Phosphorylation controls spatial and temporal activities of motor‐PRC1 complexes to complete mitosis

Abstract During mitosis, spindle architecture alters as chromosomes segregate into daughter cells. The microtubule crosslinker protein regulator of cytokinesis 1 (PRC1) is essential for spindle stability, chromosome segregation and completion of cytokinesis, but how it recruits motors to the central spindle to coordinate the segregation of chromosomes is unknown. Here, we combine structural and cell biology approaches to show that the human CENP‐E motor, which is essential for chromosome capture and alignment by microtubules, binds to PRC1 through a conserved hydrophobic motif. This binding mechanism is also used by Kinesin‐4 Kif4A:PRC1. Using in vitro reconstitution, we demonstrate that CENP‐E slides antiparallel PRC1‐crosslinked microtubules. We find that the regulation of CENP‐E ‐PRC1 interaction is spatially and temporally coupled with relocalization to overlapping microtubules in anaphase. Finally, we demonstrate that the PRC1–microtubule motor interaction is essential in anaphase to control chromosome partitioning, retain central spindle integrity and ensure cytokinesis. Taken together our findings reveal the molecular basis for the cell cycle regulation of motor‐PRC1 complexes to couple chromosome segregation and cytokinesis.


Introduction
In cell division, the spindle has a crucial role in ensuring chromosomes are correctly partitioned into daughter cells.Antiparallel microtubules are essential for bipolar spindle stability during mitosis.In anaphase, sister chromatids are pulled to opposite poles.During that stage, re-modelling and elongation of the spindle reduces the risk of DNA damage to lagging chromosomes and aneuploidy, by moving chromosomes away from the cleavage plane.They are physically separated by the central spindle, or midzone, which is a stable structure of antiparallel microtubules that specifies the plane of division.
At the start of mitosis, CENP-E localizes to unattached kinetochores, where it associates with BubR1 and the outer corona (a fibrous expanded structure) of chromosomes (Yen et al, 1991;Cooke et al, 1997;Ciossani et al, 2018;Legal et al, 2020).Kinetochore-bound CENP-E enables kinetochore capture and lateral attachment to microtubules.CENP-E moves chromosomes along the spindle to the metaphase plate before kinetochore biorientation (Fig 1A, reviewed in Craske et al, 2022).The CENP-E motor relocalizes from kinetochores to the central spindle, at the metaphase to anaphase transition (Yao et al, 1997;Kurasawa et al, 2004).This relocalization is dependent on PRC1 (protein regulator of cytokinesis: 1) a non-motor microtubule-binding protein essential for central spindle assembly.CENP-E has a substantial role in chromosome alignment in early mitosis, but its PRC1-dependent recruitment from kinetochores to the central spindle, during the metaphase-toanaphase transition, is less well understood.Depletion or inhibition of CENP-E results in accumulation of misattached polar chromosomes, and spindle checkpoint arrest in metaphase, making studies on CENP-E function in anaphase challenging (Schaar et al, 1997;Chan et al, 1998Chan et al, , 1999;;Qian et al, 2010).Small molecule inhibition of CENP-E in anaphase and telophase results in spreading and delocalization of PRC1 on the central spindle.This observation led to a proposed role for CENP-E in organizing overlapping microtubules and the central spindle (Liu et al, 2020).
PRC1 is a dimeric, non-motor, microtubule-binding protein present on bundled spindle microtubules (Jiang et al, 1998;Kajtez et al, 2016).It then is enriched on the central spindle in anaphase and the midbody in telophase and is essential for the organization of the central spindle (Jiang et al, 1998;Mollinari et al, 2002;Verbrugghe & White, 2004).PRC1 preferentially binds to antiparallel overlapping microtubules (Bieling et al, 2010;Subramanian et al, 2010).Antiparallel microtubules compact to form a central spindle, facilitate chromosome separation and specify the division plane.The timing of PRC1 recruitment coincides with the rapid dephosphorylation of the proteome during the metaphase-to-anaphase transition and is controlled by mitotic phosphorylation and dephosphorylation (Mollinari et al, 2002;Hu et al, 2012).Several motors-the Kinesin-4 Kif4A, Kif14A, MKLP1/ Kif23 and CENP-E-are recruited to overlapping microtubules in a PRC1-dependent manner in anaphase, and interact with PRC1 in cell extracts (Kurasawa et al, 2004;Gruneberg et al, 2006;Glotzer, 2009;Douglas & Mishima, 2010;Hornick et al, 2010).
Association of PRC1 with motor proteins controls the organization and the length of microtubule overlaps in the central spindle (Kurasawa et al, 2004;Zhu & Jiang, 2005;Gruneberg et al, 2006;Lee et al, 2015;Poser et al, 2019).Interestingly, Kif4A is bound to chromatin in early mitosis.It relocalizes in anaphase to the PRC1-marked central spindle (Wang & Adler, 1995;Kurasawa et al, 2004).In vitro, PRC1 and Kif4A organize microtubules into bundles that resemble Source data are available online for this figure.

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The EMBO Journal 42: e113647 | 2023 Ó 2023 The Authors overlapping microtubule arrays in the central spindle.Kif4A enables motorized sliding of microtubules past each other in the presence of PRC1 (Bieling et al, 2010;Subramanian et al, 2013;Hannabuss et al, 2019).
In order to understand how PRC1 recruits and interacts with motors to assemble the central spindle and enable the timely completion of mitosis, we combine cell biology and structural approaches to dissect the molecular mechanism of the PRC1-motor interaction, focusing on how CENP-E is recruited to PRC1 in anaphase, for which little is known.We show that human CENP-E interacts directly with PRC1 using a bipartite ΦΦ motif at their C terminus, and this mechanism is also used by Kif4A to bind PRC1.We applied AlphaFold 2 to identify a region of PRC1 that is predicted to bind to CENP-E and validated our predictions using site-directed mutagenesis.We used in vitro reconstitution and TIRF microscopy to show that full-length CENP-E slides PRC1-crosslinked microtubules past each other.We showed that the CENP-E:PRC1 interaction is spatially and temporally regulated by a phosphoswitch, which we propose, enables rapid relocalization of CENP-E from kinetochores to the central spindle during the metaphase-to-anaphase transition.Finally, we reveal a key role of motor-PRC1 interactions in the completion of mitosis.
Our findings provide a framework for understanding how phosphorylation controls the spatial and temporal activities of kinesin motors using CENP-E as a paradigm to enable completion of mitosis.

Results
The C terminus of CENP-E co-localizes with PRC1 throughout mitosis CENP-E localizes to the central spindle and midbody in anaphase and telophase (Kurasawa et al, 2004).Previous work indicated that this process requires the C terminus of CENP-E and is dependent on PRC1 (Fig 1B;Ohashi et al, 2016).We hypothesized that the function of CENP-E in anaphase is independent of its kinetochore function.We have previously mapped the kinetochore-targeting domain (a.a. 2055-2608;Chan et al, 1998;Legal et al, 2020).Thus, we hypothesized the region of CENP-E that targets the central spindle and PRC1 would be the region C-terminal to the kinetochore-targeting domain.
In order to mimic full-length CENP-E which is homodimeric, we dimerized CENP-E 2605-2701 by fusing a GST-tag N-terminal to CENP-E 2605-2701 , as previously reported (Legal et al, 2020).To test whether the C-terminal fragment of CENP-E 2605-2701 localized to overlapping microtubules in the central spindle during anaphase, and to the midbody during telophase when PRC1 is present, we imaged GST-GFP-CENP-E 2605-2701 in mitosis.We found GST-GFP-CENP-E 2605-2701 weakly co-localized with PRC1 to the centre of the metaphase spindle, and more strongly localized to PRC1-crosslinked microtubule bundles on the central spindle and midbody (Fig 1C).This is similar to the localization of full-length CENP-E in anaphase and telophase (Kurasawa et al, 2004).

A conserved CENP-E motif is required for PRC-1 binding
An alignment of full-length CENP-E from nine mammalian species and Xenopus laevis revealed high levels of sequence conservation in the last 100 amino acids of CENP-E, C-terminal to the kinetochoretargeting domain (Fig 1B and D).This C-terminal domain contains the sequence motif RYFDNSSL (amino acids 2659-2666), which was previously reported to be essential for localization of CENP-E to the midbody.The localization of the CENP-E C terminus is also dependent on PRC1 (Ohashi et al, 2016).
We mutated the strongly conserved residues FDN (F2661, D2662, N2663) or YF (Y2660, F2661) to LTT and AA respectively.We then imaged cells in mitosis transiently expressing wild-type or mutant GFP-CENP-E 2605-2701 using live-cell imaging to preserve dynamic interactions.GFP-CENP-E 2605-2701 did not display any dominant negative phenotype, unlike the CENP-E kinetochore-targeting domain (Legal et al, 2020).Microtubules were stained with the SiRtubulin dye, well suited for live-cell imaging.Both GFP-CENP-E 2605-2701 mutants failed to localize to the central spindle (Fig 1E).Interestingly, we also observed a similar, highly conserved (FFD) motif upstream, at positions 2644-2646 (Fig 1D) (Fig 1D).To test the contribution of these two motifs to CENP-E recruitment to the central spindle, we generated a series of mutations in CENP-E that had altered motifs (either one motif, or the other, or both were mutagenized-alone or in tandem, Table 1).Mutation 2644 FF 2645 to AA caused a significant reduction in the localization of CENP-E to the midbody, whereas mutation of 2660 YF 2661 to AA completely abolished CENP-E localization to the midbody (Fig 1E and F).We concluded that the second motif present in CENP-E, 2660 YF 2661 , is essential for midbody localization, and that the upstream 2644 FF 2645 motif strongly contributes to targeting to the midbody.Taken together, our data reveal that the hydrophobic motif, which we describe as ΦΦ motif, is essential for CENP-E recruitment to overlapping microtubules, and to PRC1 in vivo.

CENP-E binds PRC1 in vitro
Next, we tested whether CENP-E and PRC1 interact in vitro.We expressed the C terminus of CENP-E as a monomeric MBP fusion, named MBP-CENP-E 2605-2701 and a PRC1 1-168 fragment, previously reported to bind to Kif4A (Subramanian et al, 2013; Table 1).After mixing them together in an equimolar ratio and carrying out sizeexclusion chromatography and SDS-PAGE analysis, we observed comigration, indicating that these proteins assemble into a complex in solution (Fig 2A).We hypothesized that disruption of the second motif, which is essential for CENP-E recruitment to the central spindle, might abrogate the interaction of CENP-E with PRC1.In order to test this, we purified MBP-CENP-E 2605-2701 FDN and MBP-CENP-E 2605-2701 YF.Size-exclusion chromatography of MBP-CENP-E 2605-2701 FDN mixed with PRC1 1-168 in a 1:1 molar ratio followed by SDS-PAGE analysis revealed that the two proteins no longer interacted (Fig 2B).We observed the same results with size-exclusion chromatography of PRC1 1-168 and MBP-CENP-E 2605-2701 YF (Fig EV1A).This confirms that the region flanking the second ΦΦ motif is essential for PRC1-CENP-E to interact in vitro (Figs 2B and EV1A).

PRC1 binds dimeric the CENP-E C terminus with high affinity
In cell extracts, PRC1 interacts with Kif4A, Kif14, MKLP1 and CENP-E (Kurasawa et al, 2004;Gruneberg et al, 2006).The PRC1-Kif4A interaction has been reconstituted in vitro (Bieling et al, 2010;Subramanian et al, 2013) but the mechanism underlying the interaction of PRC1 with kinesin motors has not been reported.Hence, we sought to delineate the mechanism by which PRC1 binds to CENP-E by quantifying the affinity of CENP-E for PRC1 1-168 (Fig 2A).First, we measured the affinity of the CENP-E peptides containing the two ΦΦ motifs for PRC1 1-168 separately to understand the contributions of these two sites.Isothermal calorimetry (ITC) measurement of CENP-E peptide 1, containing the first ΦΦ motif (PKSC 2644 FF 2645 DSRSK), and peptide 2, containing the second ΦΦ motif (PVR 2660 YF 2661 DNSSLG) affinity for PRC1 1-168 revealed a very weak affinity of each peptide for PRC1 (Figs 2C,and EV1B and C).Next, we determined the affinity of the 98 amino acid C-terminal fragment of CENP-E (CENP-E 2605-2701 ), which contains both ΦΦ motifs in tandem in their native CENP-E sequence (Fig EV1D ) with PRC1 1-168 .We measured an affinity of 19.3 lM (Fig 2C).The C-terminal domain of CENP-E is predicted to be disordered using AlphaFold2 (Jumper et al, 2021), so binding to PRC1 would likely involve a large entropic penalty associated with a reduction in conformational flexibility in the protein upon binding to PRC1.Overall, this interaction is relatively weak.However, CENP-E and PRC1 are both dimers in vivo.So, in order to more closely represent the    in vivo interaction, we purified GST-CENP-E 2605-2701 which is dimeric and measured the affinity of GST-CENP-E 2605-2701 for PRC1 1-168 using ITC (Fig 2C and D).Dimerization led to a 12-fold increase in affinity between GST-CENP-E 2605-2701 for PRC1 1-168 to 1.5 lM, similar to the binding affinity reported for the Kif4A:PRC1 measured using binding assays (Subramanian et al, 2013).Overall, these data indicate multiple ΦΦ motifs increase the affinity of the CENP-E:PRC1 interaction through an avidity effect.
no aspartate follows the ΦΦ motif.We expressed the 32-amino-acid region of Kif4A containing the ΦΦ motif as a GST fusion (GST-Kif4A 1133-1165 ; Table 1).Unlike the C terminus of CENP-E, GST-Kif4A 1133-1165 did not have any affinity for PRC1, as measured by ITC (Fig EV1E).In vivo, GFP-GST-Kif4A 1133-1165 did not localize to overlapping microtubules (Fig 3B).We then searched for a second motif that could increase Kif4A binding to PRC1, similarly to CENP-E.There is a second ΦΦ motif in Kif4A (F1220, F1221) downstream of the published PRC1-binding region (F1154, F1155) (Fig 3A).We hypothesized that this second motif might contribute to the PRC1-Kif4A interaction, and that the ΦΦ motif (F1154, F1155) is essential but not sufficient for PRC1 binding, in common with CENP-E (Fig EV1).To test whether Kif4A and CENP-E bind PRC1 using a similar mechanism, we expressed a dimeric fragment of Kif4A that contains both A Sequence alignment of the C terminus of human Kif4A with Kif4A of other metazoans.Amino acid numbering is relative to the human Kif4A sequence.The two PRC1 putative motifs ΦΦ are highlighted with asterisks (*).Published phosphorylated residues are marked.Those following the CDK and Aurora kinase consensus sites are marked with an orange and blue circle respectively.Green circles represent sites that are phosphorylated but do not fit a kinase consensus site.The sequences were aligned using the program Clustal Omega (EBI) and formatted with ESPRIPT (Gouet et al, 1999).Source data are available online for this figure.
A CENP-E-PRC1 complex slides microtubules CENP-E has been proposed to slide microtubules in mitosis using its non-motor microtubule=binding domain (Steblyanko et al, 2020).It is also possible that CENP-E slides antiparallel microtubules that are crosslinked by PRC1, similar to Kif4A (Bieling et al, 2010;Subramanian et al, 2013).To distinguish between these two models, we carried out an in vitro reconstitution experiment (Fig 4).We previously reconstituted motility of both truncated and full-length CENP-E in vitro (Craske et al, 2022).The challenge in analysing the contribution of CENP-E to microtubule sliding is that about 10% purified full-length CENP-E is motile, with the long coiled-coil stalk interfering with its activity (Craske et al, 2022).In order to determine whether CENP-E slides microtubules alone, or only slides those crosslinked by PRC1, we first analysed whether CENP-E was  Next, we analysed whether full-length human CENP-E could slide microtubules apart in the presence of PRC1 in vitro.We incubated surface-immobilized microtubules with full-length human PRC1 to allow coating of the microtubule lattice with PRC1, then added GMPCPP-stabilized rhodamine microtubules, which led to microtubule bundling (Fig 4E).When 2.5 nM PRC1 alone was added, pairs of overlapping microtubules formed (Fig EV2B).Overlaps remained constant over time, and no sliding of microtubules was observed throughout the experiment lasting 20 min (Fig EV2C).In contrast, we did not observe overlapping microtubule pairs when we added 50 nM full-length CENP-E, ATP and microtubules (Fig EV2B).When we added 50 nM CENP-E and 2.5 nM PRC1, free microtubules were crosslinked and transported unidirectionally along the coverslip-immobilized microtubules (Figs 4F and G, and EV2B, Movie EV1).CENP-E-driven microtubule sliding was slow, with an average velocity of 10.4 AE 2.5 nm/s (Fig 4H).This sliding velocity is comparable to that of Kif4A, around 11 nm/s in the presence of 1 nM PRC1 (Wijeratne & Subramanian, 2018).Slowing down of microtubule sliding over time was observed (Fig 4F and G).
Together, these data suggest that a CENP-E-PRC1 complex is able to slide antiparallel microtubules relative to each other.The sliding velocity may be regulated by frictional forces that are either generated by the accumulation over time of PRC1 on cross-linked microtubules, similar to Kif4A/PRC1 sliding (Wijeratne & Subramanian, 2018), or by the fraction of inactive or paused microtubule-bound CENP-E motors that can still bind to PRC1 (Craske et al, 2022).

Phosphorylation of CENP-E controls its PRC1 microtubule-binding activity
CENP-E is strongly recruited to overlapping antiparallel microtubules, crosslinked by PRC1 in anaphase.Before anaphase, CENP-E is primarily localized to unattached kinetochores in prometaphase and remains localized to kinetochores in smaller amounts in metaphase.We hypothesized that the interaction between PRC1 and CENP-E might be regulated by post-translational modifications to enable rapid temporal and spatial relocalization of CENP-E from kinetochores to PRC1-bound microtubules in the central spindle.Of note, mitotic kinase activity is high in prometaphase, contributed by CDK, Aurora, Mps1 and Plk1 kinases.In particular, CDK activity drops dramatically during the metaphase-to-anaphase transition.Multiple phosphoproteomic studies have previously reported that the C terminus of CENP-E is phosphorylated in mitosis and identified the phosphorylated residues in vivo (Nousiainen et al, 2006;Dephoure et al, 2008;Malik et al, 2009;Kettenbach et al, 2011;Santamaria et al, 2011;Sharma et al, 2014).We noted six of these phosphorylated residues were close to the PRC1-binding motif (Fig 1D).Two serines phosphorylated at positions 2639 and 2654 fit the CDK consensus site (S/T-P) and a serine 2651 phosphorylated by the Aurora kinases close to the FF motifs was reported multiple times (Nousiainen et al, 2006;Kettenbach et al, 2011;Santamaria et al, 2011;Sharma et al, 2014;Fig 1D).S2647, S2649 and S2664 were also reported as phosphosites (Sharma et al, 2014).
In order to test whether phosphorylation of the C terminus of CENP-E affects its interaction with PRC1, we generated phosphomimetic (amino acid substitutions that mimic a phosphorylated version of the amino acid) mutants of GST-CENP-E 2605-2701 .We mutated S2639 and S2654 to generate GST-CENP-E 2605-2701 2SD (mimicking two phosphorylated amino acids), and S2639, S2647, S2649, S2651, S2654 and S2664 for GST-CENP-E 2605-2701 6SD (mimicking six phosphorylated amino acids), and measured their affinity for PRC1 using ITC.There was a small decrease in affinity of GST-CENP-E 2605-2701 2SD for PRC1 1-168 .The Kd increased from 1.5 lM for control versus 2.4 lM for 2SD (Fig 5A).GST-CENP-E 2605-2701 6SD displayed no binding to PRC1 (Fig 5B and C).Further phosphorylation of CENP-E could also contribute to reducing the PRC1: CENP-E interaction in vivo.
Next, we analysed how phosphorylation of the C terminus of CENP-E affected association with PRC1 at overlapping microtubules in cells.We examined the localization of the CENP-E C terminus in metaphase (Fig 5D).GFP-CENP-E 2605-2701 was mostly cytoplasmic, but dimeric GFP-GST-CENP-E 2605-2701 (to mimic full-length CENP-E, which functions as a dimer in vivo and would be representative of CENP-E), and was enriched on interpolar overlapping microtubules, close to the chromosomes.GST-CENP-E 2605-2701 was not observed uniformly on microtubules, indicating it is unlikely to bind microtubules directly (Fig 5D).We observed GFP-GST-CENP-E 2605-2701 2SD localized weakly to interpolar microtubules, but we did not observe association of GFP-CENP-E 2605-2701 2SD and GFP-GST-CENP-E 2605- 2701 6SD with microtubules.We frequently observed GFP-CENP-E 2605-2701 2SA, albeit in small amounts (weak fluorescence) on interpolar microtubules in metaphase.GFP-GST-CENP-E 2605-2701 2SA, which is dimeric, was observed on interpolar microtubules, and GFP-GST-CENP-E 2605-2701 6SA was also enriched there (Fig 5D).
We surmise that phosphorylation of the CENP-E C terminus prevents association with PRC1.Taken together these data reveal that phosphorylation of the C terminus of CENP-E inhibits recruitment to PRC1 at overlapping microtubules in early mitosis, by reducing the affinity of CENP-E for PRC1.The phosphorylation state of CENP-E during mitosis therefore regulates its interactions, both spatially and temporally, to enable CENP-E to associate with the outer corona of kinetochores in early mitosis, where it mediates chromosome 8 of 18 The EMBO Journal 42: e113647 | 2023 Ó 2023 The Authors The EMBO Journal Agata Gluszek-Kustusz et al capture and alignment, and then to associate with PRC1 later in mitosis.

Structural features of CENP-E-PRC1 interactions
We used AlphaFold2 to predict how CENP-E might interact with PRC1, using CENP-E 2605-2701 and PRC1 1-168 dimers as inputs for our analysis (Jumper et al, 2021;Mirdita et al, 2022).AlphaFold2 predicted that CENP-E could interact with the rod and dimerization interface of PRC1 with high confidence, and identified 2660 YFD 2661 in CENP-E as important for that interaction (Fig 6A Overall, these data indicate that kinesin motors bind the dimerization rod domain of PRC1 using their bipartite ΦΦ motifs.

PRC1-motor interactions are essential for cytokinesis
PRC1 has dual-molecular functions: it crosslinks microtubules, and it associates with kinesin motors, such as CENP-E and Kif4A.These functions allow assembly of the central spindle and ensure the final steps of mitosis.In order to distinguish the contribution (s) of PRC1 to central spindle formation, which could occur either by crosslinking microtubules or by recruiting kinesin motors, we engineered cell lines expressing GFP-PRC1-WT or GFP-PRC1-MEE (which does not bind the ΦΦ motif in kinesin motors; Fig 7A).Both cell lines were stable, indicating that these constructs did not have a dominant effect.Both cell lines also expressed constitutively a guide RNA that targets endogenous PRC1, with Cas9 expressed using an inducible promoter, so that we could induce PRC1 knockout by addition of doxycycline (McKinley & Cheeseman, 2017), as an alternative to siRNA knockdown (Fig 7A).
We observed that GFP-PRC1-WT localizes to overlapping microtubules in the metaphase spindle, the central spindle and the midbody, as previously reported (Fig 7A and B;Subramanian et al, 2013;Kajtez et al, 2016;Pamula et al, 2019).We found that GFP-PRC1-WT localization was slightly reduced when endogenous PRC1 was knocked down, most likely due to the N-terminal GFP-tagging of PRC1, which places the tag close to the dimerization interface and the motor-binding interface.However, we observed that endogenous CENP-E was present at overlapping structures ◀ Figure 5. Regulation by phosphorylation of the PRC1-CENP-E interaction.PRC1-MEE was reduced on the central part of the spindle compared with that observed for GFP-PRC1-WT (Fig 7A and B).The central spindle, which is usually marked by a high density of antiparallel microtubules, was absent or severely disrupted in cells expressing GFP-PRC1-MEE and lacking endogenous PRC1.Very few microtubules were observed between the two segregating half-spindles.
CENP-E was not present on the central spindle in these cells (Fig 7A and C).We also observed Kif4A was recruited to GFP-PRC1-WT, but was largely absent from the abscission site in the presence of GFP-PRC1-MEE (Fig 7D and E).Under these conditions, we observed hypersegregation of chromosomes in the presence of GFP-PRC1-MEE, with the distance between the chromosome mass significantly greater than in cells expressing GFP-PRC1-WT (Fig 7A and F).This phenotype is similar to that seen in cells depleted for PRC1 (Pamula et al, 2019).
To better understand how PRC1-motor interactions affect chromosome segregation and cell division, we carried out time-lapse imaging on cells expressing GFP-PRC1-WT or GFP-PRC1-MEE in the absence of endogenous PRC1, using dyes to demarcate cell membrane, DNA and microtubules.We observed that the speed of the chromosome and spindle pole mass to the daughter cells, marked by DNA and tubulin dyes, respectively, was similar in cells expressing GFP-PRC1-MEE compared with those expressing GFP-PRC1-WT (Fig 7G).We measured the accumulation of GFP-PRC1-WT on the central spindle over time (Fig 7H).GFP-PRC1-MEE was weakly recruited to overlapping microtubules (Fig 7I ), unlike GFP-PRC1-WT, which accumulated in the central spindle throughout anaphase and telophase.However, there were less antiparallel microtubules and the fibres appear thicker, indicating an abnormal regulation of microtubule bundling in the presence of GFP-PRC1-MEE (Fig 7G).The staining of GFP-PRC1-MEE was more diffuse than for GFP-PRC1-WT, and the distribution of GFP-PRC1-MEE was not constrained to the central spindle (Fig 7G and I).Additionally, GFP-PRC1-marked bundles seemed to move away from each other and make thicker bundles, which were easier to distinguish during spindle elongation in anaphase.It is also possible that the PRC1-MEE-marked bundles were severed or broken at the site of furrow ingression (Fig 7G).
PRC1 is essential for cytokinesis (Jiang et al, 1998;Mollinari et al, 2005).Next, we analysed whether the motor recruitment properties of PRC1 contribute to cytokinesis.We depleted endogenous PRC1 in cells expressing GFP-PRC1-WT or GFP-PRC1-MEE and imaged them after 72 h.In cells expressing GFP-PRC1-MEE, there was a significant increase in binucleated cells, indicating they had failed cytokinesis and were tetraploid (Fig 7J and K).Overall, these results indicate the motor recruitment properties of PRC1 are critical to ensure the completion of cytokinesis and support successful cell division.Future work will be needed to determine the contributions of individual PRC1-motor interactions to anaphase and cytokinesis.

Discussion
In this manuscript, we report the mechanistic basis of PRC1microtubule motor interactions, and recapitulate microtubule sliding by a CENP-E:PRC1 complex.We reveal the functional contribution of PRC1-interacting microtubule motors to spindle elongation in anaphase and the completion of chromosome segregation.We identify the temporal and spatial features of these regulated interactions, and show that these features are required for correct timing of cytokinesis.
In early mitosis, CENP-E is present at unattached kinetochores, and moves laterally attached kinetochores along microtubules.The kinetochore-bound CENP-E slides microtubules by pushing microtubules relative to kinetochores and promoting spindle flux (Steblyanko et al, 2020).CENP-E has also been proposed to slide spindle microtubules past each other (Risteski et al, 2021).Some motors, such as the Kinesin-14 dimeric motor HSET, use both its motor and non-motor microtubule-binding domains to slide microtubules past each other (Cai et al, 2009;Braun et al, 2017).We demonstrate that CENP-E, unlike Kinesin-14 HSET, does not slide antiparallel microtubules on its own in vitro.Instead, CENP-E promotes microtubule sliding in the presence of PRC1 in vitro.This suggests that it may function in a similar manner to Kif4A in anaphase (Bieling et al, 2010;Subramanian et al, 2013; Figs 2  and 4).
Previous work on the CENP-E C-terminal tail included part of the kinetochore targeting domain (Gudimchuk et al, 2013).In vitro and in vivo, we did not observe any binding of the CENP-E C-terminal domain to microtubules in the absence of CENP-E interaction with PRC1 (Fig 4A).The unstructured C terminus of CENP-E is phosphorylated in metaphase (Dephoure et al, 2008).Therefore, its affinity for microtubules in the context of the full-length motor is likely to be weak and non-specific.The data we present in this manuscript rule out microtubule-sliding activity of CENP-E via its Cterminal tail.
The timing of the PRC1-motor interaction is important because Kif4A and CENP-E are involved in chromosome organization and alignment in early mitosis (reviewed in Samejima et al, 2012;Craske et al, 2022).PRC1 is phosphorylated by CDK1/cyclin B on T470 and T481, in the region important for microtubule binding, at the junction between the unstructured microtubule-binding tail and the spectrin domain (Jiang et al, 1998).The microtubule bundling activity of PRC1 has been proposed to be downregulated by CDK1 and Plk1 phosphorylation (Mollinari et al, 2002;Hu et al, 2012).We show here that mitotic phosphorylation of CENP-E also reduces the strength of the PRC1-CENP-E interaction.It ensures that CENP-E associates with kinetochores to promote their alignment in early mitosis and does not associate with PRC1 (Jagric et al, 2021).At the metaphase to anaphase, cyclin B degradation leads to a decrease in mitotic kinase activity.As chromosomes segregate, we conclude CENP-E is dephosphorylated, which increases its affinity for PRC1 and facilitates its recruitment to the central spindle.Interestingly, the two ΦΦ motifs in the Kif4A motor are also flanked by threonines and serines (Nousiainen et al, 2006;Huttlin et al, 2010;Olsen et al, 2010;Kettenbach et al, 2011;Fig 3A).Thus, mitotic phosphorylation of the C terminus of Kif4A may regulate the Kif4A:PRC1 interaction temporally and spatially.
The motor recruiting function of PRC1, via the ΦΦ binding site, is crucial to the correct completion of cytokinesis and chromosome segregation (Fig 7).When this interaction is abrogated, the chromosomes separate further.Ultimately, cells fail cytokinesis and become multinucleated (Fig 7).It is possible that the other kinesins such as Kif14, MKLP2 and MKLP1 use an ΦΦ motif for PRC1 recruitment to the central spindle.However, we could not identify a PRC1 binding site from their primary sequence with confidence.MKLP1 forms a heterotetramer with the RhoGAP Cyk4/ MgcRacGAP, which has a hydrophobic motif important for PRC1 binding Caenorhabditis elegans and is highly conserved (Lee et al, 2015).If the MKLP2-PRC1 interaction is disrupted, MKLP2dependent transport of the CPC (chromosomal passenger complex) to the central spindle would be compromised and prevent cytokinesis completion (Gruneberg et al, 2004;Adriaans et al, 2020;Serena et al, 2020).During anaphase, we observe that the central spindle starts to assemble, but the antiparallel microtubule bundles, marked by GFP-PRC1-MEE, are reduced and no longer concentrated at the central spindle.GFP-PRC1-MEE still has a strong preference for antiparallel microtubule fibres and crosslinks microtubules within the spindle overlap.However, GFP-PRC1-MEE is not concentrated at the plus end of overlaps, highlighting that motors are essential for concentrating PRC1 and marking the central spindle and midbody (Subramanian et al, 2013;Wijeratne & Subramanian, 2018;Hannabuss et al, 2019).The PRC1-marked bundles also lose their coherent behaviour within the spindle (Fig 7).Recent work proposes that microtubule bundles in the central spindle are connected to each other (Carlini et al, 2022).Our data reveal that PRC1-interacting proteins that bind to the dimerization domain contribute to interbundle stability by crosslinking different sets of microtubule bundles.This may reinforce their stiffness.
The central spindle is proposed to act as a break counteracting forces that drive spindle elongation (Janson et al, 2007;Lee et al, 2015).The forces generated by single PRC1 molecules on microtubules are low, in the 0.1 pN range (Forth et al, 2014).At higher density, PRC1-crosslinked microtubules can produce significant resistance during microtubule sliding that scale with velocity of microtubule sliding, in the range 5-20 pN for sliding velocities of 25-200 nm/s (Gaska et al, 2020).Our results suggest that the brake forces produced by the microtubule-crosslinking activity of PRC1 do not fully oppose forces that drive chromosome separation because chromosomes hypersegregate in the presence of PRC1 which does not bind motors (Fig 7).This has also been reported for cells lacking PRC1 in which two half spindles became disconnected and were pulled apart (Pamula et al, 2019;Vukusic et al, 2021).Because controlled microtubule sliding does not occur when PRC1 is not bound to the kinesin motors, the outwards spindle and cortical-generated forces are likely to dominate the system.We propose that PRC1 acts both as a break and signalling adaptor.Kinesin motors associate with PRC1 via the conserved ΦΦ motifs and either generate breaking forces on the spindle or recruit other signalling molecules to regulate cytokinesis (Neef et al, 2007).Kif4A, CENP-E, MKLP1 and MKLP2 all interact with PRC1 across species.Future work will address how these PRC1-interacting motors work collectively to complete cell division.
Failed cytokinesis is a hallmark of cancer cells, leading to chromosome instability.Fast-growing polyploid cancer cells are particularly vulnerable to cytokinesis failure (McKenzie & D'Avino, 2016).
Our work may open up opportunities to interfere with cytokinesis completion and induce cytokinesis failure in cancer cells as a therapeutic cancer target to increase chromosome instability and cell death (Lens & Medema, 2019).

Protein expression, purification and assays
All constructs for bacterial expression were transformed in Escherichia coli BL21-CodonPlus (DE3)-RIL.Cultures were induced with 0.5 mM IPTG when OD 600 = 0.6 for 4 h at 25°C or overnight at 18°C for 18-20 h.Cells expressing his 6 -proteins (PRC1 1-168 , PRC1 fulllength) were re-suspended in lysis buffer (50 mM HEPES pH 7.5, 500 mM NaCl, 40 mM imidazole and 5 mM b-mercaptoethanol) supplemented with 1 mM PMSF and cOmplete EDTA-free protease inhibitor cocktail (Roche) and lysed by sonication.The lysate was cleared by centrifugation (50 min, 58,440 g) in a JA 25.50 rotor (Beckman Coulter), filtered and loaded onto a HisTrap HP column (Cytiva).His 6 -tagged proteins (from Sf9 cells and bacteria) were eluted in elution buffer (lysis buffer containing 250 mM imidazole).Constructs containing a 3C protease cleavage site were incubated overnight in dialysis buffer (25 mM HEPES pH 7.5, 300 mM NaCl, 10 mM imidazole, 1 mM EDTA and 5 mM b-mercaptoethanol) with 3C protease and then loaded onto a HisTrap HP column (Cytiva).MBP-CENP-E 2605-2701 was purified using the same lysis buffer without imidazole and an MBP-Trap HP column (Cytiva).For ITC, the MPB tag was cleaved overnight using Factor Xa (NEB) in dialysis buffer and loaded again on an MBP-Trap HP column.GST proteins were purified as previously described (Legal et al, 2020).Recombinant proteins were then concentrated and loaded on a Superdex 200 Increase 10/300 GL (Cytiva) pre-equilibrated in size-exclusion chromatography buffer: 20 mM HEPES pH 7.5, 300 mM NaCl, 1 mM EDTA and 1 mM DTT. Labelling of 647His 6 -GST-CENP-E was performed according to the manufacturer's instructions with the AlexaFluor647 (A20173A, Invitrogen).Degree of labelling was estimated as 1:3.
Full-length CENP-E was expressed in Sf9 insect cells and purified as previously published (Craske et al, 2022).Freshly purified CENP-E was used for in vitro sliding assays in Fig 4 due to deterioration in activity after freezing.Porcine brain tubulin was purified as described (Castoldi & Popov, 2003) and stored in liquid nitrogen long term.

Isothermal titration calorimetry
ITC experiments were carried out to determine the affinity and stoichiometry of PRC1:CENP-E constructs and Kif4A, known to bind PRC1.CENP-E peptides were synthesized by Lifetein, LLC.PRC1 1- 168 , CENP-E constructs and GST-Kif4A 1133-1165 were extensively dialysed into ITC buffer (20 mM HEPES pH 7.5, 150 mM NaCl, 0.005% Tween-20 and 0.5 mM TCEP); prior to the experiment to minimize heats of dilution upon titration.Peptides were directly diluted into ITC buffer.Protein concentrations were determined by absorption at 280 nm; extinction coefficients e were as follows: PRC1 , respectively, at 25°C in 16 aliquots: 1 of 0.5 ll followed by 15 × 2.5 ll.The concentration was calculated for the monomeric CENP-E constructs.For protein-peptide ITC experiments, 557 lM of PRC1 1-168 (calculated for monomeric PRC1) was titrated into 15 lM peptide 1 or peptide 2 at 25°C in 16 aliquots: 1 of 0.5 ll followed by 15 × 2.5 ll.The reference power was set to 3 lcal/s.The enthalpy of binding was analysed with correction for heat of dilution using the software package provided by the instrument manufacturer (Auto-iTC200 microcalorimeter; Malvern Instruments).Data were fit to a simple binding model with one set of sites.

Sample preparation for TIRF microscopy and TIRF microscopy imaging
For PRC1 and CENP-E, microtubule-binding assays, 0.2 mg/ml GMPCPP (Jena Biosciences) microtubule seeds containing 7% rhodamine-tubulin (Cytoskeleton Inc., TL590M-B) were polymerized in BRB80 (80 mM PIPES pH 6.9, 1 mM EGTA and 1 mM MgCl 2 ) for 1 h at 37°C, followed by centrifugation at 17,000 g for 10 min and then resuspended in BRB80.Anti-tubulin antibodies (Sigma, T7816) at a 1:10 dilution in BRB80 were first introduced to the chamber.Next, 40 ll of 1% Pluronic F-127 (Sigma Aldrich) in BRB80 was washed through the chamber and incubated for 5 min.Chambers were then washed with 40 ll of BRB80, then 40 ll 1 mg/ml casein (Sigma Aldrich) before adding the final mixture of GMP-CPP microtubules and PRC1 and/or CENP-E in final assay mix at indicated concentrations (80 mM PIPES pH 6.9, 5 mM MgCl 2 , 1 mM DTT and an oxygen scavenger mix: 0.2 mg/ml glucose oxidase, 0.035 mg/ml catalase, 4.5 mg/ml glucose and 0.1% b-mercaptoethanol).
Sliding assays were carried out in flow chambers consisting of functionalized glass coverslips coated with PEG-biotin.Firstly, chambers were washed with BRB80.Next, 40 ll of 50 lg/ml Neutravidin was washed through the chamber and left to incubate for 5 min.GMPCPP polymerized biotinylated tubulin (HiLyte647 labelled) was washed into the chamber and left for 5 min.Next, 50 ll of purified full-length PRC1 at 2.5 nM was added to coat the microtubules.This was left for 10 min.Chambers were then washed with BRB80, followed by flowing through with a final assay mix containing GMPCPP non-biotinylated microtubules, 2 mM ATP, 0.5 mg/ml casein, oxygen scavenger and CENP-E motor at indicated concentration (or buffer as a control).Microscopy was carried out immediately following this step.For microtubule sliding assays, images of free rhodamine microtubules and immobilized HiLyte 647-biotinylated microtubules using the red and far-red channels, respectively, were taken every 2 s for a total of 20 min.Imaging was performed on a Zeiss Axio Observer Z1 TIRF microscope using a Zeiss 100 × NA 1.46 objective and either a Photometrics Evolve Delta electron-multiplying charge-coupled device camera or a Photometrics Prime 95B sCMOS camera controlled by Zeiss Zen Blue software.

Image analysis
Quantification was done in Omero (OME, or ImageJ; National Institutes of Health; Allan et al, 2012;Schneider et al, 2012).Linescans for measurement of intensity across the central spindle were generated for cells at a stage of cell division defined by taking the width of the spindle of around 10-12 pixels, visualized by tubulin staining with SiR dye (1:40,000 at a final concentration of 25 nM, for 90-120 min, Spirochrome).For the measurement of the chromosome separation in telophase, the maximum distance between chromosome masses along the spindle axis was measured after maximumintensity projection of images.Cell stages were assessed by DNA morphology; telophase was distinguished from cytokinesis by the state of chromosome condensation and the shape of the cell; analysis was done in late anaphase and telophase cells, excluding cytokinesis.For quantification of midbody integrity, cells in cytokinesis were identified morphologically with a bundle of microtubules between neighbouring cells, marked by GFP-PRC1.For cells expressing PRC1-MEE in the absence of endogenous CENP-E, the bundle was generally partially or fully missing, or distorted, and GFP-PRC1 was absent or on the remnant midbody, but chromosomes and microtubules could be seen between the two cells.Midbody and abscission site were defined as a distinct PRC1 signal between the future daughter cells.

Statistics and reproducibility
Statistical analyses were performed using GraphPad Prism 9.0.Data normality was checked.No statistical method was used to predetermine sample size.No data were excluded and no blinding was done.

AlphaFold analysis
The PRC1:CENP-E dimeric complex structure was predicted using AlphaFold2 in the multimer version.The EMBO Journal Agata Gluszek-Kustusz et al

Figure 1 .
Figure 1.A hydrophobic motif is essential for recruitment of CENP-E to overlapping microtubules in mitosis.A Schematic diagram showing the metaphase to anaphase transition, during which kinesin motors Kif4A (blue) and CENP-E (orange) relocalize from chromosomes and kinetochores (pink) to PRC1 (black) on crosslinked microtubules.B Schematic diagram showing the different functional domains of full-length CENP-E, including the C terminus of CENP-E used in this study.C Representative images of HeLa cells transiently transfected with GST-GFP-CENP-E 2605-2701 and immunostained with PRC1 and CENP-C, scale bar 10 lm (n = 4).D Sequence alignment of the C terminus of human CENP-E with eight mammalian and Xenopus laevis CENP-E sequences.Amino acid numbering is relative to the human CENP-E sequence.The two PRC1 putative motifs ΦΦ are highlighted with asterisks (***).The following negatively charged amino acid is also highlighted.Phosphorylated residues following the CDK and Aurora kinase consensus sites are marked with an orange and blue circle respectively.Green circles represent sites that are phosphorylated but do not fit a kinase consensus site.The sequences were aligned using the program Clustal Omega (EBI) and formatted with ESPRIPT (Gouet et al, 1999).E Top, Representative images of live HeLa cells in cytokinesis transiently transfected with GFP-CENP-E 2605-2701 and mutants (green), incubated with SiR-tubulin (red).Scale bar, 10 lm.Bottom, linescans showing the fluorescence intensity average and standard error of the mean (SEM) for the GFP-CENP-E 2605-2701 and mutants and tubulin across the cell midbody.For GFP-CENP-E 2605-2701 , n is the number of cells.n = 11 and for the GFP-CENP-E 2605-2701 mutants, FDN 2661 LTT, YF 2660 AA and FF 2644 AA, n = 15, 16 and 25 respectively.Biological independent replicates were, respectively, 2, 3, 2 and 1. F Graph showing the quantification of GFP peak fluorescence intensity for cells transfected with GFP-CENP-E 2605-2701 constructs and quantified in (E).Mean and peak intensities for each cell are represented for each mutant, ordinary one-way ANOVA test was performed to test significance.

Figure 4 .
Figure 4. CENP-E slides anti-parallel microtubules in the presence of PRC1.A Representative images of GFP-PRC1 (magenta) mixed with rhodamine microtubules.Fire blue-green intensity LUT is used to show tubulin intensity and microtubule overlaps.B Representative images of 647 GST-CENP-E 2639-2671 (yellow) mixed with rhodamine microtubules.C Representative images of GFP-PRC1 and GST-CENP-E 2639-2671 mixed with rhodamine microtubules.D Representative immunofluorescence images of HeLa cells stained for DNA, microtubules, PRC1 and with Alexa647-labeled GST-CENP-E 2639-2671 showing it also recognizes PRC1 in cells.Experiments were repeated > 3 times.E Schematic representation of a microtubule sliding assay in a reconstituted system.The biotinylated microtubule, immobilized to the surface, is represented in yellow.The free microtubule is represented in magenta.F Representative kymograph showing microtubule-microtubule sliding in the presence of 2.5 nM PRC1 and 50 nM full-length CENP-E.G Example kymograph showing a free microtubule sliding until reaching the end of the immobilized microtubule where it slows down to a stall.H Graph showing the quantification of microtubule-microtubule sliding velocity exhibited by free microtubules transported in the presence of 2.5 nM PRC1 and 50 nM full-length CENP-E, n = 28, with median velocity and standard error reported.Data are represented from two independent experiments.

A
, B Characterization by isothermal titration calorimetry (ITC) of binding between PRC1 1-168 and GST-CENP-E 2605-2701 2SD (A) and GST-CENP-E 2605-2701 6SD (B).The y-axis indicates kcal/mole of injectant.C Table summarizing the affinity of the CENP-E constructs for PRC1 1-168 .D Live-cell imaging of metaphase spindles in HeLa cells transiently transfected wild-type, phosphomimetic and non-phosphorylatable mutants of GFP-CENP-E 2605- 2701 (monomeric) and GFP-GST-CENP-E 2605-2701 (dimeric) and stained for tubulin using SiR-Tubulin.The fraction of cells localizing to the overlapping microtubules is represented as a percentage.Scalebar, 10 lm.E Live-cell imaging of the midbody in HeLa cells transfected with wild-type, phosphomimetic and non-phosphorylatable mutants of GFP-GST-CENP-E 2605-2701 and stained for tubulin.Scalebar, 10 lm.Data represented from three independent experiments.F Linescans showing the mean fluorescence intensity and standard error (SEM) for the GFP-CENP-E 2605-2701 wild-type constructs and SA and SD mutants and tubulin across the cell midbody.n (cells) = 27, 21 and 20 respectively.Two to three biological replicates were collected.G Bar graph showing mean and standard error for GFP fluorescence intensity at peak fluorescence for GFP-GST-CENP-E 2605-2701 and mutants at 9.7 lm, quantified in (F).Asterisks indicate ordinary one-way ANOVA test significance value.****P < 0.0001.Source data are available online for this figure.

▸Figure 6 .
Figure 6.Molecular basis for the PRC1-CENP-E interaction.A AlphaFold2 prediction of the CENP-E/PRC1 interaction identifies the PRC1 residues important in CENP-E binding.B, C Elution profile from a size-exclusion chromatography (SEC, black line, left y-axis) run with subsequent multi-angle light scattering (MALS, right y-axis) analysis for PRC1 1-168 and PRC1 1-168 MEE.Outcome of the MALS analysis for the peak is presented in pink (molecular weight, right y-axis).D Fire purple-yellow intensity LUT used to show tubulin intensity and microtubule overlaps.Microtubules are shown alone or incubated with 2.5 nM full-length PRC1 WT or PRC1 MEE.Scalebar, 10 lm.Experiment was replicated two times.E SEC elution profile of PRC1 1-168 MEE (pink), MBP-CENP-E 2605-2701 (green) and MBP-CENP-E 2605-2701 /PRC1 1-168 MEE (orange) (black line, left y-axis).Source data are available online for this figure.
bound by GFP-PRC1-WT, indicating that GFP-PRC1-WT was able to interact with the ΦΦ motif of CENP-E and recruit CENP-E (Fig 7Aand C).When endogenous PRC1 was knocked down, cells expressing GFP-PRC1-MEE still progressed through mitosis and chromosome segregated in anaphase, meaning that checkpoint silencing must have taken place.In anaphase, the amount of GFP-

Figure 7 .
Figure 7.The interaction of PRC1 with motors is critical for the integrity of the central spindle.A Representative immunofluorescence images of HeLa cells in late anaphase and telophase, expressing GFP-PRC1-WT or -MEE and depleted for endogenous PRC1 using a PRC1 siRNA and a PRC1 sgRNA after doxycycline-induced Cas 9 expression.Microtubules, GFP and CENP-E are in white, green and red respectively.DNA is in blue.B Graph showing the percentage of cells with a PRC1 localized at the site of abscission for cells treated in (A).Mean and standard deviation are presented, n = 156 and 141 for cells expressing PRC1-WT and -MEE respectively.Data are from four biological replicates and one technical replicate.Asterisks indicate a T-test significance value.****P < 0.0001.C Graph showing the percentage of cells with CENP-E localized at the abscission site for cells treated in (A), mean and standard deviation are presented, n = 58 and 66 for cells expressing PRC1-WT and -MEE respectively.Data are from two biological replicates.P-value (P = 0.11) calculated for an unpaired T-test.D Representative immunofluorescence images of HeLa cells in telophase, expressing GFP-PRC1-WT or -MEE and depleted for endogenous PRC1 using a PRC1 siRNA and a PRC1 sgRNA after doxycycline-induced Cas 9 expression.Microtubules, GFP and Kif4A are in white, green and red respectively.DNA is in blue.E Graph showing the percentage of cells with Kif4A localized at the abscission site for cells treated in (D).Mean and standard deviation are presented, n = 90 and 78 for cells expressing PRC1-WT and -MEE respectively.Asterisks indicate a T-test significance value for an unpaired T-test.****P < 0.0001.Data from two biological replicates and one technical replicate.F Interchromosome distance in telophase in cells expressing GFP-PRC1-WT and GFP-PRC1-MEE in the absence of endogenous PRC1 (n = 60 and n = 53, respectively).Median and 95% confidence intervals are presented.Data from two biological replicates.Asterisks indicate a T-test significance value for an unpaired T-test.****P < 0.0001.G Representative live-cell images of HeLa cells expressing GFP-PRC1-WT or -MEE and depleted for endogenous PRC1 using a PRC1 siRNA and a PRC1 sgRNA after doxycycline-induced Cas 9 expression.Microtubules (SiR-Tubulin) and DNA (SPY650) are shown in red.The cell membrane (CellMask) is highlighted in white and GFP-PRC1 is in green.Scalebar, 10 lm.H, I Graph showing the change in fluorescence intensity for DNA and microtubules along the longitudinal axis of the spindle from metaphase (red) to anaphase and cytokinesis (dark blue) for cells expressing GFP-PRC1-WT (H, n = 10) or -MEE (I, n = 10) in the absence of endogenous PRC1.J Representative immunofluorescence images of cells expressing GFP-PRC1-WT or -MEE after 72 h siRNA depletion and doxycycline-induced knockout of endogenous PRC1.DNA, microtubules and GFP-PRC1/GFP-PRC1-MEE are in blue, red and green respectively.Scalebar, 10 lm.Quantification was from two biological replicates but experiment was also repeated using in (G).K Quantification of the number of cells mononucleated and binucleated from experiment in (J).n = 633 and 724 for cells expressing GFP-PRC1 WT and GFP-PRC1-MEE respectively.Data are from two independent experiments.Asterisks indicate a T-test significance value.****P < 0.0001.Source data are available online for this figure.

Table 1 .
Constructs generated in this study.