Rab2 Utilizes Glyceraldehyde-3-phosphate Dehydrogenase and Protein Kinase Cι to Associate with Microtubules and to Recruit Dynein*

Rab2 requires glyceraldehyde-3-phosphate dehydrogenase (GAPDH) and atypical protein kinase Cι (aPKCι) for retrograde vesicle formation from vesicular tubular clusters that sort secretory cargo from recycling proteins returned to the endoplasmic reticulum. However, the precise role of GAPDH and aPKCι in the early secretory pathway is unclear. GAPDH was the first glycolytic enzyme reported to co-purify with microtubules (MTs). Similarly, aPKC associates directly with MTs. To learn whether Rab2 also binds directly to MTs, a MT binding assay was performed. Purified Rab2 was found in a MT-enriched pellet only when both GAPDH and aPKCι were present, and Rab2-MT binding could be prevented by a recombinant fragment made to the Rab2 amino terminus (residues 2-70), which directly interacts with GAPDH and aPKCι. Because GAPDH binds to the carboxyl terminus of α-tubulin, we characterized the distribution of tyrosinated/detyrosinated α-tubulin that is recruited by Rab2 in a quantitative membrane binding assay. Rab2-treated membranes contained predominantly tyrosinated α-tubulin; however, aPKCι was the limiting and essential factor. Tyrosination/detyrosination influences MT motor protein binding; therefore, we determined whether Rab2 stimulated kinesin or dynein membrane binding. Although kinesin was not detected on membranes incubated with Rab2, dynein was recruited in a dose-dependent manner, and binding was aPKCι-dependent. These combined results suggest a mechanism by which Rab2 controls MT and motor recruitment to vesicular tubular clusters.

The small GTPase Rab2 is essential for membrane trafficking in the early secretory pathway and associates with vesicular tubular clusters (VTCs) 2 located between the endoplasmic reticulum (ER) and the cis-Golgi compartment (1,2). VTCs are pleomorphic structures that sort anterograde-directed cargo from recycling proteins and trafficking machinery retrieved to the ER (3)(4)(5)(6). Rab2 bound to a VTC microdomain stimulates recruitment of soluble factors that results in the release of vesicles containing the recycling protein p53/p58 (7). In that regard, we have previously reported that glyceraldehyde-3phosphate dehydrogenase (GAPDH) and atypical PKC (aPKC) are Rab2 effectors that interact directly with the Rab2 amino terminus and with each other (8,9). Their interaction requires Src-dependent tyrosine phosphorylation of GAPDH and aPKC (10). Moreover, GAPDH is a substrate for aPKC (11). GAPDH catalytic activity is not required for ER to Golgi transport indicating that GAPDH provides a specific function essential for membrane trafficking from VTCs independent of glycolytic function (9). Indeed, phospho-GAPDH influences MT dynamics in the early secretory pathway (11).
GAPDH was the first glycolytic enzyme reported to co-purify with microtubules (MTs) (12) and subsequently was shown to interact with the carboxyl terminus of ␣-tubulin (13). The binding of GAPDH to MTs promotes formation of cross-linked parallel MT arrays or bundles (14,15). GAPDH has also been reported to possess membrane fusogenic activity, which is inhibited by tubulin (16). Similarly, aPKC associates directly with tubulin and promotes MT stability and MT remodeling at specific intracellular sites (17)(18)(19)(20)(21). It may not be coincidental that these two Rab2 effectors influence MT dynamics because recent studies indicate that the cytoskeleton plays a central role in the organization and operation of the secretory pathway (22).
MTs are dynamic structures that grow or shrink by the addition or loss of ␣and ␤-tubulin heterodimers from the ends of protofilaments (23). Their assembly and stability is regulated by a variety of proteins traditionally referred to as microtubuleassociated proteins (MAPs). In addition to the multiple ␣/␤ isoforms that are present in eukaryotes, MTs undergo an assortment of post-translational modifications, including acetylation, glycylation, glutamylation, phosphorylation, palmitoylation, and detyrosination, which further contribute to their biochemical heterogeneity (24,25). It has been proposed that these tubulin modifications regulate intracellular events by facilitating interaction with MAPs and with other specific effector proteins (24). For example, the reversible addition of tyrosine to the carboxyl terminus of ␣-tubulin regulates MT interaction with plus-end tracking proteins (ϩTIPs) containing the cytoskeleton-associated protein glycine-rich (CAP-Gly) motif and with dynein-dynactin (27)(28)(29). Additionally, MT motility and cargo transport rely on the cooperation of the motor pro-teins kinesin and dynein (30). Kinesin is a plus-end directed MT motor, whereas cytoplasmic dynein is a minus-end MT-based motor, and therefore the motors transport vesicular cargo toward the opposite end of a MT track (31).
Although MT assembly does not appear to be directly regulated by small GTPases, Rab proteins provide a molecular link for vesicle movement along MTs to the appropriate target (22,(32)(33)(34). In this study, the potential interaction of Rab2 with MTs and motor proteins was characterized. We found that Rab2 does not bind directly to preassembled MTs but does associate when both GAPDH and aPKC are present and bound to MTs. Moreover, the MTs predominantly contained tyrosinated ␣-tubulin (Tyr-tubulin) suggesting that a dynamic pool of MTs that differentially binds MAPs/effector proteins/motors associates with VTCs in response to Rab2. To that end, we determined that Rab2-promoted dynein/dynactin binding to membranes and that the recruitment required aPKC.
MT Binding Assay-MTs were assembled from 1 g of pure bovine brain tubulin (Cytoskeleton, Inc., Denver, CO) in 20 l of Buffer B (100 mM Pipes (pH 6.8), 2 mM MgCl 2 , and 0.5 mM EGTA) containing 20 M paclitaxel (Sigma) for 20 min at 37°C. The MTs were then incubated with purified recombinant Rab2, His 6 -aPKC, or His 6 -GAPDH (200 ng) in a total volume of 50 l for 30 min at 37°C. The reaction mixtures were layered onto 250 l of a 20% sucrose cushion in Buffer B containing 20 M paclitaxel, and then centrifuged for 30 min at 100,000 ϫ g in a Sorvall M120 Discovery ultra-microcentrifuge using a S120-AT2 rotor. The resultant supernatant and pellet were separated by SDS-PAGE and transferred to nitrocellulose. The blot was probed with the appropriate antibody as indicated under "Results," washed, further incubated with horseradish peroxidase-conjugated anti-mouse or anti-rabbit antibody, developed with ECL, and then quantified by densitometry, as above.
Construction of the Rab2 Amino-terminal Fragment/Deletion Mutant-The Rab2 amino-terminal domain was generated by PCR using the 5Ј oligonucleotide primer, 5Ј-CACCAT-GGCGTACGCCTATCTC-3Ј, in tandem with the 3Ј antisense oligonucleotide, 5Ј-AATAGTTATCATTCGAGCACCGAA-3Ј. The amplified product was subcloned into pET102/D-TOPO (C-term) (Invitrogen), and the sequence was verified by DNA sequence analysis. BL21 (DE3) pLysS cells (EMD Biosciences, La Jolla, CA) transformed with the clone were grown at 37°C to 0.6 A 600 and then induced with 0.4 mM isopropyl ␤-D-thiogalactopyranoside for 3 h at 37°C. The liquid culture was centrifuged at 6,000 rpm for 30 min, and the pellet was resuspended in 50 mM Tris (pH 7.4), 1 mM dithiothreitol, 1 mM EDTA, 1% Triton X-100, and 1 mM phenylmethylsulfonyl fluoride; sonicated; centrifuged at 22,000 ϫ g for 30 min; and then the supernatant was applied to a 1-ml column of Ni 2ϩ -nitrilotriacetic acid-agarose (Qiagen, Valencia, CA) equilibrated in Buffer A (10 mM Hepes (pH 7.9), 5 mM MgCl 2 , 0.1 mM EDTA, 50 mM NaCl, and 0.8 mM imidazole). The column was washed with 10 volumes of Buffer A containing 25 mM imidazole. The tagged protein was eluted with Buffer A supplemented with 200 mM imidazole. An aliquot of the collected fractions (100 l) was analyzed by SDS-PAGE and immunoblotted with an anti-His 6 monoclonal antibody (Cell Signaling). His 6 -Rab2 fragment enriched fractions were pooled and concentrated, and the protein concentration was determined by Micro BCA protein assay reagent (Pierce). The Rab2 amino-terminal deletion mutant was generated, as outlined previously (9).

Rab2 Requires GAPDH and aPKC to Associate with MTs-
To learn if Rab2 binds directly to MTs, an in vitro MT binding assay was performed in which purified recombinant Rab2 was incubated with paclitaxel assembled MTs for 30 min at 37°C. The binding reaction was centrifuged through a 20% sucrose cushion, and then the pellet containing MTs and associated protein and the supernatant containing unbound protein were analyzed by SDS-PAGE and Western blot. As shown in Fig. 1A, Rab2 was found almost exclusively in the high speed supernatant, which contained a negligible amount of tubulin. In contrast, when the MT binding assay was performed with purified aPKC or with purified GAPDH, both proteins co-sedimented with MTs in the high speed pellet consistent with previous reports that showed GAPDH and aPKC interact directly with MTs (12,13,17,38). Because GAPDH and aPKC bind directly to the Rab2 amino terminus, we determined whether either protein could promote Rab2-MT association by supplementing the assay with either purified GAPDH or purified aPKC (Fig.  1B). As observed previously, GAPDH and aPKC independently bound to MTs, whereas Rab2 displayed no binding affinity for MTs and fractionated with the supernatant. However, Rab2 was found in the MT-enriched pellet when the MT binding assay was conducted in the presence of both GAPDH and aPKC (Fig. 1B). Rab2 indirect association with MTs was prevented when the binding assay was supplemented with a recombinant protein fragment corresponding to the Rab2 amino terminus (residues 2-70) that directly interacts with GAPDH and aPKC ( Fig. 1C) (8,9). The amount of Rab2 bound to MTs was reduced ϳ50% in the presence of Rab2 (residues 2-70) (125 ng), and ϳ70% of Rab2 was found in the high speed supernatant when co-incubated with 250 ng of the Rab2 fragment (Fig. 1C). Moreover, Rab2 (residues 2-70) was found in the GAPDH-aPKC-MT pellet indicating that the recombinant fragment interfered with Rab2-MT binding by competition for GAPDH and aPKC interaction. These combined results suggest that Rab2 requires and utilizes both GAPDH and aPKC as adaptor/scaffolding proteins to indirectly associate with MTs.
Rab2 via aPKC Preferentially Recruits Tyrosinated ␣-Tubulin and Dynein to Membranes-Tubulin can undergo a variety of post-translational modifications, including removal of the tyrosine residue from the carboxyl terminus of ␣-tubulin and subsequent tyrosine re-addition (detyrosination/tyrosination cycle) that influences interaction with specific MAPs and motor proteins (25). It is notable that GAPDH has been reported to bind specifically to the carboxyl terminus of ␣-tubulin (13). Therefore, we analyzed the distribution of Rab2 recruited tyrosinated ␣-tubulin (Tyr-tubulin) versus detyrosinated ␣-tubulin (Glu-tubulin) to VTCs by performing a quantitative membrane binding assay (10,39). Salt-washed HeLa cell membranes were incubated with rat liver cytosol and GTP␥S in the absence or presence of increasing Rab2 concentrations. The reaction was then centrifuged through a 20% sucrose cushion, and the pellet containing membranes and associated proteins, including MTs, was subjected to SDS-PAGE and Western blot analysis. The relative level of Tyr-and Glu-tubulin recruited to membranes is reported as percent of total pool because of the use of two monoclonal antibodies with different binding affinities. As shown in Fig. 2A, Rab2 promoted a dose-dependent increase in membrane-bound Tyr-tubulin. From the total pool of cytosolic Tyr-tubulin added to the binding assay and therefore available for Rab2-dependent recruitment, ϳ9 -11% of Tyr-tubulin became membrane-associated after co-incubation with Rab2 (75 ng), and addition of a higher Rab2 concentration (150 ng) resulted in ϳ17-20% increase in membrane-bound Tyr-tubulin. In contrast, ϳ3-6% of Glu-Tyr was bound to Rab2-incubated membranes regardless of the Rab2 concentration.
Because Rab2-treated membranes contained a significant amount of Tyr-tubulin, HeLa cells were transfected with Rab2 cDNA, and the distribution of Rab2 and Tyr-tubulin in vivo was analyzed by indirect immunofluorescence. Cells ectopically expressing Rab2 displayed prominent Rab2-and Tyr-tubulin-labeled pleomorphic elements (boxed area; Manders coefficient of 0.942) that were primarily juxtaposed to the nucleus as well as smaller Tyr-tubulin-labeled punctate structures dispersed throughout the cell periphery (Fig. 2B). These Tyr-tubulin/ Rab2-containing entities did not stain with anti-Glu-tubulin antibody (data not shown) but did co-distribute with GAPDH (boxed area; Manders coefficient of 0.921) and aPKC (boxed area; Manders coefficient of 0.925) (Fig. 2C). Importantly, the Tyr-tubulin/Rab2 structures co-labeled with anti-p53/ p58 (boxed area; Manders coefficient of 0.928) demonstrating that the pleomorphic elements are VTCs and not tubulin aggregates (Fig. 2D).
In that regard, we observed in Rab2overexpressing cells VTCs associated with and aligned with long MT tracks (Fig. 2C).
Rab2 recruits GAPDH upstream of aPKC, and aPKC membrane association requires GAPDH. Interestingly, increasing amounts of GAPDH added to the binding assay did not significantly increase the level of membrane-associated Tyrtubulin, indicating that GAPDH is not a limiting factor (data not shown). However, the ability of Rab2 to promote Tyr-tubulin membrane binding was eliminated when purified recombinant Rab2 NЈ⌬19, a mutant protein that fails to recruit aPKC to membranes, was added to the assay (8) (Fig. 3A). This truncation in Rab2 reduces association with GAPDH but does not abolish Rab2-GAPDH interaction (9). To learn whether aPKC played a specific role in Tyr-tubulin recruitment, the membrane binding assay was supplemented with purified recombinant aPKC. In this case and unlike GAPDH, increasing amounts of mem- . ␣-Tubulin recruited to Rab2-treated membranes is predominantly tyrosinated. A, quantitative membrane binding assay was performed as described under "Experimental Procedures." Salt-washed HeLa microsomes were incubated with cytosol and GTP␥S in the presence or absence of purified Rab2 (75 or 150 ng) for 12 min at 32°C. The membrane pellet was subjected to SDS-PAGE and transferred to nitrocellulose, and the blot was probed with anti-Tyr-tubulin monoclonal antibody and with anti-Glu-tubulin polyclonal antibody. The pool indicates total Tyr-and Glu-tubulin present in the cytosol added to each binding reaction. Results are presented as percent of total pool for each tubulin subtype. A representative Western blot from one of five independent experiments is shown. HeLa cells were mock-transfected or transfected with Rab2 cDNA. Thirty six hours post-transfection, cells were permeabilized, fixed, and then labeled with anti-Rab2 and anti-Tyrtubulin (B) or with anti-Tyr-tubulin and anti-p53/p58 (D), as described under "Experimental Procedures." C, high magnification of Rab2 cDNA-transfected cells labeled with anti-Tyr-tubulin and anti-aPKC or anti-GAPDH. Boxed areas (yellow indicates co-localization) were analyzed using the Manders overlap co-localization, as described under "Experimental Procedures" and reported under "Results." Rab2, GAPDH, aPKC, and p53/p58 co-distribute with Tyr-tubulin-labeled VTCs. FEBRUARY 27, 2009 • VOLUME 284 • NUMBER 9 brane-associated aPKC caused ϳ5-8-fold increase in membrane-bound Tyr-tubulin and a minimal increase (ϳ1-1.5-fold) in the amount of membrane-bound Glu-tubulin (Fig. 3B). The putative role of aPKC in Tyr-tubulin binding was further assessed in the binding reaction by adding anti-aPKC. Fig. 3C shows that increasing amounts of anti-aPKC reduced membrane association of aPKC and Tyr-tubulin; however, anti-PKC had no effect on Glu-tubulin recruitment. These combined biochemical results are highly suggestive that membrane-bound aPKC influences dynamic MTs enriched in Tyrtubulin to associate with VTCs.

PKC Is Essential for Dynein and Tyr-MTs on VTCs
Rab proteins regulate MT motor protein recruitment, and MT motor proteins preferentially bind to either Glu or Tyr-MTs (22,33,34,40,41). Therefore, we examined whether Rab2 recruited a motor protein to membranes in the binding assay.
Although kinesin has been reported to be present on the intermediate compartment (42)(43)(44), we did not detect any kinesin or any Rab2-recruited kinesin on the membranes (data not shown). In contrast, Rab2 promoted a dose-dependent increase in membrane-associated dynein as determined by probing the blot with anti-dynein intermediate chain (Fig.  4A). Similarly, Rab2 stimulated membrane association of p50/dynamitin, a component of the dynactin complex (Fig. 4A). However, addition of Rab2 NЈ⌬19 to the assay failed to increase dynein or p50/dynamitin binding to membranes suggesting that aPKC was necessary for their downstream recruitment (Fig. 4A). To investigate the potential role of aPKC in dynein/ dynactin recruitment, anti-GAPDH or anti-aPKC was added to the membrane binding assay. The anti-GAPDH reagent blocked membrane association of GAPDH, and consequently aPKC and dynein/dynamitin, whereas anti-PKC inhibited aPKC and dynein/dynamitin membrane binding but had no effect on GAPDH recruitment (Fig. 4B). Because aPKC-dependent GAPDH phosphorylation plays a role in MT binding to membranes, we determined whether aPKC kinase activity was required for dynein/dynamitin recruitment by incubating membranes with kinase-dead PKC (K274W) (36). As we observed for MTs, aPKC kinase activity was necessary because supplementing the membrane binding assay with PKC (K274W) failed to stimulate Rab2dependent dynein/dynamitin recruitment (Fig. 4C).
This apparent biochemical relationship between aPKC and dynein was evaluated in vivo by indirect immunofluorescence microscopy. In interphase HeLa cells overexpressing aPKC, the anti-dynein antibody predominantly labeled perinuclear pleomorphic structures that co-stained with anti-aPKC (boxed area; Manders coefficient of 0.959) as well as small vesicles scattered throughout the cytosol (Fig. 5A). In addition to the juxtanuclear position, aPKC displayed a MT-like distribution that was evident in cells co-labeled for aPKC and Tyr-MTs (Fig. 5C). As expected based on the biochemical results, dynein was also found to co-distribute with Rab2 on large vesicular elements (boxed area; Manders coefficient of 0.951) that were concentrated near the Golgi region in HeLa cells overexpressing Rab2 (Fig. 5B). . aPKC is required for Tyr-tubulin membrane association. A, quantitative membrane binding assay was performed as described under "Experimental Procedures." Salt-washed HeLa microsomes were incubated without or with 75 or 150 ng of purified recombinant Rab2 NЈ⌬19, cytosol, and GTP␥S for 12 min at 32°C, as described under "Experimental Procedures." The membrane pellet was subjected to SDS-PAGE and transferred to nitrocellulose, and the blot was probed with anti-Tyr-tubulin. A representative Western blot from one of three independent experiments is shown. cont, control. B, salt-washed HeLa microsomes were incubated without or with 100 or 200 ng of purified recombinant aPKC and incubated as above. The membrane pellet was processed as above, and the blot was probed with anti-Tyr-tubulin and with anti-Glu-tubulin. The pool indicates total Tyrand Glu-tubulin present in the cytosol added to each binding reaction. Results are presented as percent of total pool for each tubulin subtype. A representative Western blot from one of three independent experiments is shown. C, salt-washed HeLa microsomes were incubated without or with 150 ng of purified recombinant Rab2, cytosol, and GTP␥S in the presence or absence of increasing concentrations of anti-PKC for 12 min at 32°C. The membrane pellet was processed as above, and the blot was probed with the specific and indicated primary antibodies. A representative Western blot from one of three independent experiments is shown.

DISCUSSION
Microtubules undergo dynamic alterations in organization and distribution during various cellular events, including mitosis and cell migration. Although MT assembly does not appear to be directly regulated by Rab proteins, these small GTPases provide a molecular link between vesicle cargo, motor proteins, and the cytoskeleton (22,30). Indeed, by using an in vitro MT binding assay, we found that Rab2 can only associate with MTs when both GAPDH and aPKC are present despite Rab2 directly interacting with GAPDH and aPKC and GAPDH and aPKC binding directly and independently to MTs. A Rab2 amino-terminal recombinant fragment corresponding to the first 70 residues can disrupt the indirect interaction of Rab2 with MTs. Because GAPDH and aPKC associate with Rab2 via residues 1-50, it was not surprising that the recombinant fragment competitively inhibited Rab2-GAPDH-aPKC-MT association in the MT binding assay. The Rab2 amino-terminal domain like Rab2 promotes GAPDH and aPKC recruitment to membranes (8,45). However, the peptide fragment does not promote vesicle formation indicating that the intact protein is required for full Rab2 activity at the VTC (7).
Our finding that GAPDH promotes Rab2 interaction with MTs is reminiscent of the role of GAPDH in facilitating MT interaction with the EF-hand Ca 2ϩ -binding protein p22, which like Rab2 is required for membrane traffic (46,47). GAPDH was the first glycolytic enzyme found associated with tubulin and binds to the carboxyl terminus of ␣-tubulin (12,13). MT assembly is not influenced by GAPDH; however, the enzyme is known to modulate the cytoskeleton by promoting MT bundling and cross-linking (12,14,38). This alteration in the spatial organization of the intracellular milieu could have profound consequences on organelle position and cargo transport by selectively bundling parallel or anti-parallel MTs and thereby providing a directional cue. Indeed, we observed VTCs containing Rab2-GAPDH-aPKC associated with and aligned with MTs enriched in Tyr-tubulin in HeLa cells overexpressing Rab2. Additionally/alternatively, MT bundles can function as supportive entities that provide structural organization within FIGURE 4. Rab2-recruited aPKC is required for dynein binding to membranes. A, quantitative membrane binding assay was performed as described under "Experimental Procedures." Salt-washed HeLa microsomes were incubated without or with 75 or 150 ng of purified recombinant Rab2 or purified recombinant Rab2NЈ⌬19, cytosol, and GTP␥S for 12 min at 32°C. The membrane pellet was subjected to SDS-PAGE and transferred to nitrocellulose, and the blot was probed with anti-dynein and with anti-p50/dynamitin. A representative Western blot from one of three independent experiments is shown. cont, control. B, salt-washed HeLa microsomes were incubated without or with 175 ng of purified recombinant Rab2, cytosol, and GTP␥S in the presence or absence of anti-GAPDH (2.5 g) or anti-PKC (2.5 g) for 12 min at 32°C. The membrane pellet was processed as above, and the blot was probed with the specific and indicated primary antibodies. A representative Western blot from one of three independent experiments is shown. C, salt-washed HeLa microsomes were incubated without or with 150 ng of purified recombinant Rab2, cytosol, and GTP␥S in the presence or absence of purified recombinant aPKC (200 ng) or purified recombinant aPKC (Lys-274) (200 ng) for 12 min at 32°C. The membrane pellet was processed as above, and the blot was probed with the specific and indicated primary antibodies. A representative Western blot from one of three independent experiments is shown. the cell (15). This potential role of MT bundles at the VTC is also consistent with the finding of Ben-Tekaya et al. that the endoplasmic reticulum-Golgi intermediate compartment is a stationary compartment and not a collection of mobile carriers (48). In either case, many proteins reported to bundle or to cross-link MTs are immunologically related to MAPs or associate with MAPs (15). For example, it was recently reported that GAPDH binds to the heavy chain of MAP1b in adult brain (49). Likewise, GAPDH was shown to co-immunoprecipitate with the MT-binding protein Tau located in neurofibrillary tangles (50). Unlike brain tissue, we did not detect in the rat liver cytosol used in our assays Tau, MAP1b, or any immunologically related proteins to Tau and MAP1b recruited to membranes by Rab2 (data not shown). The role of GAPDH in association with MAPs is unknown; however, the suggestion that MAP-GAPDH interaction could ultimately provide ATP for cytoskeleton regulation (49) is contrary to our results that showed GAPDH glycolytic activity is not required for ER to Golgi complex transport (9).
The results reported here are consistent with the previous findings that aPKC interacts with MTs (17,18). Although aPKC can bind to MTs in vitro independently of GAPDH, the presence of Src-dependent tyrosine-phosphorylated GAPDH on the VTC as well as Src phosphorylation of a PKC is required for aPKC association with those membranes indicating multi-ple levels of upstream regulation (10,39). We have proposed that Rab2-Src-aPKC-GAPDH are components of a signaling complex that defines and regulates the site of vesicle budding from VTCs in association with MT-directed vesicle movement to the acceptor compartment (39). This interpretation is compatible with other studies indicating that aPKC influences MT dynamics. For example, aPKC has been reported to control adherens junction symmetry by regulating MT organization (20). Additionally, aPKC regulates the synaptic skeleton in Drosophila by facilitating association of the MAP1B-related protein Futsch to MTs (19). Furthermore, aPKC acts in concert with Par3 and Par6 where it localizes to cilia and is required for MT organization during ciliogenesis (51). Interestingly, aPKC like GAPDH has been found in Taupositive neurofibrillary inclusions (52). Moreover, Tau overexpression decreases Glu-tubulin levels and causes a concomitant increase in Tyr-tubulin (53). It may not be coincidental that HeLa cells overexpressing Rab2 contain VTCs enriched in Tyr-tubulin. ␣-Tubulin is synthesized with a carboxyl-terminal tyrosine. The residue is removed by a tubulin tyrosine carboxypeptidase and enzymatically re-added to the carboxyl-terminal glutamate by tubulin tyrosine ligase in what constitutes a cycle of detyrosination/tyrosination (54). Tubulin tyrosine carboxypeptidase acts preferentially on assembled MTs, and phosphorylation may regulate tubulin tyrosine carboxypeptidase-tubulin interaction suggesting a potential role for protein kinase(s) (55,56). Although numerous in vivo and in vitro studies have been performed to address the role of ␣-tubulin tyrosination/detyrosination, the specific function has not been elucidated (54). Because Tyr-MTs are more dynamic with a t1 ⁄ 2 of 10 min compared with Glu-MTs that have a t1 ⁄ 2 of 1 h, it has been proposed that Glu-tubulin imparts MT stability (57,58). However, recent studies indicate that the detyrosination/tyrosination cycle differentially affects recruitment of MT-binding proteins and molecular motors to MTs, which as a consequence influences MT stability and motility. In that regard, kinesin-1 preferentially binds to Glu-MTs, whereas p150 glued/dynactin and ϩTIPs prefer Tyr-MTs (28,59,60).
Dynactin is a multisubunit protein complex containing p50/ dynamitin that binds directly to and is required for cytoplasmic dynein motile function and for membrane association (61). Live cell imaging studies have demonstrated that overexpression of p50/dynamitin blocks ER to Golgi transport (62). There are FIGURE 5. Rab2 and aPKC co-distribute with dynein. HeLa cells were transfected with either Rab2 cDNA or PKC cDNA, as described under "Experimental Procedures." aPKC overexpressing cells were permeabilized, fixed, and then co-stained with anti-dynein (intermediate chain) and fluorescein isothiocyanate-anti-Xpress (A) or fluorescein isothiocyanate anti-Xpress and anti-Tyr-tubulin (C). B, Rab2 overexpressing cells processed as above were co-labeled with anti-dynein (intermediate chain) and anti-Rab2. Boxed areas (yellow indicates co-localization) were analyzed using the Manders overlap co-localization, as described under "Experimental Procedures" and reported under "Results." Both Rab2 and aPKC co-distribute with dynein in perinuclear pleomorphic entities. two forms of cytoplasmic dynein, cytoplasmic dynein 1 and cytoplasmic dynein 2. Cytoplasmic dynein 1 is found in all MTcontaining cells and has been shown to co-localize with p53/ p58 and ␤-COP in cells incubated at 15°C to accumulate VTCs (43,63). We found that Rab2 recruited dynein and p50/dynamitin to membranes in the quantitative membrane binding assay. Additionally, HeLa cells overexpressing Rab2 displayed large perinuclear pleomorphic structures that co-labeled with Rab2 and dynein. The Rab2 downstream effector aPKC appears to be a limiting factor for dynein/dynactin association with membranes because interfering with aPKC membrane binding and aPKC kinase activity concomitantly decrease membrane-bound dynein and p50/dynamitin. Harris and Peifer (20) have also found that aPKC regulates dynein association with the adherens junction in a Drosophila aPKC mutant. This relationship between aPKC and dynein was further evidenced in HeLa cells overexpressing PKC that displayed extensive co-distribution of the kinase with dynein in the Golgi region. The specific recruitment of dynein by Rab2 versus the motor protein kinesin would preferentially promote Tyr-MTs binding to subdomains of the VTC engaged in protein sorting and recycling. Indeed, we found that membranes treated with Rab2 contained more Tyr-tubulin (ϳ3-fold) than Glu-tubulin.
Rab2 joins the list of other Rab proteins reported to utilize dynein, including Rab4 (40) and Rab6 (33,41). Interestingly, the phylogenetic tree of the Ras superfamily shows that Rab2 is most closely related to Rab4 (64), and both Rab4 and Rab6 are involved in recycling/retrograde transport (65,66). Although we have found dynein on Rab2-generated vesicles (data not shown), it is possible that dynein motor function is inactive and recycles back to the ER on Rab2 vesicles for use in COPII vesicle transport (26). Alternatively, because dynein is a minus-end directed motor, it could be that Rab2 retrograde-directed vesicles use Tyr-MTs derived from the ER as tracks for retrieval to the ER. Studies are in progress to delineate between these two possibilities.