Cullin-dependent E3 ubiquitin ligases (CDL) are key regulators of protein destruction that participate in a wide range of cell biological processes. The Roc subunit of CDL contains an evolutionarily conserved RING domain that binds ubiquitin charged E2 and is essential for ubiquitylation. Drosophila melanogaster contains three highly related Roc proteins: Roc1a and Roc2, which are conserved in vertebrates, and Roc1b, which is specific to Drosophila. Our previous genetic data analyzing Roc1a and Roc1b mutants suggested that Roc proteins are functionally distinct, but the molecular basis for this distinction is not known.
Using co-immunoprecipitation studies we show that Drosophila Roc proteins bind specific Cullins: Roc1a binds Cul1-4, Roc1b binds Cul3, and Roc2 binds Cul5. Through domain swapping experiments, we demonstrate that Cullin binding specificity is strongly influenced by the Roc NH2-terminal domain, which forms an inter-molecular β sheet with the Cullin. Substitution of the Roc1a RING domain with that of Roc1b results in a protein with similar Cullin binding properties to Roc1a that is active as an E3 ligase but cannot complement Roc1a mutant lethality, indicating that the identity of the RING domain can be an important determinant of CDL function. In contrast, the converse chimeric protein with a substitution of the Roc1b RING domain with that of Roc1a can rescue the male sterility of Roc1b mutants, but only when expressed from the endogenous Roc1b promoter. We also identified mutations of Roc2 and Cul5 and show that they cause no overt developmental phenotype, consistent with our finding that Roc2 and Cul5 proteins are exclusive binding partners, which others have observed in human cells as well.
Citation: Reynolds PJ, Simms JR, Duronio RJ (2008) Identifying Determinants of Cullin Binding Specificity Among the Three Functionally Different Drosophila melanogaster Roc Proteins via Domain Swapping. PLoS ONE 3(8): e2918. https://doi.org/10.1371/journal.pone.0002918
Editor: Francois Schweisguth, Institut Pasteur, France
Received: May 16, 2008; Accepted: July 12, 2008; Published: August 13, 2008
Copyright: © 2008 Reynolds et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: This study was supported by American Cancer Society grant RSG-04-179-01-DDC. ACS had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript
Competing interests: The authors have declared that no competing interests exist.
Many aspects of cell and developmental biology require the regulation of protein function via ubiquitin-mediated protein destruction. Protein ubiquitylation requires the action of three families of proteins: E1 Ubiquitin Activators (Uba), E2 Ubiquitin Conjugators (Ubc), and E3 Ubiquitin Ligases (Ubl) , . Ubiquitin monomers are activated through conjugation via a thiolester linkage to an internal cysteine in E1, which then transfers the ubiquitin to a cysteine residue of an E2 protein. The E2 interacts with an E3 to mediate covalent attachment of ubiquitin onto substrate proteins. Repeated rounds of E2/E3-mediated ubiquitin transfer result in polyubiquitylation, allowing substrate proteins to be recognized and destroyed by the proteasome. Vertebrates and sea urchins have two distinct E1 enzymes, and most other organisms are thought to only have a single E1 , . While there are considerably more E2's, much of the modularity of the ubiquitin-proteasome pathway comes from the large number of different E3 ligases.
E3's can be broadly categorized as either HECT domain or RING domain. Ubiquitin is directly conjugated to an internal cysteine residue of HECT domain E3's before being transferred onto the substrate protein . RING E3's do not conjugate ubiquitin, but rather stimulate its transfer from the E2 to the substrate , . RING domains contain conserved cysteine and histidine residues that chelate zinc ions to provide a structure that interacts with an E2 , . Several RING domain structures have been solved, and they share extensive structural conservation , , , , . At least two of these RING proteins, c-Cbl and Rbx1/Roc1, use a similar hydrophobic groove in the protein to bind an E2. All of the Zn++ chelating residues of the RING domain (as well as the Zn++ ions) are required for proper folding and function of the protein , , , , . The importance to E3 ligase function of residues or domains outside of the RING domain is not currently understood.
RING E3's can be further categorized as either single or multi-protein complexes. Single protein E3's, like c-Cbl, perform the entire function of the E3 within the context of one polypeptide . Multi-protein RING E3 ligases, like the Anaphase Promoting Complex (APC) and Cullin-Dependent Ligases (CDL), use a complex of many different proteins to facilitate ubiquitin transfer . CDL are composed of three modules (Cullin, Roc, substrate adapter/receptor), each with a distinct role . The Cullin serves as a scaffold, binding a Roc protein at its COOH-terminus and a substrate adapter/receptor module at its NH2-terminus. The Roc protein serves as an interaction surface for ubiquitin-bound E2, and thereby recruits charged ubiquitin to the E3 ligase machinery. The substrate adapter/receptor module (a single protein in Cul3 CDL and multiple proteins in all other CDL) binds directly and specifically to one or a small subset of proteins targeted for polyubiquitylation and destruction. Large gene families encode these substrate adapter/receptor modules, which are thought to provide most of the CDL substrate specificity , . For instance, the F-box family (33 members in Drosophila ) contains a diverse group of proteins that recruit specific substrates to the Cul1 E3 ligase via the Skp1 adaptor, which binds both the NH2-terminus of Cul1 and the F-box domain , .
The RING domain-containing Roc proteins are essential for CDL function and are also encoded by a gene family . Humans and C. elegans contain two Roc proteins, Roc1 and Roc2, while there has been a radiation of the Roc1 family in Drosophilid species (T.D. Donaldson and R.J.D., unpublished). For instance, Drosophila melanogaster encodes three Roc proteins named Roc1a, Roc1b and Roc2 . The level of functional redundancy among metazoan Roc proteins has remained largely unexplored. We have been addressing this issue in Drosophila melanogaster by generating and characterizing mutations in the Roc genes. We previously showed that Roc1a mutants are lethal, while Roc1b mutants are male sterile , . These different phenotypes suggest that the Rocs are not redundant in function, even though Roc1a and Roc1b are 78% identical in the RING domain. Moreover, this lack of redundancy is not a result of tissue specific expression, since full compensation of Roc1a mutant phenotypes in wing imaginal cells cannot be achieved via over-expression of either Roc1b or Roc2 . These data suggest that there exist intrinsic differences in the highly related Roc proteins. Here we show that each Drosophila Roc protein binds a distinct set of Cullin proteins. We analyze chimeras between the three Roc proteins to map binding determinants, and demonstrate that both the RING and NH2-terminus of the Roc proteins can influence Cullin binding. Further, we show that not all RING domains of the individual Roc proteins are functionally interchangeable in vivo. This suggests that rather than simply providing an E2 binding interface for Cullin proteins, the Roc proteins are structurally distinct and specific RING domains play an important role in determining overall CDL function during development.
Roc proteins bind specific Cullins
We previously detected Roc-Cullin interactions in vivo by immunoprecipitating Flag-tagged Roc1a, Roc1b, and Roc2 proteins from transgenic embryo extracts and identifying interacting proteins by mass spectrometry . For these experiments, each Roc protein was expressed using the ubiquitous Roc1a promoter . The data indicated that Roc1a bound Cul1-4 and that Roc2 bound Cul5, but could not eliminate the possibility that certain Roc-Cullin complexes were undetectable by the IP/mass spec analysis. To more comprehensively test for the presence of Roc-Cullin complexes, we assembled a panel of anti-Cullin antibodies (see methods) and used these in IP/immunoblot analyses. Anti-FLAG immunoprecipitates of extracts made from transgenic embryos expressing FLAG-tagged Roc1a, Roc1b, or Roc2 proteins from the Roc1a promoter were probed with antibodies that specifically recognize each Cullin (Figure 1A). The data indicate that Roc1a binds Cullins 1–4, but not Cul5, that Roc1b binds strongly only to Cul3, and that Roc2 binds only to Cul5. This is consistent with our previous mass spec results  and shows that Rocs have strong Cullin binding preferences in vivo.
A, Flag-Roc protein complexes were immunoprecipitated from extracts prepared from wild type (−), Flag-Roc1a, Flag-Roc1b, and Flag-Roc2 transgenic embryos, and co-precipitating Cullin proteins were detected by immunoblotting. B, Alignment of Drosophila Roc proteins, indicating how we designated NH2-terminal and RING domains. Asterisks indicate the Zn++ chelating residues of the RING domain that are essential for ligase function, and the carets indicate amino acids that make important contacts with Cullins. These assignments are based on the Cul1-Rbx1 structure of Zheng et al .
The Roc Protein NH2-terminus can determine Cullin binding specificity
Available crystal structures of Roc-Cullin complexes (e.g. Roc1-Cul1 and Roc1-Cul4) reveal that the ∼110 amino acid Roc proteins contain two general domains, an NH2-terminal β-strand of between 41 and 56 amino acids and a globular RING domain that chelates 3 zinc ions (Fig. 1B) , . Deletion of the NH2-terminal β-strand of human Roc1 abrogates binding to Cul1 , indicating that this domain is required for Cullin binding. Both the NH2-terminal β-strand and the RING domain make close contacts with the Cullin homology domain at the Cullin COOH-terminus, and thus could potentially mediate specific Cullin-Roc interaction (Fig. 1B) . However, because the sequence of the RING domain is more highly conserved than the NH2-terminal β-strand, we hypothesized that the NH2-terminus of Roc proteins is responsible for mediating specific Cullin interactions. For instance, the Roc1a and Roc1b RING domains are 78% identical (Fig. 1B), yet Roc1b binds strongly only to Cul3 while Roc1a binds strongly to Cullins 1–4 (Fig. 1A). To determine whether one of these two domains in Roc proteins is responsible for specific Cullin binding, we created a series of chimeric constructs that join the NH2-terminus of one Roc protein to the COOH-terminal RING domain of another (RING-swap constructs, Fig. 2A). For example, AN2R contains the Roc1a NH2-terminus fused to the Roc2 RING domain. All constructs have an NH2-terminal V5 epitope tag and are expressed with the Roc1a promoter. If the NH2-terminus is sufficient to confer Cullin binding specificity, all chimeras with the same NH2-terminal Roc sequence should bind the same Cullins, regardless of the RING domain to which they are fused.
A, Schematic representation of the RING swap constructs. All constructs are expressed with the Roc1a promoter and regulatory regions, and the chimeric proteins contain an amino-terminal V5 tag. B, Control Roc1a and Roc1b or ANBR and BNAR constructs were transfected into S2 cells and cellular extracts were immunoprecipitated with anti-V5 antibodies and probed for the presence of Cul1 and Cul3 by immunoblotting. C, Control Roc1a and Roc2 or AN2R and 2NAR constructs were transfected into S2 cells and cellular extracts were immunoprecipitated with anti-V5 antibodies and probed for the presence of Cul1 and Cul5 by immunoblotting. D, AN2R and 2NAR chimeras were tested for interaction with Cul3 as in B, C.
We transfected these constructs into S2 cells and determined Cullin binding by IP/immunoblot. Because we had already observed that Roc1a binds Cul1 and Cul3 but not Cul5, that Roc1b binds only Cul3, and that Roc2 binds only Cul5 (Fig. 1A), we focused our analysis on these interactions. The ANBR chimera showed the same binding preference as Roc1a: it bound both Cul1 and Cul3 (Fig. 2B). Similarly, the BNAR chimera displayed the same binding specificity as Roc1b: it bound Cul3 but not Cul1 (Fig. 2B). These data indicate that the NH2-terminus of a Roc protein can direct specific Cullin binding.
Chimeras between Roc1a and Roc2 behaved slightly differently than the ANBR and BNAR proteins. For instance, AN2R failed to bind any Cullin, even though it could be stably expressed (shown for Cul1 and Cul5 in Fig. 2C). There could be several reasons why AN2R fails to bind Cullin. There may be amino acids in the Roc1a RING domain necessary for Cul1 binding that are not present in the Roc2 RING domain. We swapped several potential specificity residues in the RING domain between Roc1a and Roc2, but were unable to alter the Cullin binding (data not shown). Alternatively, since ANBR binds to Cul1, the Roc2 RING domain may contain amino acids that prevent binding to Cul1. However, we show below that the AN2R protein is not active as an E3 ligase (for example, see Fig. 6 below), and thus this protein chimera is functionally inactive perhaps because it does not fold properly. In the reciprocal experiment, 2NAR bound strongly to Cul5, and more weakly to Cul1 (Fig. 2C). Interestingly, we could also detect some binding of 2NAR to Cul3 (Figure 2D). These data indicate that the Roc2 NH2-terminus confers strong binding preference to Cul5, and that the Roc1a RING domain contributes somewhat to the selection of Cul1 and Cul3.
To confirm some of these observations in vivo, we generated multiple AN2R and 2NAR transgenic lines and analyzed embryo extracts by IP-Western analysis as in Figure 1. We consistently obtained similar results as in S2 cells; AN2R bound no Cullin, while 2NAR bound Cul5 but not Cul1 as did normal Roc2 (Fig. 3A). In addition, 2NAR also bound Cul3 (Fig. 3B). Thus, the Roc NH2-terminus provides a strong determinant for Cullin binding specificity, but is not always sufficient. In addition, since full length Roc2 does not bind either Cul1 or Cul3, our data suggest that the RING domain of Roc1a plays a more important role in Cullin binding specificity than the RING domain of Roc2.
A, RING-swap chimeric proteins were immunoprecipitated from transgenic embryo extracts and tested for interaction with Cul1 and Cul5 by immunoblotting. Two independent transgenic lines of AN2R and 2NAR are shown. B, Two 2NAR transgenic lines were tested for interaction with Cul3.
Nedd8 is a small ubiquitin-like protein that is conjugated to the K720 residue of Cul-1 (and to an homologous lysine in all other Cullins as well) using Uba3 (E1), Ubc12 (E2), and Roc1 (E3) , , , . This modification is in turn cleaved off by the multi-subunit COP9 Signalosome (CSN) , . Since mutations in the pathways that conjugate and remove Nedd8 are detrimental, the current model is that cycles of neddylation and de-neddylation are necessary for the proper function of CDL , , . We observed both the unmodified and the less abundant, slower migrating neddylated form of Cullin in some of our experiments (e.g. Fig. 1 Cullins 1–3). Because Roc1 can influence Cullin neddylation, we examined our co-immunoprecipitation data paying particular attention to whether association with different Roc chimeras affects the steady state amount of Cullin neddylation. We could find no consistent correlation between Cullin neddylation and a particular domain of one of the Roc proteins.
The Roc1b RING domain cannot provide all Roc1a function
Since the ANBR protein displays the same binding specificity as Roc1a, we wanted to determine whether it could rescue the lethality caused by the null Roc1aG1 mutation . Roc1a is located on the X chromosome, and thus Roc1aG1 males are not viable. We set up an experiment where fathers carrying an autosomally located Roc1a (as control) or ANBR transgene (expressed with the Roc1a promoter) were crossed to Roc1aG1/FM7 mothers and scored for the presence of rescued Roc1aG1 males. While the wild type Roc1a transgene was able to rescue the lethality of the Roc1aG1 mutation, none of 5 different ANBR transgenic insertions were able to do so (Fig. 4A). This was not a result of expression level differences, because all 5 of the ANBR proteins accumulated to a level comparable to the control Roc1a transgenic protein (Fig. 4B). Thus, while ANBR binds Cul1 (Fig. 2) and Cul2-4 (not shown) similarly to Roc1a, it is unable to function the same as Roc1a. This was somewhat surprising, considering that Roc1a and Roc1b share 78% protein identity in the RING domain. One possibility is that the Roc1b RING domain is unable to interact with the same E2's as the Roc1a RING domain when assembled into Cullin complexes, which would suggest that at least one essential target of a Roc1a E3 ligase is dependent on the specific RING domain sequence of Roc1a. The AN2R construct was also unable to rescue Roc1aG1 lethality (data not shown), consistent with the failure of the AN2R protein to bind Cullin.
A, Transgenes expressing chimeric ANBR proteins were tested for rescue of Roc1aG1 lethality (see Methods for genetics). All F1 progeny contain a single copy of the transgene. The transgenes are expressed under control of the Roc1a regulatory sequences. The percentage of progeny with each genotype is indicated, as is the total number of progeny scored (n). B, V5 immunoblot of extracts prepared from adult males containing the indicated transgenes. (−) indicates non-transgenic wild type control.
In several of these rescue experiment crosses we detected a small number of unbalanced male progeny that did not display the sn phenotype, and thus that did not contain the Roc1aG1 mutant chromosome (Fig. 4A). We do not unambiguously know the origin of these males, but since they were invariably sterile they are likely XO male progeny resulting from meiotic non-disjunction events in the Roc1aG1/FM7 females. This raises the possibility that reduction of Roc1a gene dose in females affects meiotic chromosome segregation.
Chimeric Roc proteins can function in vivo
Recently, Arama et al. showed that a testes-specific Cul3 isoform forms an E3 ligase with Roc1b in the testes, and Roc1b mutant males are sterile because of a failure to complete the late stages of sperm differentiation . Since the BNAR construct displays the same binding specificity as Roc1b, we tested whether the BNAR chimera could rescue the male sterility caused by the Roc1bdc3 null mutation (Fig. 5). Male fertility was measured by determining the proportion of eggs that hatched into first instar larvae after mating to wild type females. Three different transgenic lines expressing V5 epitope-tagged Roc1b under the control of the Roc1b promoter were able to rescue the male sterile phenotype (Fig. 5A). Six different BNAR lines rescued the male sterility defect, five of them to the level of the control Rob1b transgenes (Fig. 5A). The BNAR chimeric proteins were expressed from the Roc1b promoter at levels comparable to normal Roc1b (Figure 5b). Because BNAR binds to Cul3, we conclude that the Roc1a RING domain can provide Roc1b function during spermatogenesis. This is consistent with our previous observations indicating the forced expression of normal Roc1a from the Roc1b promoter can partially rescue the Roc1b male fertility defect . When considered together with the failure of ANBR to rescue the Roc1a mutant, these results suggest that, within the context of the male germ line-specific Cul3 E3 ligase complex, the Roc1a RING domain can productively interact with the same E2s as Roc1b, while Roc1b cannot do so with all of the E2s that function with Roc1a.
A, Egg hatching was assessed for progeny of Roc1bdc3 homozygous mutant males containing the indicated transgene. “Control” indicates Roc1bdc3/+ genotype. (−) indicates no transgene; i.e. a Roc1bdc3 homozygous mutant. 1A::1B indicates Roc1b driven by the Roc1a regulatory sequences. All other lines are under control of the Roc1b regulatory sequences. 500 eggs were analyzed for each line. B, V5 immunoblot of extracts prepared from adult males containing the indicated transgenes.
Interestingly, expression of wild type Roc1b from the Roc1a promoter was unable to rescue male sterility (Fig. 5A). This suggests that while the Roc1a promoter is active in the male body , it is not expressed in the male germ line in a manner appropriate to provide Roc1b function. Thus, the Roc1b regulatory sequence appears to confer expression in the testes that cannot be duplicated by the Roc1a promoter.
Chimeric Roc proteins have E3 ligase activity in vitro
Although ANBR binds Cul1-4, it does not rescue the lethality of Roc1a mutation. A possible explanation for this result is that the ANBR chimera protein is deficient in E3 ligase activity. To test this, we expressed all of the Drosophila Roc proteins and chimeras as GST fusion proteins in E. coli and purified them (Fig. 6A). We then tested them for E3 ligase activity using a previously described in vitro assay that detects E2- and GST-Roc-dependent polyubiquitin formation in the absence of either Cullin or a particular substrate , . The ANBR protein was fully functional in this assay (Fig. 6B). Thus, ANBR can bind Cullin and function as an E3 ligase, but it cannot provide all the function of Roc1a in vivo.
A, Coomassie stained gel of purified GST-Roc proteins used in the ligase assays. Bracket indicates GST-Roc proteins. Asterisk indicates GST. Lower bands are degradation products. B, All Drosophila Roc proteins and chimeras were assessed for ligase activity in a substrate free assay. Briefly, 250 ng of Roc protein (or control GST) were added to a ubiquitin ligase mixture containing UbcH5, ubiquitin, and ligase buffer and incubated for 45 minutes. “−” and “+” indicate the absence or presence of UbcH5 in the reaction, respectively. Ubiquitin conjugates were detected by Western using an anti-Ub antibody (bracket indicates poly-ubiquitin chains), and GST-Roc proteins were detected using an anti-GST antibody.
Roc1a and Roc2 displayed high E3 ligase activity, whereas Roc1b showed a weaker ability to promote poly-ubiquitylation (Fig. 6B). Comparing this activity with that of the chimeras, a pattern emerges: Roc1a and ANBR promote extensive polyubiquitylation, while that of Roc1b and BNAR is lower. Similarly, Roc2 and the 2NAR chimera are both highly active in this assay (Fig. 6B). Thus, even though the RING domain is known to mediate most of the physical interaction with the E2 , the Roc NH2-terminus may play a significant role in determining the efficiency of poly-ubiquitylation with a particular E2. As noted above, in addition to its inability to bind Cullin (Fig. 2C & 2D), the AN2R protein is non-functional as an E3 ligase in this assay (Fig. 6B).
Roc2 and Cul5 Mutant Analysis
Because Roc2 and Cul5 bind only to each other, we hypothesized that a Roc2-Cul5 complex would function independently of other Roc-Cullin complexes and that mutations of each gene would cause the same phenotype. In addition, this hypothesis predicts that the Roc2 mutant phenotype would be different than the phenotype we previously determined for Roc1a and Roc1b mutants , . The Roc2 locus is complex, with two protein coding exons separated by an intron greater than 25 kb in length (Fig. 7A). Within this intron are two predicted genes (CG8234 or CG30035) that encode sugar transporters transcribed from the strand opposite Roc2 transcription (Fig. 7A). We analyzed several transposon insertion lines for expression of Roc2 and identified two mutant alleles, both of which are viable. The Roc2KG P element insertion is within the large intron, while the Roc2pBac piggyBac insertion is in a smaller intron upstream of the first protein-coding exon (Fig. 7A). RT-PCR analysis of embryonic mRNA (from mating homozygous males and virgin females) revealed that the Roc2KG allele expresses no detectable mRNA, while the Roc2pBac allele expresses a reduced amount of mRNA compared to wild type (Fig. 7C). Neither insertion reduces the expression of the CG8234 or CG30035 genes (Fig. 7C). The Roc2KG allele also produces no detectable Roc2 protein as measure by immunoblotting of embryonic protein extracts (Fig. 7E), and thus it is a strong loss of function mutation. Roc2KG mutant animals develop normally, and we could detect no obvious phenotype, except for a slight reduction in female fecundity.
A, Schematic of the Roc2 locus. CG8234 and CG30035 are genes of unknown function as annotated by FlyBase (putative sugar transporters). B, Schematic of the Cul5 locus. Right angle arrows indicate start of transcription. Open arrow heads show the position of primers used for RT-PCR. Larger black triangles are P-element or piggyBac insertions. The boxes indicate exons, and the shaded regions represent the open reading frame. Dotted line indicates splicing. C, RT-PCR analysis of the Roc2 alleles. KG and pBac are homozygous for the insertions, and KG/pBac is a transheterozygote. Ribosomal protein 49 (rp49) was used as a positive control. D, RT-PCR analysis of the Cul5 allele. −RT indicates that no reverse transcriptase was added. E, Immunoblot comparing Roc2 protein levels in wild-type (w1118) and homozygous Roc2KG embryos. F, Immunoblot comparing Cul5 protein levels in wild-type and homozygous Cul5EY embryos. In each case the embryos were derived from crosses between mutant mothers and fathers. G, Embryo extracts from Cul5 and Roc2 mutants were blotted with antibodies against the respective proteins.
The Cul5 locus is simpler than that of Roc2, and the Cul5 transcript includes 7 exons and 6 introns. We identified a P element (Cul5EY) that is inserted into the second exon of Cul5 at amino acid D346 of the predicted open reading frame (Fig. 7B). RT-PCR analysis of embryonic mRNA (from homozygous mutant males and virgin females) revealed a reduced level of Cul5 mRNA in Cul5EY (Fig. 7D), and we were unable to detect Cul5 protein by immunoblotting of protein extracts from the same mating (Fig. 7F), indicating that Cul5EY is a strong loss of function allele. As with Roc2, Cul5EY mutants develop normally and do not display any overt morphological defects. That Roc2 and Cul5 mutant animals are viable and display no obvious developmental defects is consistent with our analysis of Roc-Cullin interactions indicating that Roc2 and Cul5 bind exclusively to each other. Indeed, Roc2 and Cul5 accumulation in vivo is interdependent: Roc2 was undetectable in Cul5 mutant embryo extracts, and Cul5 was greatly reduced in Roc2 mutant embryo extracts (Fig. 7G).
While Roc1a does not bind Cul5 when Roc2 protein is present, it is possible that we were unable to observe a phenotype in Roc2 mutants because Roc1a can bind Cul5 in the absence of Roc2, and thereby functionally substitute for Roc2. We tested this by introducing a Roc1a transgene into the Roc2KG mutant background. Even in this genotype, Roc1a bound to Cul1 but not detectably to Cul5 (Fig. 8). Moreover, as we show in Fig. 6G, the pool of Cul5 available for binding Roc1a is greatly reduced in Roc2 mutant animals relative to wild type. Thus, the Cul1 and Cul5 E3 ligase complexes form independently of one another and do not compete for the same pool of Roc proteins.
A, Extracts were prepared from embryos with either a wild-type (Gen = +) or Roc2 mutant (Gen = Roc2KG) background and the indicated transgene. The immunoprecipitated FLAG-Roc protein is indicated at the top. (−) indicates no transgene.
In this study we show that the Roc proteins play a part in the functional modularity of Cullin-dependent E3 ligases. Our data show that selective Roc-Cullin interactions occur in vivo in D. melanogaster, and that the highly conserved Roc proteins serve distinct roles as members of different Cullin E3 ligase complexes.
Roc-Cullin interaction determinants
The Roc NH2-terminus is necessary for binding to Cullin protein  and forms a β-strand that makes an inter-molecular β-sheet with the Cullin protein , . Our analysis of “RING swap” protein chimeras indicates that in some instances the Roc NH2-terminal β-strand is the primary contributor to Roc-Cullin binding specificity. Both fusing the Roc2 NH2 terminus to the Roc1a RING domain (2NAR) and fusing the Roc1a NH2-terminus to Rob1b (ANBR) results in proteins that primarily display the Cullin binding preferences of Roc2 and Roc1a, respectively. However, our data clearly indicate that the RING domain also makes a contribution to Cullin binding preference. While a full length Roc1a construct bound Cul1-4 (Fig. 1a), a construct consisting of the Roc1a NH2 terminus fused to the RING domain of the more distantly related Roc2 (AN2R) was unable to bind any Cullin. Substituting in the Roc1b RING domain, however, was able to restore Cullin binding, and the resulting ANBR protein displayed a Cullin binding profile identical to Roc1a. This suggests that a region of the RING domain that is more similar between Roc1a and Roc1b than Roc2 participates in Roc1a-Cullin binding preferences. Roc1a is 78% identical to Roc1b across the RING domain, while it only shares 45% identity with Roc2 in this region. In addition, the 2NAR protein bound detectably to Cul3 while normal Roc2 protein did not, again suggesting that the Roc1a RING domain influences Cullin selection. Taken together, we conclude from our data that the Roc NH2-terminal β-strand makes a relatively stronger contribution to Cullin binding preference than the RING domain.
The lethality of Roc1a mutants is presumably caused by the inappropriate accumulation of at least one target of a Roc1a-containing Cullin dependent E3 ligase . The ANBR protein cannot rescue the lethality of Roc1a mutants even though it binds all of the Cullins that Roc1a does. Thus, even though ANBR can activate polyubiquitin formation in vitro, fusion of the Roc1a NH2 terminus with the Roc1b RING domain does not create a fully biologically active Roc1a protein. One possible interpretation of this result is that in vivo the Roc1b RING domain cannot productively interact (i.e. stimulate ubiquitylation of critical targets) with all of the E2s that Roc1a does. This may occur at the level of direct binding, such that there are some E2s that only bind the RING domain of Roc1a and not Roc1b, or at the level of stimulating ubiquitin transfer to substrate in the context of a fully assembled CDL.
A similar observation was previously reported for TRAF3 and TRAF5 RING domain proteins . TRAF5 can activate the NF-κB pathway when over-expressed, while TRAF3 cannot. This is dependent on the RING domain, as mutation of a key RING cysteine inhibits this activation. A construct that fuses portions of the RING domains of TRAF3 and TRAF5 is also incapable of NF-κB activation. The authors proposed that these chimeric proteins might not be able to chelate zinc ions or fold properly. This may explain why AN2R is unable to bind any Cullin. However, the other Roc chimeras we constructed were able to bind Cullin and were active as E3 ligases. Moreover, the rescue of male sterility by the ANBR chimera (see below) indicates that Roc protein chimeras can be functional in vivo.
In the Drosophila male germ line, Roc1b forms a complex with a testes-specific Cul3 isoform and the BTB protein KLH10 to regulate caspase activation during spermatid differentiation . Consequently, Roc1b mutants are male sterile . Interestingly, the BNAR chimera, which binds well to Cul3, effectively rescues Roc1b mutant male sterility. This is consistent with our previous data showing that normal Roc1a can partially rescue the male sterility of Roc1b mutants when expressed from the Roc1b promoter . These data suggest that in the context of the testes specific Cul3 complex, the RING domains of Roc1a and Roc1b can productively interact with a similar set of E2s. Thus, our genetic rescue experiments with Roc1a and Roc1b mutants can be explained if Roc1b interacts with a subset of all the E2s that interact with Roc1a. Finally, the functional redundancy of Roc1a and Roc1b in the male germ line is only detected with the Roc1b promoter, suggesting that the Roc1a and Roc1b genes are expressed differently during spermatogenesis.
Function of the Roc2-Cul5 E3 ligase
We show that Roc2 and Cul5 only bind to each other, and that knocking out one protein greatly reduces the level of the other. The Roc2-Cul5 complex is conserved in other species including C. elegans and humans , . What is the function of the Roc2-Cul5 complex in vivo? A previous Drosophila study used viable P element insertions in the 5′UTR of Cul5 for over-expression experiments that suggested Cul5 is involved in cell fate specification and bouton formation in the larval CNS . This study indicated that the insertion alleles were very weakly hypomorphic, and consistent with this we were not able to detect a difference in the Cul5 mRNA levels of these alleles by RT-PCR (data not shown). Here we report the identification of Roc2 and Cul5 transposon insertion alleles in which we cannot detect protein by immunoblot analysis of mutant embryos. These mutants develop into morphologically normal adults. Thus, Roc2-Cul5 is not required for development.
It is possible that Roc2-Cul5 is redundant with other CDL. A recent paper showed that Roc1-Cul2 and Roc2-Cul5 complexes may act redundantly during meiotic cell cycle progression in C. elegans . RNAi knockdown of Roc2 or Cul5 did not reveal an obvious phenotype, consistent with our results. However, RNAi knockdown of either Roc2 or Cul5 mRNA in a cul-2 mutant background caused complete sterility, whereas cul-2 mutants only display partial sterility. We occasionally observed a small, but inconsistent reduction in female fecundity in both the Drosophila Roc2 and Cul5 mutants, perhaps reflecting such redundancy. Cul2- and Cul5-based E3 ligases use similar substrate adapter machinery, consisting of ElonginB, ElonginC, and a variable BC box protein , , , suggesting that Cul2 and Cul5 complexes could have overlapping substrates in some organisms. Drosophila Cul2 forms a complex with Rbx1, Elongins B and C, and VHL that supports polyubiquitin chain formation in vitro, and that is capable of ubiquitylating the HIF-1a transcription factor as occurs in mammals , , . Our data indicate that any potential redundancy between Cul2 and Cul5 in Drosophila must occur by utilizing different Roc proteins, as Roc1a is not part of a Cul5 complex, and Roc2 is not part of the Cul2 complex. Whether redundancy exists or not, that the Cul5-Roc2 complex has been evolutionarily conserved suggests that it plays an important role in many organisms.
Materials and Methods
Cell Culture and Transfection
S2 cells were maintained in Schneider's medium supplemented with 10% FBS and 100 U/ml penicillin and 100 ug/ml streptomycin. Cells were transfected using Effectene according to the manufacturer's instructions (Qiagen), and protein lysates were obtained 48 hours later. All transfected DNA's were cloned into the pCaSpeR-4 vector.
The RING swap constructs were made by using the CAICR protein sequence that is common to all Drosophila Roc proteins (see Fig. 1B) as a region of overlap for primer design. Chimeras were expressed with either a Roc1a- or Roc1b-grf (genomic rescue fragment). The Roc1a-grf was previously described  and contains 980 bp upstream of the Start codon and 620 bp downstream of the stop codon. A FLAG- or V5- tag was inserted in frame immediately downstream of the initiating methionine. The Roc1b-grf, containing 840 bp upstream from the Start codon and 330 bp downstream from the Stop codon, was also previously described , and here we inserted an in frame V5 tag downstream of the Start codon.
Creation of GST-fusion Proteins
Using the pCaSpeR-4 Roc constructs as template , PCR products were made using primers that added EcoR1 sites on either side, and the product was then cloned into pGEX-1 (GE Healthcare) and confirmed by sequencing. Primers used are as follows. Roc1a 5′Eco: 5′-CAGAGGAATTCGAAGTCGACGAGGATGGATAC-3′. Roc1a 3′Eco: 5′-CAGAGGAATTCTTAGTGGCCGTACTTC-3′. Roc1b 5′Eco: 5′-TCATTAGAATTCGCCGAGGAGATAGAGGTTG-3′. Roc1b 3′Eco: 5′-CAGAGGAATTCACCGGTCTAGCGGCCGTACTTC-3′. Roc2 5′Eco: 5′-TGACAGGAATTCGCTGATGATCCAGAAAACTC-3′. Roc2 3′Eco: 5′-CAGAGGAATTCACCGGTTTATTTTCCCATGCG-3′.
Protocol used for isolation of GST fusion proteins was previously described . Constructs were transformed into BL21DE3 bacteria and induced by adding IPTG to 0.4 mM. GST-Roc proteins were purified using Glutathione-Sepharose 4B beads (GE Healthcare). Protein concentration was determined by Coomassie stain using BSA standards.
Ubiquitin Ligase Assay
Ligase assays were performed essentially as described  for 45 minutes at 37°C with the following components: 50 mM Tris-HCl pH 7.5, 5 mM MgCl2, 2 mM NaF, 0.6 mM DTT, 2 mM ATP, 10 nM Okadaic Acid, 40 ng rabbit Ube1 (Boston Biochem), 300 ng UbcH5, 12 µg bovine Ub (Sigma), and 250 ng GST-Roc. Samples were run by SDS-PAGE on a 12% gel followed by Western blotting for Ubiquitin.
RNA was extracted from embryos using TRIzol (Sigma-Aldrich) according to the manufacturer's instructions. RT-PCR was previously described .
Primer sequences used for RT-PCR are as follows. CG8234: 5′-CACCCATGTGTCCTTCTCCGT-3′ and 5′-TGACCACGGTTCACAAACCAG-3′. CG30035: 5′-GAGAACATCCGTCATGCGGTG-3′ and 5′-GAGCAGGATGCCTATGTTACC-3′. Cul5: 5′-CACAAAGTTCATTTGACGAGGCG-3′ and 5′-TGTGGCCAGGCGGAGATTCTC-3′. Roc2: 5′-CAGAGACCGGTATGGCTGATGATCCAGAA-3′ and 5′-CCCATGCGCTGAATGGACCA-3′.
Immunoprecipitations and Western Blotting
For embryo lysates, overnight egg collections (0–16 hrs) were dechorionated for 3 minutes in 50% bleach and dounce homogenized with 10 volumes of NP-40 lysis buffer (50 mM Tris pH 8.3, 150 mM NaCl, 0.5% NP-40, 1 ng/ml leupeptin, 0.5 ng/ml pepstatinA, 1 mM PMSF). Lysates were centrifuged at 14,000 rpm for 10 min at 4°C and the supernatant was collected. For immunoprecipitations, 25 µl protein-A beads were washed 3× with 1 ml NP-40 lysis buffer, and then pre-incubated with antibody for 2 h before adding to 1 ml of lysate (1 mg/ml protein). Immunoprecipitations were performed overnight at 4°C.
The following antibodies were used: rabbit anti-Cul1 (Zymed), rabbit anti-Cul2 (gift of Dr. Yue Xiong, UNC), guinea pig anti-Cul3 (gift of Dr. Jim Skeath, Washington University), rabbit anti-Cul4 , affinity purified rabbit anti-Cul5, guinea pig anti-Roc2 whole serum, mouse anti-FLAG (Invitrogen), mouse anti-V5 (Invitrogen), and Rabbit anti-Ub (Covance). Anti-peptide antibodies against Roc2 and Cul5 were generated using synthetic peptides (Invitrogen) coupled to KLH (Pierce). The peptide sequences are CADDPENSVDRPTDD (Roc2) and CKRDRDIFEEVWPDK (Cul5). Injections and serum withdrawal were performed at Pocono Rabbit Farm & Laboratory, Inc. High titer bleeds of anti-Cul5 were purified with the same peptide using the Sulfolink Kit (Pierce).
Stocks and Genetics
The Roc1aG1 and Roc1bdc3 alleles have been described previously , . The Roc2KG07982, Roc2pBacf00911, and Cul5EY21463 alleles were obtained from the Bloomington stock center. To test for rescue of Roc1a lethality, Roc1aG1, sn, FRT/FM7, Act-GFP females were mated to males that expressed a specific transgene (V5-Roc1a or V5-ANBR) under control of the Roc1a promoter. Rescue was scored by the presence of sn males in the progeny. To test for rescue of Roc1b male sterility, males of the genotype Roc1bdc3/TM3, Sb and containing a transgene insertion on the second chromosome (V5-Roc1b, V5-ANBR, or V5-BNAR) were mated to Roc1bdc3/TM3, Sb females. w+ (indicating the presence of the transgene), Sb+, Roc1bdc3/Roc1bdc3 male progeny were then mated with w1118 virgin females to assay for rescue of sterility. Five batches of 100 eggs from this cross were transferred onto individual grape juice plates, and the numbers of hatched eggs quantified 36 h later.
We thank Lisa Wolff for technical assistance, Dr. Tim Donaldson for generating useful early versions of Roc chimera constructs, Drs. Yue Xiong, Jim Skeath, and Sima Zacharek for reagents, and Ashley Godfrey for comments.
Conceived and designed the experiments: PJR RD. Performed the experiments: PJR JS. Analyzed the data: PJR JS RD. Wrote the paper: PJR RD. The PI: RD. Performed an experiment for part of one figure: JS. Helped write the paper and design experiments: RD.
- 1. Hershko A, Ciechanover A (1998) The ubiquitin system. Annu Rev Biochem 67: 425–479.A. HershkoA. Ciechanover1998The ubiquitin system.Annu Rev Biochem67425479
- 2. Pickart CM (2001) Mechanisms underlying ubiquitination. Annu Rev Biochem 70: 503–533.CM Pickart2001Mechanisms underlying ubiquitination.Annu Rev Biochem70503533
- 3. Jin J, Li X, Gygi SP, Harper JW (2007) Dual E1 activation systems for ubiquitin differentially regulate E2 enzyme charging. Nature 447: 1135–1138.J. JinX. LiSP GygiJW Harper2007Dual E1 activation systems for ubiquitin differentially regulate E2 enzyme charging.Nature44711351138
- 4. Pelzer C, Kassner I, Matentzoglu K, Singh RK, Wollscheid HP, et al. (2007) UBE1L2, a novel E1 enzyme specific for ubiquitin. J Biol Chem 282: 23010–23014.C. PelzerI. KassnerK. MatentzogluRK SinghHP Wollscheid2007UBE1L2, a novel E1 enzyme specific for ubiquitin.J Biol Chem2822301023014
- 5. Scheffner M, Nuber U, Huibregtse JM (1995) Protein ubiquitination involving an E1-E2-E3 enzyme ubiquitin thioester cascade. Nature 373: 81–83.M. ScheffnerU. NuberJM Huibregtse1995Protein ubiquitination involving an E1-E2-E3 enzyme ubiquitin thioester cascade.Nature3738183
- 6. Deshaies RJ (1999) SCF and Cullin/Ring H2-based ubiquitin ligases. Annu Rev Cell Dev Biol 15: 435–467.RJ Deshaies1999SCF and Cullin/Ring H2-based ubiquitin ligases.Annu Rev Cell Dev Biol15435467
- 7. Lorick KL, Jensen JP, Fang S, Ong AM, Hatakeyama S, et al. (1999) RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination. Proc Natl Acad Sci U S A 96: 11364–11369.KL LorickJP JensenS. FangAM OngS. Hatakeyama1999RING fingers mediate ubiquitin-conjugating enzyme (E2)-dependent ubiquitination.Proc Natl Acad Sci U S A961136411369
- 8. Borden KL (2000) RING domains: master builders of molecular scaffolds? J Mol Biol 295: 1103–1112.KL Borden2000RING domains: master builders of molecular scaffolds?J Mol Biol29511031112
- 9. Liu HL, Yang CT, Zhao JH, Huang CH, Lin HY, et al. (2007) Molecular dynamics simulations to investigate the effects of zinc ions on the structural stability of the c-Cbl RING domain. Biotechnol Prog 23: 1231–1238.HL LiuCT YangJH ZhaoCH HuangHY Lin2007Molecular dynamics simulations to investigate the effects of zinc ions on the structural stability of the c-Cbl RING domain.Biotechnol Prog2312311238
- 10. Goldenberg SJ, Cascio TC, Shumway SD, Garbutt KC, Liu J, et al. (2004) Structure of the Cand1-Cul1-Roc1 complex reveals regulatory mechanisms for the assembly of the multisubunit cullin-dependent ubiquitin ligases. Cell 119: 517–528.SJ GoldenbergTC CascioSD ShumwayKC GarbuttJ. Liu2004Structure of the Cand1-Cul1-Roc1 complex reveals regulatory mechanisms for the assembly of the multisubunit cullin-dependent ubiquitin ligases.Cell119517528
- 11. Zheng N, Schulman BA, Song L, Miller JJ, Jeffrey PD, et al. (2002) Structure of the Cul1-Rbx1-Skp1-F boxSkp2 SCF ubiquitin ligase complex. Nature 416: 703–709.N. ZhengBA SchulmanL. SongJJ MillerPD Jeffrey2002Structure of the Cul1-Rbx1-Skp1-F boxSkp2 SCF ubiquitin ligase complex.Nature416703709
- 12. Zheng N, Wang P, Jeffrey PD, Pavletich NP (2000) Structure of a c-Cbl-UbcH7 complex: RING domain function in ubiquitin-protein ligases. Cell 102: 533–539.N. ZhengP. WangPD JeffreyNP Pavletich2000Structure of a c-Cbl-UbcH7 complex: RING domain function in ubiquitin-protein ligases.Cell102533539
- 13. Angers S, Li T, Yi X, MacCoss MJ, Moon RT, et al. (2006) Molecular architecture and assembly of the DDB1-CUL4A ubiquitin ligase machinery. Nature 443: 590–593.S. AngersT. LiX. YiMJ MacCossRT Moon2006Molecular architecture and assembly of the DDB1-CUL4A ubiquitin ligase machinery.Nature443590593
- 14. Angers S, Li T, Yi X, MacCoss MJ, Moon RT, et al. (2006) Molecular architecture and assembly of the DDB1-CUL4A ubiquitin ligase machinery. Nature 443: 590–593.S. AngersT. LiX. YiMJ MacCossRT Moon2006Molecular architecture and assembly of the DDB1-CUL4A ubiquitin ligase machinery.Nature443590593
- 15. Chen A, Wu K, Fuchs SY, Tan P, Gomez C, et al. (2000) The conserved RING-H2 finger of ROC1 is required for ubiquitin ligation. J Biol Chem 275: 15432–15439.A. ChenK. WuSY FuchsP. TanC. Gomez2000The conserved RING-H2 finger of ROC1 is required for ubiquitin ligation.J Biol Chem2751543215439
- 16. Kamura T, Koepp DM, Conrad MN, Skowyra D, Moreland RJ, et al. (1999) Rbx1, a component of the VHL tumor suppressor complex and SCF ubiquitin ligase. Science 284: 657–661.T. KamuraDM KoeppMN ConradD. SkowyraRJ Moreland1999Rbx1, a component of the VHL tumor suppressor complex and SCF ubiquitin ligase.Science284657661
- 17. Ohta T, Michel JJ, Schottelius AJ, Xiong Y (1999) ROC1, a homolog of APC11, represents a family of cullin partners with an associated ubiquitin ligase activity. Mol Cell 3: 535–541.T. OhtaJJ MichelAJ SchotteliusY. Xiong1999ROC1, a homolog of APC11, represents a family of cullin partners with an associated ubiquitin ligase activity.Mol Cell3535541
- 18. Jackson PK, Eldridge AG, Freed E, Furstenthal L, Hsu JY, et al. (2000) The lore of the RINGs: substrate recognition and catalysis by ubiquitin ligases. Trends Cell Biol 10: 429–439.PK JacksonAG EldridgeE. FreedL. FurstenthalJY Hsu2000The lore of the RINGs: substrate recognition and catalysis by ubiquitin ligases.Trends Cell Biol10429439
- 19. Petroski MD, Deshaies RJ (2005) Function and regulation of cullin-RING ubiquitin ligases. Nat Rev Mol Cell Biol 6: 9–20.MD PetroskiRJ Deshaies2005Function and regulation of cullin-RING ubiquitin ligases.Nat Rev Mol Cell Biol6920
- 20. Willems AR, Schwab M, Tyers M (2004) A hitchhiker's guide to the cullin ubiquitin ligases: SCF and its kin. Biochim Biophys Acta 1695: 133–170.AR WillemsM. SchwabM. Tyers2004A hitchhiker's guide to the cullin ubiquitin ligases: SCF and its kin.Biochim Biophys Acta1695133170
- 21. Lee J, Zhou P (2007) DCAFs, the missing link of the CUL4-DDB1 ubiquitin ligase. Mol Cell 26: 775–780.J. LeeP. Zhou2007DCAFs, the missing link of the CUL4-DDB1 ubiquitin ligase.Mol Cell26775780
- 22. Ho MS, Tsai PI, Chien CT (2006) F-box proteins: the key to protein degradation. J Biomed Sci 13: 181–191.MS HoPI TsaiCT Chien2006F-box proteins: the key to protein degradation.J Biomed Sci13181191
- 23. Schulman BA, Carrano AC, Jeffrey PD, Bowen Z, Kinnucan ER, et al. (2000) Insights into SCF ubiquitin ligases from the structure of the Skp1–Skp2 complex. Nature 408: 381–386.BA SchulmanAC CarranoPD JeffreyZ. BowenER Kinnucan2000Insights into SCF ubiquitin ligases from the structure of the Skp1–Skp2 complex.Nature408381386
- 24. Noureddine MA, Donaldson TD, Thacker SA, Duronio RJ (2002) Drosophila Roc1a encodes a RING-H2 protein with a unique function in processing the Hh signal transducer Ci by the SCF E3 ubiquitin ligase. Dev Cell 2: 757–770.MA NoureddineTD DonaldsonSA ThackerRJ Duronio2002Drosophila Roc1a encodes a RING-H2 protein with a unique function in processing the Hh signal transducer Ci by the SCF E3 ubiquitin ligase.Dev Cell2757770
- 25. Donaldson TD, Noureddine MA, Reynolds PJ, Bradford W, Duronio RJ (2004) Targeted disruption of Drosophila Roc1b reveals functional differences in the Roc subunit of Cullin-dependent E3 ubiquitin ligases. Mol Biol Cell 15: 4892–4903.TD DonaldsonMA NoureddinePJ ReynoldsW. BradfordRJ Duronio2004Targeted disruption of Drosophila Roc1b reveals functional differences in the Roc subunit of Cullin-dependent E3 ubiquitin ligases.Mol Biol Cell1548924903
- 26. Furukawa M, Ohta T, Xiong Y (2002) Activation of UBC5 ubiquitin-conjugating enzyme by the RING finger of ROC1 and assembly of active ubiquitin ligases by all cullins. J Biol Chem 277: 15758–15765.M. FurukawaT. OhtaY. Xiong2002Activation of UBC5 ubiquitin-conjugating enzyme by the RING finger of ROC1 and assembly of active ubiquitin ligases by all cullins.J Biol Chem2771575815765
- 27. Hu J, Zacharek S, He YJ, Lee H, Shumway S, et al. (2008) WD40 protein FBW5 promotes ubiquitination of tumor suppressor TSC2 by DDB1-CUL4-ROC1 ligase. Genes Dev in press. J. HuS. ZacharekYJ HeH. LeeS. Shumway2008WD40 protein FBW5 promotes ubiquitination of tumor suppressor TSC2 by DDB1-CUL4-ROC1 ligase.Genes Dev in press
- 28. Kamura T, Conrad MN, Yan Q, Conaway RC, Conaway JW (1999) The Rbx1 subunit of SCF and VHL E3 ubiquitin ligase activates Rub1 modification of cullins Cdc53 and Cul2. Genes Dev 13: 2928–2933.T. KamuraMN ConradQ. YanRC ConawayJW Conaway1999The Rbx1 subunit of SCF and VHL E3 ubiquitin ligase activates Rub1 modification of cullins Cdc53 and Cul2.Genes Dev1329282933
- 29. Morimoto M, Nishida T, Nagayama Y, Yasuda H (2003) Nedd8-modification of Cul1 is promoted by Roc1 as a Nedd8-E3 ligase and regulates its stability. Biochem Biophys Res Commun 301: 392–398.M. MorimotoT. NishidaY. NagayamaH. Yasuda2003Nedd8-modification of Cul1 is promoted by Roc1 as a Nedd8-E3 ligase and regulates its stability.Biochem Biophys Res Commun301392398
- 30. Hori T, Osaka F, Chiba T, Miyamoto C, Okabayashi K, et al. (1999) Covalent modification of all members of human cullin family proteins by NEDD8. Oncogene 18: 6829–6834.T. HoriF. OsakaT. ChibaC. MiyamotoK. Okabayashi1999Covalent modification of all members of human cullin family proteins by NEDD8.Oncogene1868296834
- 31. Lammer D, Mathias N, Laplaza JM, Jiang W, Liu Y, et al. (1998) Modification of yeast Cdc53p by the ubiquitin-related protein rub1p affects function of the SCFCdc4 complex. Genes Dev 12: 914–926.D. LammerN. MathiasJM LaplazaW. JiangY. Liu1998Modification of yeast Cdc53p by the ubiquitin-related protein rub1p affects function of the SCFCdc4 complex.Genes Dev12914926
- 32. Lyapina S, Cope G, Shevchenko A, Serino G, Tsuge T, et al. (2001) Promotion of NEDD-CUL1 conjugate cleavage by COP9 signalosome. Science 292: 1382–1385.S. LyapinaG. CopeA. ShevchenkoG. SerinoT. Tsuge2001Promotion of NEDD-CUL1 conjugate cleavage by COP9 signalosome.Science29213821385
- 33. Zhou C, Seibert V, Geyer R, Rhee E, Lyapina S, et al. (2001) The fission yeast COP9/signalosome is involved in cullin modification by ubiquitin-related Ned8p. BMC Biochem 2: 7.C. ZhouV. SeibertR. GeyerE. RheeS. Lyapina2001The fission yeast COP9/signalosome is involved in cullin modification by ubiquitin-related Ned8p.BMC Biochem27
- 34. Cope GA, Deshaies RJ (2003) COP9 signalosome: a multifunctional regulator of SCF and other cullin-based ubiquitin ligases. Cell 114: 663–671.GA CopeRJ Deshaies2003COP9 signalosome: a multifunctional regulator of SCF and other cullin-based ubiquitin ligases.Cell114663671
- 35. von Arnim AG (2003) On again-off again: COP9 signalosome turns the key on protein degradation. Curr Opin Plant Biol 6: 520–529.AG von Arnim2003On again-off again: COP9 signalosome turns the key on protein degradation.Curr Opin Plant Biol6520529
- 36. Wolf DA, Zhou C, Wee S (2003) The COP9 signalosome: an assembly and maintenance platform for cullin ubiquitin ligases? Nat Cell Biol 5: 1029–1033.DA WolfC. ZhouS. Wee2003The COP9 signalosome: an assembly and maintenance platform for cullin ubiquitin ligases?Nat Cell Biol510291033
- 37. Arama E, Bader M, Rieckhof GE, Steller H (2007) A ubiquitin ligase complex regulates caspase activation during sperm differentiation in Drosophila. PLoS Biol 5: e251.E. AramaM. BaderGE RieckhofH. Steller2007A ubiquitin ligase complex regulates caspase activation during sperm differentiation in Drosophila.PLoS Biol5e251
- 38. Dadgostar H, Cheng G (1998) An intact zinc ring finger is required for tumor necrosis factor receptor-associated factor-mediated nuclear factor-kappaB activation but is dispensable for c-Jun N-terminal kinase signaling. J Biol Chem 273: 24775–24780.H. DadgostarG. Cheng1998An intact zinc ring finger is required for tumor necrosis factor receptor-associated factor-mediated nuclear factor-kappaB activation but is dispensable for c-Jun N-terminal kinase signaling.J Biol Chem2732477524780
- 39. Sasagawa Y, Sato S, Ogura T, Higashitani A (2007) C. elegans RBX-2-CUL-5- and RBX-1-CUL-2-based complexes are redundant for oogenesis and activation of the MAP kinase MPK-1. FEBS Lett 581: 145–150.Y. SasagawaS. SatoT. OguraA. Higashitani2007C. elegans RBX-2-CUL-5- and RBX-1-CUL-2-based complexes are redundant for oogenesis and activation of the MAP kinase MPK-1.FEBS Lett581145150
- 40. Kamura T, Maenaka K, Kotoshiba S, Matsumoto M, Kohda D, et al. (2004) VHL-box and SOCS-box domains determine binding specificity for Cul2-Rbx1 and Cul5-Rbx2 modules of ubiquitin ligases. Genes Dev 18: 3055–3065.T. KamuraK. MaenakaS. KotoshibaM. MatsumotoD. Kohda2004VHL-box and SOCS-box domains determine binding specificity for Cul2-Rbx1 and Cul5-Rbx2 modules of ubiquitin ligases.Genes Dev1830553065
- 41. Ayyub C, Sen A, Gonsalves F, Badrinath K, Bhandari P, et al. (2005) Cullin-5 plays multiple roles in cell fate specification and synapse formation during Drosophila development. Dev Dyn 232: 865–875.C. AyyubA. SenF. GonsalvesK. BadrinathP. Bhandari2005Cullin-5 plays multiple roles in cell fate specification and synapse formation during Drosophila development.Dev Dyn232865875
- 42. Duan DR, Pause A, Burgess WH, Aso T, Chen DY, et al. (1995) Inhibition of transcription elongation by the VHL tumor suppressor protein. Science 269: 1402–1406.DR DuanA. PauseWH BurgessT. AsoDY Chen1995Inhibition of transcription elongation by the VHL tumor suppressor protein.Science26914021406
- 43. Kibel A, Iliopoulos O, DeCaprio JA, Kaelin WG Jr (1995) Binding of the von Hippel-Lindau tumor suppressor protein to Elongin B and C. Science 269: 1444–1446.A. KibelO. IliopoulosJA DeCaprioWG Kaelin Jr1995Binding of the von Hippel-Lindau tumor suppressor protein to Elongin B and C.Science26914441446
- 44. Aso T, Yamazaki K, Aigaki T, Kitajima S (2000) Drosophila von Hippel-Lindau tumor suppressor complex possesses E3 ubiquitin ligase activity. Biochem Biophys Res Commun 276: 355–361.T. AsoK. YamazakiT. AigakiS. Kitajima2000Drosophila von Hippel-Lindau tumor suppressor complex possesses E3 ubiquitin ligase activity.Biochem Biophys Res Commun276355361
- 45. Iwai K, Yamanaka K, Kamura T, Minato N, Conaway RC, et al. (1999) Identification of the von Hippel-lindau tumor-suppressor protein as part of an active E3 ubiquitin ligase complex. Proc Natl Acad Sci U S A 96: 12436–12441.K. IwaiK. YamanakaT. KamuraN. MinatoRC Conaway1999Identification of the von Hippel-lindau tumor-suppressor protein as part of an active E3 ubiquitin ligase complex.Proc Natl Acad Sci U S A961243612441
- 46. Lisztwan J, Imbert G, Wirbelauer C, Gstaiger M, Krek W (1999) The von Hippel-Lindau tumor suppressor protein is a component of an E3 ubiquitin-protein ligase activity. Genes Dev 13: 1822–1833.J. LisztwanG. ImbertC. WirbelauerM. GstaigerW. Krek1999The von Hippel-Lindau tumor suppressor protein is a component of an E3 ubiquitin-protein ligase activity.Genes Dev1318221833
- 47. Mehle A, Goncalves J, Santa-Marta M, McPike M, Gabuzda D (2004) Phosphorylation of a novel SOCS-box regulates assembly of the HIV-1 Vif-Cul5 complex that promotes APOBEC3G degradation. Genes Dev 18: 2861–2866.A. MehleJ. GoncalvesM. Santa-MartaM. McPikeD. Gabuzda2004Phosphorylation of a novel SOCS-box regulates assembly of the HIV-1 Vif-Cul5 complex that promotes APOBEC3G degradation.Genes Dev1828612866
- 48. Yu X, Yu Y, Liu B, Luo K, Kong W, et al. (2003) Induction of APOBEC3G ubiquitination and degradation by an HIV-1 Vif-Cul5-SCF complex. Science 302: 1056–1060.X. YuY. YuB. LiuK. LuoW. Kong2003Induction of APOBEC3G ubiquitination and degradation by an HIV-1 Vif-Cul5-SCF complex.Science30210561060
- 49. Liu B, Sarkis PT, Luo K, Yu Y, Yu XF (2005) Regulation of Apobec3F and human immunodeficiency virus type 1 Vif by Vif-Cul5-ElonB/C E3 ubiquitin ligase. J Virol 79: 9579–9587.B. LiuPT SarkisK. LuoY. YuXF Yu2005Regulation of Apobec3F and human immunodeficiency virus type 1 Vif by Vif-Cul5-ElonB/C E3 ubiquitin ligase.J Virol7995799587
- 50. Luo K, Xiao Z, Ehrlich E, Yu Y, Liu B, et al. (2005) Primate lentiviral virion infectivity factors are substrate receptors that assemble with cullin 5-E3 ligase through a HCCH motif to suppress APOBEC3G. Proc Natl Acad Sci U S A 102: 11444–11449.K. LuoZ. XiaoE. EhrlichY. YuB. Liu2005Primate lentiviral virion infectivity factors are substrate receptors that assemble with cullin 5-E3 ligase through a HCCH motif to suppress APOBEC3G.Proc Natl Acad Sci U S A1021144411449
- 51. Mehle A, Thomas ER, Rajendran KS, Gabuzda D (2006) A zinc-binding region in Vif binds Cul5 and determines cullin selection. J Biol Chem 281: 17259–17265.A. MehleER ThomasKS RajendranD. Gabuzda2006A zinc-binding region in Vif binds Cul5 and determines cullin selection.J Biol Chem2811725917265