Formation of one procentriole next to each pre-existing centriole is essential for centrosome duplication, robust bipolar spindle assembly and maintenance of genome integrity. However, the mechanisms maintaining strict control over centriole copy number are incompletely understood. Here we show that Plk4 and STIL, the key regulators of centriole formation, form a protein complex that provides a scaffold for recruiting HsSAS-6, a major component of the centriolar cartwheel, at the onset of procentriole formation. Furthermore, we demonstrate that phosphorylation of STIL by Plk4 facilitates the STIL/HsSAS-6 interaction and centriolar loading of HsSAS-6. We also provide evidence that negative feedback by centriolar STIL regulates bimodal centriolar distribution of Plk4 and seemingly restricts occurrence of procentriole formation to one site on each parental centriole. Overall, these findings suggest a mechanism whereby coordinated action of three critical factors ensures formation of a single procentriole per parental centriole.
Centrosomes are the major microtubule organizing centre in most of animal cells and composed of a pair of centrioles surrounded by pericentriolar material. Centriole formation is indispensable for centrosome duplication and must be tightly coordinated with cell cycle progression to ensure robust formation of bipolar mitotic spindles and proper chromosome segregation. Centriole formation begins with the assembly of the cartwheel structure that mainly dictates the universal radial ninefold symmetry of centrioles, followed by attachment of peripheral centriolar microtubules and further centriole elongation1,2,3. Despite the recent notable progress in our understanding of the molecular and structural principles of centriole assembly, the mechanisms ensuring formation of only one procentriole at the base of each parental centriole per cell division cycle remain incompletely understood.
An evolutionarily conserved core pathway for centriole assembly includes the following five major components: Cep192/DSpd-2/SPD-2, Plk4/Sak/ZYG-1, HsSAS-6/DSas-6/SAS-6, STIL/Ana2/SAS-5 and CPAP/DSas-4/SAS-4 (refs 1, 2, 3). Among these components, Plk4 (refs 4, 5), HsSAS-6 (refs 6, 7) and STIL8,9,10,11 particularly may play an important role in controlling centriole number, since their overexpression induces concurrent formation of multiple procentrioles around a parental centriole8,9,10,12,13.
The conserved proteins of SAS-6 family are known to be a crucial element of a centriolar cartwheel structure14,15,16,17. Whereas it seems that nine of SAS-6 rod-shaped homodimers self-assemble into the central part of the cartwheel14,15,16, there could be additional factors strictly regulating this process or other cartwheel components facilitating SAS-6 self-assembly at the onset of procentriole formation. Given that Plk4 acts upstream of HsSAS-6 and STIL8,9,10,12,13, and also that HsSAS-6 and STIL appear to be interdependent for their loading to the centrioles8,9,10, Plk4 and STIL are plausible candidates for regulating HsSAS-6 oligomerization for cartwheel assembly. Although their relationship in other species appears to be mostly conserved6,7,18,19,20,21,22,23,24, how their collaborative action regulates the onset of centriole formation remains elusive. Moreover, the critical substrates of Plk4, a key kinase for centriole duplication, and how the kinase reaction triggers the onset of procentriole formation remain to be discovered.
In this study, we identify STIL as a critical substrate of Plk4, and show that the phosphorylation event leads to formation of the STIL/HsSAS-6 complex and initiation of procentriole assembly. Furthermore, we demonstrate negative feedback in which centriolar recruitment of the STIL/HsSAS-6 complex in turn limits distribution of centriolar Plk4 through the ubiquitin–proteasome pathway. This coordinated action of the three key factors triggers the onset of procentriole formation and, concurrently, restricts the occurrence of procentriole formation to one site per parental centriole.
Plk4 recruits STIL to the centrioles by direct binding
First, to investigate the physical interactions between the three key factors for centriole assembly, we conducted co-immunoprecipitation analysis with human 293T cells expressing FLAG-tagged full-length Plk4 or Plk4ΔPEST lacking the first PEST destruction motif25, and tested whether the Plk4 proteins interact with endogenous STIL or HsSAS-6 proteins. This analysis revealed that Plk4-FLAG full-length interacts with endogenous STIL, but not with HsSAS-6 (Fig. 1a). Furthermore, we found that a higher amount of endogenous STIL could be co-immunoprecipitated with Plk4ΔPEST-FLAG owing to the increase in the expression levels of Plk4ΔPEST-FLAG compared with those of Plk4-FLAG full length (Fig. 1a). However, we could not detect such a robust interaction in the case of a kinase-dead mutant of Plk4ΔPEST-FLAG, suggesting that STIL preferentially interacts with Plk4 wild-type (WT) rather than the kinase dead. We also found that the interaction requires the two tandem polo boxes, PB1 and PB2, but not the C-terminal PB3 of Plk4 (Supplementary Fig. 1a–d)5,26. Using human influenza hemagglutinin (HA) tagged deletion constructs of STIL, we narrowed down the STIL domain that is required for Plk4 binding to the short conserved coiled-coil domain23 (Fig. 1b–d and Supplementary Fig. 1e,f). Moreover, yeast two-hybrid and in vitro binding assays established that Plk4 directly bound to the STIL fragments containing the CC domain presumably in a kinase-activity-dependent manner (Fig. 1e and Supplementary Fig. 1g,h).
We therefore reasoned that the physical interaction between the two proteins might be needed for centriolar recruitment of STIL. We depleted endogenous STIL using short interfering RNAs (siRNAs) against the 3′-untranslated region (3′UTR) and expressed STIL full-length or deletion constructs tagged with HA at comparable levels in human U2OS cells (Supplementary Fig. 1a). We found that whereas centriole numbers were reduced in the majority of interphase cells upon depletion of endogenous STIL, expression of exogenous full-length STIL could functionally rescue this phenotype (~26% and ~57% of cells with ≥4 centrioles, respectively; Fig. 1f) and frequently induced formation of multiple procentrioles next to each pre-existing centriole. In contrast, expression of the N-terminal fragment of STIL rescued centriole formation in only ~13% of cells (Fig. 1f) even though this fragment efficiently localized to the centrioles, indicating that the C-terminal region of STIL is crucial for centriole formation. Importantly, we determined that STIL proteins lacking the CC domain did not localize to the centrioles (~21% of cells with centriolar STILΔCC, compared with ~76% of cells with centriolar STIL FL; Fig. 1f) and failed to rescue centriole formation. Overall, these findings indicate that STIL is recruited to the centrioles by direct binding to Plk4 through its conserved CC domain, and that this interaction is necessary for centriole formation.
STIL STAN motif is crucial for HsSAS-6 centriolar targeting
We then investigated how the C-terminal region of STIL contributes to centriole formation. Since centriolar loading of HsSAS-6 is dependent on STIL8,9,10, we monitored whether HsSAS-6 proteins are present at centrioles when the C-terminal region or the conserved STAN motif23 of STIL was depleted. We first confirmed that whereas centriolar loading of HsSAS-6 was significantly reduced upon depletion of endogenous STIL, expression of STIL full length restored the localization of HsSAS-6 around the mother centriole (~40% and ~85% of cells with centriolar HsSAS-6, respectively; Fig. 2a). Intriguingly, we found that the STIL proteins lacking the STAN motif failed to recruit HsSAS-6 to the centrioles even though they robustly localized to the centrioles (~5% of cells with centriolar HsSAS-6; Fig. 2a and Supplementary Fig. 2a,b). These data indicate that the STAN motif is crucial for centriolar targeting of HsSAS-6.
Plk4 kinase activity promotes STIL/HsSAS-6 interaction
It has been shown that the functional homologues of STIL: SAS-5 in Caenorhabditis elegans7 and Ana2 in Drosophila melanogaster23, can directly bind to SAS-6 proteins. However, in recent studies, a direct interaction between STIL and HsSAS-6 could not be detected9,10. We therefore hypothesized that Plk4 might regulate the mode of their interaction in human cells. To test this idea, we conducted co-immunoprecipitation experiments using 293T cells expressing Plk4ΔPEST-FLAG and Myc-HsSAS-6 proteins. Interestingly, we found that endogenous STIL was detected in the immunoprecipitated fraction of HsSAS-6 in cells expressing Plk4ΔPEST-FLAG and Myc-HsSAS-6, whereas this was not the case in cells expressing kinase-dead Plk4ΔPEST-FLAG and Myc-HsSAS-6 (Fig. 2b). This result prompted us to address whether phosphorylation of STIL by Plk4 facilitates a direct interaction between STIL and HsSAS-6.
To examine this, we used a combined biochemical approach using in vitro kinase assays with recombinant STIL N3C and Plk4ΔPEST-FLAG, followed by in vitro pull-down assays with recombinant maltose-binding protein (MBP) tagged HsSAS-6 (Fig. 2c). We found that Plk4ΔPEST efficiently phosphorylates STIL N3C in vitro (Supplementary Fig. 3c). Remarkably, we demonstrated that the phosphorylated STIL N3C directly bound to MBP-HsSAS-6 in vitro (Fig. 2d and Supplementary Fig. 2c,d). By contrast, this interaction was abolished when the STAN motif was removed from STIL N3C (Fig. 2e). This is in line with the observation that the STAN motif is crucial for centriolar loading of HsSAS-6 (Fig. 2a). To further narrow down the region of STIL for directly binding to HsSAS-6, we generated several deletion mutants within the C-terminal fragment of STIL (Fig. 2f,g and Supplementary Fig. 2e). As expected, amino acid (a.a.) 1,061–1,083 and a.a. 1,106–1,147 regions in the STAN appeared to be required for the interaction between the phosphorylated STIL and HsSAS-6 (Fig. 2f and Supplementary Figs 2e and 3a). Furthermore, we demonstrated that the STIL STAN motif phosphorylated by Plk4 is sufficient for binding to HsSAS-6 (Fig. 2g). Overall, these findings support the notion that phosphorylation of STIL by Plk4 facilitates the direct interaction between the conserved STAN motif of STIL and HsSAS-6, leading to centriolar loading of HsSAS-6.
STIL is phosphorylated by Plk4 in vitro and in vivo
We next sought to analyse the phosphorylation of STIL by Plk4 to further investigate its biological relevance for centriole formation. We first conducted in vitro kinase assays with Plk4ΔPEST-FLAG and the indicated four STIL fragments, and found that the fragments STIL N3 and C were efficiently phosphorylated by Plk4ΔPEST-FLAG in vitro (Fig. 3a). Intriguingly, we found a significant shift in the mobility of the phosphorylated STIL C fragment due to hyper-phosphorylation by Plk4ΔPEST (Fig. 3a,b). Using mass spectrometry (MS) analysis and phospho-specific antibodies, we identified seven and five phosphorylated serine/threonine residues within the N3 and C fragments, respectively (Fig. 3a,c and Supplementary Fig. 3a–c). We next investigated whether STIL is also phosphorylated by Plk4 in vivo. We observed a shift in the mobility of endogenous STIL when expressing Plk4ΔPEST-FLAG in U2OS cells (Fig. 3d). The shift was abolished upon treatment of the cell lysate with λ-phosphatase, indicating that endogenous STIL proteins were phosphorylated by Plk4 in vivo (Fig. 3d). Similarly, we found a significant band shift of STIL N3C fragment in U2OS cells expressing Plk4ΔPEST-FLAG, which is suggestive of the occurrence of multiple phosphorylations on the STIL fragment (Fig. 3e). Importantly, in addition, the shift of STIL N3C was drastically attenuated by mutating all the identified phosphorylated residues to alanine, indicating that these sites can be phosphorylated in vivo (Fig. 3e).
We then set out to examine the biological relevance of these phosphorylation sites for STIL function. We first found that the mutation of all seven S/T residues in the STIL N3 region or all five S/T residues in the STIL C region to alanine did not affect the interaction between Plk4 and STIL (Supplementary Fig. 4a–d,f). Moreover, since the N3 region of STIL is sufficient for binding to Plk4 (Fig. 1e), we further analysed deletion mutants within the N3 and confirmed that the conserved coiled-coil domain is essential for the Plk4/STIL interaction (Fig. 1b–d and Supplementary Fig. 4a–c,f). However, when mutating the sole S/T residue, T727, within the CC to alanine, we still detected the Plk4/STIL interaction (Supplementary Fig. 4a,g). These data suggest that while Plk4 kinase activity itself seems to be critical for the interaction, the phosphorylation of STIL by Plk4 is possibly dispensable for the interaction. We speculate that Plk4 autophosphorylation27,28 can modulate the state of Plk4 self-assembly, leading to the direct binding to the CC domain of STIL.
Critical sites in the STAN for HsSAS-6 centriolar targeting
Given that the phosphorylated STAN motif of STIL itself is sufficient for interacting with HsSAS-6 in vitro (Fig. 2f,g), we reasoned that S1061 and S1116 that are within the STAN motif and phosphorylated by Plk4 in vitro could be critical residues to mediate the STIL/HsSAS-6 interaction (Fig. 4a). To address this idea, we first conducted an alanine mutational scan for the S/T sites within the STAN motif, which led to the identification of three critical sites (S1061, S1116 and T1119) for the STIL/HsSAS-6 interaction in vitro (Fig. 4b and Supplementary Fig. 5a). As we could not find any evidence of phosphorylation at T1119 by MS, we assume that T1119 could be important for the structural arrangement of the STAN motif rather than being a phosphorylation site. Interestingly, S1061 and S1116 are the specific residues that are highly conserved from human STIL to Drosophila Ana2 (Fig. 4a), implying their biological significance throughout evolution. Second, we investigated whether alanine substitution mutants of the two phosphorylation sites of STIL have the ability to rescue the defect in the centriolar loading of HsSAS-6 and centriole formation when endogenous STIL proteins are depleted. Strikingly, we found that although mutating both residues to alanine did not affect centriolar targeting of STIL (Fig. 4c,d), expression of the S1061A, S1116A or 2A double mutant of STIL failed to rescue centriolar loading of HsSAS-6 and centriole formation in the cells depleted of endogenous STIL (centriolar HsSAS-6; ~4% for STIL 2A and ~78% for STIL WT: ≥4 centrin foci; ~2% for STIL 2A and ~50% for STIL WT; Fig. 4c,d and Supplementary Fig. 5b–f). On the other hand, expression of the STIL alanine mutants at three other MS-identified phosphorylation sites (S1181, T1238 or T1250) or the STIL deletion mutant lacking all the seven MS-identified phosphorylation sites in the N3 region mostly rescued the phenotype provoked by depletion of endogenous STIL (Supplementary Figs 4e and 5d–f). To further characterize the two critical phosphorylation sites in STIL, S1061 and S1116, we generated phosphomimetic mutants at these residues and investigated their function for centriole formation. Importantly, we found that expression of a phosphomimetic STIL mutant at S1061 under an attenuated human cytomegalovirus (CMV) promoter induced centriole overduplication more efficiently than that of STIL WT in the same condition (Supplementary Fig. 6a,b). Consistently, a phosphomimetic mutant at S1061 of the STIL STAN could interact with MBP-HsSAS-6 in vitro even without being phosphorylated by Plk4 (Supplementary Fig. 6c). On the other hand, introducing of a phosphomimetic mutation at S1116 impaired Plk4-mediated STIL/HsSAS-6 interaction in vitro, and centriolar targeting of HsSAS-6 in human cells (Supplementary Fig. 6d and data not shown). Given that the MS analysis revealed that this residue was phosphorylated by Plk4 in vitro and also that it is found to be phosphorylated in mammalian cells (PhosphoSitePlus database), we favour the possibility that substitution of S1116 to D/E could not mimic the phosphorylation state, but rather reduced the function of STIL. However, alternatively, it is also possible that S1116 is just critical for structural integrity of the STAN motif and/or its function independently of being phosphorylated. Taken together, we propose that S1061 and S1116 of STIL can be the most important phosphorylation sites for the STIL/HsSAS-6 interaction and resulting centriolar targeting of HsSAS-6 in procentriole formation.
Bimodal centriolar distribution of Plk4 during cell cycle
We next hypothesized that the interaction between Plk4 and STIL might have an influence on the centriolar recruitment and/or maintenance of Plk4. To explore this possibility, we examined the distribution of endogenous Plk4 (ref. 29) in U2OS cells released from a nocodazole arrest and fixed at successive time points. Intriguingly, we found a bimodal distribution of Plk4 at centrioles depending on the cell cycle progression (Fig. 5a–c, Supplementary Figs 1b and 7a,b). As previously reported30,31, we observed that most of the cells exhibited one intense focus of Plk4 on each parental centriole during prophase/metaphase (~90%, ~0.3 μm in diameter; Fig. 5a–c and Supplementary Fig. 7a,b), and also that the signal intensity of the foci substantially declined around telophase. However, in the next cell cycle, we detected endogenous Plk4 localized in a ring-like manner around the parental centrioles (~0.62 μm in diameter; Fig. 5a–c and Supplementary Fig. 7a) and partially overlapped with a Cep152 ring, as a marker for parental centrioles (Fig. 5a)32,33. Quantitative analyses indicated that the majority of cells in G1 phase harboured a ring-like pattern of endogenous Plk4 (~65% at 8–10 h after the release; Fig. 5a,c). Remarkably, we further found that the ring-like pattern of centriolar Plk4 changed back into a dot on the parental centriole wall in G1/S phase (~52% as a dot at 13 h after the release; Fig. 5a,c). Co-staining of endogenous Plk4 and STIL revealed that when STIL localized to centrioles in G1/S phase, centriolar distribution of Plk4 was always restricted to a spot and largely overlapped with centriolar STIL foci (Fig. 5a–c). We could hardly detect the existence of a ring-like pattern of Plk4 with STIL foci at centrioles, suggesting that they are mutually exclusive. In addition, we noted that STIL and HsSAS-6 appeared to be loaded to the centrioles almost concomitantly and precisely co-localized with each other (data not shown)31. We therefore assumed that the existence of STIL and HsSAS-6 might allow the conversion of the centriolar Plk4 ring into a dot.
To test this, we examined the centriolar distribution of Plk4 when STIL or HsSAS-6 was depleted from U2OS cells. Interestingly, we found that most of the interphase cells depleted of STIL or HsSAS-6 harboured the ring-like arrangement of centriolar Plk4 while the cell cycle progression was not affected (Plk4 ring; ~18% for siCnt, ~91% for siHsSAS-6 and ~71% for siSTIL; Fig. 5d,e, and Supplementary Figs 1a and 7c,d). In addition, the expression of STIL ΔCC in STIL siRNA-treated cells did not suppress the increase in the number of cells with a ring-like pattern of centriolar Plk4 (~59% for siSTIL+empty vector and ~60% for siSTIL+ΔCC; Fig. 5e and Supplementary Fig. 7e), indicating that the existence of STIL and HsSAS-6 at centrioles is required for the conversion of the centriolar Plk4 ring into a dot.
The interaction of Plk4 with STIL protects centriolar Plk4
Given that the expression levels of Plk4 are known to be regulated by trans-autophosphorylation that induces proteolytic degradation by the E3 ubiquitin ligase Skp-Cullin-F-box containing complex, SCFSlimb/β-TrCP and the ubiquitin–proteasome-dependent pathway in D. melanogaster and mammalian cells27,28,34,35, we hypothesized that the conversion of centriolar Plk4 followed by centriolar STIL/HsSAS-6 loading might involve protein degradation through the ubiquitin–proteasome pathway mediated by the SCF complex or other E3 ligases. To address this, we synchronized U2OS cells in G1/S phase with aphidicolin and transiently treated with MG132, a proteasome inhibitor. In the cells treated without MG132, endogenous Plk4 localized mostly as a dot and resided with STIL foci at centrioles (Plk4 ring; ~8%; Fig. 6a,b and Supplementary Fig. 7f). In stark contrast, when treated with MG132, majority of the cells harboured a complete ring of Plk4 with STIL foci at the centrioles, which we could hardly detect in normal cycling cells (Plk4 ring; ~93%; Fig. 6a,b and Supplementary Fig. 7c,f). In this situation, Plk4 proteins were primarily enriched at the position overlapping with STIL foci as compared with the rest of the ring. This implies that centriolar STIL could interact with and protect Plk4 proteins from protein degradation, whereas the residual centriolar Plk4 proteins are normally degraded.
To address this model, we next investigated whether overexpression of STIL full-length or mutant proteins stabilizes centriolar Plk4. We found that whereas low expression of HA-STIL full length in the cells depleted of endogenous STIL restored the population of cells containing Plk4 dots at the centrioles, overexpression of HA-STIL full-length, ΔSTAN or 5A mutant proteins stabilized centriolar Plk4 as a ring overlapping with the STIL proteins (Fig. 6c). Considering that the centriolar loading of HsSAS-6 and procentriole formation were inhibited in the cells expressing HA-STIL ΔSTAN or 5A mutant, this result suggests that centriolar presence of STIL might be sufficient for stabilizing centriolar Plk4 in this situation. Intriguingly, when expressing the PACT-STIL ΔCC mutant that fails to interact with Plk4, but still localizes to centrioles, we found that expression of the STIL mutant proteins maintained centriolar Plk4 as a ring overlapping with the STIL mutant proteins and recruited HsSAS-6 to centrioles (Fig. 6c and Supplementary Fig. 7g). This result suggests that PACT-STIL ΔCC can bypass the requirement of STIL function for centriolar loading of HsSAS-6, and also that close-range presence of STIL and Plk4 at centrioles, or their transient interaction could be critical for protecting centriolar Plk4 from protein degradation and for centriolar recruitment of HsSAS-6. However, we cannot exclude the possibility that residual binding activity of overexpressed STIL ΔCC to Plk4 somehow managed to facilitate those events.
Using biochemical analysis in human 293T cells, we next sought to investigate whether STIL protects Plk4 from protein degradation. Importantly, we demonstrated that expression of STIL efficiently inhibited ubiquitination of Plk4ΔPEST-FLAG WT (Fig. 6d). Given that the first PEST domain of Plk4 contains the site recognized by the SCF complex25,34, the degradation of Plk4ΔPEST proteins might be regulated by another E3 ubiquitin ligase. Furthermore, we found that expression of STIL full-length stabilized Plk4ΔPEST-FLAG WT, whereas that was not the case when co-expressing STILΔN3, which lacks the binding region to Plk4 (Fig. 6e). We also noted that STIL seemed to stabilize activated Plk4ΔPEST-FLAG WT proteins (p-Plk4ΔP) (Fig. 6e and Supplementary Fig. 7h). This is in agreement with the observation that STIL preferentially interacts with Plk4 WT rather than the kinase dead (Fig. 1). Taken together, these data suggest that the interaction between STIL and Plk4 protects Plk4 from protein degradation mediated by the ubiquitin–proteasome pathway.
In conclusion, our findings uncover a molecular basis for the onset of centriole formation by demonstrating that direct association of STIL with Plk4 and STIL phosphorylation by Plk4 lead to centriolar loading of HsSAS-6 for cartwheel assembly (Fig. 7). Furthermore, our study suggests a negative feedback model in which centriolar STIL/HsSAS-6 recruitment limits centriolar distribution of Plk4 to one site per parental centriole (Fig. 7 and Supplementary Fig. 7i). This coordinated action promotes formation of a single procentriole and, concurrently, could inhibit formation of another procentriole, thus presumably contributing to maintenance of one procentriole next to each parental centriole.
How could phosphorylated STIL facilitate cartwheel assembly by direct binding to HsSAS-6? It could be structurally critical for the spatial arrangement and connection between HsSAS-6 homodimers. Indeed, it has been shown in D. melanogaster that co-overexpression of DSas-6 and Ana2 induces formation of highly ordered tubules with the structures reminiscent of the centriolar cartwheel hub20. However, to drive centriole overduplication through efficient centriolar recruitment of extra DSas-6 and Ana2, additional co-expression with Plk4/Sak is needed20. These observations are compatible with our findings, implying that the interplay between the three key factors that we demonstrated may underlie the centriole assembly pathway across species. On the other hand, in C. elegans, given that the interaction between SAS-5 and SAS-6 seems to be detectable presumably even in the absence of ZYG-1 (refs 7, 36), and also that ZYG-1 can directly bind to37 and phosphorylate SAS-6 (ref. 38) for centriole assembly, the regulatory mechanism for cartwheel assembly may be somehow different in this organism along with its structural divergence of the centriole structure.
It has been recently shown that the expression levels of Plk4 are regulated by trans-autophosphorylation that mediates proteolytic degradation by the E3 ubiquitin ligase SCFSlimb/β-TrCP and the ubiquitin–proteasome-dependent pathway in D. melanogaster39,40 and mammalian cells27,28. The reduction of centriolar Plk4 followed by centriolar recruitment of the STIL/HsSAS-6 complex seems to involve protein degradation through the ubiquitin–proteasome pathway (Fig. 5d). It will be therefore important in the future study to further investigate the detailed mechanisms how the recruitment of STIL/HsSAS-6 allows SCFSlimb/β-TrCP and/or other E3 ubiquitin ligases to target for degradation of centriolar Plk4 proteins that do not form a complex with STIL. Considering that physical association and co-localization of Plk4 and STIL at one site on the parental centriole wall is dependent on the kinase activity of Plk4, it is possible that a complex formation between active Plk4 and STIL prevents Plk4 from undergoing protein degradation. Alternatively, any other protein that STIL brings to centrioles may protect Plk4 from the protein degradation. Furthermore, given that the presence of the SAS-5/SAS-6 complex at centrioles is needed for the diminution of centriolar ZYG-1 during interphase18, it is tempting to speculate that the feedback mechanism that we demonstrated in this study is a conserved system for tight control of centriole copy number throughout evolution.
Based on the findings in this study, further study will be needed to establish the structural model how the sequential physical interactions between Plk4/STIL/HsSAS-6 proteins lead to the assembly of a core structure for initiating cartwheel assembly.
Cell culture and cell lines
Human U2OS and HEK293T cells were obtained from the European Collection of Cell Culture (ECACC). U2OS cells stably expressing GFP-centrin1 were gifted from Bornens41. These cells were cultured in DMEM supplemented with 10% fetal bovine serum at 37 °C in 5% CO2 incubator.
Cell cycle synchronization and flow cytometry analysis
For cell synchronization at prometaphase, cells were treated with 100 ng ml−1 nocodazole for 14 h, washed three times with PBS and released in fresh medium. For cell cycle arrest in G1/S phase, cells were treated with 2 μg ml−1 aphidicolin for 24 h.
For flow cytometry analyses, cells cultured on dishes were trypsinized, washed twice with PBS and fixed in 70% cold ethanol at −20 °C at each time point. The fixed cells were washed with PBS twice and incubated with Muse Cell Cycle reagents at room temperature (RT) for 30 min. The DNA contents of the cells were then measured using Muse Cell Analyzer (Merck Millipore). Flow cytometry analysis was repeated at least two times.
Molecular biology and RNA interference
The following siRNAs were used: Stealth siRNA (Life Technologies) against 3′UTR of HsSAS-6 (5′-GAGCUGUUAAAGACUGGAUACUUUA-3′) and negative control Low GC Duplex no. 2 (12935110); custom siRNA (Sigma Genosys) against 3′UTR of Plk4 (5′-CTCCTTTCAGACATATAAG-3′); custom siRNA (JBios) against 3′UTR of STIL (5′-GTTTAAGGGAAAAGTTATT-3′).
pcDNA3 constructs encoding Plk4 full-length FLAG, a kinase-dead Plk4 [K41M]-FLAG, Plk4Plk4ΔPEST-FLAG and Plk4[K41M]ΔPEST-FLAG were gifts from Dr Hiroyuki Mano. The mammalian expression constructs for HA-STIL full-length, deletion mutants, alanine substitution mutants and phosphomimetic mutants were created by insertion of subcloned fragments into SpeI-digested modified pCMV5-HA vector or using PrimeSTAR mutagenesis basal kit (TaKaRa). pcDNA3-Plk4ΔPEST–[ΔPB1]/[ΔPB2]/[ΔPB3]–FLAG expression constructs were created using PrimeSTAR mutagenesis basal kit (TaKaRa). Since expression levels of Plk4ΔPΔPB3-FLAG were high compared with those of the other Plk4 mutants used in Supplementary Fig. 1d, the Plk4ΔPΔPB3-FLAG plasmid was transfected into cells with half the amount of the other Plk4 plasmids.
Transfection of siRNA or DNA constructs into U2OS and HEK293T cells was performed using Lipofectamine RNAiMAX (Life Technologies) or Lipofectamine 2000 (Life Technologies) according to the manufacturer’s instructions. Unless otherwise noted, transfected cells were analysed 48–72 h after transfection with siRNA and 24 h after transfection with DNA constructs.
The following primary antibodies were used in this study: rabbit polyclonal antibodies against STIL (Abcam, ab89314, indirect immnunofluorescence (IF) 1:500, western blotting (WB) 1:1,000), Cep152 (Bethyl Laboratories, A302-480A, IF 1:1,000), HA-tag (Abcam, ab9110, IF 1:1,000, WB 1:1,000); mouse monoclonal antibodies against centrin-2 (Millipore, 20H5, IF 1:1,000), HsSAS-6 (Santa Cruz Bio-technology, Inc., sc-81431, WB 1:1,000), Plk4 (Merck Millipore, clone 6H5, MABC544, IF 1:500), FLAG-tag (Sigma, F1804, IF 1:1,000, WB 1:1,000), HA-tag (Covance, MMS-101P, WB 1:500) and α-tubulin (Sigma, DM1A, WB 1:2,000). P-S1061 rabbit antibodies were raised against C+NGVDL[pS]MEAN, where [pS] is a phosphorylated serine residue (Eurofins Operon). The following secondary antibodies were used: Alexa Fluor 488 goat anti-mouse IgG (H+L) (Molecular Probes, 1:500), Alexa Fluor 568 goat anti-rabbit IgG (H+L) (Molecular Probes, 1:500) for IF; goat polyclonal antibodies horseradish peroxidase against mouse IgG (Promega, W402B, 1:5,000), rabbit IgG (Promega, W401B, 1:5,000) for WB.
Indirect immunofluorescence and immunoblotting
For indirect immunofluorescence microscopy, the cells cultured on coverslips were fixed using −20 °C methanol for 10 min. The cells were then permeabilized with PBS/0.05% Triton X-100 (PBSX) for 5 min, washed with PBS three times and incubated for blocking in 1% BSA in PBSX for 30 min at RT. The cells were then incubated with primary antibodies for 3 h at RT, washed with PBSX three times and incubated with secondary antibodies for 1 h at RT. The cells were thereafter washed with PBSX twice, stained with 0.2 μg ml−1 Hoechst 33258 (Dojindo) in PBS for 5 min at RT, washed again with PBSX and mounted onto glass slides. Counting the number of immunofluorescence signals was performed by using an Axioplan2 fluorescence microscope (Carl Zeiss) with a × 100/1.4 numerical aperture plan-APOCHROMAT objective. Data acquisition for the images and quantification of the signal intensity were performed using DeltaVision Personal DV-SoftWoRx system (Applied Precision) equipped with a CoolSNAP CH350 CCD camera. The images were acquired as serial sections along the z axis and stacked using the ‘quick projection’ algorithm in SoftWoRx. The signal intensities of centriolar Plk4, STIL and HsSAS-6 were quantified using the Data Inspector tool in SoftWorx. The captured images were processed with Adobe Photoshop CS5.1 (version 12.1). We assessed cells from several fields for each experiment, and we were normally blinded to the sample ID during experiments and outcome assessment. Once a field was determined, we counted all cells that matched with the criteria within the field. In the experiments using the cells expressing HA-tagged full-length or mutants of STIL, we counted cells adequately expressing the STIL proteins at comparable levels and excluded cells expressing the STIL proteins at low levels or cells excessively expressing the STIL proteins.
For preparation of human cell lysates for immunoblotting, cells were collected, washed in PBS and lysed by vortexing at 4 °C in lysis buffer (20 mM Tris/HCl pH 7.5, 50 mM NaCl, 1% Triton X-100, 5 mM EGTA, 1 mM dithiothreitol (DTT), 2 mM MgCl2 and 1/1,000 protease inhibitor cocktail (Nakalai Tesque)). Lysates were cleared by centrifugation for 10 min at 13,000 r.p.m. at 4 °C and the supernatant was collected. SDS–polyacrylamide gel electrophoresis (SDS–PAGE) was performed using 7–12% polyacrylamide gels, followed by transfer on Immobilon-P membrane (Millipore Corporation). The membrane was probed with the primary antibodies, followed by incubation with their respective horseradish peroxidase-conjugated secondary antibodies (Promega). Washes were performed in PBS containing 0.02% Tween. The signal was detected as Chemi Doc XRS+ (Bio-Rad). Signal intensity of immunoreactive bands was measured using Adobe Photoshop. Full scan images of the western blots and gels used in the main figures are shown in Supplementary Fig. 8. Unless otherwise specified, the experiments of western blotting were repeated at least three times. In Figs 3c,e and 4b, and Supplementary Figs 2c–e, 4b,c, 5a and 6a were repeated at least two times.
For preparing whole-cell lysates of HEK293T cells, cells were washed by PBS and lysed in ice-cold lysis buffer. The lysates were vortexed for 40 min at 4 °C, and insoluble material was removed after centrifugation for 10 min. For immunoprecipitation of FLAG-tagged Plk4 proteins, whole-cell lysates were incubated with FLAG antibody-conjugated M2 agarose (Sigma) for 2 h at 4 °C. Since the expression levels of FLAG-Plk4 proteins in the cells were very low, we monitored them by using the Flag immunoprecipitation instead of using the input materials. For HsSAS-6 immunoprecipitation, whole-cell lysates were incubated with protein G sepharose for 1 h at 4 °C for preclear, and then incubated for 2 h at 4 °C with protein G agarose that had been incubated with anti-HsSAS-6 antibodies. In both cases, the beads were washed at least four times with lysis buffer and resuspended in SDS sample buffer before loading onto a SDS–PAGE gel.
In vitro kinase assay and MBP pull-down assay
For in vitro kinase assay, HEK293T cells were transfected with Plk4ΔPEST-FLAG WT or kinase-dead using Lipofectamine 2000 (Invitrogen). After 24 h, cells were harvested, treated with lysis buffer (20 mM Tris/HCl, pH 7.5, 150 mM NaCl, 0.5% Triton X-100, 1 mM DTT, 2 mM MgCl2 and 1/1,000 protease inhibitor cocktail (Nacalai Tesque)) and the lysates were immunoprecipitated with beads conjugated to FLAG antibodies. The beads were washed four times with lysis buffer supplemented with additional 500 mM NaCl and twice with kinase buffer (20 mM Tris HCl (pH 7.5), 150 mM NaCl and 1 mM DTT). The beads were then incubated with bacterially expressed recombinant proteins of STIL fragments thereof in 30 μl kinase buffer containing 10 mM MgCl2 and 30 μM ATP without or with 5 μ Ci [γ-32P] ATP. Kinase reactions were performed at 30 °C for 15–90 min and terminated by adding SDS sample buffer. Proteins were separated by SDS–PAGE, stained with SimplyBlue Safe (Invitrogen) and phosphorylation was visualized by autoradiography (Typhoon FLA 9000, GE Healthcare). After the kinase reaction, the resulting materials were subsequently processed for in vitro binding assay with MBP-HsSAS-6 proteins. In vitro kinase assays for Fig. 3a and Supplementary Fig. 3b were repeated three times.
For in vitro MBP pull-down assays in Fig. 2d,e and Supplementary Fig. 2c, after the kinase reaction, the supernatant and eluted fraction with FLAG peptides (Sigma) both of which contained phosphorylated STIL N3C proteins were collected. For other in vitro MBP pull-down assays, only the supernatant was collected. The resulting fractions were then incubated with MBP-HsSAS-6 full length purified from baculovirus/insect cell expression system and thereafter pulled down using amylose resin (New England Biolabs). Input and the protein complexes pulled down with the resins were analysed by western blotting using STIL, HA, FLAG or HsSAS-6 antibodies.
DNAs encoding fragments of human STIL were cloned in pGEX system vectors (GE Healthcare) encoding for glutathione S-transferase (GST) tags. The recombinant protein expression of the fragments was performed in E. coli strain BL21 gold (DE3) in LB medium. Protein expression was induced at 22 °C by addition of 0.3 mM isopropyl-β-D-thiogalactoside and allowed to proceed for 18 h. Cell pellets were lysed by lysozyme treatment and sonication, resuspended in lysis buffer containing 50 mM Tris HCl (pH 7.5), 150 mM NaCl, 2 mM MgCl2, 5 mM EDTA, 1 mM DTT, 1:500 protease inhibitor cocktail (Nacalai Tesque) and 0.5% Triton X-100. The lysates were incubated with Glutathion sepharose beads (GE Healthcare). The beads were then washed 10 times with lysis buffer supplemented with additional 500 mM NaCl. For preparing STIL fragments, proteins were eluted from the beads by removal of the GST tags by PreScission Protease (GE Healthcare) in a cleave buffer containing 20 mM Tris HCl (pH 7.5), 150 mM NaCl and1 mM DTT. For in vitro MBP pull-down assays in Figs 2g and 4b, and Supplementary Figs 2e and 6c,d, GST-fused STIL fragments were eluted by 10 mM glutathione in the cleave buffer.
Since it was not feasible to obtain soluble fraction of GST-fused HsSAS-6 full-length proteins from bacteria, we generated MBP-fused HsSAS-6 full-length proteins using Baculovirus Expression System with Gateway Technology (Invitrogen). In brief, DNA encoding HsSAS-6 full length was cloned into a modified pENTR-1A-5Myc-MBP vector. The expression clone was obtained from the entry clone and a pDEST vector through gateway cloning strategy. The recombinant bacmid was then obtained from DH10Bac E. coli cells transformed with the expression vector, and subsequently transfected to Sf9 insect cells with Cellfectin II reagent (Invitrogen). The titre of recombinant baculovirus was amplified by repeated infection to Sf9 cells. MBP-5Myc-HsSAS-6 full-length proteins were purified from 1 l (~2 × 106 ml–1) culture of the Sf9 cells infected with sufficiently amplified baculovirus for 3 days. The procedure for protein purification was similarly done with amylose resin as described above for GST-fusion proteins.
For MS analysis, to identify Plk4-phosphorylated residues of STIL, the STIL proteins phosphorylated by Plk4ΔPEST-FLAG in vitro were digested into shorter peptides in solution by trypsin. The peptides were subsequently desalted and analysed by a nanoLC-linear ion trap-orbitrap mass spectrometer. MS analysis was repeated two times.
Yeast two-hybrid analysis
Yeast strain L40 (a gift from Masato Kanemaki) was grown in complete medium (yeast extract peptone dextrose; (YPD)) and transformed with a modified version of the vectors pSM671 (bait) and pSM378 (prey; gifts from Satoru Mimura) that contained full length or fragments of Plk4 or STIL. Positive colonies were cultured on yeast plate without leucine and tryptophan (SD–L/–W) in the presence of histidine overnight. On the next day, cells were streaked on SD–L/–W without histidine plates supplemented with 50 mM 3-amino-triazol. Two independent colonies were streaked per sample. Plates were placed at 30 °C for 3 days. Yeast two-hybrid analysis was repeated at least three times.
How to cite this article: Ohta, M. et al. Direct interaction of Plk4 with STIL ensures formation of a single procentriole per parental centriole. Nat. Commun. 5:5267 doi: 10.1038/ncomms6267 (2014).
Gönczy, P. Towards a molecular architecture of centriole assembly. Nat. Rev. Mol. Cell Biol. 13, 425–435 (2012).
Avidor-Reiss, T. & Gopalakrishnan, J. Building a centriole. Curr. Opin. Cell Biol. 25, 72–77 (2013).
Brito, D. A., Gouveia, S. M. & Bettencourt-Dias, M. Deconstructing the centriole: structure and number control. Curr. Opin. Cell Biol. 24, 4–13 (2012).
Bettencourt-Dias, M. et al. SAK/PLK4 is required for centriole duplication and flagella development. Curr. Biol. 15, 2199–2207 (2005).
Habedanck, R., Stierhof, Y. D., Wilkinson, C. J. & Nigg, E. A. The Polo kinase Plk4 functions in centriole duplication. Nat. Cell Biol. 7, 1140–1146 (2005).
Dammermann, A. et al. Centriole assembly requires both centriolar and pericentriolar material proteins. Dev. Cell 7, 815–829 (2004).
Leidel, S., Delattre, M., Cerutti, L., Baumer, K. & Gönczy, P. SAS-6 defines a protein family required for centrosome duplication in C. elegans and in human cells. Nat. Cell Biol. 7, 115–125 (2005).
Vulprecht, J. et al. STIL is required for centriole duplication in human cells. J. Cell Sci. 125, 1353–1362 (2012).
Tang, C. J. et al. The human microcephaly protein STIL interacts with CPAP and is required for procentriole formation. EMBO J. 30, 4790–4804 (2011).
Arquint, C., Sonnen, K. F., Stierhof, Y. D. & Nigg, E. A. Cell-cycle-regulated expression of STIL controls centriole number in human cells. J. Cell Sci. 125, 1342–1352 (2012).
Kitagawa, D. et al. Spindle positioning in human cells relies on proper centriole formation and on the microcephaly proteins CPAP and STIL. J. Cell Sci. 124, 3884–3893 (2011).
Strnad, P. et al. Regulated HsSAS-6 levels ensure formation of a single procentriole per centriole during the centrosome duplication cycle. Dev. Cell. 13, 203–213 (2007).
Kleylein-Sohn, J. et al. Plk4-induced centriole biogenesis in human cells. Dev. Cell 13, 190–202 (2007).
Nakazawa, Y., Hiraki, M., Kamiya, R. & Hirono, M. SAS-6 is a cartwheel protein that establishes the 9-fold symmetry of the centriole. Curr. Biol. 17, 2169–2174 (2007).
Kitagawa, D. et al. Structural basis of the 9-fold symmetry of centrioles. Cell 144, 364–375 (2011).
van Breugel, M. et al. Structures of SAS-6 suggest its organization in centrioles. Science 331, 1196–1199 (2011).
Kilburn, C. L. et al. New Tetrahymena basal body protein components identify basal body domain structure. J. Cell Biol. 178, 905–912 (2007).
Delattre, M., Canard, C. & Gönczy, P. Sequential protein recruitment in C. elegans centriole formation. Curr. Biol. 16, 1844–1849 (2006).
Pelletier, L., O'Toole, E., Schwager, A., Hyman, A. A. & Muller-Reichert, T. Centriole assembly in Caenorhabditis elegans. Nature 444, 619–623 (2006).
Stevens, N. R., Roque, H. & Raff, J. W. DSas-6 and Ana2 coassemble into tubules to promote centriole duplication and engagement. Dev. Cell 19, 913–919 (2010).
Rodrigues-Martins, A., Riparbelli, M., Callaini, G., Glover, D. M. & Bettencourt-Dias, M. Revisiting the role of the mother centriole in centriole biogenesis. Science 316, 1046–1050 (2007).
Rodrigues-Martins, A. et al. DSAS-6 organizes a tube-like centriole precursor, and its absence suggests modularity in centriole assembly. Curr. Biol. 17, 1465–1472 (2007).
Stevens, N. R., Dobbelaere, J., Brunk, K., Franz, A. & Raff, J. W. Drosophila Ana2 is a conserved centriole duplication factor. J. Cell Biol. 188, 313–323 (2010).
Kitagawa, D. et al. PP2A phosphatase acts upon SAS-5 to ensure centriole formation in C. elegans embryos. Dev. Cell 20, 550–562 (2011).
Yamashita, Y. et al. Sak serine-threonine kinase acts as an effector of Tec tyrosine kinase. J. Biol. Chem. 276, 39012–39020 (2001).
Slevin, L. K. et al. The structure of the Plk4 cryptic polo box reveals two tandem polo boxes required for centriole duplication. Structure 20, 1905–1917 (2012).
Guderian, G., Westendorf, J., Uldschmid, A. & Nigg, E. A. Plk4 trans-autophosphorylation regulates centriole number by controlling betaTrCP-mediated degradation. J. Cell Sci. 123, 2163–2169 (2010).
Holland, A. J., Lan, W., Niessen, S., Hoover, H. & Cleveland, D. W. Polo-like kinase 4 kinase activity limits centrosome overduplication by autoregulating its own stability. J. Cell Biol. 188, 191–198 (2010).
Cizmecioglu, O. et al. Cep152 acts as a scaffold for recruitment of Plk4 and CPAP to the centrosome. J. Cell Biol. 191, 731–739 (2010).
Sillibourne, J. E. et al. Autophosphorylation of polo-like kinase 4 and its role in centriole duplication. Mol. Biol. Cell 21, 547–561 (2010).
Sonnen, K. F., Schermelleh, L., Leonhardt, H. & Nigg, E. A. 3D-structured illumination microscopy provides novel insight into architecture of human centrosomes. Biol. Open 1, 965–976 (2012).
Lukinavicius, G. et al. Selective chemical crosslinking reveals a Cep57-Cep63-Cep152 centrosomal complex. Curr. Biol. 23, 265–270 (2013).
Fu, J. & Glover, D. M. Structured illumination of the interface between centriole and peri-centriolar material. Open Biol. 2, 120104 (2012).
Cunha-Ferreira, I. et al. Regulation of autophosphorylation controls PLK4 self-destruction and centriole number. Curr. Biol. 23, 2245–2254 (2013).
Klebba, J. E. et al. Polo-like kinase 4 autodestructs by generating its slimb-binding phosphodegron. Curr. Biol. 23, 2255–2261 (2013).
Qiao, R., Cabral, G., Lettman, M. M., Dammermann, A. & Dong, G. SAS-6 coiled-coil structure and interaction with SAS-5 suggest a regulatory mechanism in C. elegans centriole assembly. EMBO J. 31, 4334–4347 (2012).
Lettman, M. M. et al. Direct binding of SAS-6 to ZYG-1 recruits SAS-6 to the mother centriole for cartwheel assembly. Dev. Cell 25, 284–298 (2013).
Kitagawa, D., Busso, C., Fluckiger, I. & Gönczy, P. Phosphorylation of SAS-6 by ZYG-1 is critical for centriole formation in C. elegans embryos. Dev. Cell 17, 900–907 (2009).
Rogers, G. C., Rusan, N. M., Roberts, D. M., Peifer, M. & Rogers, S. L. The SCF Slimb ubiquitin ligase regulates Plk4/Sak levels to block centriole reduplication. J. Cell Biol. 184, 225–239 (2009).
Cunha-Ferreira, I. et al. The SCF/Slimb ubiquitin ligase limits centrosome amplification through degradation of SAK/PLK4. Curr. Biol. 19, 43–49 (2009).
Piel, M., Meyer, P., Khodjakov, A., Rieder, C. L. & Bornens, M. The respective contributions of the mother and daughter centrioles to centrosome activity and behavior in vertebrate cells. J. Cell Biol. 149, 317–330 (2000).
We are grateful to Hiroyuki Mano for Plk4 constructs, Satoru Mimura for constructs for Y2H assay, Ingrid Hoffmann for Plk4 antibodies, Mikiko Takahashi for a PACT plasmid, Michel Bornens for U2OS cells stably expressing GFP-centrin1, Yuji Tanno and Yuya Yamagishi for their technical advise of CMV promoter, as well as the members of Kitagawa laboratory and Akshari Gupta for their discussion and critical reading of the manuscript. We thank Pierre Gönczy for constructs and fruitful discussions. This work was supported by Grant-in-Aid for Japan Society for the Promotion of Science Fellows, Grant-in-Aid for Young Scientists (A) and for Scientific Research on Innovative Areas from the Ministry of Education, Science, Sports and Culture of Japan, by Improvement of Research environment for young researchers grant from Japan Science and Technology Agency, by Takeda Science Foundation and by the Mitsubishi foundation.
The authors declare no competing financial interests.
About this article
Cite this article
Ohta, M., Ashikawa, T., Nozaki, Y. et al. Direct interaction of Plk4 with STIL ensures formation of a single procentriole per parental centriole. Nat Commun 5, 5267 (2014). https://doi.org/10.1038/ncomms6267
Journal of Biomedical Science (2022)
Communications Biology (2020)
Nature Communications (2019)
Cep131 overexpression promotes centrosome amplification and colon cancer progression by regulating Plk4 stability
Cell Death & Disease (2019)
Cell Death & Disease (2019)