Mitotic Regulator Mis18β Interacts with and Specifies the Centromeric Assembly of Molecular Chaperone Holliday Junction Recognition Protein (HJURP)*

Background: HJURP is a molecular chaperone essential for the deposition of the centromere marker CENP-A. Results: Mis18β binds with and specifies the centromere localization of HJURP. Conclusion: Mis18β governs centromere assembly via the Mis18β-HJURP-CENP-A axis. Significance: Our finding reveals a novel mechanism underlying CENP-A incorporation into the centromere. The centromere is essential for precise and equal segregation of the parental genome into two daughter cells during mitosis. CENP-A is a unique histone H3 variant conserved in eukaryotic centromeres. The assembly of CENP-A to the centromere is mediated by Holliday junction recognition protein (HJURP) in early G1 phase. However, it remains elusive how HJURP governs CENP-A incorporation into the centromere. Here we show that human HJURP directly binds to Mis18β, a component of the Mis18 complex conserved in the eukaryotic kingdom. A minimal region of HJURP for Mis18β binding was mapped to residues 437–460. Depletion of Mis18β by RNA interference dramatically impaired HJURP recruitment to the centromere, indicating the importance of Mis18β in HJURP loading. Interestingly, phosphorylation of HJURP by CDK1 weakens its interaction with Mis18β, consistent with the notion that assembly of CENP-A to the centromere is achieved after mitosis. Taken together, these data define a novel molecular mechanism underlying the temporal regulation of CENP-A incorporation into the centromere by accurate Mis18β-HJURP interaction.

somes and spindle microtubules. In eukaryotic organisms, the centromere is epigenetically specified by nucleosomes containing a unique histone H3 variant, CENP-A, with the exception of budding yeast (1)(2)(3)(4). CENP-A orthologues present in all known eukaryotes. It is the most important epigenetic marker of the centromere (5)(6)(7)(8)(9) and is required for the correct localization of most centromere-and kinetochore-related proteins (5, 10 -17). Very recently, Cleveland and colleagues (17) unambiguously demonstrated that CENP-A is the epigenetic marker to maintain and propagate the centromere identity and function through gene targeting in human cells and fission yeast. Biochemically, the centromere-targeting domain of CENP-A is sufficient to direct its centromere incorporation, whereas the assembly of a functional kinetochore requires the N-terminal and C-terminal tails of CENP-A (17).
Unlike typical histone proteins, the deposition of CENP-A to the centromere occurs in early G 1 phase (18). Several proteins have been reported to be essential to the deposition and maintenance of CENP-A, including CENP-C, CENP-N, RbAp46/48, Mis18 complex (Mis18␣, Mis18␤, and Mis18BP1), RSF (remodeling and spacing factor) complex, and HJURP 3 (3, 19 -28). Among these proteins, HJURP is of great importance for CENP-A deposition. In yeast, the HJURP homologue Scm3 is required for the deposition of centromeric Cse4 nucleosome (29 -33). Down-regulation of HJURP impairs the deposition of newly synthesized CENP-A in mammalian cells (26 -27). As a molecular chaperone of CENP-A, HJURP forms a prenucleosomal complex with the CENP-A/H4 heterodimer via its highly conserved Scm3 domain (25, 34 -36). However, although the Scm3 domain is sufficient to facilitate the formation of CENP-A nucleosomes in vitro, the Scm3 domain itself is not sufficient to localize on the centromere (22). The Mis18 complex, composed of Mis18␣, Mis18␤, and Mis18BP1, is required for the deposi-tion of CENP-A (19 -20). A recent study showed that the centromere localization of HJURP is dependent on the Mis18 complex (22). However, the mechanism by which Mis18 directs HJURP recruitment to centromere is still unclear.
In this study, we report that Mis18␤ is a novel binding partner of HJURP. A minimal region of HJURP (residues 437-460) is required for the direct interaction with Mis18␤. A central fragment of HJURP (residues 401-490) is sufficient for the centromere recruitment of HJURP. In contrast, a mutant of HJURP lacking residues 437-460 failed to localize on the centromere. Depletion of Mis18␤ by siRNA perturbed the recruitment of HJURP to the centromere. Furthermore, we demonstrated that phosphorylation of HJURP by CDK1 reduced its binding affinity to Mis18␤. Our findings provide novel insights into how centromere deposition of CENP-A occurs in a cell cycle-dependent manner.

MATERIALS AND METHODS
Plasmid Construction-The cDNA of RbAp46, Mis18␣, and CENP-N were amplified from the human testis cDNA library (Clontech) using a standard PCR protocol. The cDNA of Mis18␤, Mis18BP1 (Knl-2), and RbAp48 were purchased from GeneCopoeia. The cDNA of HJURP was purchased from Proteintech Group. The cDNA of CENP-C was a gift from Dr. Andrea Musacchio (European Institute of Oncology, Milan, Italy). Constructs of AD and BD fusion proteins were generated by subcloning the indicated cDNAs into pGADT7 and pGBKT7 (Clontech), respectively. Constructs of 3ϫFLAG, GFP, GST, and His 6 -tagged proteins were generated by subcloning the indicated cDNAs into p3XFLAG-myc-CMV-24 (Sigma), pEGFP-C1 (Clontech), pGEX-5X-3 (GE Healthcare), and pET-28a (Novagen), respectively.
To generate mCherry-Mis18␤, cDNA of GFP in GFP-Mis18␤ was replaced by cDNA of mCherry. All constructs of HJURP truncations were generated by ligating restriction enzyme-digested PCR products and corresponding vectors. Point mutations were introduced using the QuikChange sitedirected mutagenesis kit (Agilent). All plasmids were verified by sequencing.
Yeast Two-hybrid Assay-Yeast two-hybrid assays were performed as described previously (37,38). Briefly, the plasmids of BD-tagged protein and AD-tagged protein were co-transformed into yeast strain AH109. The co-transformed yeast were grown on SD medium with X-␣-Gal but lacking Leu, Trp, His, and Ade.
Recombinant Protein Production and Pull-down Assays-Recombinant protein preparation and pull-down assays were performed as described (39). Briefly, the GST fusion protein in bacteria in the soluble fraction was purified by using glutathione-agarose chromatography and chromatography, and histidine-tagged protein was purified using nickel-nitrilotriacetic acid-agarose beads. In the purification of GST-tagged proteins and pull-down assays, we used PBS containing 0.2% Triton X-100.
Immunoprecipitation-For FLAG immunoprecipitation, 293T cells transiently transfected to express FLAG fusion proteins were lysed in IP buffer (50 mM Tris-HCl, pH 8.0, 150 mM NaCl, 1 mM EDTA, 1 mM DTT, protease inhibitors (Roche Applied Science), 0.2% Triton X-100) on ice for 10 min. The cell lysates were centrifuged at 12,000 ϫ g for 15 min. To prepare nuclear extract, cells were homogenized in 0.1ϫ IP buffer. Homogenized extracts were centrifuged at 350 ϫ g for 5 min. The pellet was suspended in IP buffer, sonicated, and centrifuged at 12,000 ϫ g for 15 min to produce a chromatin-free extract. Cell lysates or nuclear extracts were incubated with anti-FLAG M2 affinity beads (Sigma) at 4°C for 3 h. After washing with IP buffer three times, proteins associated with beads were eluted by boiling in SDS sample buffer. Protein samples were separated by SDS-PAGE and analyzed by Western blotting. For GFP tag immunoprecipitation, GFP-Trap_A (Chromotek) was used to incubate with cell lysate of GFP-HJURP stable cell line in 1ϫ NEBuffer for PMP (New England Biolabs).
In Vitro Kinase Assay-Recombinant GST-HJURP-C1 and GST-HJUP-C1-S3A were incubated with 2 units of CDK1-cyclin B (New England Biolabs) in kinase buffer (50 mM Tris-HCl, 10 mM MgCl 2 , 1 mM EGTA, 2 mM dithiothreitol, 0.01% Brij 35, pH 7.5) containing 100 M ATP at 30°C for 30 min. Protein samples were separated by SDS-PAGE. The phosphorylated proteins were detected by staining the gel by the Diamond Phosphoprotein Gel Stain Kit (Invitrogen). Then the level of protein was visualized by Coomassie Blue staining of the same gel.
Cell Culture and Cell Cycle Synchronization-HeLa and 293T cells, from the American Type Culture Collection (Manassas, VA) were maintained as subconfluent monolayers in Dulbecco's modified Eagle's medium (Invitrogen) with 10% FBS (Hyclone, Logan, UT) and 100 units/ml penicillin plus 100 g/ml streptomycin (Invitrogen) at 37°C with 8% CO 2 . To obtain the cell lines stably expressing GFP-HJURP and GFP-HJURP-S3D, respectively, HeLa cells were transfected with GFP-HJURP or GFP-HJURP-S3D plasmid using Lipo-fectamine2000 (Invitrogen). Both cell lines were selected in complete medium containing 800 g/ml G418 and then maintained in complete medium containing 200 g/ml G418. For synchronization in prometaphase, HeLa cells were treated for 16 h with 50 ng/ml nocodazole. For synchronization in early G 1 phase, HeLa cells were treated for 16 h with 2 mM thymidine, washed three times with PBS, and released in complete medium for 8 h and then assayed.
Deconvolution images were collected using a Deltavision wide field deconvolution microscope system built on an Olympus IX-71 inverted microscope base. For imaging, a ϫ100, 1.35 numerical aperture lens was used, and optical sections were taken at intervals of 0.3 m. Images for display were generated by projecting single optical sections as described previously (38).
For live cell imaging, cells were cultured in MatTek glassbottom microwell dishes (MatTek) in CO 2 -independent medium (Invitrogen) containing 10% (v/v) FBS, 100 units/ml penicillin, and 100 g/ml streptomycin. A z-series of three images at 0.5-m intervals was acquired every 5 min using the same equipment. Image stacks were deconvolved and projected with SoftWorx (Applied Precision) and mounted onto figures with Photoshop and Illustrator (Adobe).
Fluorescence Intensity Quantification-Quantification of the level of centromere-localizing signal was conducted as described by Liu et al. (37). In brief, the average pixel intensities from at least 100 centromeres from 10 cells were measured, and background pixel intensities were subtracted. The pixel intensities at each centromere were then normalized against ACA pixel values to account for any variations in staining or image acquisition. The values of specific siRNA-treated cells were then plotted as a percentage of the values obtained from cells transfected with a control scramble siRNA duplex. The values of GFP-HJURP full-length and deletion mutant were expressed as arbitrary units.
Data Analyses-To determine significant differences between means, unpaired t tests assuming unequal variance were performed; differences were considered significant when p was Ͻ0.05.

RESULTS
Identifying Mis18␤ as a Binding Partner of HJURP-To identify proteins that recruit HJURP to centromeres through direct interaction, we tested the interaction between HJURP and factors that are essential for CENP-A deposition and maintenance via a yeast two-hybrid assay because most recombinant centromeric proteins are either less soluble or unstable (37,38). As shown in Fig. 1A, our assay showed that HJURP interacts with Mis18␤ but not Mis18␣, Mis18BP1, RbAp46, RbAp48, CENP-C, and CENP-N. To confirm this interaction, a GST pull-down assay using purified GST-HJURP and His-Mis18␤ was performed (Fig. 1B). Indeed, HJURP directly binds to Mis18␤ in vitro, as judged by Western blotting of Mis18␤ in the GST-HJURP-bound fraction (Fig. 1B, bottom, lane 5). No Mis18␤ was retained on GST-Sepharose beads, suggesting that the interaction between Mis18␤ and HJURP is specific. To test if Mis18␤ and HJURP form a cognate complex, we carried out immunoprecipitation using cell lysates from 293T cells transiently transfected to express FLAG-HJURP protein. As shown in Fig. 1C, FLAG immunoprecipitation successfully pulled down FLAG-HJURP based on Western blotting using an anti-FLAG antibody (top, lane 4). Western blotting analysis with an anti-Mis18␤ antibody confirmed the existence of Mis18␤ protein in the FLAG-HJURP immunoprecipitates (Fig. 1C, bottom,  lane 4), confirming the existence of HJURP-Mis18␤ complex in cells.
There are two Mis18 isoforms (␣ and ␤) in mammalian cells (19). To probe whether HJURP forms a cognate complex with Mis18 protein in an isoform-selective manner, we carried out immunoprecipitation using lysates from 293T cells transiently transfected to express FLAG-Mis18␣ and FLAG-Mis18␤, respectively. As shown in Fig. 1D, both FLAG-Mis18␣ and FLAG-Mis18␤ proteins expressed at a comparable level in together with different AD constructs, were co-transformed into yeast cells and cultured on a selective plate containing X-␣-Gal but lacking uracil, tryptophan, leucine, and histidine. Control is the cells cotransformed with BD-p53 and AD-T as a positive control. B, GST-HJURP directly binds to His-Mis18␤ in vitro. Purified His-Mis18␤ was incubated with purified GST-HJURP immobilized on glutathione-agarose. After exclusive wash, proteins associated with glutathione-agarose were separated by SDS-PAGE and analyzed by Coomassie Blue staining or Western blotting with anti-Mis18␤ antibody. C, nuclear extracts from 293T cells expressing FLAG-HJURP were subjected to anti-FLAG immunoprecipitation followed by Western blotting using antibodies against Mis18␤ and FLAG, respectively. Lysate of untransfected 293T cells was used as a negative control. D, nuclear extracts from 293T cells expressing FLAG-Mis18␣ or FLAG-Mis18␤ were subjected to anti-FLAG immunoprecipitation followed by Western blotting using antibodies against HJURP, tubulin, and FLAG, respectively. Lysate of untransfected 293T cells was used as a negative control (lane 1).
293T cells judged by Western blotting analysis (bottom, lanes 2 and 3). Anti-FLAG immunoprecipitation brought down equivalent amount of FLAG-Mis18␣ and FLAG-Mis18␤ proteins (bottom, lanes 5 and 6). As predicted, HJURP protein is only present in the Mis18␤ immunoprecipitates (top, lane 6), which is consistent with the outcome from an early yeast two-hybrid assay. The absence of tubulin protein in any of the FLAG immunoprecipitates confirmed the specificity of the immunoprecipitation. Thus, we conclude that HJURP directly binds to Mis18␤ and forms a cognate complex with Mis18␤ in cells.
Mapping the Binding Interface between HJURP and Mis18␤-To delineate the structure-functional relationship of the HJURP-Mis18␤ interaction, we sought to ask which region of HJURP is required for interaction with Mis18␤. To this end, a series of HJURP truncations as illustrated in Fig. 2A were generated, and then the yeast two-hybrid assay was carried out using Mis18␤ as bait. HJURP-C (residues 401-748) mediates the interaction with Mis18␤ (Fig. 2B). In contrast, HJURP-N (residues 1-400) interacts with Mis18␤ weakly in our assay. Next, a GST pull-down assay was carried using GST-Mis18␤ as affinity matrix to absorb lysates of cells expressing different GFP-HJURP truncations. Indeed, Mis18␤ pulls down HJURP-C strongly (Fig. 2C, lane 15). On the contrary, it pulls down HJURP(1-200) less efficiently (Fig. 2C, lane 12). To pinpoint the minimal region of HJURP required for binding to Mis18␤, interactions of Mis18␤ with a series of smaller HJURP fragments were tested via a yeast two-hybrid assay. The results showed that the minimal region of HJURP required for binding to Mis18␤ is the fragment encompassing residues 401-490 of HJURP (Fig. 2D). In addition, both C2a(421-580) and C2b(437-580) fragments interact with Mis18␤. However, the C2c(461-580) fragment failed to interact with Mis18␤ (Fig.  2D). This result suggests that the region of amino acids 437-460 is essential for HJURP-Mis18␤ interaction. Consistent with our prediction, deletion of residues 437-460 from HJURP disrupted HJURP-Mis18␤ interaction (Fig. 2E). However, deleting residues 437-446 or 447-460 from HJURP did not disrupt HJURP-Mis18␤ interaction. Thus, we conclude that the region containing residues 437-460 of HJURP is the minimal region required for its interaction with Mis18␤.
HJURP Is Recruited to Centromere via a Direct Binding to Mis18␤-To map the region of HJURP responsible for its centromere localization, GFP-tagged HJURP truncations were transiently transfected to express in HeLa cells, and their localization was examined by immunofluorescence microscopy. GFP-tagged full-length HJURP localizes on centromeres in early G 1 phase (Fig. 3A). Consistent with a recent report (40), the C-terminal HJURP(401-748) localizes to centromeres (Fig.  3A), whereas the N-terminal HJURP(1-400) failed to localize to centromeres (Fig. 3A). Interestingly, HJURP-C1(401-490), the fragment essential for binding Mis18␤, is capable of localizing to the centromere ( Fig. 3A; see Fig. 3B for quantitative analysis). However, the HJURP-C4 fragment (aa 491-748) failed to localize to centromeres. Collectively, the deletion analyses demonstrate that the deletion mutant HJURP-C1 (aa 401-490) is essential and sufficient for localizing HJURP to the centromere. Because our biochemical characterization demonstrated that the HJURP-C1 fragment of HJURP physically inter-acts with Mis18␤, we reason that HJURP is recruited to the centromere through a direct interaction with Mis18␤. If this is true, mutation of HJURP unable to bind Mis18␤ would not be able localize to the centromeres. Consistent with our speculation, an immunofluorescence assay demonstrated that HJURP deletion mutant (HJURP⌬437-460) failed to localize onto centromeres (Fig. 3, C and D), which is consistent with the outcome from our yeast two-hybrid assay (Fig. 2E).
Interestingly, our yeast two-hybrid assay showed that a shorter deletion, such as HJURP⌬447-460 or HJURP⌬438 -446, remains active in binding to Mis18␤ (Fig. 2E). Because GFP-HJURP⌬447-460, but not GFP-HJURP⌬438 -446, is localized on centromeres, (Fig. 3, C and D), we conclude that the region containing amino acids 438 -446 is critical for HJURP localization via its interaction with Mis18␤. Interestingly, deletion of residues 438 -446 from HJURP-C did not , together with two BD constructs as indicated, were co-transformed into yeast cells and cultured on a selective plate containing X-␣-Gal but lacking uracil, tryptophan, leucine, and histidine. Control is the cells co-transformed with BD-p53 and AD-T as a positive control. C, purified GST-Mis18␤ was immobilized on glutathioneagarose and incubated with extracts of 293T cells expressing GFP-tagged HJURP fragments. After extensive wash, proteins associated with glutathione-agarose were eluted and separated by SDS-PAGE followed by transfer to nitrocellulose membrane for Western blotting analyses (IB) with anti-GFP and anti-GST antibody, respectively. D and E, AD-Mis18␤, together with different BD constructs of different HJURP truncations, were co-transformed into yeast cells and cultured on selective plate containing X-␣-Gal but lacking uracil, tryptophan, leucine, and histidine. Control is the cells co-transformed with BD-p53 and AD-T as a positive control. Note that deletion of 24 amino acids (aa 437-460) from HJURP abolished the interaction between HJURP and Mis18␤.
completely abolish its ability to localize to the centromere, although its fluorescence intensity was significantly impaired (Fig. 3, E and F; p Ͻ 0.01).
Given the possibility that HJURP can form dimer (40), we tested whether the low level centromere localization of GFP-HJURP⌬437-460 is due to heterodimerization between endogenous HJURP and exogenous GFP-HJURP⌬437-460. To this end, we carried out a co-immunoprecipitation assay using lysates from 293T cells transiently transfected to express FLAG-HJURP and deletion mutants of GFP-HJURP. As shown in Fig. 4A, the removal of amino acids 437-460 from GFP-HJURP did not alter its interaction with FLAG-HJURP (Fig. 4A,  lane 7). Thus, we conclude that HJURP dimerization facilitates its localization to centromere.
Both Mis18 complex assembly and HJURP localization to the centromere occur in late mitosis and early G 1 phase of the following cycle (20, 26 -27). If Mis18␤ recruits HJURP to centromeres, Mis18 complex should concentrate to centromeres before HJURP. Consistent with an earlier report (27), live cell imaging showed that mCherry-Mis18␤ started to appear at the centromeres during anaphase B. However, GFP-HJURP exhibits a diffused localization in cytoplasm (Fig. 4B), demonstrating the temporal order of centromere localization. Thus, the centromere loading sequence of Mis18 complex and HJURP is consistent with our hypothesis that HJURP is recruited to centromeres by Mis18␤.
To test the requirement of Mis18␤ for HJURP centromere targeting, we sought to suppress Mis18␣ and Mis18␤ protein levels using siRNA. As shown in Fig. 4, C and D, both siRNAs against Mis18␣ and Mis18␤ effectively suppress the protein expression of Mis18␣ and Mis18␤, respectively. Quantitative analyses show that our siRNA protocol gives typically ϳ87 Ϯ  MARCH 21, 2014 • VOLUME 289 • NUMBER 12 JOURNAL OF BIOLOGICAL CHEMISTRY 8331 5% and 83 Ϯ 4% reduction in the amount of Mis18␣ and Mis18␤ protein, respectively, although the levels of tubulin showed no fluctuation in siRNA-treated cells (Fig. 4E; p Ͻ 0.01). When we treated GFP-HJURP stable cell line with siRNA against Mis18␣ or Mis18␤, the centromere localization of HJURP largely disappeared (Fig. 4, F and G). Because Mis18␣, Mis18␤, and Mis18BP1 are mutually dependent for their centromeric localization (20), it is not surprising that depletion of Mis18␣ or Mis18BP1 exhibits the same perturbation effect on HJURP localization that was also seen in the Mis18␤-depleted cells. Thus, we conclude that HJURP is recruited to centromeres by the Mis18 complex through its direct interaction with Mis18␤.

Mis18 Complex Recruits HJURP to Centromere
Regulation of HJURP to Centromeres by CDK1 Phosphorylation-It has been reported that the temporal restriction of CENP-A incorporation is mediated by CDK1 activity. One possible molecular pathway of this restriction is phosphorylation of Mis18BP1 inhibiting its centromere recruitment via CENP-C (41)(42). Because HJURP plays a key role in CENP-A incorporation, its recruitment to centromeres may also be temporally controlled by CDK1 activity. Using a mitotic phosphorylation-specific antibody, MPM2, we showed that HJURP is highly phosphorylated in mitosis (Fig. 5A). A phosphoproteome screen has identified at least eight phosphorylation sites of HJURP during mitosis (43). Three phosphorylation sites that conform to CDK1 consensus sites (Ser-412, Ser-448, and Ser-473) localized in the HJURP-C1 (aa 401-490) fragment. Because HJURP-C1 (aa 401-490) mediates interaction with Mis18␤, we hypothesize that CDK1 may control the temporal interaction between HJURP and Mis18␤ through phosphorylation of these sites. To address this possibility, an in vitro kinase assay using purified GST-HJURP(401-490) as substrate was performed (Fig. 5B). Our data showed that CDK1 can phosphorylate GST-HJURP(401-490) in vitro. When Ser-412, Ser-448, and Ser-473 were mutated to alanines, phosphorylation of HJURP-3A was undetectable (Fig. 5B, top panel, lane 4). To examine if the phosphorylation of HJURP affects the binding between HJURP and Mis18␤, different GST-tagged HJURP constructs were used as affinity matrix to pull down His-Mis18␤. Indeed, compared with wild type HJURP, HJURP-3D, in which Ser-412, Ser-448, and Ser-473 were mutated to aspartic acid to mimic the phosphorylation state, pulled down a much lesser amount of Mis18␤ (Fig. 5C).
Next, we examine the localization of phosphomimetic HJURP-3D in HeLa cells. For this purpose, we generated HeLa cell lines stably expressing GFP-HJURP and GFP-HJURP-S3D, respectively (Fig. 5D). Although GFP-HJURP-S3D can still localize at centromeres in early G 1 phase, its signal intensity significantly diminished, compared with cells expressing GFP-HJURP-WT (Fig. 5, E and F). It is likely that there are additional phosphorylation sites on HJURP or Mis18␤ that affect their interactions. The other possibility is that HJURP-3D may be recruited to centromeres by dimerization with endogenous HJURP. Next, we asked if the phosphorylation of HJURP affects the centromere incorporation of CENP-A. Our siRNA against HJURP effectively inhibits HJURP protein expression at 48 h after transfection, which yielded a typical 87 Ϯ 5% suppression of HJURP protein (Fig. 5, G and H; p Ͻ 0.01).
As predicted, suppression of HJURP resulted in a significant reduction of CENP-A level at the centromere (Fig. 5, I and J). Ectopically expression of wild type HJURP rescued the assembly of CENP-A efficiently (Fig. 5J). However, expression of HJURP-3D was unable to recover the efficient incorporation of CENP-A (Fig. 5, I and J). Thus, we conclude that the temporal control of HJURP phosphorylation in mitosis by CDK1 is essential for achieving a correct assembly of CENP-A protein to centromeres for faithful mitosis.

DISCUSSION
Faithful genome segregation depends on the functions of the eukaryotic centromere, which is characterized by a unique histone 3 variant, CENP-A. Given the crucial role of CENP-A in centromere specification, discovering the mechanism of CENP-A nucleosome assembly is of great importance for our understanding of epigenetic inheritance of centromere. Earlier studies show that the Mis18 complex is required for newly CENP-A assembly in human cells, and the loading time of the Mis18 complex is slightly earlier than CENP-A loading (18,20,27). However, the precise molecular mechanism by which the Mis18 complex directs CENP-A nucleosome assembly has remained elusive. Recent studies show that CENP-C can bind to Mis18BP1, a component of the Mis18 complex, to facilitate CENP-A nucleosome assembly (41,44). Among all of the proteins that are required for CENP-A loading, only CENP-C and CENP-N can directly bind to CENP-A nucleosome (23,24).
Here, we delineate the molecular mechanism by which Mis18 complex recruits prenucleosomal CENP-A complex. We believe that our findings fit the known knowledge and fill a missing gap of the CENP-A assembly pathway. Based on our own findings and the previous publications in the field, we propose a roadmap of CENP-A assembly (Fig. 6). This model demonstrates a special relationship between old CENP-A and new CENP-A. The old CENP-A nucleosome recruits CENP-C through direct interaction between the CENP-A C-terminal tail and CENP-C. CENP-C recruits the Mis18 complex at late anaphase when CDK1 activity is sharply reduced. As a consequence, the Mis18 complex recruits prenucleosomal CENP-A complex through directly binding between Mis18␤ and HJURP. Scm3, the homolog of HJURP in fission yeast, can physically interact with Mis18 in vitro (33)(34). This indicates that the mechanism of HJURP-mediated CENP-A protein assembly is conserved from fission yeast to humans.
It is reported that the cell cycle control of CENP-A nucleosome assembly to the centromere is mediated by CDK activity, and inhibition of CENP-A nucleosome assembly by CDK activity is probably exerted through phosphorylation of CENP-A assembly factors, including Mis18BP1 (42). However, aberrant centromere targeting of the non-phosphorylatable mutant Mis18BP1 S24A did not result in premature CENP-A nucleosome assembly. This indicates that other factors directing CENP-A assembly are also under the CDK phospho-regulation (42). Consistent with this notion, our data indicate that phosphorylation of HJURP by CDK1 alleviates the interaction affinity between HJURP and Mis18␤ and inhibits premature CENP-A assembly. Given the fact that GFP-HJURP-S3D remains localizing to the centromeres to a certain extent, we FIGURE 5. HJURP recruitment to centromeres is regulated by CDK1. A, immunoprecipitation was performed using GFP antibody-coupled Sepharose beads using lysates from HeLa cells stably expressing GFP-HJURP treated as indicated. Nocodazole was added to block cells in mitosis. Extract of mitotic cells were treated with -phosphatase (-PPase) before immunoprecipitation to dephosphorylate proteins. The immunopurified products were probed with anti-GFP antibody and MPM2 antibody, respectively. B, an in vitro kinase assay was performed using CDK1 as kinase and purified GST-tagged HJURP fragment or the fragment harboring point mutations as illustrated above. The top panel shows the gel staining with a Pre-Q diamond phosphor-protein staining kit. The bottom panel shows Coomassie Blue-stained gel. C, different purified GST fusion HJURP mutants were used as affinity matrix to pull down purified His-Mis18␤. The pull-downs were examined by anti-HJURP and anti-Mis18␤ antibody, respectively. D, immunoblots of lysates from normal HeLa cells, HeLa cells stably expressing GFP-HJURP-WT, and HeLa cells stably expressing GFP-HJURP-3D probed with the indicated antibodies. E, representative images of cells stably expressing GFP-HJURP or GFP-HJURP-S3D. Cells were fixed and co-stained for ACA (red), microtubule (magenta), and DNA (blue). Cells with midbody were selected to show that they were in early G 1 phase. Scale bar, 5 m. F, bar graph showing quantification of GFP fluorescence intensity at centromeres for the immunofluorescence assay described in D. The data represent mean Ϯ S.E. (error bars) of three independent experiments. More than 70 centromeres (from 10 cells) were quantified for each group. Student's t test was used to calculate the p value for comparison of HJURP-3D and HJURP-WT. G, immunoblots of lysates from cells transfected with siRNA against HJURP or a scramble sequence siRNA (a negative control) probed with the indicated antibodies. 48 h after siRNA transfection, cells were collected and assayed by Western blotting. H, quantification of HJURP protein suppression by siRNA. Values represent the means Ϯ S.D. (error bar) from three independent experiments. I, representative images of different cells as indicated treated with a control siRNA (si-ctrl) or siRNA against HJURP twice. 96 h after transfection, cells were fixed and stained for CENP-A (red) and DNA (blue). Scale bar, 5 m. J, bar graph showing quantification of CENP-A fluorescence intensity at centromeres for siRNA treatments described in I. The data represent mean Ϯ S.E. of three independent experiments. More than 200 centromeres (from 20 cells) were quantified per condition. Student's t test was used to calculate p value for comparison between the indicated groups.
reason that other CDK1 phosphorylation sites on HJURP or other CENP-A loading factors may also play an important role in regulating CENP-A assembly. It would be of great interest down the road to identify and characterize those regulatory mechanisms.
The kinetochore is a complex structure that functions as a molecular machine to power chromosome movement and as a signaling device to govern chromosome segregation and cell cycle control. We have recently developed an expanded palette of optical sensors to visualize and quantify dynamic phosphorylation (45), methylation (46), and acetylation (39) in live cell mitosis. The dynamics of centromere methylation is tightly coupled to mitotic phosphorylation to ensure chromosome plasticity during cell division (46). It has been reported that Mis18 deficiency leads to perturbed histone methylation and liberation of DNMT3A/B from the centromere (47). Given the cross-talk and interdependence between lysine 9 methylation and phosphorylation of serine 10 seen in histone 3 during the cell division cycle (48), it would be of great interest to probe whether and how methylation and phosphorylation gradients govern HJURP-mediated CENP-A loading to the centromere during mitosis and whether the mitotic phosphorylation also affects the assembly dynamics and plasticity of other histone fold-containing proteins, such as CENP-S/X complex, in cen-tromere plasticity (we refer to centromere plasticity as reversible assembly and disassembly of functional centromere) control (49).
In summary, we demonstrate that Mis18␤ governs the centromere loading of CENP-A by recruiting CENP-A chaperone HJURP. We have also demonstrated that the phosphorylation of HJURP by CDK1 inhibits the centromere deposition of CENP-A, providing mechanistic insight into a better understanding of spatiotemporal dynamics underlying CENP-A deposition during early G 1 phase. Our findings provide novel insights for better understanding the molecular pathway underlying HJURP-directed CENP-A loading to the centromere.