The Drosophila MCPH1-B isoform is a substrate of the APCCdh1 E3 ubiquitin ligase complex

ABSTRACT The Anaphase-Promoting Complex (APC) is a multi-subunit E3 ubiquitin ligase that coordinates progression through the cell cycle by temporally and spatially promoting the degradation of key proteins. Many of these targeted proteins have been shown to play important roles in regulating orderly progression through the cell cycle. Using a previously described Drosophila in vitro expression cloning approach, we screened for new substrates of the APC in Xenopus egg extract and identified Drosophila MCPH1 (dMCPH1), a protein encoded by the homolog of a causative gene for autosomal recessive primary microcephaly in humans. The dMCPH1-B splice form, but not the dMCPH1-C splice form, undergoes robust degradation in Xenopus interphase egg extract in a Cdh1-dependent manner. Degradation of dMCPH1-B is controlled by an N-terminal destruction box (D-box) motif as its deletion or mutation blocks dMCPH1-B degradation. dMCPH1 levels are increased in Drosophila morula (APC2) mutant embryos, consistent with dMCPH1 being an APC substrate in vivo. Using a purified, reconstituted system, we show that dMCPH1-B is ubiquitinated by APCCdh1, indicating that the effect of APC on dMCPH1-B ubiquitination and degradation is direct. Full-length human MCPH1 (hMCPH1) has been predicted to be an APC substrate based on its interaction with the APC subunit Cdc27. We were not able to detect changes in hMCPH1 levels during the cell cycle in cultured human cells. Overexpression of hMCPH1 (or dMCPH1-B) in developing Xenopus embryos, however, disrupts cell division, suggesting that proper regulation of hMCPH1 and dMCPH1-B activity plays a critical role in proper cell-cycle progression.


INTRODUCTION
The Anaphase-Promoting Complex (APC) is a multi-subunit E3 ubiquitin ligase that catalyzes ubiquitin-mediated proteasomal degradation of target proteins. A major function of the APC is to promote degradation of key cell-cycle proteins so as to coordinate orderly progression through the cell cycle (Peters, 2006). Human and yeast APC are each composed of 14-15 identified subunits and two primary co-activators, Cdc20 and Cdh1 (Kulkarni et al., 2013). Destruction of APC substrates is required in eukaryotes for the initiation of anaphase and exit from mitosis. Cdc20 associates with the APC in early mitosis, leading to the destruction of proteins that control the onset of anaphase, whereas Cdh1 promotes degradation of APC substrates that control late mitosis and the following G1 phase. These co-activators provide APC substrate specificity by facilitating the recognition of specific destruction motifs (e.g. degrons) such as the D-box (RxxLxxxxN) or KEN box (Lys-Glu-Asn) (King et al., 1996;Min and Lindon, 2012;Pfleger and Kirschner, 2000). Mutations of these motifs block the recognition of the protein by the APC, preventing their APC-mediated destruction.
Xenopus egg extract contains many of the components necessary for ubiquitin-mediated degradation such as E1, E2, and E3 enzymes, ubiquitin, and the proteasome. Moreover, biochemical regulation of APC Cdc20 -and APC Cdh1 -mediated degradation has been well studied and characterized in this system. Xenopus egg extract lacks Cdh1, and Cdc20 is the primary activator of APC (Lorca et al., 1998). Addition of exogenous human Cyclin B lacking its N-terminal D-box (CycBD90) to interphase Xenopus egg extract drives the extract into mitosis and promotes the degradation of APC Cdc20 substrates (Glotzer et al., 1991). Addition of exogenous Cdh1 to interphase Xenopus egg extract similarly promotes the degradation of APC Cdh1 substrates (Pfleger and Kirschner, 2000).
The in vitro expression cloning (IVEC) strategy involves generating [ 35 S]methionine-labeled proteins by in vitro-coupled transcription and translation of small, random pools of cDNAs; these radiolabeled proteins can then be used for biochemical screening in a powerful approach that allows for rapid isolation of relevant cDNAs corresponding to ''hits'' in the screen (King et al., 1997). IVEC has been successfully used in Xenopus egg extract to identify important APC substrates such as Geminin, Securin, Xkid, Tome-1, and Sororin (Ayad et al., 2003;Funabiki and Murray, 2000;McGarry and Kirschner, 1998;Rankin et al., 2005;Zou et al., 1999). A weakness of the original IVEC strategy, however, is that, depending on the cDNA library being used, certain genes are over-represented whereas other genes are under-represented in the library. Thus, the same substrate is often identified over and over again, and substantial screening is necessary to identify relevant rare clones. Furthermore, the pools of cDNAs used for IVEC screening must be deconvoluted in order to isolate single hits as the identities of the clones in the pools are unknown.
To overcome these limitations, we previously modified the IVEC methodology to generate radiolabeled protein pools from Release 1 of the Drosophila Gene Collection (DGC), an annotated unigene set of 5,849 full-length cDNA clones representing 43% of the fly genome (Lee et al., 2005;Stapleton et al., 2002). Clones were individually arrayed in 17 6 384-well plates, and in vitro transcription and translation was performed on small pools containing equivalent amounts of cDNA (or mRNA) for each gene. This Drosophila IVEC (DIVEC) approach has allowed for efficient genome-scale screening to identify substrates of the Pan Gu kinase and binding partners of p53 (Lee et al., 2005;Lunardi et al., 2010).
Given the conservation across phyla between cell cycle proteins, we herein applied the DIVEC approach to perform a biochemical screen for APC substrates in Xenopus interphase egg extract and identified Drosophila Microcephalin (dMCPH1) as a candidate. Human MCPH1 (hMCPH1) is a causative gene of autosomal recessive primary microcephaly (MCPH), a neurodevelopment disorder characterized by reduced brain size (Jackson et al., 2002;Woods et al., 2005). In humans, MCPH1 has been shown to prevent premature mitotic entry by regulating centrosomal recruitment of Chk1 at the G2/M transition as well as premature chromosome condensation by negatively regulating the activity of condensin II (Gruber et al., 2011;Tibelius et al., 2009;Trimborn et al., 2006;Yamashita et al., 2011). hMCPH1 has also been reported to have several functions in the DNA damage response (Gavvovidis et al., 2012;Lin et al., 2005;Peng et al., 2009;Rai et al., 2006;Tibelius et al., 2009;Trimborn et al., 2006;Yamashita et al., 2011;Yang et al., 2008). We previously reported that Drosophila syncytial embryos derived from mcph1-null females exhibit Chk2-mediated mitotic arrest in response to damaged or incompletely replicated DNA (Rickmyre et al., 2007). Because mcph1 mutants contain an intact DNA checkpoint, and MCPH1 has been shown to regulate premature chromosome condensation in other systems, we previously proposed that dMCPH1 prevents accumulation of DNA damage by delaying chromosome condensation until DNA replication is completed. Although MCPH1 is reported to function in multiple cellular processes, its regulation is not well understood. In this report, we demonstrate that dMCPH1 is a substrate of the critical cell cycle regulator, APC Cdh1 .

MATERIALS AND METHODS
cDNA clones and mutagenesis cDNA clones encoding dMCPH1-B (clone LD42241), dMCPH1-C (clone LP15451), or p78 (GH13229) were obtained from the Drosophila Gene Collection Release 1 or the Drosophila Genomics Resource Center (Indiana University, Bloomington, IN), respectively. cDNA clones encoding hMCPH1, Cyclin B, NT-Cyclin B, Mos, Luciferase, and GFP were gifts from Marc Kirschner's lab (Harvard Medical School, Boston, MA). dMCPH1-B and dMCPH1-C were subcloned into vector pCS2 for in vitro transcription and translation reactions. dMCPH1-B DN , dMCPH1-B DboxMut , and dMCPH1-B 1-64 were generated from CS2-dMCPH1-B by mutagenesis to remove the first 40 amino acids, replace amino acids 36-40 with alanines, or remove the last 762 amino acids, respectively. dMCPH1-B, dMCPH1-B DboxMut , and hMCPH1 were also subcloned into pCS2 derivatives encoding six N-or C-terminal Myc tags.

DIVEC screen and APC degradation assay
Xenopus interphase egg extract was prepared as previously described (Pfleger and Kirschner, 2000). Baculoviruses encoding human His6tagged CDH1 and His6-tagged Cyclin BD90 (gifts from Marc Kirschner's lab) were expressed in Sf9 cells by baculovirus infection and purified over nickel beads. For the DIVEC screen, radiolabeled protein pools were generated from pools of cDNAs from the Drosophila Gene Collection Release 1 by transcription and translation in reticulocyte lysates using a Gold TNT T7 kit according to the manufacturer's protocol (Promega, Madison, WI) as previously described (Lee et al., 2005). The identity of positive clones was confirmed by DNA sequencing.
For testing individual proteins in the APC degradation assay, 1 ml of radiolabeled protein was added to 10 ml of Xenopus egg extract supplemented with energy mix (1 mM HEPES, pH 7.7, 1 mM ATP, 10 mM creatine phosphate, and 1 mM MgCl 2 ) and 10 mg/ml ubiquitin. Egg extract was incubated with Xenopus Buffer control (100 mM KCl, 1 mM MgCl 2 , 0.1 mM CaCl 2 , 10 mM HEPES, 50 mM sucrose, 5 mM EGTA), His6-Cyclin BD90 (60 mg/ml), or His6-CDH1 (0.4 nM) prior to starting the reaction with addition of radiolabeled proteins, and reactions were allowed to proceed at room temperature as previously described (Ayad et al., 2003). All radiolabeled, in vitro-translated protein migrated at the expected size as assessed by SDS-PAGE/autoradiography. For radiolabeled degradation assays, loading controls were not necessary as equivalent volumes (0.5 ml) were removed at the indicated times for processing by SDS-PAGE/autoradiography. NT-Cyclin B peptide 100 mM was prepared as previously described (Pfleger and Kirschner, 2000). Pixel intensity measurements of autoradiograms were performed using ImageJ and statistical analysis was performed using the paired equal variance two-tailed t-test.
In vitro ubiquitination assay APC was purified by immunoprecipitation of Cdc27 from Xenopus interphase egg extract using Protein G Sepharose beads (GE Healthcare Life Sciences, Pittsburgh, PA) and anti-Cdc27 antibodies (AF3.1; Santa Cruz Biotechnology, Dallas, TX) as previously described (Wei et al., 2004). For each ubiquitination reaction, 5 ml of APC-bound beads was incubated with 0.75 mM purified E1 (Boston Biochem, Cambridge, MA), 2 mM His-UbcH10 (Boston Biochem), 7.5 mg/ml ubiquitin (Boston Biochem), 0.5 ml 206 Energy Regeneration Mix (2 mg/ml creatine phosphokinase, 20 mM ATP, 200 mM Creatine Phosphate, 20 mM HEPES, 20 mM MgCl 2 , 0.1% BSA), 5 mM ubiquitin aldehyde (Boston Biochem), and 10 mM DTT. 1 ml of in vitro transcription/translation reaction product and 0.4 nM His-Cdh1 or equal volume of Cdh1 dialysis buffer was incubated in each reaction for 90 minutes. Reaction products were separated by SDS-PAGE and visualized by autoradiography.

Xenopus embryo injection, immunostaining, and immunoblotting
Capped mRNA encoding Mos, GFP, hMCPH1, dMCPH1-B, or dMCPH1-B DboxMut was generated by in vitro transcription reactions using the mMessage mMachine kit per manufacturer's instructions (Life Technologies, Carlsbad, CA). Embryos were injected at the 2-or 4-cell stage with 2 ng of RNA and fixed in MEMFA (100 mM MOPS pH 7.4, 2 mM EGTA, 1 mM MgSO 4 , and 3.7% formaldehyde) after 4 hours. After fixation, embryos were washed 26in PBS and dehydrated stepwise (1 hour/step) in 75% PBS/25% methanol, 50% PBS/50% methanol, and 100% methanol and stored at 4˚C. The percentage of injected embryos exhibiting cell-cycle defects was quantified and statistical analysis was performed using the Fisher exact test.
For immunoblotting, capped mRNA encoding C-terminally Myc-tagged hMCPH1, dMCPH1-B, or dMCPH1-B DboxMut was generated, and 1 ng of RNA was injected into each cell of a two-cell staged Xenopus embryo. At 4 hours post-injection, the embryos were lysed in 66Sample Buffer (300 mM Tris pH 6.8, 12% w/v SDS, 30% w/v glycerol, 600 mM DTT, and 0.01% w/v bromophenol blue). One quarter of each lysate was analyzed by SDS-PAGE and immunoblotting using standard techniques. Primary antibodies used included mouse anti-Myc-tag (1:500, 9E10) and mouse anti-a-tubulin (1:2000, DM1a, Sigma-Aldrich, St Louis, MO). HRP-conjugated secondary antibodies were used to detect primary antibodies by chemiluminescence.
All Xenopus experiments conform to institutional and national animal welfare policies.

DIVEC screen for APC substrates
In order to identify APC Cdc20 or APC Cdh1 substrates using DIVEC, bacterial stocks containing cDNA clones from the Drosophila Gene Collection Release 1 were individually grown and their plasmids purified and pooled (Fig. 1A). Pooled clones (24 clones/ pool) were used to generate radiolabeled proteins in rabbit reticulocyte lysate as previously described (Lee et al., 2005). To test proteins for their capacity to undergo APC CDC20 -or APC Cdh1mediated degradation, protein pools were incubated in Xenopus interphase egg extract supplemented with Xenopus buffer (XB), human CycBD90, or Cdh1. Candidate APC substrates were identified by their decreased band intensity after incubation in CycBD90 or Cdh1-supplemented extract relative to the buffer control as revealed by SDS-PAGE and autoradiography.
We identified two candidate substrates of APC in Xenopus egg extract using the DIVEC approach (Fig. 1B). We initially named these candidates ''p78'' and ''p91'' based on their apparent SDS-PAGE mobility. In the primary screen that involved the use of radiolabeled protein pools, both candidates were stable in the presence of XB and CycBD90 (mitotic extract containing activated APC Cdc20 ), but they degraded in Xenopus egg extract supplemented with Cdh1, suggesting that they are substrates of APC Cdh1 and not APC Cdc20 . In addition, both candidates exhibited decreased mobility on SDS-PAGE when incubated in Cyclin BD90-supplemented (mitotic) extract, suggesting that they may be phosphorylated during mitosis.
The corresponding cDNA clones for the two candidate substrates were identified based on the predicted molecular weights of their encoded proteins and retesting in the degradation assay. We confirmed that the protein products generated by in vitro transcription and translation of these individual cDNA clones were degraded in Cdh1-supplemented Xenopus egg extract (Fig. 1C,D). p91 is encoded by clone LD43341 and corresponds to the Drosophila mcph1 gene (Brunk et al., 2007;Rickmyre et al., 2007). p78 is encoded by clone GH13229 and corresponds to CG32982, an uncharacterized Drosophila gene. Cyclin B, a well-characterized APC substrate, was not identified in our screen because it is not present in the Drosophila Gene Collection Release 1. Radiolabeled Cyclin B, however, was used as a positive control in our screen and was shown to degrade in both mitotic (activated APC Cdc20 ) and Cdh1-supplemented interphase Xenopus egg extract (data not shown).

Drosophila MCPH1-B stability is regulated by APC
We previously identified a requirement for dMCPH1 during early embryogenesis in Drosophila (Rickmyre et al., 2007). Two distinct isoforms of Drosophila MCPH1 (referred to as MCPH1-B and MCPH1-C) are produced by alternative splicing (Rickmyre et al., 2007). Both isoforms are present in larval brains and imaginal discs. Drosophila MCPH1-B (dMCPH1-B) is predominantly expressed in the ovaries and syncytial embryos, whereas MCPH1-C (dMCPH1-C) is expressed primarily in the testes. The two isoforms differ primarily at their N-and Ctermini. dMCPH1-B contains an additional 47 amino acids at its N-terminal end and lacks 200 amino acids at its C-terminal end when compared to the dMCPH1-C isoform (supplementary Schematic of the DIVEC screen strategy to identify APC substrates. 35 S-radiolabeled proteins were produced from pools of cDNA clones from the Drosophila Gene Collection Release 1 as previously described (Lee et al., 2005). Radiolabeled protein pools were incubated in Xenopus interphase egg extract supplemented with Xenopus buffer (XB), non-degradable Cyclin B (CycBD90), or Cdh1. Reaction products were analyzed by SDS-PAGE and autoradiography to identify proteins degraded via APC-Cdc20 or APC-Cdh1. (B) p91 and p78 are candidate APC substrates. Autoradiogram of two protein pools containing p91 and p78. Both p91 and p78 exhibited an upward electrophoretic mobility shift in CycBD90-supplemented (mitotic) extract and decreased band intensity in Cdh1-supplemented extract. Asterisks mark proteins in the pools that did not exhibit decreased intensity in the supplemented extract and therefore served as negative controls. (C,D) Retesting of radiolabeled p91 and p78 (prepared from individual cDNA clones) by incubation in Xenopus interphase egg extract in the presence of Cdh1 confirmed that the clones encode putative APC substrates.

RESEARCH ARTICLE
Biology Open (2014) 3, 669-676 doi:10.1242/bio.20148318 material Fig. S1A). Both isoforms contain an N-terminal BRCT domain. Only dMCPH1-C, however, contains an additional pair of BRCT domains at its C-terminal end. We identified the B isoform of dMCPH1 as a hit in our DIVEC screen for APC substrates. To demonstrate that the degradation of dMCPH1-B in Xenopus egg extract was specific to APC Cdh1 activity, we tested whether Cdh1-mediated degradation of dMCPH1-B in Xenopus interphase egg extract could be inhibited by addition of an N-terminal peptide of Cyclin B (NT-Cyclin B) containing a functional D-box ( Fig. 2A). NT-Cyclin B is degraded in Cdh1-supplemented egg extract and competitively blocks APC Cdh1 -mediated degradation of Cdc20 (Pfleger and Kirschner, 2000). Similarly, if dMCPH1-B degradation in Cdh1-supplemented Xenopus interphase egg extract were mediated by APC Cdh1 , addition of excess NT-Cyclin B should inhibit its degradation. Consistent with this model, we found that addition of NT-Cyclin B potently blocked dMCPH1-B degradation in Cdh1-supplemented extract ( Fig. 2A).
We next asked if the MCPH1-C isoform is also a substrate of APC Cdh1 . We incubated radiolabeled dMCPH1-C in Xenopus interphase egg extract in the absence or presence of Cdh1 and assessed its levels after 30 and 60 minutes by performing SDS-PAGE/autoradiography ( Fig. 2B; supplementary material Fig.   S1B). For dMCPH1-B and Cyclin B (positive control), we detected robust turnover in Cdh1-supplemented Xenopus interphase egg extract. Although we detected statistically significant Cdh1-mediated degradation for dMCPH1-C, it was not nearly as robust as that of dMCPH1-B or Cyclin B.
During our characterization of dMCPH1-B degradation, we found that an N-terminally Myc-tagged, but not a C-terminally Myc-tagged, version of dMCPH1-B degraded in Xenopus interphase egg extract (Fig. 2C), suggesting that the N-terminal Myc-tag might mask a nearby degron. These findings were consistent with a model in which the first 47 amino acids of dMCPH1-B that is not shared with dMCPH1-C contains the relevant degron that mediates degradation by APC Cdh1 . To test this possibility, we generated an N-terminal truncation mutant of dMCPH1-B (dMCPH1-B DN ) in which the first 40 amino acids was deleted. We found that this mutant was stable in Cdh1supplemented extract, indicating that the N-terminal end of dMCPH1-B contains a degron necessary for APC Cdh1 -mediated degradation (Fig. 2C).
We identified a putative D-box motif (RRPLHDSN) within the first 40 amino acids of dMCPH1-B and generated a mutant in which the first four amino acids of this sequence were replaced with alanines (dMCPH1-B DboxMut ). We found that, in contrast to the wild-type protein, dMCPH1-B DboxMut was stable in Cdh1supplemented extract (Fig. 2C). These data indicate the D-box sequence found within the N-terminal 40 amino acids of dMCPH1-B mediates its APC Cdh1 -dependent degradation.
Mutants of the Drosophila morula (mr) gene, which encodes the homolog of the vertebrate APC2 subunit of APC, have increased levels of Cyclin B due to reduced APC activity (Reed and Orr-Weaver, 1997). Syncytial embryos laid by females transhetersozygous for mr 1 and mr 2 alleles (mr 1 /mr 2 ) arrest in mitosis shortly after a few cell cycles. dMCPH1-B is primarily expressed in syncytial embryos (Brunk et al., 2007;Rickmyre et al., 2007). If dMCPH1-B were an APC substrate, we reasoned that its levels should be increased in morula mutant flies. To test this possibility, we prepared lysates from 0-1 hour syncytial embryos derived from wild-type or mr 1 /mr 2 females and assessed endogenous dMCPH1, Cyclin B (positive control), and alpha-tubulin (loading control) levels by immunoblotting (Fig. 2D). Embryos derived from mr 1 /mr 2 females had increased levels of both dMCPH1-B and Cyclin B compared to wild type, suggesting that dMCPH1-B is an APC substrate in vivo. mr 1 / mr 2 -derived embryos also contain dMCPH1, which exhibits slower mobility on SDS-PAGE (Fig. 2D). Because mr 1 /mr 2derived embryos are reported to arrest in mitosis, it is possible that this form of dMCPH1 is the result of mitotic phosphorylation.

dMCPH1-B is ubiquitinated by APC
We next sought to determine whether dMCPH1-B is a direct substrate of APC Cdh1 using a purified system as previously described (King et al., 1995;Pfleger and Kirschner, 2000). The APC was purified from Xenopus interphase egg extract by immunoprecipitation using an antibody against the Cdc27 subunit. Purified APC was then used for in vitro ubiquitination reactions containing recombinant human E1, E2 (UbcH10), Cdh1, and ubiquitin. The radiolabeled NT-Cyclin B peptide (positive control) was polyubiquinated as evidenced by the presence of higher molecular weight laddering on SDS-PAGE (Fig. 3A). In contrast, no laddering was detected for firefly luciferase (negative control). We next tested whether dMCPH1-B was ubiquitinated in our purified system and whether addition of Cdh1 would enhance ubiquitination. We found that ubiquitination of dMCPH1-B and NT-Cyclin B (positive control) was dramatically enhanced in the presence of Cdh1 in our reconstituted ubiquitination system, consistent with dMCPH1-B being an APC Cdh1 substrate (Fig. 3B). Ubiquitination of the D-box mutant, dMCPH1-B DboxMut , was observed in the presence of Cdh1, albeit at a much reduced level (Fig. 3B). This phenomenon has been observed with other APC substrates in the purified system (Araki et al., 2005;Fang et al., 1998b;Pfleger and Kirschner, 2000), and the low level of ubiquitination observed likely reflects the fact that the purified system lacks many regulatory proteins present in an extract or cell. To further confirm that the Nterminal end of dMCPH1-B contains a functional D-box, we showed that the first 64 amino acids of dMCPH1-B (dMCPH1-B 1-64 ) was ubiquitinated in the purified system and that ubiquitination was enhanced in the presence of Cdh1 (Fig. 3B). These results indicate that dMCPH1-B is a direct substrate of APC Cdh1 in vitro and that the N-terminal D-box of dMCPH1-B plays a major role in mediating its ubiquitination by APC.
Steady state-levels of hMCPH1 do not change in a cell cycledependent manner in cultured human cells Human MCPH1 (hMCPH1) contains one N-terminal and two Cterminal BRCT domains and is more similar to dMCPH1-C in organization than dMCPH1-B (supplementary material Fig.  S1A). Although hMCPH1 lacks an N-terminal degron similar to dMCPH1-B, it contains several putative D-boxes and a candidate KEN box. To determine if hMCPH1 is also degraded via APC Cdh1 , radiolabeled hMCPH1 was incubated in Xenopus interphase egg extract in the absence or presence of Cdh1. In contrast to dMCPH1-B, hMCPH1 did not degrade in Cdh1supplemented extract (supplementary material Fig. S2A). The observed doublet is consistent with an alternative translation initiation downstream (35 amino acids) of the canonical start site using the rabbit reticulocyte translation system. It is possible that the incapacity of Xenopus interphase egg extract to support hMCPH1 degradation by APC Cdh1 is due to differences between the amphibian and human systems.
We next assessed the steady-state levels of hMCPH1 throughout the cell cycle in cultured human cells. HeLa cells were synchronized by nocodazole block and release, and aliquots were taken at two-hour time points in order to assess endogenous levels of hMCPH1, Cyclin B, Cyclin A, p27, and Cdk1 by immunoblotting (supplementary material Fig. S2B). From 2-10 hours after nocodazole release, p27 levels were elevated, and Cyclin A and Cyclin B levels were decreased, consistent with cell-cycle progression into G1. By 10 hours after nocodazole release, p27 levels were decreased, whereas Cyclin A and Cyclin B levels were increased, indicating cell-cycle progression through S, G2, and M-phase. Throughout the time course, hMCPH1 levels remained constant. Taken together, these data suggest that the overall cellular levels of hMCPH1 do not fluctuate in an APCdependent manner.

Overexpression of hMCPH1 or dMCPH1-B results in cell-cycle defects
Because APC-mediated degradation of substrates is required for cell-cycle progression, we sought to determine if increasing MCPH1 levels would lead to disruption of cell division. The Xenopus embryo system has been previously used as an in vivo readout of cell cycle progression (Fang et al., 1998a;Ivanovska et al., 2004;McGarry and Kirschner, 1998;Pfleger et al., 2001a;Pfleger et al., 2001b;Rankin et al., 2005). An advantage of the Xenopus embryo system is that the non-injected cells act as a negative control within the same embryo.
We tested whether injecting mRNAs encoding hMCPH1 or dMCPH1-B into developing Xenopus embryos at the 2-4 cell stage would lead to disruption of cell division. Because Cdh1 is absent in the early embryo, levels of injected MCPH1 should not be regulated by APC, leading to inappropriate activity during these early embryonic cell cycles (Lorca et al., 1998). Injected embryos were allowed to develop, fixed, and assessed for cell division defects (Fig. 4A,B). Mos (a component of cytostatic factor; positive control) is required to maintain metaphase arrest during meiosis II by inhibiting APC activity (Tunquist and Maller, 2003). Injection of Mos mRNA resulted in a block in cell division in the injected half of the embryo. Injection of GFP (negative control) had no observable cell cycle effect on the injected cells. In contrast, 92% of embryos injected with hMCPH1 and 67% of those injected with dMCPH1-B exhibited reduced cell number and increased cell size, likely due to cellcycle arrest. The levels of the human and Drosophila MCPH1 proteins expressed in embryos are nearly equivalent as assessed by immunoblotting (supplementary material Fig. S3). Thus, we attribute the difference in potency between hMCPH1 and dMCPH1-B to be due to differences in sequence identity between the insect and vertebrate proteins. Finally, injections of the D-box mutant of dMCPH1-B also result in embryos with cell cycle arrest (Fig. 4A,B). As expected, levels of the mutant are comparable to that of the wild-type dMCPH1-B protein (not degraded due to the absence of Cdh1 in the early embryo) (supplementary material Fig. S3).
Embryos injected with hMCPH1 were fixed and stained for tubulin and DNA to further examine the cell-cycle defects associated with hMCPH1 overexpression (Fig. 4C). In contrast to the uninjected cells, hMCPH1-injected cells contained abnormal spindle arrangements, free centrosomes, lack of DNA, and/or DNA trapped between daughter blastomeres. These findings are consistent with a previous study in which Sororin, another substrate of APC Cdh1 , was overexpressed in Xenopus embryos (Rankin et al., 2005).

DISCUSSION
In our DIVEC screen for APC substrates in Xenopus egg extract, we identified two candidates: the protein encoded by CG32982, a previously uncharacterized Drosophila gene, and dMCPH1-B, a splice variant of Drosophila mcph1, the homologue of a human microcephaly gene. We show that dMCPH1-B undergoes Cdh1dependent degradation in Xenopus egg extract and not Cdc20dependent degradation. We show that APC-mediated degradation of dMCPH1 is restricted primarily to the splice variant dMCPH1-B, which contains an N-terminal D-box sequence required for Cdh1-mediated degradation. This restriction may allow for tissueor developmental-specific regulation of dMCPH1 levels during the cell cycle. Consistent with this idea, we show that dMCPH1 levels are up-regulated in syncytial embryos with reduced APC activity (mr 1 /mr 2 ), a developmental stage in which dMCPH1-B is preferentially expressed. The low level of dMCPH1-C degradation may reflect cryptic APC Cdh1 site(s) that is recognized in our optimized system. Alternatively, our system may be missing a co-factor required for efficient turnover of dMCPH1-C by APC Cdh1 in Drosophila embryos that allows for differential regulation of dMCPH1-B and dMCPH1-C by the APC.
Because dMCPH1-B is preferentially expressed during Drosophila syncytial embryogenesis and is down-regulated by the APC, one would predict that dMCPH1-B levels would oscillate throughout the cell cycle during this developmental stage. However, oscillations in total levels of APC substrates, such as mitotic cyclins, are not observed until the later cycles of syncytial embryogenesis (Raff et al., 2002). In fact, localized degradation of Cyclin B by the APC is proposed to control cellcycle progression during these syncytial cycles (Raff et al., 2002). Thus, it is not surprising that Brunk et al. observed no change in total levels of dMCPH1 during the cell cycles of syncytial embryogenesis (Brunk et al., 2007). It is possible that dMCPH1-B, like Cyclin B, is targeted for degradation in a localized manner.
In vitro ubiquitination assays also revealed that the N-terminal D-box of dMCPH1-B is sufficient for APC Cdh1 -mediated ubiquitination. The finding that the N-terminal D-box is also not required for APC Cdh1 -mediated ubiquitination suggests that dMCPH1-B contains additional degrons. This finding is not surprising because many APC substrates have been shown to contain multiple APC-targeting motifs (Min and Lindon, 2012). Although dMCPH1-B contains multiple predicted D-box motifs, we show that deletion of the N-terminal D-box is sufficient to significantly block its Cdh1-dependent degradation in Xenopus interphase egg extract. dMCPH1-C also contains many of these putative D-boxes motifs, as well two motifs in the C-terminal region that are not shared with dMCPH1-B. These motifs potentially mediate the low level of degradation in APC Cdh1activated Xenopus egg extract.
Two isoforms of human MCPH1 produced by alternative splicing have been previously described and are structurally similar to Drosophila dMCPH1-B and C (Gavvovidis et al., 2012). The full-length form of hMCPH1 (used in the current study) contains an N-terminal and two C-terminal BRCT domains, whereas the short form lacks the C-terminal paired BRCT domain region. A previous report has shown that the Cterminal paired BRCT domains of full-length hMCPH1 interact with Cdc27, a subunit of the APC, and the authors hypothesized that hMCPH1 is a substrate of the APC or may regulate APC activity (Singh et al., 2012). In our current study, however, we were not able to observed changes in bulk steady-state hMCPH1 levels in cultured human cells during the cell cycle.
MCPH1 has been shown to be a rapidly evolving gene that exhibits low sequence similarity between homologs (Ponting and Fig. 4. Overexpression of dMCPH1-B or hMCPH1 results in cell-cycle defects. (A) Representative images of whole Xenopus embryos fixed four hours after injection of Mos, GFP, full-length human MCPH1 (hMCPH1), dMCPH1-B, or dMCPH1-B DboxMut RNA at the 2-4cell stage. Arrows indicate injected halves of embryos. (B) Quantification of Xenopus embryos displaying cell division defects 4 hours postinjection. Total number of embryos injected is indicated in parentheses. *p,0.005 (C) Confocal sections of the uninjected (left) and injected (right) areas of a representative whole embryo following injection with hMCPH1 mRNA. Microtubules, green; DNA, red. Scale bar: 100 mm. Jackson, 2005). Therefore, it is perhaps not surprising that several functions of MCPH1 appear to be species-specific. For example, only hMCPH1 has been shown to regulate condensin IIdependent chromosome condensation (Yamashita et al., 2011). Thus, it is possible that APC-dependent regulation of Drosophila MCPH1 is not a conserved feature in humans. Alternatively, similar to the situation with Cyclin B in early embryos of Drosophila, levels of hMCPH1 may be regulated locally. Alternatively, the activity of hMCPH1 could be regulated via its binding partners/effectors. Indeed, binding partners, SET/ Phosphatase Inhibitor 2 and E2F1, are potential or known APC substrates, respectively (Brautigan et al., 1990;Budhavarapu et al., 2012;Leung et al., 2011;Peart et al., 2010;Yang et al., 2008). Thus, the regulation of these two MCPH1 binding partners by the APC could serve as a mechanism to regulate MCPH1 activity in a cell cycle-dependent manner in vertebrates.
We show herein that overexpression of either hMCPH1 or dMCPH1-B in Xenopus embryos, an assay that has been previously used to characterize important cell-cycle regulators, leads to cell-cycle defects (Fang et al., 1998a;Ivanovska et al., 2004;McGarry and Kirschner, 1998;Pfleger et al., 2001a;Pfleger et al., 2001b;Rankin et al., 2005). This finding suggests that tight regulation of the levels of MCPH1 may be required for proper cell-cycle progression. Because hMCPH1 is known to negatively regulate mitotic entry and chromosome condensation, the cell-cycle defects we observe in Xenopus embryos overexpressing MCPH1 may be due to misregulation of these processes (Alderton et al., 2006;Tibelius et al., 2009;Trimborn et al., 2006;Yamashita et al., 2011). Although MCPH1 has been implicated in many cellular processes, regulation of its activity is not well understood. Future studies to elucidate how the activities and/or levels of MCPH1 are controlled will be important to fully understand how this evolutionarily conserved, highly evolving protein functions in regulating critical processes within the developing organism.