUB1 and RZZ as part of separate branches.

Our results are consistent with the role for BUB1 in recruiting the RZZ complex to kinetochores in human cells (Caldas et al., 2015; Zhang et al., 2015). They are based on a careful quantification of ZWL-1^Zwilch::GFP at kinetochores over time in presence or absence of BUB-1 (Figure 4B and Figure 4—figure supplement 1A,B). In contrast, the conclusion from Essex et al., 2009 was drawn from immunofluorescent staining in two-cell stage embryos with activated SAC through monopolar spindles (Figure 4G) and this staining was not specifically quantified. Furthermore, a significant reduction and premature disappearance of kinetochore-localized GFP::CZW-1^ZW10 (another member of the RZZ complex) was in fact visible in absence of BUB-1 at kinetochores in our previous work on the central spindle (Supplementary Figure 3C, Maton et al., 2015). At the time, we did not focus on this phenotype associated with the KNL-1 Δ85-505 mutant, as the effect of this mutant on HCP-1/2^CENP-F and CLS-2^CLASP kinetochore localizations was a lot more potent. However, in light of our new results presented in the current manuscript, these previous data are fully consistent with a role for kinetochore-localized BUB-1 in the recruitment of the RZZ complex. We have thus edited our revised manuscript to cite this previous work where appropriate.

6) The authors should address the apparent discrepancy that they assume that all the functions of CLASP and HCP1/2 originate from their role at kinetochores via BUB1, but in BUB-1 RNAi + BUB1^ΔKD embryos, HCP1/2/CENP-F are not present at kinetochores and chromosome segregation is normal (Figure 3—figure supplement 1). Nevertheless, when HCP1/2 are depleted, merotelic chromosomes appear. This would suggest that HCP1/2 do not require to be brought to kinetochores by BUB1 to prevent merotelic attachments.

We thank the reviewers and editors for bringing this concern to our attention and we apologize for being unclear about this in the original version of our manuscript. We in fact do not assume that all functions of CLASP and HCP-1/2 are at the kinetochore, and we even have evidence (as suggested by the Reviewers and Editors: the higher rate of merotely in absence of HCP-1/2 in the BUB1^ΔKD mutant) against this premise. Our results are consistent with the idea that CLASP and HCP-1/2 have roles both at and outside the kinetochore. As our current study does not focus precisely on the function of CLASP and HCP-1/2, we did not elaborate on that specific point, but we have tried to clarify this in the revised version of our manuscript.

https://doi.org/10.7554/eLife.40690.057

Article and author information

Author details

Frances Edwards

Institut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, Paris, France

Contribution
Conceptualization, Formal analysis, Investigation, Writing—original draft, Writing—review and editing

Competing interests
No competing interests declared
Gilliane Maton

Institut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, Paris, France

Contribution
Conceptualization

Competing interests
No competing interests declared
Nelly Gareil

Institut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, Paris, France

Contribution
Resources, Methodology

Competing interests
No competing interests declared
Julie C Canman

Department of Pathology and Cell Biology, Columbia University, New York, United States

Contribution
Conceptualization

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0001-8135-2072
Julien Dumont

Institut Jacques Monod, CNRS, UMR 7592, University Paris Diderot, Sorbonne Paris Cité, Paris, France

Contribution
Conceptualization, Funding acquisition, Writing—original draft, Writing—review and editing

For correspondence
julien.dumont@ijm.fr

Competing interests
No competing interests declared

"This ORCID iD identifies the author of this article:" 0000-0001-5312-9770

Funding

Fondation ARC pour la Recherche sur le Cancer (Doctorant en 4e année de thèse)

Frances Edwards

Ministère de l'Enseignement supérieur, de la Recherche et de l'Innovation

Frances Edwards

National Institutes of Health (R01GM117407)

Julie C Canman

Fondation pour la Recherche Médicale (DEQ20160334869)

Julien Dumont

Mairie de Paris (Emergence)

Julien Dumont

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Acknowledgements

We thank all members of the Pintard and Dumont labs for support and advice. We thank Déborah Bourc’his for critical reading and editing of the manuscript. We are grateful to Patricia Moussounda, Soilihi Madi Ali and Christie Ouaddi for providing technical support. We thank Arshad Desai, Reto Gassmann and Dhanya Cheerambathur for worm strains. Some strains were provided by the CGC, which is funded by NIH Office of Research Infrastructure Programs (P40 OD010440). FE was supported by a PhD fellowship from the French Ministry of Research and from the Association pour la Recherche sur le Cancer (ARC). This work was supported by CNRS and University Paris Diderot, by grant NIH-R01GM117407 to JCC, and by grants from the Mairie de Paris (Emergence) and the Fondation pour la Recherche Médicale (FRM DEQ20160334869) to JD.

Senior Editor

Anna Akhmanova, Utrecht University, Netherlands

Reviewing Editor

Jon Pines, Institute of Cancer Research Research, United Kingdom

Version history

Received: August 1, 2018
Accepted: December 13, 2018
Accepted Manuscript published: December 14, 2018 (version 1)
Version of Record published: December 21, 2018 (version 2)
Version of Record updated: March 8, 2019 (version 3)

Copyright

This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.