|Home | About | Journals | Submit | Contact Us | Français|
Selective proteolysis in plants is largely mediated by the ubiquitin (Ub)/proteasome system in which substrates, marked by the covalent attachment of Ub, are degraded by the 26 S proteasome. The 26 S proteasome is composed of two subparticles, the 20 S core protease (CP) that compartmentalizes the protease active sites and the 19 S regulatory particle that recognizes and translocates appropriate substrates into the CP lumen for breakdown. Here, we describe an affinity method to rapidly purify epitope-tagged 26 S proteasomes intact from Arabidopsis thaliana. In-depth mass spectrometric analyses of preparations generated from young seedlings confirmed that the 2.5-MDa CP-regulatory particle complex is actually a heterogeneous set of particles assembled with paralogous pairs for most subunits. A number of these subunits are modified post-translationally by proteolytic processing, acetylation, and/or ubiquitylation. Several proteasome-associated proteins were also identified that likely assist in complex assembly and regulation. In addition, we detected a particle consisting of the CP capped by the single subunit PA200 activator that may be involved in Ub-independent protein breakdown. Taken together, it appears that a diverse and highly dynamic population of proteasomes is assembled in plants, which may expand the target specificity and functions of intracellular proteolysis.
Plants, like other eukaryotes, rely on the selective removal of abnormal/nonfunctional polypeptides and key short lived regulatory proteins to maintain homeostasis and control their physiology, growth, and development. Arguably, the main protease in plants is the 26 S proteasome, a 2.5-MDa complex responsible for the bulk of ubiquitin (Ub)4-mediated proteolysis (for reviews see Refs. 1, 2). Although the accumulated knowledge of the 26 S proteasome is mainly derived from the analysis of yeast and mammalian complexes, emerging studies indicate that a similar complex exists in plants (3, 4). Its intricate architecture is generated by a 28 subunit core protease (CP) capped at both ends by an 18 subunit or more regulatory particle (RP). The CP is a self-compartmentalized multicatalytic protease created by the assembly of four stacked heptameric rings of α and β subunits in a α1–7/β1–7/β1–7/α1–7 configuration. A central chamber encloses the active sites for peptidylglutamyl-peptide-hydrolyzing, trypsin-like, and chymotrypsin-like activities provided by the β1, β2, and β5 subunits, respectively. Access to this chamber is guarded by an axial pore created by each α subunit ring, which employs a sophisticated gating mechanism to restrict access such that only unfolded proteins may enter the catalytic chamber (2, 5).
The RP binds to one or both ends of the CP and sits directly over the α ring pore. It is composed of two subcomplexes as follows: a base containing six related AAA-ATPases (designated RPT1–6 for regulatory particle triple-A ATPases) and three non-ATPase subunits (designated RPN1, RPN2, and RPN10, for regulatory particle non-triple-A ATPases), and a lid that contains at least 12 additional RPN subunits (RPN1–3 and -5–13) (1,–3). The functions of only some of the RP subunits are known. The six RPT subunits form a ring that consumes ATP to facilitate channel opening, and target protein unfolding and translocation into the CP (5, 6). The RPN10 and RPN13 subunits function as the major Ub receptors to identify appropriate substrates bearing poly-Ub chains (7,–10). RPN1 has been shown to interact with ubiquitin-binding shuttle proteins and thus may also assist in substrate recognition (11). RPN11 has a deubiquitylating activity that can remove Ub moieties bound to target proteins during their breakdown (12). The possible roles of the remaining subunits include the assembly and maintenance of structural integrity, substrate selection, processing steps to ready a target for breakdown, target import, discharge of amino acid/peptide products from the CP lumen, and Ub recycling (2, 13).
In addition to core subunits, a number of other factors associate substoichiometrically with the 26 S proteasome. Given the complicated design of this multisubunit particle, it is not surprising that some act transiently as chaperone-like factors to promote assembly (14,–16). Others appear to aid in polyubiquitylating substrates (e.g. E3s), the delivery of these substrates to the complex, and/or Ub recycling during substrate breakdown (2, 17, 18). In the most extreme case, novel complexes have been identified in yeast and mammals that consist of the CP capped on one or both ends by the hexameric PA28/11S regulator (19) or the single proteasome activator (PA)-200 protein (Blm10 in yeast) (20,–22).
In the past few years, great strides have been made in defining the 26 S proteasome from plants and identifying most of its core subunits (3, 4). Both genomic analyses and biochemical studies of purified preparations have shown that the complex is more heterogeneous than in most other eukaryotes. For example, wheras each core CP and RP subunit is encoded by a single gene in yeast, most Arabidopsis and rice subunits are encoded by gene pairs, some of which are sufficiently different in sequence (23,–26) and/or genetic impact (13, 27,–32) to suggest distinct functions. Unfortunately, all previous biochemical analyses of plant proteasomes used conventional chromatographic approaches to isolate the particle (25, 26, 33). Based on studies with the yeast complex, these purifications may have missed less tightly bound core and accessory components (e.g. RPN13, UPL7 (Hul5 in yeast), UBP6, ECM29, and PA200) (34, 35). At least for the Arabidopsis particle, the time-consuming protocol also generated preparations contaminated with breakdown products for individual subunits (e.g. RPN10), thus compromising conclusions drawn from their analysis (26).
To better define the activity and subunit composition of the 26 S proteasomes in plants, we developed an affinity-based strategy to effectively purify the holoenzyme intact from Arabidopsis. Mass spectrometric (MS) analysis of the complex isolated from young seedlings allowed us to more accurately catalog the subunit composition, post-translation modifications, and proteasome-interacting proteins. Particles assembled with all but three of the potential core subunit isoforms were detected, indicating that a heterogeneous collection of 26 S proteasomes is assembled in planta. In addition, a number of CP and RP subunits were found to undergo one or more post-translational modifications, including partial proteolytic cleavage, acetylation, and ubiquitylation. Finally, we identified several other proteins that associate with the Arabidopsis proteasome, including the PBAC2 assembly chaperonin, the associated DSS1/Sem1/RPN15 protein, the deubiquitylating enzyme UBP16, and the alternative activator PA200. Our results indicate that plants assemble a highly diverse population of proteasomes that likely expands the functionality of these proteolytic particles.
The pag1-1 (SALK_114864) and pa200-1–6 (SALK_103341, SALK_ 095870, SALK_070184, SALK_035070, SALK_007570, and SALK_151948, respectively) T (transfer)-DNA insertion mutants in the Arabidopsis thaliana ecotype Col-0 were identified in the Signal T-DNA collection and obtained from the Arabidopsis Biological Resource Center (Columbus, OH). The pag1-1, pa200-2, and pa200-3 alleles were tracked by genomic PCR using the T-DNA-specific left border primer (Lba1) in combination with the gene-specific primers P11, P13, and P15, respectively (see supplemental Table 1 for all primer sequences used in this study). RT-PCR of the T-DNA insertion lines used the primer pairs P1 + P2 (pag1-1), P12 + P13 (pa200-2) and P14 + P15 (pa200-3) in combination with total seedling RNA as described previously (18). The rpn12a-1 mutant was described by Smalle et al. (30). The mutants were backcrossed three times to the Col-0 parent and then made homozygous by selfing. Unless otherwise noted, plants were grown under sterile conditions on solid Gamborg's B-5 growth medium containing 2% sucrose and 0.7% agar (Invitrogen).
For MG132 treatments, plants were grown on growth medium agar containing 2% sucrose for 4 days under long day conditions. Seedlings were then transferred to liquid growth medium containing 2% sucrose and 100 μm MG132 (N-(benzyloxycarbonyl)-Leu-Leu-Leu-al; Enzo Life Sciences, New York) and incubated for 30 h under continuous light with gentle shaking (28).
The genomic region encompassing the full coding sequence of PAG1 plus the 2-kbp sequence upstream of the ATG translation start site was PCR-amplified from A. thaliana ecotype Col-0 genomic DNA, using the primer pair P9 and P10, and cloned into the pENTR/D-TOPO entry vector (Invitrogen). The sequence-confirmed clone was recombined in-frame into the appropriate destination vectors containing the various C-terminal fusion tags, including FLAG (DYKDDDDK), Myc (EQKLISEEDL), and HA (YPYDVPDYA) (pEarleyGate302, 303, and 301, respectively (36)). These constructions were transformed into pag1-1/+ heterozygous plants by the Agrobacterium-mediated floral dip method. Double heterozygous T1 progeny were selected by Basta resistance and confirmed by genomic PCR to contain the pag1-1 allele and the PAG1 transgenes using primers P1 + P2 (wild type), P3 + Lba1 (pag1-1 T-DNA), and P3 + P5 (PAG1 transgenes). Homozygous pag1-1 T3 plants rescued with the various tagged PAG1 transgenes were confirmed by immunoblot analysis with anti-PAG1 antibodies.
The full-length PAG1 cDNA was PCR-amplified using primers P5 and P6 and cloned into the pDONR221 entry vector (Invitrogen). The sequence-confirmed cDNA was recombined into pDEST17 to express the protein with an N-terminal His6 tag in Escherichia coli strain BL21. Following a 3-h induction with 0.4 mm isopropyl 1-thio-β-d-galactopyranoside, the expressed protein was collected from the insoluble fraction by centrifugation, dissolved in 8 m urea, and bound to nickel-nitrilotriacetic acid agarose (Qiagen, Valencia, CA) followed by elution with 250 mm imidazole. PAG1 protein was further purified by preparative SDS-PAGE; gel pieces containing the 27-kDa protein (visualized by Coomassie Blue staining) were excised, rinsed, and injected directly into rabbits (Harlan BioProducts, Madison, WI).
PA200 antibodies were generated against a partial fragment encompassing residues 840–1140. The corresponding cDNA sequences were obtained by RT-PCR amplification of total seedling RNA using the primer pairs P7 + P8 and subcloned into pET23b (Novagen, San Diego). The protein fragment was expressed in BL21 cells, purified, and injected into rabbits as described for PAG1. Immunoblot analyses were performed according to Smalle et al. (30). Antibodies against CSN4 and CSN5, eIF3b and eIF3-e, HSC70, Rubisco large subunit, and nitrilase-1 were provided by Drs. Xing-Wang Deng, Daniel Chamovitz, Charles Guy, Archie Portis, and Mark Estelle, respectively. Antibodies against PBA1, RPN1, RPN5, RPN10, RPN12a, RPT2a, and Ub were as described previously (26, 30). Anti-FLAG M2 antibodies were obtained from Sigma.
PAG1-FLAG pag1–1−/− seedlings were grown 10 days under continuous light in liquid growth medium containing 2% sucrose. The seedlings (5 g of fresh weight) were pulverized at liquid nitrogen temperatures using a mortar and pestle and extracted with 7.5 ml of Buffer A (50 mm Tris-HCl (pH 7.5), 25 mm NaCl, 2 mm MgCl2, 1 mm EDTA, and 5% (v/v) glycerol), with 10 mm ATP, 6 μm chymostatin, and 2 mm phenylmethylsulfonyl fluoride added just before use. Extracts were filtered through Miracloth (Calbiochem) and clarified at 25,000 × g for 20 min. The supernatant was immediately applied three times to a column containing 50 μl of anti-FLAG M2 affinity beads (Sigma) and then washed three times with 2 ml of Buffer A. Bound protein was eluted by a 20-min rotation at 4 °C with 250 μl of Buffer A containing 500 ng/μl of the FLAG peptide (DYKDDDDK; University of Wisconsin Biotech Center, Madison, WI). The RP subcomplex was selectively released by incubation of bead-bound 26 S proteasomes with Buffer A plus 800 mm NaCl.
Glycerol gradient centrifugation and activity assay were performed as described previously (13). CP peptidase activity in the absence or presence of MG132 was measured using the substrate succinyl-Leu-Leu-Val-Tyr-7-amido-4-methylcoumarin (BioMol, Plymouth Meeting, PA) (26). Other protease inhibitors were obtained from Sigma. Nondenaturing PAGE followed the protocol of Yang et al. (26). For two-dimensional native/SDS-PAGE, the gel lanes from native PAGE were incubated with 1% SDS and 1% 2-mercaptoethanol for 30 min and then subjected to SDS-PAGE in the second dimension.
For the protease inhibitor assays, seedlings were extracted as above with the inclusion of various inhibitors. Concentrations used were as follows: Roche Applied Science complete mini protease inhibitor mixture, 1 tablet/10 ml; aprotinin, 800 nm; antipain, 100 μm; benzamide, 4 mm; chymostatin, 6 μm; E-64, 10 μm; leupeptin, 10 mm; MG132, 50 μm; N-ethylmaleimide, 1 mm; pepstatin, 1 μg/ml; and phenylmethylsulfonyl fluoride, 2 mm. Extracts were incubated at 25 °C for 1 h.
Samples purified by the anti-FLAG affinity chromatography were treated with 50 mm dithiothreitol and 55 mm iodoacetamide, digested overnight at 37 °C with 20 ng/μl sequencing grade trypsin (Promega, Madison, WI), or 25 ng/μl lysyl endopeptidase C (LysC; Wako, Richmond, VA) in 100 mm ammonium bicarbonate (pH 8.0), and then vacuum dried. Samples were reconstituted in 100 μl of 5% acetonitrile and 0.1% formic acid, desalted using C18 pipette tips (OMIX tip C18, Varian, Lake Forest, CA), and dried again. The vacuum-dried samples were reconstituted in 10 μl of 5% acetonitrile and 0.1% formic acid prior to liquid chromatographic separation. For affinity purification after MG132 treatments, plants were grown as stated above for 9 days and then treated for 30 h with 100 μm MG132.
High energy collision dissociation (HCD) and electron transfer dissociation (ETD) MS analyses employed a capillary liquid chromatography-MS/MS system consisting of a high performance liquid chromatograph (HPLC) (Waters NanoAcquity, Milford, MA) connected to an electrospray ionization (ESI) FT/ion-trap mass spectrometer (LTQ Orbitrap Velos, Thermo Fisher Scientific, San Jose, CA) (37, 38). A fritless 100 × 365-μm fused silica capillary micro-column was prepared by pulling the tip of the capillary to ~1 μm with a P-2000 laser puller (Sutter Instruments, Novato, CA) and packing the capillary with 10 cm of 5-μm diameter C18 beads (Western Analytical Products, Inc., Murrieta, CA). The peptides were loaded over 20 min at a flow rate of 1 μl/min and eluted over 115 min at a flow rate of 200 nl/min with a gradient of 2–45% acetonitrile in 0.1% formic acid. For the trypsin-digested samples, a full mass scan was performed in the FT Orbitrap between 300 and 1500 m/z at a resolution of 60,000, followed by 10 MS/MS HCD scans of the 10 highest intensity parent ions at 45% relative collision energy. The HCD scans were also analyzed in the FT Orbitrap detector at a resolution of 7500. Dynamic exclusion was enabled with a repeat count of 2 over a duration of 15 min and excluded for 30 min. For the LysC-digested samples, the same chromatography and full mass scan parameters were used, with ETD analysis of the 10 most intense ions in the ion trap. The ETD activation time was 70 ms, with charge-state screening enabled and the singly and doubly charged ions excluded from analysis.
Proteins purified by anti-FLAG affinity chromatography were separated by SDS-PAGE. Following visualization of the lanes with Coomassie Blue, a total of 17 gel bands was excised and subjected to in-gel trypsin digestion. The tryptic peptides extracted from each gel slice were dried, desalted, and reconstituted as above and loaded onto the C18 capillary microcolumn described above. MS analysis employed a capillary liquid chromatography-MS/MS system consisting of an HPLC connected to an ESI ion-trap MS (Surveyor HPLC and LCQ deca XPplus; Thermo Fisher Scientific, San Jose, CA) (39). The peptides were eluted over 150 min at a flow rate of 300 nl/min with a gradient of 5–80% acetonitrile in 0.1% formic acid. A full mass scan was performed between 400 and 2000 m/z, followed by three MS/MS collision-induced dissociation (CID) scans of the three highest intensity parent ions at 45% relative collision energy.
The acquired MS and MS/MS spectra were searched against the A. thaliana ecotype Col-0 protein database (IPI Database version 3.61, September 2009) using the SEQUEST program (Thermo Fisher Scientific). Sequences for trypsin, LysC, and human keratin were added to the database to decrease the false-positive discovery rate. Masses for both precursor and fragment ions were treated as mono-isotopic. Oxidized methionine (+16 Da), carbamidomethylated cysteines (+57 Da), acetylation (+42 Da), myristoylation (+210 Da), and phosphorylation (+80 Da) were included as variable modifications. In addition, a mass shift of 114.1 Da for lysine residues was included as a variable modification to identify possible Ub footprints (40, 41). The initial search also allowed for up to two missed trypsin cleavages given that ubiquitylated lysines are often resistant to digestion, with a follow-up analysis that permitted this cleavage (42). The data were filtered using a 1% false discovery rate (43). For the Orbitrap MS/MS datasets, parent ion masses were initially matched with a mass tolerance of 15 ppm for precursor masses and 0.1 Da for HCD fragments; peptides were then filtered using Xcorr versus charge state (+1 > 1.5, +2 > 2.0, +3 > 2.25, +4 > 2.5, +5 > 2.75, +6 > 3.0), and an Sp score >200. For the ion trap MS/MS dataset, parent ion masses were initially matched with a mass tolerance of 1.4 Da for precursor masses and 1 Da for CID fragments; peptides were then filtered using Xcorr versus charge state (+1 > 1.5, +2 > 2.0, +3 > 2.5). A minimum identification of two unique peptides was required for confident identification of the parent protein.
Genes encoding orthologs for various Arabidopsis proteasome subunits were identified by BLAST searches of the Phytozome and NCBI databases (blast.ncbi.nlm.nih.gov) using the Arabidopsis protein sequence as the query (accession numbers are provided in supplemental Dataset 1). Orthologs were confirmed by reciprocal BLAST searches of the Arabidopsis protein database. Protein sequences were then aligned using ClustalW2 (supplemental Dataset 2). Phylogeny was determined by Bayesian estimation using the Mr.Bayes 3.1.2 program (44) with a mixed model. Specific commands for Mr.Bayes were as follows: lset nst = 6 rates = invgamma. Each group was run for 100,000 generations with sampling every 100 cycles for a total of 1000 samples. The sump and sumt commands were used to tabulate posterior probabilities of positive selection for each amino acid site and to build consensus trees. The first 250 cycles were discarded to remove results of estimations obtained before the process reached convergence. Trees were rooted with obvious non-plant orthologs and were viewed and edited using FigTree version 1.3.1.
Sequence data from this study can be found in supplemental Dataset 2.
To enrich for Arabidopsis proteasomes containing the common CP subcomplex, we adopted a strategy first successful in yeast that involves replacing one of the 14 CP polypeptides with a tagged version and then exploiting the tag for rapid affinity purification (34, 35). The most attractive candidate in Arabidopsis was the α7 subunit, which is encoded by the single PAG1 gene (At2g27020) (23). The 249-amino acid PAG1 protein (27 kDa) has high sequence identity to orthologs from other plants (Oryza sativa (84%), Zea maize (86%), Glycine max (87%), Populus trichocarpa (91%), Physcomitrella patens (82%), and Vitis vinifera (90%)), as well as animals (Homo sapiens (61%) and Drosophila melanogaster (51%)) and yeast (Saccharomyces cerevisiae (Pre10, 49%)). As part of the α ring, PAG1 does not directly participate in proteolysis but, through its N terminus, plays a role in gating the axial pore that guards the CP catalytic chamber (5, 6). The crystal structure of the yeast CP shows that the C terminus of PAG1 is solvent-exposed (45), thus allowing us to append tags to this end potentially without perturbing CP assembly.
As a first step in PAG1 replacement, we identified a null mutation (pag1-1) in the A. thaliana ecotype Col-0 T-DNA insertion collection that interrupts the 5th intron (Fig. 1A). Homozygous pag1-1 progeny could not be generated from a self-crossed heterozygous parent (supplemental Table 2), indicating that the α7 subunit is essential in plants as it is in yeast (46). We also did not detect aborted embryos in siliques from selfed heterozygous pag1-1 plants, suggesting that the barrier occurs early in reproduction. This barrier was pinpointed to a defect in male gametogenesis from the analysis of reciprocal crosses between pag1-1/+ and wild-type flowers. Whereas the pag1-1 allele was readily transmitted through the egg, no transmission was detected through pollen (supplemental Table 2).
To engineer an affinity-tagged proteasome, we introduced into heterozygous pag1-1 plants transgenes controlled by the native PAG1 promoter that express the full-length PAG1 protein bearing a variety of C-terminal epitopes (e.g. FLAG, HA, Myc, and TAP). When we tested for their ability to rescue homozygous pag1-1 plants in selfed T2 populations, we failed to identify rescued lines using the PAG1-TAP transgene, potentially because this 309-residue tag is too large to retain PAG1 functionality. Fortunately, successful rescue was achieved with the smaller tags, FLAG, HA, and Myc, which added only 23, 23, and 24 residues, respectively. Immunoblot analysis of these lines with anti-PAG1 antibodies confirmed the substitutions. Whereas a doublet of PAG1 protein could be seen in heterozygous pag1-1 plants expressing the tagged PAG1 transgenes, only the higher molecular mass, tagged versions could be seen when the pag1-1 allele was made homozygous (see Fig. 1B for an example). pag1-1 plants rescued with either PAG1-FLAG, PAG1-HA, or PAG1-Myc were phenotypically indistinguishable from wild type when grown under normal conditions and were fully fertile (Fig. 1C), strongly suggesting that these tagged proteins faithfully replaced their wild-type counterpart.
Initial attempts at affinity purification suggested that the FLAG epitope provided the most robust enrichment and was used in all the subsequent studies. Importantly, the PAG1-FLAG protein successfully integrated into the 26 S proteasome complex without perturbing CP/RP assembly. When crude extracts from wild-type plants were subjected to glycerol gradient centrifugation, we could detect the 26 S proteasome as a peak of peptidase activity using the substrate succinyl-Leu-Leu-Val-Tyr-7-amido-4-methylcoumarin (26), which was sensitive to the CP inhibitor MG132 (Fig. 1D). This activity co-sedimented with known subunits of the CP and RP as judged by immunoblot analyses with a library of anti-CP (PAG1 (α7) and PBA1 (β1)) and anti-RP antibodies (RPN1, RPN5, RPT2, RPN10, and RPN12a) (Fig. 1E). Nearly identical sedimentation profiles for peptidase activity and for CP and RP subunits were observed for extracts generated with PAG1-FLAG pag1-1 plants (Fig. 1E). This co-sedimentation also included the FLAG epitope attached to PAG1-FLAG protein.
During the glycerol gradient fractionations, we noticed that the PAG1-FLAG protein is sensitive to post-homogenization proteolysis, which removes over time most, if not all, of the FLAG sequence. Tests with a variety of protease inhibitors discovered that this in vitro cleavage is sensitive to the chymotrypsin inhibitor chymostatin and MG132 but not to many others (Fig. 1F). Consequently, chymostatin was routinely included in the purification protocol to minimize release of the FLAG tag.
Using a homozygous PAG1-FLAG pag1-1 line, we developed a rapid and robust protocol to enrich for the 26 S proteasome directly from crude seedling extracts. It involved an initial homogenization of liquid-grown seedlings in a nondenaturing buffer containing chymostatin, clarification to remove cell debris, and incubation of the soluble material with beads conjugated with anti-FLAG antibodies. Following a wash with a low salt (25 mm NaCl) buffer, proteasomes were competitively released from the antibodies under gentle, nondenaturing conditions simply by incubating the beads with an excess of the 8-amino acid FLAG peptide (DYKDDDDK). Ten mm ATP was routinely included in all buffers to maintain association of the RP and CP subcomplexes (26, 47). Approximately 12 μg of proteasomes could be isolated from 5-g fresh weight of seedlings. In total, the procedure took ~2 h, which is substantially faster than the 2-day conventional protocol described by us previously that involved two precipitation steps and two chromatography steps, one of which employed a high salt elution that can release loosely bound subunits/cofactors (26, 35).
SDS-PAGE and peptidase assays demonstrated that this single-step affinity purification is highly effective in isolating reasonably intact 26 S proteasomes. As compared with a FLAG-peptide eluate generated with wild-type plants, that obtained from PAG1-FLAG pag1-1 plants was enriched for MG132-sensitive peptidase activity (Fig. 2D), and for a collection of proteasome proteins reminiscent of that obtained by conventional methods (26), including a 24–32-kDa set that encompasses the α and β subunits of the CP and a set between 24 and 110 kDa that encompasses most RP subunits (Fig. 2A). Importantly, two abundant contaminants of conventionally purified proteasomes (tripeptidyl peptidase-II and fatty acid α-dioxygenase-1 (26, 48)) were absent in the affinity-purified preparations. In agreement with the need for ATP to maintain RP-CP binding and the sensitivity of this association to high salt (34, 35), the abundance of the RP subunits was substantially reduced if ATP was omitted from all steps of the purification (Fig. 2A), or if proteasomes bound to the anti-FLAG antibody resin in the presence of ATP were first washed with high salt (800 mm NaCl) before FLAG peptide elution (Fig. 2B).
Subsequent immunoblot analyses confirmed the presence of specific subunits for both the CP and RP (Fig. 2C). In particular, full-length RPN10 without substantial contamination by breakdown products was detected in the affinity preparations, which contrasted results from the conventional method where most RPN10 was degraded during purification (26). In agreement with the need for ATP to maintain 26 S proteasome integrity, levels of the RP subunits (RPN1, RPN5, RPN10, RPN12a, and RPT2) but not the CP subunits (PAG1 (α7) and PBA1 (β1)) were substantially lower when we attempted to purify the complex without ATP (Fig. 2C).
In addition to expected CP and RP subunits, we detected several other proteins that could represent: (i) other, yet to be identified, components of the Arabidopsis 26 S complex based on studies with yeast particle; (ii) assembly chaperonins; (iii) various accessory proteins; or (iv) other complexes previously shown (eIF3 complex) or proposed (COP9 signalosome (CSN)) to interact with the RP or CP (14, 21, 34, 35, 49,–51). The unidentified protein at 200 kDa (Fig. 2, A and B) was of special interest because it matched the molecular mass of PA200, a previously described activator of the CP in mammals (22) and yeast (Blm10 (21, 52)). Its identity as PA200 was subsequently confirmed using antibodies generated against a portion of the 1781-residue Arabidopsis protein (Fig. 2C). The abundance of PA200 in the affinity preparations was unaffected by omitting ATP during the purification, implying that its association with the CP is ATP-independent (Fig. 2C). Conversely, immunoblotting with antibodies against two eIF3 subunits (eIF3-b and eIF3-e) failed to detect this complex in our affinity preparations even though these proteins could be readily seen in crude Arabidopsis extracts (Fig. 2C and data not shown). Likewise, we failed to detect CSN4 or CSN5 in the affinity preparations, strongly suggesting that the eight-subunit CSN complex evolutionarily related to the RP lid does not form a CP-RP(base)-CSN particle by replacing the lid as proposed (51).
Experiments with wild-type plants indicated that our affinity method also enriched for several proteins nonspecifically (supplemental Table 3). One substantial contaminant at 38 kDa matched the mass of nitrilase, previously shown by us to stick to agarose beads, possibly via its avidity for the aliphatic nitrile groups used to cross-link the resin (40). Its confirmation as nitrilase was subsequently provided by both immunoblot analysis with anti-nitrilase antibodies and by MS/MS sequencing of preparations from both wild-type and PAG1-FLAG pag1-1 plants (Fig. 2C and supplemental Table 3). HSC70 and Rubisco were also confirmed as contaminants of the affinity procedure by MS and by overexposure of immunoblots prepared with wild-type and PAG1-FLAG pag1-1 samples and probed with anti-HSC70 and anti-Rubisco large subunit antibodies.
Native PAGE of the affinity preparations followed by immunoblot analyses of representative subunits or by SDS-PAGE in the second dimension demonstrated that the collection of CP and RP proteins assembled into their respective subcomplexes (Fig. 3, A and B). In addition, several forms of the 26 S proteasome containing both CP and RP were evident. The fastest mobility form likely represented the CP capped by one RP, whereas the middle form likely represented a CP doubly capped with RP. The slowest migrating form is unknown; intriguingly, it could represent the doubly capped RP-CP complex assembled with a host of other factors as seen for the yeast complex (35). We also detected a new complex of slightly slower mobility as compared with the CP. Subsequent immunoblot analysis with anti-PA200 antibodies and SDS-PAGE in the second dimension revealed that it consists of the CP capped by only PA200 and no RP subunits, and thus it represents a heretofore unknown proteasome type in plants (Fig. 3, A and B).
We comprehensively determined the subunit composition of the affinity-purified proteasomes using a variety of MS/MS techniques and spectrometers, with a special focus on the presence of the various subunit isoforms and their possible post-translational modifications. The deepest dataset was generated by in-solution trypsinization of unfractionated samples followed by analysis with an LTQ-Orbitrap Velos mass spectrometer using HCD for peptide fragmentation. For a second approach, we separated the polypeptides by SDS-PAGE followed by in-gel trypsinization of gel slices, and we analyzed the peptides with an LCQ-deca XPplus ion-trap mass spectrometer using CID for peptide fragmentation. As a third approach, we digested the polypeptides with LysC in-solution and detected the peptides with the Orbitrap mass spectrometer using ETD for peptide fragmentation. False-positive peptide spectrum matches to the Arabidopsis proteome were eliminated upon filtering the data to maintain a false discovery rate below 1%. We also purged proteins identified from wild-type seedlings subjected to the same affinity protocol (e.g. nitrilase, the small and large subunits of Rubisco, and HSC70 (supplemental Table 3)), which presumably bound nonspecifically to the anti-FLAG antibody beads. The combined results for expected RP and CP subunits are summarized in Table 1. Taken together, we confirmed the complete subunit composition of the “core” Arabidopsis 26 S proteasome, which includes all 7 α (PAA-PAG) and all 7 β (PBA-PBG) subunits of the CP, all 6 RPT subunits, and 11 of the RPN subunits (RPN1–3, RPN5–12, the exception being RPN13). The MS/MS dataset yielded remarkable sequence coverage for most subunits (42–100%), with a 74% average for all 53 polypeptides (Table 1).
In addition to high sequence coverage, a large number of unique peptides allowed unambiguous identification of nearly every subunit paralog predicted by genome annotations (23, 24, 26, 30, 53). Of the 22 subunits potentially expressed by two Arabidopsis genes, we matched specific peptides to both predicted isoforms for all but the following three: PAC2(α3), RPT1b, and RPN12b (Table 1). The predicted amino acid sequence for PAC2 is highly divergent from that for PAC1. The C-terminal regions of this pair are co-linear but the N-terminal region for PAC2 contains a large insertion of unrelated sequence. The expressed sequence tags for PAC2 only match this insertion, suggesting that the bulk of the locus is not transcribed. Together with the absence of PAC2 protein in the purified 26 S complex, it is highly likely that the PAC2 locus is a pseudogene. The RPN12b locus encodes a substantially truncated protein as compared with RPN12a and lacks expression support (30). Our failure to unambiguously find the RPN12b protein strongly supports the conclusion that this locus is also a pseudogene. We failed to identify the RPT1b isoform but readily detected its paralog RPT1a. Expressed sequence tag data estimate that the RPT1b gene is expressed at a much lower level than RPT1a (5 versus 141 expressed sequence tags (Table 1)). Combined with its low amino acid identity to RPT1a (81%), which is eclipsed only by PAC1/2 and RPN12a/b among 22 proteasome protein pairs in Arabidopsis, it is possible that RPT1b is also a pseudogene or, more intriguingly, that it is expressed only under specific conditions.
Studies with yeast and mammalian 26 S proteasomes and preliminary analysis of the rice complex showed that a number of core subunits are or may be affected by various post-translational modifications, including proteolytic processing, acetylation (N-terminal and side chain), myristoylation, and phosphorylation, which may affect their assembly, localization, and/or activity (25, 54,–59). In addition, at least one 26 S proteasome subunit (RPN1) may be modified by Ub from the global MS analysis of Arabidopsis ubiquitylated proteins (40, 41). Here, we exploited our deep sequence coverage to interrogate more thoroughly the entire Arabidopsis proteasome population for such modifications.
Like subunits of yeast and animal 26 S proteasomes (54, 55), a number of Arabidopsis subunits are N-acetylated. Of the 53 proteins that compose the core complex, we detected peptides at or close to the predicted initiator methionine for 19. Of these 19, 2 contained an unmodified N-terminal methionine (RPT1a and RPN11); 10 had an acetylated N-terminal methionine, and 7 began with the immediately distal residue (alanine or glycine), which was presumably exposed upon proteolytic removal of the N-terminal methionine (supplemental Table 4). We did not find any nonacetylated versions for the 10 subunits beginning with an N-acetylated methionine, suggesting that this modification is comprehensive. Several subunits were also found to be acetylated on internal residues (PAG1, PAE2, RPN1a, RPT1a, and RPT5a (Table 2)).
Our MS/MS dataset was searched for phosphoryl and myristoyl additions using SEQUEST. Unfortunately, no peptides with supra-threshold values for phosphorylated amino acids were detected. Nor were myristoylated residues identified despite reports that the plant RPT2 subunit bears this modification (25, 60).
Based on studies with the yeast 26 S proteasome, one essential post-translational modification is proteolytic processing at the N terminus of the β1, β2, and β5 subunits (PBA1, PBB1/2, and PBE1/2 in Arabidopsis, respectively). This autocatalytic cleavage occurs during CP assembly and exposes an interior threonine whose α-amino group acts as the nucleophile during peptide bond hydrolysis (61). A search of our MS/MS dataset for PBA1 and PBB1/2 identified peptides that reflect this processing in Arabidopsis. In particular, peptides beginning with the expected Thr-13 and Thr-47 residues, respectively (residues 13–31 for PBA1 and 38–58 for PBB1/2), were found in the affinity-purified proteasomes subjected to trypsinization, with no peptides detected for the upstream region (Fig. 4, A–C, and supplemental Fig. 1, A–C).
A similar processing likely occurs for PBE1/2. We failed to detect the tryptic peptides that would reflect this cleavage proximal to Thr-57 (residues 57–66). However, processing was supported indirectly by the absence of expected peptides upstream of Thr-57 in the PBE1/2 proteins despite extensive sequence coverage of the proteins downstream of this site (64/49% coverage of total sequences or 81%/62% if processed) (supplemental Fig. 1, D and E). Our preliminary catalog of tryptic peptides from PBG1 suggests that it is processed to reveal an N-terminal threonine (Thr-23); this processing is seven residues upstream of the expected position for an active-site threonine and may or may not generate an active peptidase.
Confirmation of β1 N-terminal processing in Arabidopsis was provided by examining the PBA1 protein in plants treated with MG132, which should block this proteolytic maturation (61). Whereas only processed PBA1 was detected immunologically in wild-type plants, a second higher molecular mass form was apparent upon MG132 treatment that matched the expected size of unprocessed PBA1 (23 versus 25 kDa) (Fig. 4D).
Surprisingly, ubiquitylation was the most prevalent modification we found in the affinity-purified proteasomes. Ub addition was detected by its signature tryptic footprint where the target lysine is increased in mass by an isopeptide-linked diglycine derived from the C terminus of Ub (+114 kDa). In most cases, this lysine is immune to trypsin cleavage and thus internal in the peptide (canonical) (40, 41), but in some cases, such cleavage can occur to expose the ubiquitylated lysine at the C terminus (noncanonical) (42). Eleven of the 53 Arabidopsis subunits contained a peptide with a high probability Ub footprint (residue of 242.1 m/z), nine of the canonical type and two of the noncanonical type (Table 2). The strongest evidence for ubiquitylation was generated for RPN1a; in addition to the unmodified tryptic peptide spanning residues 192–223, we found the same peptide bearing a canonical Ub footprint at Lys-218, which was abundant in our MS/MS dataset (Fig. 5C). In contrast, Ub footprints were not detected on any RPN1b peptides despite 76% coverage of its sequence, suggesting that the modification is restricted to the a isoform. Our list of ubiquitylated subunits also included three subunits of the RPT ring, RPN2a/b, RPN6, and four CP α subunits, including PAG1-FLAG. Some, but not all, of the comparable yeast subunits were also reported to be ubiquitylated from a global analysis of this modification (41).
Further evidence for subunit ubiquitylation was provided by immunoblot analysis of the affinity-purified preparations with anti-Ub antibodies. In addition to trace amounts of Ub trimers and tetramers, and a smear of high molecular mass polyubiquitylated proteins that presumably co-purified with the 26 S proteasome via their association with Ub receptors, we detected two prominent species at 115 and 100 kDa (Fig. 5A). Both their apparent molecular masses and their presence in proteasomes affinity-purified in the presence of ATP but not in the absence strongly suggested that they represent ubiquitylated forms of RPN1a and RPN2a/b (Fig. 5A). The lower molecular mass form was assigned to an RPN1 isoform by probing the SDS-polyacrylamide gels with both anti-Ub and anti-RPN1a antibodies; a 100-kDa species of similar electrophoretic mobility was detected with both antibodies (Fig. 5B). Because the ubiquitylated form of RPN1a should be ~9-kDa larger in mass, this co-migration indicated that either most of the RPN1a pool associated with the Arabidopsis 26 S proteasome is modified with Ub or that the appended Ub moiety does not change its electrophoretic mobility.
Sequence alignments of RPN1a and RPN2a/b revealed that the ubiquitylated lysines are positionally conserved in the a but not the b isoforms of RPN1 (Lys-218) and in both isoforms of RPN2a/b (Lys-165) for all plants examined (except the alga Chlamydomonas reinhardtii), but substituted for a variety of amino acids in non-plant species (Fig. 5, E and F). Such limited distributions imply that the ubiquitylation of RPN1 and RPN2 at these sites is restricted to the plant kingdom. When the ubiquitylation sites for the α subunits were mapped onto the three-dimensional structure of the yeast CP (45), those for PAE1/2 and PAF1 were found to be solvent-exposed and thus accessible to the Ub ligation machinery, whereas those for PAC1 and PAG1 were near the external surface but buried. In the absence of an RP structure, the accessibility of the ubiquitylation sites for the RP subunits is unclear.
In addition to core RP and CP subunits, we detected a number of proteasome-interacting proteins in our MS/MS dataset (supplemental Table 5). These include Ub, the assembly chaperone PBAC2 (Pba2 in yeast), the accessory factor DSS1/RPN15 (Sem1 in yeast), the UPB16 de-ubiquitylating enzyme (Ubp8/Usp42 in yeast/humans), and the CP activator PA200, which was also detected immunologically (Figs. 1D and and22C). A collection of proteins unique to plants was also present in the dataset. Confirmation that they actually associate specifically with Arabidopsis proteasomes is underway.
In a previous study, we detected immunologically in our proteasome preparations members of the RAD23 and DSK2 family, which transiently interact with the 26 S proteasome and serve as shuttles to deliver ubiquitylated substrates (18). However, none of these shuttle proteins was detected here by MS, suggesting that they interact at substoichiometric levels with the complex. We also failed to positively identify several proteasome-associated proteins first identified in yeast, including the Ub receptor RPN13, UBP6, UPL7 (yeast Hul5), and ECM29 (2, 17), even through genes encoding obvious orthologs are present in Arabidopsis. The absence of these proteins in the MS/MS dataset implies that either their interactions are too weak to even survive the mild isolation conditions used here, the bound forms of the proteins are present at very low levels, or that they do not interact with the Arabidopsis particle. Neither searches of our MS/MS dataset nor BLAST analysis of the Arabidopsis genome found obvious orthologs of the α or β subunits comprising the mammalian heterohexameric PA26/11S regulator (19), suggesting that plants do not use this alternative RP in proteasomal control.
The most intriguing proteasome-interacting protein was PA200, given our detection of the PA200-CP complex by native PAGE in the affinity-purified preparations or even following glycerol gradient centrifugation of crude Arabidopsis extracts (Figs. 3 and and11C) and the fact that it could represent an alternative proteasome in plants. The mammalian and yeast versions stimulate the peptidase activity of the CP, likely by opening the gate, and may participate in the Ub-independent degradation (17, 20, 22). Arabidopsis PA200 shares only 22% amino acid sequence identity with both its yeast and human counterparts but can be easily recognized by the organization of HEAT repeats, which help form its signature solenoid structure (Fig. 6A) (20,–22).
To better understand the functions of PA200 in plants, we developed a collection of T-DNA insertion mutants that potentially block expression of the single Arabidopsis PA200 gene (Fig. 6A). Both RT-PCR and immunoblot analysis with anti-PA200 antibodies documented that two of the mutants pa200-2 and pa200-3 failed to accumulate both the full-length PA200 mRNA and protein and thus likely represent null alleles (Fig. 6, B and C).
Surprisingly, the pa200 mutants were phenotypically indistinguishable to wild type under a variety of growth conditions, indicating that this activator is not essential in Arabidopsis (Fig. 6, D and E). These conditions included darkness, short and long day photoperiods, continuous red or far-red light, exposure to MG132, which should block CP activity, and growth in the presence of amino acid analogs, which should increase the abundance of abnormal proteins that require proteasomal removal (53). The levels of Ub, free poly-Ub chains, and Ub-protein conjugates were also unaffected in the pa200 backgrounds (±MG132) as compared with wild type, suggesting that the PA200-CP complex works independently of ubiquitylation (Fig. 6F). Whereas yeast blm10 mutants are modestly hypersensitive to the DNA-damaging agent bleomycin (21), Arabidopsis pa200-2 and pa200-3 seedlings were not more sensitive to this drug.
The only response we observed for PA200 was a substantial increase in the protein upon exposure of Arabidopsis seedlings to MG132 or in mutant backgrounds that dampen RP activity (e.g. rpn12a-1 (30)) (Fig. 6G). This rise implies that PA200 is either a proteasome substrate or more likely that PA200, like subunits of the CP and RP (26), is part of a regulatory system that coordinately responds to proteolytic demand. The increase in PA200 resulted in the assembly of more PA200-CP complexes. As compared with proteasome preparations affinity-purified via the PAG1-FLAG protein from nontreated plants, those affinity purified after MG132 treatment contained substantially more PA200 (Fig. 6H).
The proteasomal incorporation of both isoforms for most CP and RP subunits encoded by gene pairs indicates that the Arabidopsis complex is actually a heterogeneous collection of particles assembled with an assortment of isoform combinations. This heterogeneity in turn raises the possibility some pairs have subfunctionalized to generate distinct 26 S proteasome types. Recent analyses of RPN1a/b, RPN5a/b, and RPT2a/b support such nonredundancy by showing that the subunits pairs have unique expression patterns and possibly both common and nonoverlapping activities (13, 27, 29, 31, 32).
As a further test, we examined phylogenetically how several CP and RP paralogs evolved with the prediction that the earlier these duplicates appeared during plant evolution and the more they were retained in the different plant lineages, the more likely it would be that the paralogs acquired distinct functions. Our analyses included CP (PAA1/2) and RP (RPN1a/b, RPN2a/b, RPT1a/b) protein pairs from a number of eudicots (including A. thaliana and Arabidopsis lyrata), monocots, the lower plants Selaginella moellendorffii and P. patens, and the alga C. reinhardtii. The phylogenetic trees were determined via Bayesian estimation and were rooted with obvious non-plant orthologs (Fig. 7 and supplemental Fig. 2).
Comparisons of the trees revealed that the duplication of the plant CP and RP genes likely occurred not in a common ancestor but at different times during plant evolution, depending on the lineage branch. Overall, the protein pairs grouped according to the main plant lineages (eudicot, monocot, lower plant, and alga). By and large, the eudicot proteins clustered with their species paralog and separate from the orthologous pair in other eudicots, implying that each pair arose separately by relatively recent species-specific duplication events. Likely causes were the whole scale genome duplications seen for many plant species such as A. thaliana (62). In contrast, individuals from the monocot pairs commonly clustered with orthologs from other monocots and not with their paralogs, implying that these pairs appeared early during monocot evolution and were retained as the modern genomes developed. The only deviation from this pattern was RPT1, where the RPT1b isoform in both A. thaliana and A. lyrata formed a separate subclade away from the other eudicot and monocot sequences (Fig. 7B). Assuming that the RPT1b locus is a pseudogene in both A. thaliana and A. lyrata, this distinct subclade likely reflects the diminished pressure to conserve coding sequence after gene inactivation.
Taken together, it appears unlikely that plants share a common set of proteasome subunit isoforms, strongly suggesting that if isoform-specific functions do exist, they are not shared among all plants. Furthermore, the more recent evolutionary origins of the eudicot paralogs, as compared with those in monocots, imply that any nonredundant functions that do exist in eudicots should be species-specific.
Given its central position within the Ub/26 S proteasome system, the 26 S proteasome assumes a major role in the selective removal of both aberrant polypeptides and important short lived regulators. Based on estimates that plants such as Arabidopsis express >1000 different Ub-protein ligases that ubiquitylate an equal or greater number of targets (1, 3), it is expected that this self-compartmentalized protease is uniquely designed to operate with high selectivity for the appended Ub moiety but with low specificity for the sequence of the modified target. To provide insights into the organization and functions of the plant 26 S proteasome, we present here a comprehensive description of the particle from young Arabidopsis seedlings, using a robust affinity method for its isolation. MS and biochemical analyses of the resulting preparations revealed that plants actually assemble a heterogeneous collection of proteasomes that may play important roles in handling the myriad of potential targets that are committed by both Ub-dependent and -independent mechanisms.
Central to our affinity method was the genetic replacement of a CP subunit with an affinity-tagged variant followed by the use of a single, mild chromatography step based on the tag to rapidly isolate the complex directly from crude extracts. For simplicity, we focused on the PAG1 subunit given that it is encoded by a single Arabidopsis gene. In theory, many other subunits should also be amenable if they can be engineered with solvent-exposed tags.
Like various subunits of the Arabidopsis RP lid and base (13, 27,–29, 31), our genetic analysis of PAG1 revealed that the CP is also essential in Arabidopsis. Interestingly, a common theme of these CP and RP mutants is that they block male but not female gametogenesis. This block could reflect a special role for the 26 S proteasome during male meiosis as seen in an Arabidopsis deletion of the pollen-specific E3 component UBL17 (63), or more likely, it could reflect the unique development program that delivers the sperm cells to the ovule during fertilization. Although haploid egg cells missing proteasome subunits may still have sufficient levels of the 26 S proteasome provided by the maternal diploid megasporocyte, the extensive growth of the haploid pollen tube cell as it delivers the two sperm cells may eventually dilute proteasome levels below a viable threshold.
Here, we affinity-captured proteolytic complexes sharing the CP subunit PAG1, using young Arabidopsis seedlings as the source. MS/MS analyses revealed that all but three of the potential subunit paralogs based on the Arabidopsis genome are incorporated into the particle assembled in this tissue, except for the predicted products from the PAC2, RPN12b, and RPT1b loci. Consequently, we provide further support for the proposal that plants actually contain a large array of compositionally distinct proteasomes (26). They could be assembled at random to generate a wide assortment of subtly different particles or could be deliberately constructed by integrating together specific isoforms to create a more defined subset. Such deliberate matching could imply that functionally unique plant proteasomes exist. Such a scenario is exemplified by the mammalian immunoproteasome, which replaces the β1, β2, and β5 catalytic subunits of the CP with specialized isoforms that release peptides more suitable for antigen presentation (64). Work is now underway to test this possibility by affinity-purifying proteasomes containing tags appended to specific isoforms of individual CP and RP subunits.
Phylogenetic analyses of the 26 S proteasome within the plant kingdom strongly suggest that the various paralogs arose not from a common ancestor but were generated by multiple independent duplications in the various plant lineages. In particular, we predict that the monocot isoforms arose by genome duplication(s) in a common ancestor after the eudicot/monocot split, whereas the eudicot isoforms separately arose later by species-specific duplication events. Consequently, if subfunctionalization of paralogs has occurred, its consequences may not pervade the entire plant kingdom but be more restricted to individual species. The most likely scenario is subfunctionalization of expression patterns, which has already been observed between several Arabidopsis RP paralogs (13, 28, 31, 65).
For PAC2, RPT1b, and RPN12b loci for which protein products were not detected, the derived amino acid sequences have the lowest identity as compared with their incorporated paralog within the collection of Arabidopsis RP and CP proteasome subunits. The predicted PAC2 and RPN12b proteins are also substantially truncated, making it highly likely that both are pseudogenes. For RPT1b, its activity is unclear. The corresponding protein retained a high sequence identity to its RPT1a paralog (81%), but both it and its A. lyrata ortholog are clearly distinct phylogenetically from others in the plant RPT1 family. Its significantly lower expression in Arabidopsis combined with its absence in our MS/MS dataset suggest that RPT1b is either not expressed, has tissue/developmental stage-restricted expression patterns, or more remotely, is not assembled into a complex that binds the CP.
In-depth MS analyses revealed that the Arabidopsis 26 S proteasome, despite its heterogeneity, is remarkably analogous to the yeast and human versions (35, 55). In particular, we found that the PBA1(β1) and PBB1/2(β2) subunits and likely also the PBE1/2 (β5) subunit are post-translationally processed to reveal an N-terminal threonine that we presume becomes part of their active sites. Although not conclusive, the sensitivity of PBA1 cleavage to MG132 implies that the CP itself is the responsible protease as demonstrated genetically in yeast (61).
Like the yeast and mammalian subunits, the N terminus of a number of other Arabidopsis subunits is altered by N-acetylation of the initiator methionine or by N-terminal processing (supplemental Table 4). The roles of these modification/processing events in proteasome assembly/function are not yet clear. Although several studies with non-plant proteasomes identified various subunits that are modified by phosphorylation, we failed to detect this modification using ETD MS/MS methods in any of the Arabidopsis subunits. Final conclusions about phosphorylation status will ultimately require more sensitive methods to detect phosphoproteins, including the use of immobilized metal chelate chromatography to enrich for phosphopeptides.
The most surprisingly finding was the extensive modification of the Arabidopsis 26 S proteasome subunits by Ub. Prior MS/MS studies of global ubiquitylation detected a number of yeast subunits containing one or more Ub moieties, including Pre3(β1), Pup1(β2), Pre2(β5), RPN1, RPN2, RPN3, RPN5, RPN6, RPN7, RPN8, RPN9, and RPN13 (41), whereas similar studies by us in Arabidopsis detected ubiquitylated RPN1 (40). Neither study identified the site(s) of Ub addition nor was it clear whether the subunits were ubiquitylated while bound to the 26 S complex. Here, we identified Ub footprints on 11 proteasome subunits, and based on our method of enrichment, most of these subunits should contain the Ub appendage while incorporated into the 26 S proteasome.
The only exception might be the ubiquitylated form of PAG1 (as PAG1-FLAG), which could have been purified in the free form in addition to that assembled into proteasomes. In fact, the frequency with which we detected ubiquitylated PAG1 in PAG1-FLAG pag1-1 plants as compared with other subunits (Table 2) raises the possibility that this modification reflects the turnover of excess PAG1-FLAG, which failed to assemble into the CP. Such turnover has been reported previously for Arabidopsis RPN10 (53), suggesting that unassembled proteasome subunits are rapidly removed in planta.
Immunoblot analysis of the 26 S proteasome preparations with anti-Ub antibodies suggested that RPN1 and RPN2 are the most abundant ubiquitylated proteins in the Arabidopsis complex (at least in young seedlings). Although sequence alignments surrounding the Ub attachment sites (Lys-218 in RPN1a and Lys-165 in RPN12/a/b) imply that this modification is restricted to plants, the detection of ubiquitylated yeast RPN1 could indicate that the modification is more widespread (41).
What are the functions/fates of ubiquitylated 26 S proteasomes? One possibility is that they reflect the process whereby plants and other eukaryotes remove unwanted or nonfunctional complexes. Through ubiquitylation and subsequent subunit extraction, this 2.5-MDa complex could be processively disassembled followed by Ub-mediated degradation of the individual free subunits. Alternatively, Ub addition could impart new functions to specific subunits. For example, given the positions of RPN1 and RPN2 in the RP base close to its interface with the lid (49), and the proposed role of RPN1 as a Ub receptor (66), the ubiquitylation of these proteins could have important implications in lid/base binding and/or the association of ubiquitylated substrates with the RP. Contrasting possibilities are that ubiquitylation of RPN1 either blocks subsequent docking of Ub-protein conjugates by interacting with its own Ub recognition domain or that it promotes docking of conjugates via the interaction of the Ub moieties with the Ub-binding motifs of shuttle proteins such as RAD23, which deliver ubiquitylated cargo to the particle (18, 66). Clearly, the analysis of RPN1 and RPN2 mutants that inhibit Ub addition (e.g. arginine substitutions at Lys-218 and Lys-165, respectively) are needed to clarify its importance.
In addition to core CP and RP subunits, we identified a number of accessory proteins, including the PBAC2 (Pba2 in yeast) chaperonin, whose ortholog in yeast helps with assembly of the CP/RP holo-complex, DSS1/RPN15 (Sem1 in yeast), which may alter proteasome subunit composition and/or localization, and the deubiquitylating enzyme UBP16 (2, 17, 67). The closest yeast and human orthologs of UBP16 are Ubp8 and Usp42, which have been implicated in histone H2B deubiquitylation by the SAGA complex and embryogenesis, respectively (68, 69). Whether UBP16 represents a functional analog of these DUBs remains to be determined. As opposed to the yeast particle, we failed to detect the Ub receptor RPN13, ECM29, UBP6, and UPL7(Hul5) despite the presence of obvious orthologs in the Arabidopsis genome. The absence of these potential cofactors could indicate that the affinity-purified proteases characterized here are still missing important accessory proteins despite the mild conditions used for isolation. Retaining association of these cofactors could require chemical cross-linking before tissue homogenization to stabilize their weak affinity.
Another accessory protein associated with the Arabidopsis proteasomes is PA200 that forms a complex with the CP. This alternative CP activator has been implicated in Ub-independent protein breakdown, but its exact physiological role(s) remain unclear (20, 21). Like that in yeast, PA200 is not essential in Arabidopsis. In fact, null pa200 mutants were indistinguishable to wild type under a variety of growth conditions. That the level of PA200 in Arabidopsis seedlings substantially increases in response to conditions that limit 26 S proteasome activity (MG132 treatment or the rpn12a-1 mutant background) could indicate that PA200 is a proteasome substrate. Alternatively, observations that MG132 also markedly increases the levels of both the PA200 mRNA5 and the PA200-capped CP complex (Fig. 6H) raise the intriguing possibility that the PA200-CP proteasome represents a stress-induced proteolytic particle. Hopefully, the analysis of pa200 mutants in combination with 26 S proteasome RP mutants may help delineate the function(s) of the PA200-CP complex, especially under suboptimal growth conditions or situations that stress 26 S proteasome capacity.
In summary, analysis of our affinity-purified preparations has revealed that Arabidopsis and likely other plants, assemble a heterogeneous collection of proteasomes. By exploiting this purification strategy, its should now be possible to track the abundance of the various complexes and subcomplexes and their post-translational modifications in specific tissues and developmental states and, under various growth conditions, to reveal how each contributes to the architecture and functions of these proteolytic machines.
We thank Joseph Walker, Dr. Maria Hansson, and David Gemperline for technical help; Drs. Archie Portis, Xing-Wang Deng, Daniel Chamovitz, Mark Estelle, and Charles Guy for various antibodies; and the Arabidopsis Biological Resource Center for providing the expressed sequence tag clones and SALK T-DNA lines.
*The MS facility was supported in part by National Institutes of Health Grants 1P50HG004952 from NHGRI and P01GM081269 from NIGMS (to M. S. and L. M. S.). This work was supported by United States Department of Energy Basic Energy Sciences Program Grant DE-FG02-88ER13968 and National Science Foundation Arabidopsis 2010 Program Grant MCB-0115870 (to R. D. V.).
The on-line version of this article (available at http://www.jbc.org) contains supplemental Tables 1–5, Figs. 1 and 2, and Datasets 1 and 2.
5K. H. Lee and R. D. Vierstra, unpublished data.
4The abbreviations used are: