Cdc20 is a substrate adaptor and activator of the anaphase-promoting complex/cyclosome (APC/C), the E3 ubiquitin ligase whose activity is required for anaphase onset and exit from mitosis. A green fluorescent protein derivative, Cdc20–GFP, bound to centrosomes throughout the cell cycle and to kinetochores from late prophase to late telophase. We mapped distinct domains of Cdc20 that are required for association with kinetochores and centrosomes. FRAP measurements revealed extremely rapid dynamics at the kinetochores (t1/2 = 5.1 s) and spindle poles (t1/2 = 4.7 s). This rapid turnover is independent of microtubules. Rapid transit of Cdc20 through kinetochores may ensure that spindle checkpoint signaling at unattached/relaxed kinetochores can continuously inhibit APC/CCdc20 targeting of anaphase inhibitors (securins) throughout the cell until all the chromosomes are properly attached to the mitotic spindle.

Trafficking of cell cycle regulatory proteins within the mitotic spindle may be essential in controlling the accurate timing of cell division (Gorbsky et al., 1999; Gorbsky, 2001). Cdc20 is an activator and substrate-specific adaptor protein for the mitotic ubiquitin ligase called the anaphase-promoting complex/cyclosome (APC/C)* (for review see Vodermaier, 2001). Cdc20 targets the anaphase inhibitors Pds1/securin by facilitating a physical link between the APC/C and the target molecule. Mad2, Mad3/BubR1, and Bub3, members of the Mad and Bub spindle checkpoint protein families, restrain the APC/C from targeting Pds1/securin proteins before the alignment of the chromosomes at the metaphase plate. These proteins appear to inhibit APC/C by binding to Cdc20 (Fang et al., 1998; Kallio et al., 1998; Chan et al., 1999). The various checkpoint proteins may function independently or cooperatively to block the targeting of substrates by APC/CCdc20 (Sudakin et al., 2001; Tang et al., 2001; Fang, 2002).

Many of the mitotic checkpoint proteins and regulators of the APC/C, including Cdc20, Bub1, Mad3/BubR1, Bub3, Mad1, and Mad2, associate with kinetochores and centrosomes, often at specific times in the cell cycle (Chen et al., 1996; Li et al., 1997; Kallio et al., 1998; Taylor et al., 1998). These data have led to increasingly detailed models that unattached kinetochores foster the assembly of inhibitory proteins onto the APC/C and/or Cdc20, thus restraining APC/CCdc20 from targeting securins (Kallio et al., 1998; Chen et al., 1998; Sudakin et al., 2001, Sironi et al., 2002). Howell et al. (2000) used FRAP measurements to show that Mad2 is a transient component of the spindle poles and kinetochores with a turnover halftime of 24–28 s. Furthermore, the authors observed that Mad2 is transported between the kinetochores and spindle poles, and this transfer depends on intact spindle microtubules. Here, we quantitatively examine the subcellular localization and dynamics of full length and mutant Cdc20 in living cells using high-resolution fluorescence microscopy and FRAP.

Cdc20–GFP binds to Mad2, BubR1, and APC/C and does not inhibit mitotic progression in living cells

To determine whether Cdc20–GFP recapitulates the normal intermolecular association of endogenous Cdc20 we used anti-GFP antibody to immunoprecipitate Cdc20–GFP from mitotic (8–12 h in taxol or nocodazole) extracts of transiently transfected HeLa cells. When the immunoprecipitate was probed with an anti-Cdc20 antibody, a single ∼82-kD protein band was found (Fig. 1 A), which corresponds to the expected size of the Cdc20–GFP chimera. All endogenous Cdc20 remained in the supernatant, suggesting that only one copy of Cdc20 is present in checkpoint complexes in vivo. We compared anti-GFP immunoprecipitates of extracts prepared from mitotic cells expressing full-length Cdc20 or an NH2-terminal deletion, Cdc20–GFPΔ1–167, that lacks the Mad2-binding domain (Fig. 1 B). Mad2, BubR1, and the core APC/C proteins, Cdc27 and Cdc16, were detected in immunoprecipitates of full-length Cdc20 but not Cdc20–GFPΔ1–167, confirming that the NH2-terminal region of Cdc20 is required for association with Mad2, BubR1, and the APC/C (Fig. 1 C).

Cdc20–GFP associates with centrosomes throughout the cell cycle and with kinetochores in M phase

The localization and dynamics of Cdc20–GFP were analyzed in living LLC-PK cells transiently transfected with a plasmid encoding Cdc20–GFP. Chromosome movements in prometaphase and anaphase, the timing of the metaphase–anaphase transition, and exit from M phase all occurred normally in these cells, suggesting that expression of Cdc20–GFP did not impair progression through mitosis. Furthermore, Cdc20–GFP cells treated with nocodazole arrested at M phase for several hours (Fig. S1).

In interphase cells, Cdc20–GFP was concentrated in the nucleus but excluded from the nucleolus. Substantial amounts were also cytoplasmic with a strong concentration at the centrosome. Association with the centrosome persisted throughout the entire cell cycle (Fig. 2 A). In early mitosis, Cdc20–GFP accumulated at the kinetochores, at the spindle poles, and along kinetochore microtubules (Fig. 2 A). During prometaphase, kinetochores near the spindle poles were more intense compared with kinetochores near the spindle equator (Fig. 2 A). We did not detect differences in the fluorescence intensities of the leading and trailing kinetochores of prometaphase chromosomes during their migration to the metaphase plate (Fig. S2 and Video 1). The Cdc20–GFP colocalized with the Crest kinetochore marker in M phase (Fig. 2 B). When late prometaphase or metaphase cells were treated with the spindle-disrupting agent nocodazole, the intensity of all kinetochore signals increased to the maximal level (Fig. 2 C), suggesting that the amount of Cdc20 associated with kinetochores is partially and inversely dependent on microtubule occupancy. In nondrug-treated cells, the peak intensity of fluorescence at kinetochores was reached 1–3 min after nuclear envelope breakdown (NEB; Fig. 2 D), and Cdc20–GFP remained associated with the kinetochores from late prophase to late telophase (Fig. 2, B and D). After onset of anaphase, the kinetochore Cdc20–GFP signal diminished rapidly and became indistinguishable from the background as the cells exited mitosis (Fig. 2, B and D). The intensity of diffuse cytoplasmic Cdc20–GFP also decreased substantially during anaphase and telophase, consistent with the findings that Cdc20 is proteolyzed as cells progress to G1 (Weinstein, 1997). In contrast to the loss of Cdc20 at kinetochores and in the cytoplasm, the intensity of Cdc20–GFP at the spindle poles remained high throughout mitosis and after the cells had exited mitosis (Fig. 2 B).

We quantified the distribution of endogenous Cdc20 in mitotic cells by measuring fluorescence intensities after immunolabeling endogenous Cdc20 in fixed cells (n = 5) and comparing these data with measurements of Cdc20–GFP fluorescence in living, transfected cells (n = 5). In good agreement, both approaches revealed that during mitosis, >80% of Cdc20 was diffusely distributed in the cytoplasm with the remainder concentrated on the poles, spindle fibers, and kinetochores (Fig. 2 E).

Distinct domains of Cdc20 mediate localization to kinetochores and centrosomes

In cell extracts, the Cdc20 protein is found in a variety of complexes with spindle checkpoint proteins and with the APC/C. It is unclear if these different populations localize to different subcellular sites. The Cdc20 protein consists of an NH2-terminal region (amino acids 1–167) that contains putative destruction boxes and domains involved in binding to the APC/C and to the checkpoint protein Mad2 (Zhang and Lees, 2001). After that are seven WD-40 repeats that form a β-propeller structure and may be involved in binding to substrates (Hilioti et al., 2001). We found that the NH2-terminal region containing the Mad2-binding domain is required for localization to centrosomes, whereas the WD-40 repeats are necessary for localization to kinetochores and spindle microtubules (Fig. 3). A short deletion of the NH2 terminus (Δ1–110), which retains the Mad2-binding domain, had no obvious effect on localization in interphase and mitosis. In contrast, a longer NH2-terminal deletion (Δ1–167), which removes the Mad2/APC/C-binding domain eliminated binding to interphase and mitotic centrosomes but preserved localization at mitotic kinetochores (Fig. 3). A construct containing only the first 167 amino acids and lacking all WD-40 repeats (Δ168–499) showed centrosome and spindle pole localization but did not bind kinetochores. Deletion of the entire NH2 terminus, including the first WD-40 repeat, eliminated binding to both kinetochores and centrosomes. These findings indicate that association of Cdc20 with kinetochores requires the WD-40 repeats. In contrast, Cdc20 localization to centrosomes requires the Mad2/APC/C-interacting domain and thus may be due to interaction with Mad2 or APC/C concentrated there.

Cdc20–GFP turns over rapidly at kinetochores and centrosomes

Unattached kinetochores may provide a platform for the assembly/activation of spindle checkpoint complexes with the APC/C (Chen et al., 1998; Kallio et al., 1998). Howell et al. (2000) used FRAP to demonstrate that fluorescent derivatives of the checkpoint protein Mad2 transiently associate with kinetochores and spindle poles, exhibiting half-times of ∼26 s and ∼23 s, respectively. We used FRAP to analyze the turnover of Cdc20–GFP at the kinetochores and centrosomes of LLC-PK cells.

First we determined that photobleaching of Cdc20–GFP did not induce defects in chromosome movements or cell cycle progression (unpublished data). The recovery of Cdc20–GFP was very rapid at kinetochores and centrosomes with average half-times of 5.1 ± 3.6 s (n = 11) and 4.7 ± 3.6 s (n = 7), respectively (Fig. 4 A; Table I; Video 2). At kinetochores, recovery rates were similar from prometaphase to metaphase. In anaphase cells (n = 5), recovery of kinetochores was somewhat faster (t1/2 = 3.3 ± 1.4 s). Recovery of Cdc20–GFP at interphase centrosomes was also rapid (t1/2 = 6.9 ± 3.3 s, n = 7; Fig. 4 B; Table I; Video 3). The average turnover of Cdc20–GFP in the cytoplasm was significantly faster (P < 0.05, 2.7 ± 1.0 s, n = 8; Table I) than that of kinetochores and centrosomes. The total extent of recovery was from 80 to 94% at centrosomes and kinetochores (Table I), suggesting that most Cdc20 associated with these structures exchanges rapidly. The treatment of cells with microtubule drugs, nocodazole or taxol, did not significantly affect recovery at kinetochores or centrosomes (Table I; Fig. 4 C; Video 4).

Cdc20–GFP lacking the Mad2-binding domain (Δ1–167) localizes at kinetochores but not centrosomes. FRAP analysis of Cdc20–GFPΔ1–167 at kinetochores showed rapid half-times for recovery (5.2 ± 3.6 s) and high maximal recovery (82 ± 16%), numbers not different from those of full-length Cdc20–GFP (Fig. 4 D; Table I). Again, treatment of Cdc20–GFPΔ1–167-expressing cells with nocodazole did not alter recovery half-time or extent (Fig. 4 E; Table I).

The role of Cdc20 protein dynamics in the spindle checkpoint

Like Mad2, Cdc20 associates with mitotic kinetochores and spindle poles transiently. However, Cdc20 exchange occurs approximately four times as fast as the published rates for Mad2. Kinetochore-associated Cdc20 exchanges rapidly with the cytoplasmic pool, independent of spindle microtubules. Thus, the trafficking of Cdc20 is distinct from that of Mad2 and may relate to how the checkpoint signal is broadcast throughout the cell from unattached kinetochores.

Some years ago, we proposed a model whereby transient association of Cdc20 with unattached kinetochores served to maintain inhibition of the APC/C toward targets whose ubiquitylation and degradation are required for anaphase onset (Kallio et al., 1998). The work reported here and studies from other laboratories support this basic conceptual framework. We now propose refinements to this model (Fig. 5). Kinetochores lacking microtubule attachment or tension contain high concentrations of spindle checkpoint proteins (e.g., Mad1, Mad2, Bub1, BubR1, and Bub3). We suggest that Cdc20 circulates rapidly at all kinetochores, binding via its WD-40 repeats, possibly through interaction with other WD-40 proteins, such as Bub3 (Fraschini et al., 2001). Binding to the kinetochore by the WD-40 domain leaves free the Cdc20 NH2-terminal domain that contains binding sites for inhibitory checkpoint proteins Mad2 and BubR1. While at the kinetochore, Cdc20 accepts the inhibitory checkpoint proteins, and binding of anaphase inhibitors (securins) to the APC/C is blocked. In contrast, the targeting of early M phase substrates of APC/CCdc20, such as cyclin A, is not inhibited, possibly because the early substrates interact with COOH-terminal regions of Cdc20. Other kinetochore-associated checkpoint proteins (e.g., Mad1, Bub1, Mps, and CenpE) facilitate transfer of the checkpoint inhibitor proteins to Cdc20 (for Mad1 see Sironi et al., 2002). Kinetochore-bound kinases, phosphatases, or other enzymes might also modify Cdc20 or its associated proteins to inhibit APC/CCdc20 targeting of securins. Microtubule attachment or tension at kinetochores induces the dynein-mediated transport of certain checkpoint proteins from the kinetochore toward the poles along spindle fiber microtubules (Howell et al., 2001). The very high exchange rates for Cdc20 (more rapid than those of the inhibitor Mad2) may allow Cdc20 to continuously sample all kinetochores within the cell and thus maintain cell-wide inhibition of APC/CCdc20, even in cells with only one or a few unattached kinetochores. Finally, during metaphase and anaphase, the continued concentration of Cdc20 at kinetochores, centrosomes, and spindle microtubules may additionally serve to maintain high levels of the active APC/CCdc20 near substrates concentrated within the spindle.

Cdc20–GFP constructs and mutagenesis

Oligonucleotides were synthesized for the NH2- and COOH-terminal deletion mutants with an overhang sequence to allow restriction digestion after the PCR reaction. Amplified fragments were digested with HindIII and BamH1 and ligated into the pEGFP-N3 vector (CLONTECH Laboratories, Inc.) to generate fusion proteins with EGFP at the COOH-terminal end of Cdc20 mutants.

Transfection and expression of Cdc20–GFP chimeras

Cell culture was performed as previously described (Kallio et al., 1998). LLC-PK and HeLa cells were transiently transfected with plasmids encoding full-length or mutated Cdc20–GFP by LipofectAMINE PLUS reagent (Life Technologies) or Fugene 6 reagent (Roche Diagnostics Corp.) according to the manufacturer's recommendations. 24–48 h after transfection, the cells were fixed and processed for microscopic analysis or subjected to biochemical studies or live cell video analysis.

Immunoprecipitation and immunoblotting

HeLa cells expressing full-length or mutated Cdc20–GFP chimeras were treated with nocodazole or taxol for 8–12 h. Mitotic cells were collected. Cell extracts and supernatants were prepared and used for immunoprecipitation using anti-GFP antibodies (2.5 μg; Molecular Probes and Abcam Ltd.) or for Western blotting experiments as described previously (Kallio et al., 1998).

Fixation and immunofluorescence

LLC-PK cells expressing Cdc20–GFP were fixed with 3% formaldehyde in PHEM (60 mM Pipes, 25 mM Hepes, pH 6.9, 10 mM EDTA, 4 mM MgCl2) for 15 min. After washes with MBST (10 mM MOPS, 150 mM NaCl, pH 7.3, 0.05% Tween 20), DNA was stained with DAPI and the cells on coverslips were mounted with Vectashield (Vector Laboratories). For immunofluorescence, LLC-PK and HeLa cells on coverslips were simultaneously fixed and extracted for 15 min in 0.25% CHAPS in PHEM containing 2% formaldehyde and 100 nM microcystin LR. Coverslips were labeled with antibodies as previously described (Kallio et al., 1998) and analyzed with a ZEISS Axioplan IIi microscope equipped with a Hamamatsu Orca II camera and Metamorph Imaging system (Universal Imaging Corp.).

Analysis of living cells

For live cell observation, a planapochromat 60× (N.A. 1.4) objective (Nikon) was used with a SenSys CCD camera (Photometrics Ltd.) connected to a Nikon Diaphot microscope and imaged with Metamorph software. The average signal intensity of kinetochore-bound Cdc20–GFP at different mitotic phases was analyzed from 10 live cell sequences by measuring the integrated fluorescence intensity minus the background from the 10 brightest kinetochores per each cell and time point. For detailed methods on live cell analysis and FRAP see the supplemental Materials and methods .

Online supplemental material

Supplemental materials and methods, supplemental figures (Figs. S1 and S2), and Quicktime movies of the time-lapse fluorescence and phase contrast images accompanying Fig. S2 (Video 1) and Fig. 4 (Videos 2–4) are available.

We thank Dr. Patricia Wadsworth (University of Massachusetts, Amherst, MA) for providing LLC-PK cells expressing α-tubulin. We thank Dr. Ted Salmon (University of North Carolina, Chapel Hill, NC) and Dr. Tim Yen (Fox Chase Cancer Center, Philadelphia, PA) for providing antibodies.

This study was supported by grants from the Helsingin Sanomat Foundation (M.J. Kallio) and from the National Institute of General Medical Sciences (G.J. Gorbsky).

The online version of this article includes supplemental material.

Victoria A. Beardmore's present address is Medical Research Council Protein Phosphorylation Unit, School of Life Sciences, University of Dundee, Dundee, DD1 5EH, Scotland.


Abbreviations used in this paper: APC/C, anaphase-promoting complex/cyclosome; NEB, nuclear envelope breakdown.

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Supplementary data