BUB-1 targets PP2A:B56 to regulate chromosome congression during meiosis I in C. elegans oocytes

Protein Phosphatase 2A (PP2A) is a heterotrimer composed of scaffolding (A), catalytic (C), and regulatory (B) subunits. PP2A complexes with B56 subunits are targeted by Shugoshin and BUBR1 to protect centromeric cohesion and stabilise kinetochore–microtubule attachments in yeast and mouse meiosis. In Caenorhabditis elegans, the closest BUBR1 orthologue lacks the B56-interaction domain and Shugoshin is not required for meiotic segregation. Therefore, the role of PP2A in C. elegans female meiosis is unknown. We report that PP2A is essential for meiotic spindle assembly and chromosome dynamics during C. elegans female meiosis. BUB-1 is the main chromosome-targeting factor for B56 subunits during prometaphase I. BUB-1 recruits PP2A:B56 to the chromosomes via a newly identified LxxIxE motif in a phosphorylation-dependent manner, and this recruitment is important for proper chromosome congression. Our results highlight a novel mechanism for B56 recruitment, essential for recruiting a pool of PP2A involved in chromosome congression during meiosis I.


Introduction
Formation of a diploid embryo requires that sperm and egg contribute exactly one copy of each chromosome. The cell division in charge of reducing ploidy of the genome is meiosis, which involves two chromosome segregation steps after a single round of DNA replication (Marston and Amon, 2004;Ohkura, 2015). Female meiosis is particularly error prone (Hassold and Hunt, 2001), which can lead to chromosomally abnormal embryos. Therefore, understanding the molecular events that guarantee proper chromosome segregation during female meiosis is of paramount importance. Cell division is under tight control of post-translational modifications (PTMs), of which phosphorylation is the most studied. The balance between kinase and phosphatase activities plays a central role, but we still lack a clear picture of how this is achieved during meiosis, especially when compared to mitosis (Gelens et al., 2018;Novak et al., 2010).
In the present work, we used C. elegans oocytes to establish the role and regulation of PP2A during female meiosis. We found that PP2A is essential for female meiosis, and its recruitment to meiotic chromosomes and spindle is mediated by the B56 regulatory subunits PPTR-1 and PPTR-2. Targeting of the B56 subunits is mediated by the kinase BUB-1 through a canonical B56 LxxIxE motif, which targets both PPTR-1 and PPTR-2 to the chromosomes and central spindle during meiosis. Overall, we provide evidence for a novel, BUB-1-regulated role for PP2A:B56 in chromosome congression during female meiosis in C. elegans. The schematic was generated from the PDB structure 2npp (Xu et al., 2006). (B) Schematic of the timescales used throughout the paper. Metaphase I was defined as time zero and chosen as the frame prior to the one where chromosome separation was detected. (C) Microtubule and chromosome dynamics were followed in wild-type and let-92(RNAi) oocytes expressing GFP::tubulin and mCherry::histone. Magenta arrows point to defective spindle structure; the cyan arrow points to misaligned chromosomes; the yellow arrow shows an apparent separation between chromosome masses. Inset numbers represent the time relative to metaphase I in seconds. Scale bar, 2 mm. See Figure 1-video 1. (D) The number of oocytes with misaligned chromosomes in metaphase I was compared between wild-type and let-92(RNAi) oocytes and the percentage is represented (p<0.0001, Fisher's exact test). The number of oocytes analysed (n) is shown. (E) The number of oocytes with an extruded polar body (PB) after meiosis I in wild-type and let-92(RNAi) oocytes was analysed and the percentage is represented (p<0.0001, Fisher's exact test). The number of oocytes analysed (n) is shown. (F) ASPM-1 and chromosome dynamics were followed in wildtype and let-92 (RNAi) oocytes expressing GFP::ASPM-1 and mCherry::histone. Inset numbers represent the time relative to metaphase I in seconds. Cyan arrows point to spindle poles, whereas orange arrows highlight the unfocused ASPM-1 cumuli. Scale bar, 2 mm. See Figure 1-video 2. (G) The number of oocytes with defective spindle at prometaphase I in wild-type and let-92(RNAi) oocytes was analysed, and the percentage is represented (p<0.0001, Fisher's exact test). The number of oocytes analysed (n) is shown. (H) Securin IFY-1 degradation was used as a proxy for anaphase progression and followed in wild-type and let-92(RNAi) oocytes. Greyscale images of the chromosomes are shown as well as whole oocyte images using the 'fire' LUT. The intensity scale is shown in the bottom. Inset numbers represent the time relative to metaphase I in seconds. Scale bar, 2 mm. See Figure 1video 3. (I) Cytoplasmic Securin IFY-1 levels were measured throughout meiosis I, and the mean ± s.e.m is shown in the graph. The online version of this article includes the following video and figure supplement(s) for figure 1: Figure supplement 1. PP2A is essential for Meiosis I in C. elegans oocytes. Figure supplement 2. CLASP CLS-2 intensity and localisation is not affected after let-92 depletion. Figure 1-video 1. Wild type and let-92(RNAi) oocytes expressing GFP::tubulin and mCherry::histone were dissected and recorded. https://elifesciences.org/articles/65307#fig1video1 Figure 1-video 2. Wild type and let-92(RNAi) oocytes expressing GFP::ASPM-1 and mCherry::histone were dissected and recorded. https://elifesciences.org/articles/65307#fig1video2 Figure 1-video 3. Wild type and let-92(RNAi) oocytes expressing Securin IFY-1 ::GFP and mCherry::histone were dissected and recorded. https://elifesciences.org/articles/65307#fig1video3 Figure 1-video 4. Wild type and let-92(RNAi) oocytes expressing CLASP CLS-2 ::GFP and mCherry::histone were dissected and recorded. https://elifesciences.org/articles/65307#fig1video4 exact test). Similar defects were observed by depleting the sole PP2A scaffolding subunit, PAA-1 (Figure 1-figure supplement 1A-C). In let-92(RNAi) and paa-1(RNAi), oocytes microtubules do not organise into a bipolar structure ( Figure 1C, Figure 1-figure supplement 1A, magenta arrows). We then analysed the localisation of the spindle pole protein GFP::ASPM-1 (Connolly et al., 2014). GFP::ASPM-1 displays two focused poles in 100% of wild-type oocytes ( Figure 1F,G, cyan arrows). In contrast, GFP::ASPM-1 foci fail to coalesce in 95% of let-92(RNAi) oocytes, displaying a cluster of small foci ( Figure 1F, orange arrows; Figure 1G; Figure 1-video 2). We then sought to determine whether the lack of chromosome segregation was due to a defect in meiosis I progression. We measured endogenously Securin IFY-1 ::GFP levels as a readout for aAnaphase-pPromoting cComplex/cCyclosome (APC/C) activity (i.e. anaphase progression). Cytoplasmic securin IFY-1 degradation proceeded at similar rates in wild-type and LET-92-depleted oocytes ( Figure 1H,I; Figure 1-video 3), indicating that APC/C activity is largely unperturbed in the absence of PP2A. Given the similarity of this phenotype to the depletion of CLASP orthologue CLS-2 (Dumont et al., 2010;Laband et al., 2017;Schlientz and Bowerman, 2020), we analysed the localisation of CLS-2 and detected no changes in CLS-2 levels throughout meiosis (Figure 1-figure supplement 2; Figure 1-video 4).
Taken together, we have found that PP2A is required for spindle assembly, chromosome alignment, and PBE during meiosis I. Additionally, APC activity is unperturbed by PP2A depletion, but we cannot rule out an impact on other pathways acting redundantly with APC (Sonneville and Gonczy, 2004;Wang et al., 2013).

PP2A:B56 localises to meiotic chromosomes and spindle
To assess the localisation of the core PP2A enzyme (A and C subunits) in vivo, we attempted to tag endogenous LET-92 with GFP but were unsuccessful, presumably due to disruption of its native structure, in agreement with a recent report (Magescas et al., 2019). We generated a GFP-tagged version of the sole C. elegans PP2A scaffold subunit, PAA-1, and used this to assess the localisation of the core enzyme during meiosis I (Figure 2A; Figure 2-video 1). The fusion protein localised in centrosomes and P-granules during the early embryonic mitotic divisions (Figure 2-figure supplement 1A), in agreement with previous immunofluorescence data (Lange et al., 2013). During meiosis I, GFP::PAA-1 localises to spindle poles ( Figure 2A, cyan arrows) and chromosomes ( Figure 2A, magenta arrows). The chromosomal signal is a combination of midbivalent and kinetochore populations, visible when analysing single Z-planes in the time-lapses (Figure 2-figure supplement 1A, magenta and yellow arrows). As meiosis I progresses, GFP::PAA-1 signal concentrates in the central spindle between the segregating chromosomes ( Figure 2A, magenta arrowhead), finally disappearing by late anaphase I. This pattern differs substantially from that of Protein Phosphatase 1 (PP1), which localises in the characteristic cup-shaped kinetochores (Hattersley et al., 2016).
To address which regulatory subunits are involved in targeting PP2A to the meiotic spindle and chromosomes, we first assessed the localisation of the two C. elegans B56 orthologues, PPTR-1 and PPTR-2, and the single B55 orthologue, SUR-6 (Figure 2-figure supplement 2A). Live imaging of endogenous, GFP-tagged regulatory subunits revealed that both B56 orthologues, PPTR-1 and PPTR-2, localised strongly and dynamically within the meiotic spindle, whereas no spindle or chromosome localisation of B55 SUR-6 could be detected (Figure 2-figure supplement 2B). PPTR-1 has the highest sequence identity with human B56a2 (68.3%) and e3 (71.87%), whereas PPTR-2 displays the highest sequence identity with human B56d3 (66.19%) and B56g1 (68.97%) ( Table 1 and Supplementary file 1). Closer analysis of the C-terminal sequence in B56 which plays a key role in specifying centromere versus kinetochore localisation (Vallardi et al., 2019) further confirmed that PPTR-1 displays the highest sequence identity with the centromeric B56s, a and e (93.75% and 87.5%, respectively), while PPTR-2 displays the highest sequence identity with the kinetochore-localised B56, g and d (93.75% and 100%, respectively) (Figure 2-figure supplement 2C). We will henceforth refer to PPTR-1 as B56a PPTR-1 and PPTR-2 as B56g PPTR-2 . We used endogenous GFPtagged versions of B56a PPTR-1 and B56g PPTR-2 (Kim et al., 2017) and analysed their dynamic localisation pattern in greater spatial and temporal detail. B56a PPTR-1 localises mainly to the region between homologous chromosomes (midbivalent) during metaphase of meiosis I ( Figure 2B, magenta arrow; Figure 2-video 2) and faintly in kinetochores ( Figure 2B, yellow arrows). During anaphase I, B56a PPTR-1 is present exclusively on the central spindle ( Figure 2B, magenta arrowhead; Figure 2video 2). B56g PPTR-2 localises mainly in the midbivalent during metaphase of meiosis I ( Figure 2C, Figure 2. Caenorhabditis elegans B56 regulatory subunits PPTR-1 and PPTR-2 are required for normal meiosis I. (A) Top: Schematic of the paa-1 gene structure and its tagging with gfp. Bottom: The PP2A scaffold subunit GFP::PAA-1 was followed throughout meiosis I in a dissected oocyte. Magenta arrows point to the midbivalent; cyan arrows point to spindle poles; and magenta arrowhead highlights the central-spindle localisation. Inset numbers represent the time relative to metaphase I in seconds. Scale bar, 2 mm. See Figure 2-video 1. (B) Top: Schematic of the pptr-1 gene structure and its tagging with gfp. Bottom: PPTR-1 and chromosome dynamics were followed in oocytes expressing PPTR-1::GFP and mCherry::histone. The magenta arrow points to the midbivalent and the yellow arrow points to the kinetochore. Magenta arrowhead highlights the central-spindle localisation. Inset numbers represent the time relative to metaphase I in seconds. Scale bar, 2 mm. See Figure 2-video 2. (C) Top: Schematic of the pptr-2 gene structure and its tagging with gfp. Bottom: PPTR-2 and chromosome dynamics were followed in oocytes expressing PPTR-2::GFP and mCherry::histone. The magenta arrow points to the midbivalent, the yellow arrow points to the kinetochore, and the cyan arrow points to the spindle pole. Inset numbers represent the time relative to metaphase I in seconds. Scale bar, 2 mm. Magenta arrowhead highlights the central-spindle localisation, and yellow arrowhead highlights the chromosome-associated signal. See Figure 2 -video 3. (D) PAA-1 and chromosome dynamics were followed in wild-type, pptr-1(RNAi), pptr-2D, and pptr-2D+pptr-1(RNAi) oocytes expressing GFP::PAA-1 and mCherry::histone. Magenta arrows point to the absence of GFP signal on prometaphase chromosomes, and the cyan arrows point to spindle poles. The yellow arrows highlight one misaligned bivalent. Inset numbers represent the time relative to metaphase I in seconds. Scale bar, 2 mm. See Figure 2 -video 4. (E) On the left, the schematic depicts how angles were measured relative to the spindle pole-to-pole axis. On the right, the angle of bivalents at 80 s before metaphase I in wild-type, pptr-1(RNAi), pptr-2D, and pptr-2D+pptr-1(RNAi) oocytes. Violin plot includes each data point (chromosome), the median (straight black line), and the interquartile range (dashed black lines). N represents number of oocytes and n number of bivalents measured. p values shown in the figure were obtained using a Kruskal-Wallis test. (F) On the left, the schematic depicts how distances were measured relative to the centre of the spindle. On the right, the distance of bivalents 80 s before metaphase I was measured in wild-type, pptr-1(RNAi), pptr-2D, and pptr-2D+pptr-1(RNAi) oocytes. Violin plot includes each data point (chromosome), the median (straight black line), and the interquartile range (dashed black lines). N represents number of oocytes and n number of bivalents measured. p values shown in the figure were obtained using a Kruskal-Wallis test. The online version of this article includes the following video and figure supplement(s) for figure 2:     These results show that C. elegans B56 subunits, like their mammalian counterparts, display a similar but not identical localisation pattern: while both B56a PPTR-1 and B56g PPTR-2 are present in the midbivalent and central spindle, B56g PPTR-2 is also associated with chromosomes during anaphase.
Depletion of B56a PPTR-1 and B56g PPTR-2 leads to chromosome congression defects To address the role of the C. elegans B56 subunits during meiosis I, we combined a B56g PPTR-2 deletion allele (ok1467, 'pptr-2D') with RNAi-mediated depletion of B56a PPTR-1 ('pptr-1(RNAi)'), which we will refer to hereafter as 'PPTR-1/2 depletion'. While there was no significant change in GFP::PAA-1 localisation upon depletion of B56a PPTR-1 or deletion of B56g PPTR-2 , no PAA-1 signal is detected associated with chromosomes upon double PPTR-1/2 depletion ( Figure 2D, magenta arrow; Figure 2-video 4). Of note, PP2A targeting to poles was still detected ( Figure 2D, cyan arrows), indicating that B56 subunits target PP2A complex to chromosomes but are not necessary for spindle pole targeting ( Figure 2D; Figure 2-video 4). We noticed that chromosomes failed to align upon PPTR-1/2 depletion ( Figure 2D, yellow arrow), and in order to quantify this phenotype, we measured the angle between the bivalent long axis and the spindle axis ('q', Figure 2F (Hattersley et al., 2016). Both the angle (q) and the distance (d) increased significantly upon PPTR-1/2 double depletion ( Figure 2F,G). Taken together, these results indicate that B56 subunits are involved in chromosomal and central spindle targeting PP2A and play a role in chromosome congression prior to anaphase. The PAA-1 localisation and chromosome alignment defects observed upon PPTR-1/2 depletion suggest that the subunits are at least partially redundant.
Using a fluorescence polarisation-based assay, we confirmed that the LxxIxE motif of BUB-1 binds to purified recombinant PPTR-2, and this binding is abolished by the L282A,V285A mutations ( Figure 4C). While localisation of BUB-1 L282A,V285A was indistinguishable from that of wild-type BUB-1 during metaphase I (   GFP and BUB-3 is highlighted with green and blue arrows, respectively. The band corresponding to BUB-1::GFP was further analysed by mass spectrometry to look for phospho-modified peptides. (B) Serine 283 is phosphorylated in vivo. In addition, three other phosphorylation sites were Figure 5 continued on next page arrows, and Figure 4H; Figure 4-video 2). In contrast, chromosome-associated B56g PPTR-2 was less affected in the BUB-1 L282A,V285A mutant ( Figure 4G, yellow arrows). Importantly, the LxxIxE motif mutations BUB-1 L282A,V285A abrogates GFP::PAA-1 localisation in the midbivalent and central spindle ( Figure 4I, magenta arrows; Figure 4-video 3) without affecting the spindle pole PAA-1 localisation ( Figure 4I, cyan arrows; Figure 4-video 3). Some GFP::PAA-1 signal was still detected in anaphase chromosomes, consistent with the remaining B56g PPTR-2 on chromosomes ( Figure 4I,J, yellow arrows). This LxxIxE motif-dependent regulation is specific for B56 subunits because the localisation of the SAC component Mad1 MDF-1 , a known BUB-1 interactor (Moyle et al., 2014), is not disrupted after mutating the BUB-1 LxxIxE motif (Figure 4-figure supplement 2B). Mutation of the BUB-1 LxxIxE motif not only impairs B56 chromosomal targeting but also leads to alignment/congression defects ( Figure 4K,L), indicating that the BUB-1 LxxIxE motif recruits PP2A:B56 and plays an important role in chromosome congression. Lagging chromosomes were detected in 36% of oocytes in the BUB-1 L282A,V285A mutant, versus 10% in wild-type oocytes (p=0.0125, Fisher's exact test), but segregation was achieved in 100% of the cases with no PBE defects were detected. Interestingly, the newly identified LxxIxE motif specifically recruits PP2A:B56 to metaphase chromosomes and anaphase central spindle, but not anaphase chromosomes.
Phosphorylation of BUB-1 LxxIxE is important for PP2A:B56 chromosome targeting Since phosphorylation of LxxIxE motifs can increase affinity for B56 by~10 fold (Wang et al., 2016), we sought to determine whether Ser 283 within BUB-1 LxxIxE motif is phosphorylated in vivo. To this end, we immunoprecipitated endogenous, GFP-tagged BUB-1 from embryo lysates using a GFP nanobody. Immunoprecipitated material was digested with trypsin, peptides analysed by mass spectrometry and searches conducted for peptides containing phosphorylated adducts. As expected GFP-tagged, but not untagged, BUB-1 was pulled down by the GFP nanobody ( Figure 5-figure supplement 1A) along with the BUB-1 partner, BUB-3 ( Figure 5A, blue arrow). We found four phospho-sites clustered within a disordered region, one of which is Ser 283, within the LxxIxE motif ( Figure 5B; see also representative MS spectra for Ser 283 in Figure 5-figure supplement 1B). We expressed a BUB-1 fragment containing the LxxIxE motif ( Figure 5C) and performed Cdk1 kinase assays, which showed that Cdk1 can phosphorylate the 259-332 BUB-1 fragment ( Figure 5D). Western blot analysis using a phospho-specific antibody revealed that Cdk1 can phosphorylate Ser 283 in vitro ( Figure 5E). Importantly, LxxIxE motif peptides with phosphorylated Ser 283 bound recombinant B56g PPTR-2 with higher affinity than non-phosphorylated LxxIxE peptide ( Figure 5F). We generated a phospho Ser 283-specific BUB-1 antibody ( Figure 5-figure supplement 2) and observed that while BUB-1 phosphorylated in Ser 283 is detected in midbivalent and kinetochore, it is preferentially enriched in the midbivalent ( Figure 5G,H).

Discussion
In the present article, we have uncovered new roles for PP2A during oocyte meiosis in C. elegans. PP2A is essential for meiosis I: depletion of the catalytic or scaffold subunits leads to severe spindle assembly defects, lack of chromosome segregation, and failure to achieve PBE. These effects are likely brought about by a combination of different PP2A subcomplexes with varying regulatory B subunits. PP2A:B56 regulates chromosome dynamics prior to segregation since depletion of the two B56 orthologues, PPTR-1 and PPTR-2, leads to alignment defects. We have uncovered a new phospho-regulated B56 LxxIxE motif in C. elegans BUB-1 that recruits PP2A:B56 and is important for chromosome alignment during meiosis I.

Dissecting the role of PP2A during oocyte meiosis
Depletion of the sole catalytic or scaffold PP2A subunits leads to massive meiotic failure and embryonic lethality. The earliest effect we could see in our experimental set up is a failure to assemble a bipolar spindle. This will of course have a direct impact on any process that should occur after spindle assembly, including chromosome alignment and segregation, followed by PBE. However, BUB-1 depletion leads to severe spindle assembly and alignment defects, yet in the majority of cases, chromosomes segregate (with visible errors -lagging chromosomes) and polar bodies do extrude. Therefore, lack of a proper bipolar metaphase spindle is not sufficient to result in lack of segregation or PBE. PP2A complexes harbouring the B56 subunits PPTR-1 and PPTR-2 are required to target the phosphatase to chromosomes to regulate chromosome alignment in metaphase I. Furthermore, this chromosomal B56 pool is recruited by BUB-1 through its LxxIxE SLiM motif. Mutation of this motif that prevents binding to B56 subunits leads to alignment defects. B56 subunits however are not involved in spindle pole targeting of PP2A, suggesting that this spindle pole pool is the one relevant for spindle assembly. Our attempts to address a possible role for other B subunits were focused on RSA-1 and SUR-6 given their reported centrosomal roles during mitosis (Enos et al., 2018;Kitagawa et al., 2011;Schlaitz et al., 2007;Song et al., 2011). However, neither RSA-1 nor SUR-6 was required for meiotic spindle assembly. It is likely that the role of PP2A on spindle assembly is achieved by a combination of B subunits and that could also include uncharacterised B subunits (UniProt Consortium et al., 2020).

B56 targeting during different stages of meiosis I
Chromosomal PPTR-1 and PPTR-2 and the ensuing PP2A targeting prior to chromosome segregation depend on the BUB-1 LxxIxE motif. Interestingly, this dependency changes during anaphase, where PPTR-2 chromosomal targeting is BUB-1 dependent but LxxIxE motif independent and depends on the kinase domain. The regulation of protein localisation during meiosis I in C. elegans oocytes is highly dynamic, and differences have been observed between metaphase and anaphase. For example, while kinetochore localisation of the CLASP orthologue CLS-2 during metaphase depends on BUB-1, a pool of CLS-2 is able to localise in the anaphase central spindle in a BUB-1independent manner (Laband et al., 2017). In this line, since its role during meiosis was first described (Dumont et al., 2010), there has been no clear explanation as to the cause of the alignment and segregation defects upon BUB-1 depletion. Our results provide a plausible explanation for the role of BUB-1 in chromosome alignment during oocyte meiosis in C. elegans through the recruitment of PP2A:B56.
Possible function of chromosome-associated PP2A As mentioned above, the PP2A complexes are likely playing a number of important roles during meiosis. Our work uncovers a function during chromosome congression involving B56 subunits targeted by BUB-1. Similar to mice and yeast, it is therefore likely that PP2A complexes at the chromosome control proper chromosome-spindle attachments. The alignment defects we observed upon PPTR-1/ 2 depletion (or in the LxxIxE motif mutant) resemble those reported in the absence of kinetochore proteins (Danlasky et al., 2020;Dumont et al., 2010). Interestingly, PP2A:B56 complexes containing PPTR-1 and PPTR-2 are present at the meiotic kinetochore, and it is therefore possible that PP2A:B56 works in parallel to and/or regulates kinetochore protein(s). Furthermore, we detected GFP::PAA-1 on anaphase chromosomes, similar to kinetochore proteins (Danlasky et al., 2020;Dumont et al., 2010;Hattersley et al., 2016).
During meiosis in C. elegans, the Aurora B orthologue, AIR-2, concentrates in the interface between homologous chromosomes (i.e. the midbivalent; Kaitna et al., 2002;Rogers et al., 2002;Schumacher et al., 1998), and its activity is counteracted by PP1, which is recruited by the protein LAB-1 (Tzur et al., 2012). PP1 counteracts Aurora B AIR-2 during meiosis by antagonising Haspinmediated H3T3 phosphorylation in the long arm of the bivalent (Ferrandiz et al., 2018). Consistent with this, PP1 depletion leads to loss of sister chromatid cohesion during meiosis I (Kaitna et al., 2002;Rogers et al., 2002). During prometaphase and metaphase I, Aurora B AIR-2 is retained in the bivalent, whereas PP1 resides mainly in kinetochores (Hattersley et al., 2016) and it is therefore likely that other phosphatase(s) will be involved in controlling Aurora B-mediated phosphorylation events during metaphase I. Since PP2A:B56 is concentrated in the midbivalent during meiosis I, we hypothesise that it could be balancing AIR-2 activity during meiosis. In this respect, we found that serine 612 in BUB-1 is phosphorylated and this serine is embedded in a sequence (RRLSI) closely resembling the consensus for PP2A:B56 reported in Kruse et al., 2020. Furthermore, the sequence also fits into the loosely defined Aurora B consensus RRxSj (where j is a hydrophobic aa) (Cheeseman et al., 2002;Deretic et al., 2019;Kettenbach et al., 2011). Therefore, BUB-1 itself could be subjected to an Aurora B-PP2A:B56 balance and it will be very interesting to address whether BUB-1 and other meiotic proteins are regulated by the balance between Aurora B and PP2A:B56.
In a broader context, a putative LxxIxE motif has been identified in human Bub1 (Cordeiro et al., 2020;Singh et al., 2020;Wang et al., 2016). While this motif has not been tested functionally, it is interesting that this putative LxxIxE motif is preceded by a PLK1 binding motif and is important for restraining PLK1 activity during SAC activation (Cordeiro et al., 2020). While we did not find a PLK1 binding site preceding BUB-1 LxxIxE, a combination of PLK1 and B56 motifs is present in aa 516-536 of C. elegans BUB-1 (Cordeiro et al., 2020). It will be interesting to determine whether BUB-1 plays a role in regulating the PLK1-PP2A:B56 balance and also what biological role this axis plays during meiosis.
In summary, we provide evidence for a novel, BUB-1-regulated role for PP2A:B56 during female meiosis in C. elegans. It will be interesting to test in the future our hypothesis that PP2A is the main phosphatase counteracting Aurora B-mediated phosphorylation to achieve proper phosphorylation levels during meiosis I.

C. elegans strains
Strains used in this study were maintained at 20 degrees unless indicated otherwise. For a complete list of strains, please refer to Supplementary file 2. Requests for strains not deposited in the CGC should be done through the FP lab's website (https://pelischlab.co.uk/reagents/).

RNAi
For RNAi experiments, we cloned the different sequences in the L4440 RNAi feeding vector (Timmons and Fire, 1998).
All sequences were inserted into L4440 using the NEBuilder HiFi DNA Assembly Master Mix (New England Biolabs) and transformed into DH5a bacteria. The purified plasmids were then transformed into HT115(DE3) bacteria (Timmons et al., 2001). RNAi clones were picked and grown overnight at 37˚C in LB (Luria-Bertani medium) with 100 mg/ml ampicillin. Saturated cultures were diluted 1:100 and allowed to grow until reaching an OD 600 of 0.6-0.8. Isopropyl-b-d-thiogalactopyranoside (IPTG) was added to a final concentration of 1 mM, and cultures were incubated overnight at 20˚C. Bacteria were then seeded onto NGM plates made with agarose and allowed to dry. L4 worms were then plated on RNAi plates and grown to adulthood at 20˚C for 24 hr in the case of let-92(RNAi), bub-1(RNAi), and paa-1(RNAi) and 48 hr in all other cases.

CRISPR strains GFP::SUR-6
For the generation of in situ-tagged GFP::SUR-6, we used the self-excising cassette method (Dickinson et al., 2015). In brief, N2 adults were injected with a plasmid mix containing Cas9, a sgRNA targeting the N-terminus of sur-6 and a repairing template to insert the GFP sequence, along with a LoxP-flanked cassette that encoded for a hygromycin resistance gene, a sqt-1 mutant to confer a dominant roller phenotype, and heat-shock-induced Cre recombinase. After selection in hygromycin, positive integrants (evidenced by their roller phenotype) were heat-shocked to express Cre and remove the cassette.

bub-1 S283A
The wild-type sequence: TTCAACGCCAATCTAAATCCTAGAAGACGTCATCTTTCACCAGTCAGTGAGAAAACGGTT GATGATGAG was mutated to: TTCAACGCCAATCTAAATCCTAGAAGACGTCACCTTGCGCCAGTCAGTGAGAAAACGG TTGATGATGAG The introduced changes are shown in red, and synonymous mutations are shown in cyan.

Live imaging of oocytes
A detailed protocol for live imaging of C. elegans oocytes was used with minor modifications (Laband et al., 2018). Fertilised oocytes were dissected and mounted in 5 ml of L-15 blastomere culture medium (0.5 mg/ml inulin; 25 mM HEPES, pH 7.5 in 60% Leibowitz L-15 medium and 20% heatinactivated fetal bovine serum) on 24 Â 40 mm #1.5 coverslips. Once dissection was performed and early oocytes identified using a stereomicroscope, a circle of Vaseline was laid around the sample, and a custom-made 24 Â 40 mm plastic holder (with a centred window) was placed on top. The sample was imaged immediately. Live imaging was done using a 60Â/NA 1.4 oil objective on a spinningdisk confocal microscope (MAG Biosystems) mounted on a microscope (IX81; Olympus), an EMCCD Cascade II camera (Photometrics), spinning-disk head (CSU-X1; Yokogawa Electric Corporation). Acquisition parameters were controlled by MetaMorph seven software (Molecular Devices). For all live imaging experiments, partial maximum-intensity projections are presented in the figures and full maximum-intensity projections are presented in the supplementary videos. All files were stored, classified, and managed using OMERO (Allan et al., 2012). Figures were prepared using OMERO.figure and assembled using Adobe Illustrator. Representative videos shown in Supplementary material were assembled using custom-made macros in Fiji/ImageJ (Schindelin et al., 2012).

Generation of phospho-Ser 283 BUB-1 antibody
The antibody was generated by Moravian Biotec by immunising rabbits with the following peptide: RRRHL(pS)PVSEKTC. Serum was adsorbed with a non-phosphorylated peptide (RRRHLSPVSEKTC) followed by affinity purification with the antigenic, phosphorylated peptide. Different fractions were tested in immunofluorescence by incubating different dilutions (1:1,000 and 1:10,000) with 1 mM and 10 mM of either non-phosphorylated or phosphorylated peptide. Only the phosphorylated peptide compited out the signal. Additionally, we used the BUB-1 S283A strain, and no antibody signal was detected.

Immunofluorescence
Worms were placed on 4 ml of M9 worm buffer in a poly-D-lysine (Sigma, P1024)-coated slide, and a 24 Â 24 cm coverslip was gently laid on top. Once the worms extruded the embryos, slides were placed on a metal block on dry ice for >10 min. The coverslip was then flicked off with a scalpel blade, and the samples were fixed in methanol at 20˚C for 30 min. After blocking in phosphate-buffered saline (PBS) buffer plus 3% bovine serum albumin and 0.1% Triton X-100 (AbDil), samples were incubated overnight at 4˚C with anti-BUB-1 (Desai et al., 2003) and anti-tubulin (1/400, clone DM1a, Sigma-Aldrich) in AbDil. After three washes with PBS plus 0.1% Tween, secondary antibodies were added at 1/1000 (goat anti-mouse and goat anti-rabbit conjugated to Alexa Fluor 488, Alexa Fluor 594, Thermo Scientific). After 2 hr at room temperature and three washes with PBS plus 0.1% Tween, embryos were mounted in ProLong Diamond antifade mountant with DAPI (Thermo Scientific).
For the comparison of total versus phospho Ser 283 BUB-1, a total BUB-1 antibody was labelled with Alexa-488, while phospho Ser 283 BUB-1 was labelled with Alexa 647, using the APEX Alexa Fluor Antibody Labelling kits (Thermo). We used the strain HY604, which is a temperature-sensitive allele of the the APC component MAT-1, that arrests in meiosis I prior to spindle rotation when moved to the restrictive temperature.

GFP immunoprecipitation
For GFP immunoprecipitations, we followed a published protocol (Sonneville et al., 2017) with minor modifications (Pelisch et al., 2019). Approximately 1000 worms expressing GFP-tagged endogenous BUB-1 were grown for two generations at 20˚C in large 15 cm NGM plates with concentrated HT115 bacteria. Worms were bleached and embryos were laid in new 15 cm NGM plates with concentrated HT115 bacteria. Once >80% of the worm population was at the L3/L4 stage, worms were washed and placed on 15 cm agarose plates containing concentrated HT115 bacteria. After 24 hr, worms were bleached and the embryos were resuspended in a lysis buffer containing 100 mM HEPES-KOH pH 7.9, 50 mM potassium acetate, 10 mM magnesium acetate, 2 mM ethylenediaminetetraacetic acid (EDTA), 1Â protease inhibitor ULTRA (Roche), 2Â PhosSTOP (Roche), and 1 mM dithiothreitol (DTT). The solution was added drop-wise to liquid nitrogen to generate beads that were later grinded using a SPEX SamplePrep 6780 Freezer/Mill. After thawing, we added one-quarter volume of buffer containing lysis buffer supplemented with 50% glycerol, 300 mM potassium acetate, 0.5% NP40, plus DTT, protease, and phosphatase inhibitors as described above. DNA was digested with 1600U of Pierce Universal Nuclease for 30 min on ice. Extracts were centrifuged at 25,000 g for 30 min and then at 100,000 g for 1 hr. The extract was then incubated for 60 min with 30 ml of a GFP nanobody covalently coupled to magnetic beads. The beads were washed 10 times with 1 ml of wash buffer (100 mM HEPES-KOH pH 7.9, 300 mM potassium acetate, 10 mM magnesium acetate, 2 mM EDTA, 0.1% NP40, plus protease and phosphatase inhibitors) at 4˚C (cold room). Bound proteins were eluted twice using two rounds of 50 ml LDS (Lithium dodecyl sulfate) sample buffer (Thermo Scientific) at 70˚C for 15 min and stored at À80˚C.

Sample preparation for mass spectrometry
IP samples were run on 4-12% Bis-Tris sodium dodecyl sulfate gels with MOPS running buffer, and the gel was stained using Quick Coomassie Stain (Generon). Bands of interest were cut and washed with water:acetonitrile (50:50), followed by a wash with 100 mM ammonium bicarbonate. The gel pieces were then washed with 100 mM ammonium bicarbonate:acetonitrile (50:50), followed by a final wash with acetonitrile. Gel pieces were dried using a SpeedVac.
Samples were reduced with 10 mM DTT in 20 mM ammonium bicarbonate and alkilated with 50 mM IAA (iodoacetamide) in 20 mM ammonium bicarbonate. Samples were then washed sequentially with 100 mM ammonium bicarbonate, 100 mM ammonium bicarbonate:acetonitrile (50:50), and acetonitrile. Gel pieces were dried using a SpeedVac.
Trypsin solution (12.5 mg/ml stock in 20 mM ammonium bicarbonate) was added to cover the gel pieces and incubated for 30 min on a shaking platform and incubated sample overnight at 30˚C on a shaker. Peptides were extracted by standard procedures and reconstituted in 10 ml of 5% formic acid/10% acetonitrile. After vortexing for 1 min, water was added to 50 ml.

Mass spectrometry analysis
Samples were run on an Ultimate 3000 RSLCnano system (ThermoFisher Scientific) coupled with a Q-Exactive Plus Mass Spectrometer (Thermo Fisher Scientific). Peptides initially trapped on an Acclaim PepMap 100 (Thermo Fisher Scientific) and then separated on an Easy-Spray PepMap RSLC C18 column (Thermo Fisher Scientific). Sample was transferred to mass spectrometer via an Easy-Spray source with temperature set at 50˚C and a source voltage of 2.1 kV. The mass spectrometer was operated on in data-dependent acquisition mode (top 15 method). MS resolution was 70,000 with a mass range of 350-1600. MS/MS resolution was 17,500.
RAW data files were extracted and converted to mascot generic files (.mgf) using MSC Convert. Extracted data then searched against C. elegans proteome and BUB-1 specifically, using the Mascot Search Engine (Mascot Daemon Version 2.3.2). Type of search used was MS/MS Ion Search using Trypsin/P. Carbamidomethyl (C) was set as a fixed modification, and variable modifications were as follows: acetyl (N-term), dioxidation (M), Gln to pyro-Glu (N-term Q), oxidation (M), deamidation (NQ), and phosphorylation (STY).
Peptide mass tolerance was ±10 ppm (# 13C = 2) with a fragment mass tolerance of ±0.6 Da. Maximum number of missed cleavages was 2.
The mass spectrometry proteomics data have been deposited to the ProteomeXchange Consortium via the PRIDE (Perez-Riverol et al., 2019) partner repository with the dataset identifier PXD023258.

Kinase assays
Forty microlitre reactions were set up containing 40 mM Tris-HCl pH 7.5, 100 mM ATP (Adenosine triphosphate), 10 mM MgCl 2 , and 2 mg of either BUB-1 (259-332) or H1. At t = 0, 15 ng/ml Cdk1/ Cyclin B was added, before incubation at 30˚C for 30 min. Aliquots were taken immediately after Cdk1/CyclinB addition at t = 0 and then again after the 30 min incubation. All samples were then incubated at 70˚C for 15 min in a final concentration of 1Â LDS buffer. Sodium dodecyl sulfate-polyacrylamide gel electrophoresis (SDS-PAGE) was then conducted on a NuPage 4-12% Bis-Tris gel (Thermo) with MES buffer before being stained with ProQ Diamond (Thermo) and imaged using Bio-Rad ChemiDoc. Once fluorescence was recorded, Coomassie staining was performed. For the western blot, SDS-PAGE was conducted as above with 67 ng of substrate protein per well before the western was conducted using a nitrocellulose membrane (GE Healthcare) and 1Â NuPage transfer buffer (Thermo). The membrane was blocked using Intercept PBS blocking buffer (LI-COR), the primary antibodies used were anti-GST at 1:1000 (made in sheep), and anti-phospho Ser 283 1:20,000 (made in rabbit). Secondary antibodies were anti-sheep IRDye 680RD anti-rabbit 800CW (LI-COR), both at 1:50,000. The membrane was then imaged using LI-COR Odyssey CLx.
Expression and purification of PPTR-2 PPTR-2 was expressed from pHISTEV30a vector as a 6xHis-and Strep-tagged protein (plasmid fgp_445) in Escherichia coli strain BL21 (DE3) and the bacterial culture was incubated overnight at 37˚C with shaking at 220 rpm. Bacteria were grown in TB medium at 37˚C with shaking at 220 rpm until OD600 reached~0.6-0.8 and induced with 150 mM IPTG. Induction was performed at 18˚C with shaking at 220 rpm for~16 hr. Cells were pelleted and lysed by sonication in 50 mM NaP, 300 mM NaCl, 10 mM imidazole, 10% glycerol, 0.5 mM TCEP, (tris(2-carboxyethyl)phosphine) and protease inhibitors. After binding to a Ni-NTA column, protein was washed with 20 mM imidazole and then eluted with 350 mM imidazole. The tag was cleaved with 6xHis-tagged TEV (Tobacco Etch Virus Protease) protease overnight at 4˚C, and the tag and protease were removed from the sample by binding to Ni-NTA. PPTR-2 was concentrated and further purified using a HiLoad 16/600 Superdex 200 pg size exclusion column.

Fluorescence polarisation
The following peptides were synthesised by peptides and elephants GmbH: BUB-1 FITC-Ahx-NPRRRHLSPVSEKTVDDEEE, pBUB-1 FITC-Ahx-NPRRRHLphSPVSEKTVDDEEE, and LAVA FITC-Ahx-NPRRRHASPASEKTVDDEEE. Reactions (35 ml) were set up in FP buffer (50 mM NaP pH 7.5, 150 mM NaCl, 0.5 mM TCEP) containing peptide concentrations 0.5-1 mM. These were then used to create a 1:2 serial dilution series using FP buffer containing the same peptide concentrations as above as well as the indicated concentration of PPTR-2. Reactions were left for 30 min before triplicates of each dilution were aliquoted into a black 384-well plate, centrifuged (2 min, 2000 rpm), and analysed using the PheraStar FS.

Image analysis and statistics
For time-dependent analysis, metaphase I was taken as time = 0 s. This frame was chosen as the previous frame where the first indication of chromosome separation was visible. All image analysis was done in Fiji (Schindelin et al., 2012). For total intensity measurements within the meiotic spindle, images were thresholded and binary images were generated using the ReinyEntropy method and used to automatically generate the regions of interest (ROIs) for each slice (z) and time point (t) or in the sum-projected image. Going through all the slices was particularly necessary when measuring protein intensity associated with a specific structure/location, since the angle of the spindle can lead to erroneous analysis. All ROIs were recorded and, in order to get background measurements, the ROIs were automatically placed on a different oocyte region, away from the spindle. Backgroundsubstracted intensity values were then normalised to the maximum intensity value of the control video using Graphpad Prism 7.0 and are presented as mean ± s.e.m.
Central spindle to chromosome ratio for PPTR-2::GFP ( Figure 4G) was obtained as follows. Images were selected at early anaphase (t = 40 s), and to obtain the chromosome ROIs, we used the mCherry::histone channel to create a mask. These ROIs were transferred to the PPTR-2::GFP channel, and the intensity was measured as described above. The region between the chromosomes was selected intensities were measured to obtain the central spindle intensity. Background corrected values were used to obtain the ratio central spindle/chromosome. Results are shown as median with interquartile range, and differences were analysed using an unpaired two-tailed t-test with Welch's correction.
For the alignment/congression analysis, we selected videos in which the spindles were contained in a single Z-plane at À80 s. There, we established the spindle axes with a line extending from pole to pole and the 'metaphase plate' with a perpendicular line in the middle of the spindle (see Figure 2-figure supplement 3). A line was drawn on the long axes of the bivalents, and the angle between this line and the spindle axis was measured ('q'). Additionally, for each bivalent, the distance ('d') between the centre of the bivalent and the metaphase plate was measured.
Contingency tables were analysed using the Fisher's exact test (two tailed), and the p values are presented in the figures and/or in the text.

Generation of supplementary videos
The 4D TIFF files were converted to video (.avi) files using a custom-made macro that uses the Stack-Reg Fiji plugin for image registration. Videos were assembled using maximum-intensity projections; hence, the videos might not match a specific panel within the main figures, which are single slices or partial projections in order to highlight specific characteristics.