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Intraflagellar transport (IFT) machinery mediates the bidirectional movement of cargos that are required for the assembly and maintenance of cilia. However, little is known about how IFT is regulated in vivo. In this study, we show that the small guanosine triphosphatase (GTPase) adenosine diphosphate ribosylation factor–like protein 13 (ARL-13) encoded by the Caenorhabditis elegans homologue of the human Joubert syndrome causal gene ARL13B, localizes exclusively to the doublet segment of the cilium. arl-13 mutants have shortened cilia with various ultrastructural deformities and a disrupted association between IFT subcomplexes A and B. Intriguingly, depletion of ARL-3, another ciliary small GTPase, partially suppresses ciliogenesis defects in arl-13 mutants by indirectly restoring binding between IFT subcomplexes A and B. Rescue of arl-13 mutants by ARL-3 depletion is mediated by an HDAC6 deacetylase-dependent pathway. Thus, we propose that two conserved small GTPases, ARL-13 and ARL-3, coordinate to regulate IFT and that perturbing this balance results in cilia deformation.
Cilia, which act as motile or sensory devices on the surfaces of most eukaryotic cells, play essential roles in development and postnatal tissue pattern formation. Mounting evidence links defects in cilia biogenesis and/or function to a wide spectrum of human genetic disorders that have been collectively termed ciliopathies (Badano et al., 2006). Joubert syndrome (JS) is an autosomal recessive disorder characterized by abnormalities in the central nervous system and by various commonly shared ciliopathy manifestations such as cystic kidney, blindness, and polydactyly. The functions of all identified JS loci (NPHP1, AHI1, CEP290, RPGRIP1L, TMEM67/MKS3, Arl13B, and CC2D2A), as well as most other ciliopathy candidate genes, have been suggested to be cilia and/or basal body related. Nonetheless, the precise roles of these genes remain enigmatic (Pazour and Rosenbaum, 2002; for reviews see Eley et al., 2005; Fliegauf et al., 2007; Parisi, 2009).
Intraflagellar transport (IFT) builds and maintains all cilia and flagella (Rosenbaum and Witman, 2002). In Caenorhabditis elegans, the head amphid and tail phasmid sensory organs terminate with channel cilia, which are composed of middle segments containing nine peripheral doublet microtubules and distal segments containing singlet microtubules (Perkins et al., 1986). In C. elegans, IFT is regulated by two anterograde motor machineries, the canonical heterotrimeric kinesin-II and homodimeric OSM-3/KIF17, and one retrograde dynein motor (Scholey, 2008). The two kinesin motors cooperate to build the middle doublets, whereas OSM-3 acts alone to extend distal singlets (Ou et al., 2005). Kinesin-II associates with IFT subcomplex A (IFT-A), OSM-3 associates with IFT subcomplex B (IFT-B), and the Bardet–Biedl syndrome (BBS) proteins stabilize the association between IFT-A and IFT-B. In the absence of BBS-7 and BBS-8, IFT-A and IFT-B separate as a result of mechanical competition between the two kinesin motors (Ou et al., 2005). Remarkably, both kinesin-II/KIF3 and OSM-3/KIF17 homologues appear to contribute to IFT and ciliogenesis in vertebrate systems (Marszalek et al., 2000; Lin et al., 2003; Jenkins et al., 2006; Insinna et al., 2008, 2009).
ADP ribosylation factor (Arf)–like proteins (Arls) are enzymatically active small GTPases in the Ras superfamily. The family of mammalian Arf/Arl GTPases includes 29 members, and the roles of most Arf/Arls are poorly understood (for reviews see D’Souza-Schorey and Chavrier, 2006; Gillingham and Munro, 2007). In comparative genomic searches, Arl3 and Arl6 were identified as genes that are expressed exclusively in ciliated organisms (Avidor-Reiss et al., 2004; Li et al., 2004). Later, human Arl6 was identified as a locus causative for BBS syndrome, and its C. elegans homologue was found to enter the cilium and undergo IFT (Fan et al., 2004). Meanwhile, ARL-3 was found in the Chlamydomonas reinhardtii ciliary proteome (Pazour et al., 2005) and implicated in Leishmania donovani flagellum biogenesis (Cuvillier et al., 2000). The Arl3(−/−) mouse dies after birth and exhibits typical ciliopathy manifestations such as cystic kidney and photoreceptor degeneration (Schrick et al., 2006). In addition, mutations in another small GTPase, Arl13b, cause typical JS disorder, and the Arl13b(−/−) mouse shows coupled defects in cilia structure and Sonic hedgehog signaling (Caspary et al., 2007; Cantagrel et al., 2008). In C. elegans, all three ARLs are ciliary proteins (Fan et al., 2004; Blacque et al., 2005). Nonetheless, little is known about the molecular mechanisms of ARLs in cilia.
In this study, we report that in C. elegans, ARL-13 localizes exclusively to the doublet segment of the cilium in a manner dependent on its conserved proline-rich domain (PRD). Depletion of ARL-13 causes a disrupted association between IFT-A and IFT-B subcomplexes and various cilia deformities. Intriguingly, depletion of another small GTPase, ARL-3, can partially rescue ciliogenesis defects in arl-13 mutants by restoring the binding efficiency between IFT-A and IFT-B. Further analyses demonstrated that this specific rescue effect is the result of an attenuated association between IFT-B and the OSM-3 motor in ARL-3–deficient cilia and depends on the deacetylase HDAC6. Thus, our findings provide novel mechanistic insights into small GTPase-mediated regulation of IFT machinery. Moreover, the functional balance between ARL-13 and ARL-3 appears to be critical for proper assembly and maintenance of the IFT motor complex: perturbing this process compromises IFT integrity and results in general cilia deformations.
Previous analyses in zebrafish, mouse, and human suggest a highly conserved role for Arl13B protein family members in cilia (Sun et al., 2004; Caspary et al., 2007; Cantagrel et al., 2008; Duldulao et al., 2009). arl-13, the C. elegans homologue of the human Arl13b gene, is expressed exclusively in ciliated sensory neurons throughout development in both hermaphrodites (Fig. S1, A and C; Fan et al., 2004) and males (not depicted), which indicates a distinct ciliary role for ARL-13.
The subcellular localization of ARL-13 was determined by expressing full-length arl-13 cDNA fused to GFP from the 1.2-kb native promoter (ARL-13::GFP). We found that ARL-13::GFP localized robustly to amphid and phasmid cilia (Fig. 1 B). Strikingly, GFP-tagged ARL-13 was absent from the distal singlet segment of the cilium and from the rest of the neuron, including the neuronal cell body, dendrite, and axon (Fig. 1 B), which suggests that the ARL-13 protein is efficiently targeted to the cilium and plays a specific role within the middle doublet segment.
Our observations of ARL-13 ciliary localization are identical to previously published data (Blacque et al., 2005).We did not observe detectable IFT movement of ARL-13::GFP along the cilium (Fig. S2 A). Analyses of ARL-13::GFP localization in IFT motor mutant kap-1(ok676) or osm-3(p802) worms suggest that ARL-13 ciliary targeting does not require the IFT motor kinesin-II or OSM-3 (Fig. S2 B). Both ARL-13 and human Arl13B have a putative N-terminal (NT) palmitoylation motif (Zhou et al., 2006b). The C. elegans ARL-13C12-15Del protein, in which the C12–15 palmitoylation motif has been deleted, localized to both cilia and the cytosol (Fig. S1 D). Quantitation of fluorescence intensity revealed that only ~30% of the ARL-13C12-15Del protein localized to cilia compared with ~95% of wild-type ARL-13. This observation suggests that ARL-13 is a ciliary membrane-binding small GTPase.
In contrast to most small GTPases, which are ~20 kD and composed of only a GTPase domain, Arl13B has an atypical long C terminus that contains a coiled-coil helix and a PRD (Fig. 1 A). This unique structural pattern is conserved in all Arl13B protein family members from the green algae C. reinhardtii to mammals. In zebrafish, ciliary targeting of Arl13B requires both the N and C termini (Duldulao et al., 2009). To characterize the putative cilia targeting signal sequence of C. elegans ARL-13, we generated transgenic animals that express different GFP-tagged ARL-13 truncations. Interestingly, both the ARL-13 NT truncation (which retains the GTPase domain plus the coiled-coiled helix) and the ARL-13 PRD truncation (which possesses only the PRD domain) were targeted to cilia (Fig. 1 C), indicating redundant ciliary targeting signals in the N and C termini of the worm ARL-13 protein. Nonetheless, ARL-13 PRD::GFP showed restricted middle segment localization, whereas ARL-13 NT::GFP was present in both middle and distal segments. This result suggests that the PRD domain is critical for restriction of ARL-13 to the doublet segment. Although full-length ARL-13 protein was completely absent from the cell body, we observed significant GFP signals in the cytoplasmic region for ARL-13 NT::GFP and ARL-13 PRD::GFP (Fig. 1 C), which suggests that both the N and C termini are required for efficient ciliary targeting of ARL-13.
Two deletion alleles are available for the arl-13 gene, gk513 and tm2322. The gk513 allele removes a 1.1-kb DNA fragment, including the promoter and first exon (Fig. 1 A). The tm2322 allele, an in-frame deletion that removes exons 7–9, encodes a truncated protein with an intact GTPase domain (Fig. 1 A). Both arl-13(gk513) and arl-13(tm2322) animals are healthy and show no gross anatomical abnormalities. We used gk513 as a reference allele. Because of the unique expression pattern of the ARL-13 protein (Fig. 1 B), we focused our experiments on cilia.
In C. elegans, cilia integrity can be assessed by a simple and efficient dye-filling assay. In living worms, amphid and phasmid neurons take up lipophilic fluorescent dye through sensory cilia that are exposed to the outside environment (Hedgecock et al., 1985). Worm mutants with abnormal cilia cannot take up dye and are termed dye-filling defective (Dyf; Perkins et al., 1986). Under the fluorescence dissecting microscope, arl-13(gk513) amphids showed normal dye uptake, whereas ~40% of phasmids were Dyf (Fig. 2 A). Although no Dyf phenotype was observed in amphids, our transmission electron microscopy (TEM) experiments revealed that some arl-13(gk513) amphid cilia were malformed (see Fig. 4). The Dyf phenotype of arl-13 mutants could be fully rescued by introducing an ARL-13::GFP transgene (Fig. 2 A). Furthermore, overexpression of ARL-13 NT::GFP and ARL-13 PRD::GFP both caused Dyf in wild-type animals, which indicates the importance of the GTPase and PRD domains in ARL-13 ciliary function (Fig. 2 A).
We also generated a mutant ARL-13R83Q that resembles the R79Q mutation identified in human JS patients. The human ARL13BR79Q mutant retains half of the GTP-binding efficiency of the wild-type protein (Cantagrel et al., 2008). In C. elegans, ARL-13R83Q showed a wild-type ciliary localization pattern (Fig. 2 B). However, as expected, the mutant could only partially rescue the arl-13(gk513) Dyf phenotype (Fig. 2 A). Overexpression of ARL-13R83Q also caused Dyf in wild-type animals. Collectively, our data suggest a conserved role for the ARL-13 protein and its GTPase activity in ciliogenesis.
We used ciliary markers to examine cilia morphology in arl-13 mutants. To minimize differences in expression levels of the markers, we introduced each gfp transgene from wild-type strains into arl-13 mutants by genetic crossing. Expression of OSM-6::GFP, an IFT-B marker, revealed that ~40% phasmid cilia are truncated, and the cilia often show abnormal bulblike structures in the middle segments (Fig. 2 C). This ratio is comparable with the Dyf ratio of arl-13(gk513) phasmid cilia.
Further analyses revealed that IFT-B proteins (OSM-5, OSM-6, and CHE-13), the IFT-B–associated OSM-3 motor, and IFT regulators (BBS-7 and BBS-8) all accumulated in bulblike structures in middle segments, whereas the IFT-A protein CHE-11 and its associated motor KAP-1 did not exhibit bulblike accumulation along the cilium (Fig. 2 D). All observed bulblike structures were located proximal to the middle to distal transition point (Fig. 2 D, dashed arrows), which might indicate a defective transition of IFT-B subcomplexes (including associated BBS proteins and the OSM-3 motor) from middle segments to distal segments in arl-13 mutants. In transition zones (TZs; Fig. 2 D, solid arrows), all IFT markers showed similar enrichment in both arl-13 and wild-type worms.
Next, we examined IFT motility in arl-13 mutants. In wild-type animals, kinesin-II and OSM-3 cooperate in moving the same IFT particle along the middle segment at 0.7 µm/s. Then, the OSM-3 kinesin alone moves the IFT particle along the distal segment at the faster rate of 1.3 µm/s. Cytoplasmic dynein mediates retrograde movement of the IFT particle along the whole axoneme at a rate of 1.1 µm/s (Signor et al., 1999; Snow et al., 2004; Ou et al., 2005). In bbs-7 and bbs-8 mutants, kinesin-II and OSM-3 separate in the middle segment, which results in IFT-A moving with kinesin-II at a slower rate of 0.5 µm/s and IFT-B moving with OSM-3 at a faster rate of 1.3 µm/s (Ou et al., 2005).
In arl-13 mutants, anterograde IFT movement along distal singlets and retrograde IFT movement occurred at characteristic wild-type rates (Table S1). Because IFT components accumulated abnormally in middle segments, we performed detailed analyses of IFT movement in these regions. The recorded IFT velocities in phasmid cilia were distributed in a normal curve that resembled the previous observation made in amphid cilia (Fig. 2 E; Snow et al., 2004). In arl-13 mutants, the velocity curves of IFT-A and the IFT-A–associated motor kinesin-II shifted to the left (slower) side, whereas those of IFT-B and the IFT-B–associated motor OSM-3 shifted to the right (faster) side (Fig. 2 E).
To determine the molecular basis of the abnormal IFT movement in arl-13 mutants, we subtracted the transport event ratio of wild-type animals from that of arl-13 mutants at each velocity step. Analyses of the distribution curves revealed that in arl-13 cilia, IFT-A and kinesin-II moved at a rate of ~0.5 µm/s, whereas IFT-B and OSM-3 moved at ~1.3 µm/s (see Fig. 5). For all IFT reporters used in our analyses, fewer IFT particles were found to move at the normal rate of ~0.7 µm/s in arl-13 mutants than in wild-type animals. These observations suggest that in ARL-13–deficient cilia, the IFT complex tends to dissociate, and the separated subcomplexes are transported by either kinesin-II or OSM-3 alone (see Fig. 7). The dissociation of IFT-A and IFT-B may account for the ciliogenesis defects and accumulation of IFT-B subcomplexes in arl-13 mutants.
Incomplete dissociation of the IFT complex in arl-13 cilia indicates the involvement of redundant players in this process. arl-3 and arl-6, the C. elegans homologues of human Arl3 and Arl6/BBS3, are promising candidates because they are expressed exclusively in ciliated cells. Similar to ARL-13, ARL-3::GFP does not show detectable movement in cilia (Fig. S2 A), axons, or dendrites (not depicted). In contrast, ARL-6 exhibits typical IFT motility in cilia (Fan et al., 2004). Although ARL-3 was reported to be expressed exclusively in ciliated neurons, with little ciliary localization (Blacque et al., 2005), analysis of our GFP-tagged ARL-3, whose expression was driven by its own 2.5-kb promoter, revealed that a significant amount of ARL-3::GFP localized to cilia (both middle and distal segments; Fig. 3 B). We further analyzed arl-3(tm1703) mutants, which carry a genomic deletion that encompasses nearly all of the arl-3 gene (Fig. 3 A). To our surprise, not only were arl-3(tm1703) animals superficially wild type, they also had no detectable sign of cilia malformation by the dye-filling assay and IFT markers (Fig. 3, C and D).
To address the possibility that arl-3 negatively regulates ciliogenesis, we generated a transgenic strain that overexpresses ARL-3Q72L, a constitutive GTP-binding (dominant active [DA]) mutant. In accordance with our prediction, DA ARL-3Q72L overexpression caused Dyf in wild-type phasmid cilia (Fig. 3 C). We characterized the genetic interaction between arl-3 and arl-13. As shown in Fig. 3 C, arl-3; arl-13 double mutants showed less phasmid Dyf, suggesting that depletion of ARL-3 can partly rescue cilia deformations in ARL-13–deficient cilia. This result confirms that ARL-3 negatively regulates ciliogenesis. Consistently, overexpression of DA ARL-3 in arl-13 had an additive effect in causing much more severe Dyf (Fig. 3 C). Further analysis indicated that the abnormal bulblike accumulations of IFT-B components, BBS proteins, and the OSM-3 motor in arl-13 mutants were significantly rescued by the introduction of the arl-3–null allele (Fig. 3 E).
In middle segments of wild-type animals, IFT-A and IFT-B subcomplexes are transported together by kinesin-II and OSM-3 at the intermediate rate of 0.7 µm/s. According to our measurements, the length of the phasmid cilia along which IFT particles move at 0.7 µm/s is ~2.2 µm (Fig. 3 F). In arl-13 mutants, this length decreases to ~1.5 µm. As expected, the length of middle segment can be partly rescued to ~2.0 µm in arl-3; arl-13 double mutants (Fig. 3 F).
To investigate cilia deformations at the ultrastructural level, we used TEM to examine amphid cilia in various mutants (Fig. 4). Wild-type amphids contained 10 cilia bundled together (Fig. 4 A), whereas arl-13 mutants had only six to eight distal segments, likely as a result of premature truncation of the distal segments of some cilia (n = 8; Fig. 4 B). The remaining distal segments contained normal microtubule singlets. Some truncations in the distal segments continued further, usually resulting in one to two missing middle segments in the worms we sectioned (Fig. 4 F). In contrast to the normal pattern in middle segments of nine peripheral doublets adjacent to the membrane, misplaced doublets were frequently seen in the ciliary lumen of arl-13 mutants (Fig. 4, F and T, arrowheads), a phenomenon indicative of a disrupted axoneme architecture or microtubule: membrane connection.
Several other cilia deformations were observed in arl-13 mutants. For example, an abnormal membrane distortion (seen in two of eight amphids of arl-13 mutants; Fig. 4, F and R, black arrows) in middle segments may correlate with the bulblike structure observed in Fig. 2 C. Occasionally, we observed an increased number of outer doublets (14 rather than 9 doublets; Fig. 4 S) in a cilium, with most showing B-tubule seam breaks, and some doublets were seen in the ciliary lumen. This structure represents a fused cilium with misplaced doublets in the middle of the ciliary lumen. The C. elegans TZ typically contains a circular array of doublet microtubules with y links between the axoneme and ciliary membrane (Fig. 4, M–P, white arrows; Perkins et al., 1986). The number and morphology of amphid cilia in the TZ area of arl-13 mutants were comparable with those of wild-type animals (Fig. 4, I, J, M, and N).
Consistent with our finding that ARL-3 depletion can rescue various ciliary deformations in arl-13 mutants, the distal segments of arl-3; arl-13 mutants were restored to 9–10 cilia, comparable with those of wild-type worms (Fig. 4 C). The abnormal membrane distortion (Fig. 4, F and R, arrows) and uncommon ciliary fusion with broken B-tubules were not detected in any examined arl-3; arl-13 amphid cilium (n = 8), indicating a rescue effect. In accordance with the result that ARL-3 depletion could not completely rescue ciliogenesis defects in arl-13 mutants, middle segments of arl-3; arl-13 mutants possessed misplaced doublets in the ciliary lumen (Fig. 4 G, arrowhead).
However, overexpression of the ARL-3Q72L DA mutant caused a much more severe ciliogenesis defect in arl-13 animals. Only three to six middle and distal segments existed in the amphid cilia of ARL-3Q72L(Xs); arl-13 (Fig. 4, D and H). Unexpectedly, overexpression of ARL-3Q72L DA also reduced the number of cilia in the TZ area (Fig. 4 L). Checking IFT markers in ARL-3Q72L(Xs); arl-13 mutants (Fig. S4 B) and examining TEM sections deeper into the dendrite region did not reveal mispositioned TZs or cilia. Thus, we conclude that some cilia are completely missing in ARL-3Q72L(Xs); arl-13 mutants. On the basis of these results and the observation that a significant amount of ARL-3 protein is cytosolic (Fig. 3 B), we propose that ARL-3 plays a role in a very early stage of ciliogenesis, possibly before TZ formation. Collectively, the TEM data complement our previous findings and support a model in which ARL-3 and ARL-13 act in opposite directions to regulate ciliogenesis.
To gain a mechanistic insight into how ARL-3 depletion rescues ciliogenesis defects in arl-13 mutants, we performed detailed IFT analysis on arl-3 single and arl-3; arl-13 double mutants. arl-13 mutants showed a destabilized IFT complex (Fig. 2 E). To our surprise, a significant proportion of the IFT-A particles and kinesin-II motor moved at the slower rate of 0.5 µm/s in arl-3; arl-13 mutants, as they did in arl-13 mutants (Fig. 5, A and B). Moreover, the IFT-B component OSM-6 also tended to move at the slower 0.5 µm/s rate in arl-3; arl-13 double mutants (Fig. 5 C). Interestingly, in contrast to all other IFT components tested, the OSM-3 motor tended to move at a faster rate of 1.3 µm/s in arl-3; arl-13 mutants (Fig. 5 D). Thus, our data reveal that in arl-3; arl-13 mutants, IFT-A and IFT-B subcomplexes move together and OSM-3 tends to dissociate from the IFT complex and move alone in the middle segments (see Fig. 7).
ARL-3 depletion does not rescue arl-13 ciliogenesis defects by restoring the integrity of the entire IFT particle. Rather, the absence of ARL-3 destabilizes the association between IFT-B and the OSM-3 motor, which indirectly restores binding between IFT-A and IFT-B subcomplexes. A similar scenario exists in bbs mutants. In bbs single mutants, IFT-A and IFT-B subcomplexes separate, but in bbs; osm-3 double mutants, the subcomplexes move together by kinesin-II alone because of the absence of a dragging force generated by the faster OSM-3 motor (Pan et al., 2006). To support this conclusion, we examined arl-3 mutants and found that more IFT-A and IFT-B moved together at a slower rate, whereas more OSM-3 moved at a faster rate (Fig. 5). In all mutants examined, the anterograde movement in distal segments and the retrograde movement were unchanged (Table S1). Notably, although the IFT integrity in arl-3; arl-13 is reminiscent of that in arl-3, the former still show Dyf phenotype. This finding indicates that compromised IFT integrity is not the sole explanation for the ciliogenesis defects in arl-13 mutants.
Few systematic analyses of the effectors of Arl GTPases have been undertaken. One mechanistic study linked Arl3 depletion to increased tubulin acetylation in HeLa cells (Zhou et al., 2006a). Two tubulin deacetylases, HDAC6 and SIRT2, were characterized recently (Hubbert et al., 2002; North et al., 2003). Notably, HDAC6 physically interacts with a BBSome subunit, BBIP10, and is involved in BBIP10-dependent cytoplasmic tubulin acetylation (Loktev et al., 2008). To investigate whether ARL-3 and HDAC6 function in the same pathway to regulate ciliogenesis, we characterized the C. elegans HDAC6 homologue F41H10.6 (hereafter termed HDAC6). The C. elegans hdac6 gene has one available mutant allele, ok3203, which removes ~400 bp of coding sequence and may result in a prematurely terminated protein or alternatively spliced products. hdac6 mutants are superficially wild type and possess normal cilia on the basis of dye-filling experiments. hdac6 gene expression was detected in ciliated amphids and phasmids, nerve cords, intestine, and pharynx (Fig. S3). In ciliated neurons, the GFP::HDAC6 signal is diffuse in the cell body, axon, dendrite, and cilium. Interestingly, GFP::HDAC6 is retained predominantly in the middle segment, like ARL-13::GFP (Fig. 6 A).
We then generated arl-3; hdac6 double-, arl-13; hdac6 double-, and arl-3; arl-13; hdac6 triple-mutant animals. arl-3; hdac6 double mutants were normal in the dye-filling assay. As shown in Fig. 6 B, the hdac6 allele can rescue the ciliogenesis defect in arl-13 to a similar extent as the arl-3 allele. We next asked whether hdac6 and arl-3 act in the same genetic pathway to correct the ciliogenesis defects in arl-13 mutants. Epistasis analysis is commonly used to assess genetic interactions among several genes. We reasoned that if arl-3 and hdac6 act independently or redundantly, we would observe an additive rescue effect in arl-3; hdac6; arl-13 triple mutants. A dye-filling assay showed that the rescue effect in arl-3; hdac6; arl-13 triple mutants is comparable with that in arl-3; arl-13 or hdac6; arl-13 double mutants, suggesting that arl-3 and hdac6 act in the same genetic pathway to regulate cilia formation. Furthermore, TEM analyses confirmed that the distal amphid cilia number can be restored to the wild-type level in hdac6; arl-13 double mutants (n = 8; Fig. 6 C). Similar to ARL-3 DA overexpression, HDAC6 overexpression could cause Dyf (Fig. 6 B). Therefore, our data reveal that the previously reported, microtubule-associated deacetylase HDAC6 plays a novel role in the ciliogenesis pathway regulated by the small GTPase ARL-3.
Collectively, our data support the working model that ARL-13 and ARL-3, although not moved along the cilium, play novel roles in coordinating IFT (Fig. 7). Specifically, we propose that ARL-13 acts to enhance the binding force between IFT-A and IFT-B subcomplexes, and ARL-3 functions in an HDAC6–dependent manner to regulate the association between IFT-B and the OSM-3 motor. The absence of ARL-13 produces a destabilized IFT complex, which can be pulled apart into separate IFT-A–kinesin-II and IFT-B–OSM-3 particles by the dragging force generated between faster-moving OSM-3 motors and slower-moving kinesin-II motors. In arl-3 single and arl-3; arl-13 double mutants, the significantly attenuated association between IFT-B and OSM-3 reduces the dragging force and indirectly restores the binding efficiency of IFT-A and IFT-B subcomplexes.
Considerable interest exists in further defining the molecular pathways that lead to ciliopathies. Exploring the in vivo molecular mechanisms of conserved disease genes in a simple C. elegans model system has helped advance our understanding of the pathophysiologies of many ciliopathies, such as autosomal dominant polycystic kidney disease, Merkel–Gruber syndrome, nephronophthisis, and BBS syndromes (Haycraft et al., 2001; Fan et al., 2004; Barr, 2005; Badano et al., 2006; Jauregui et al., 2008; Williams et al., 2008; Bialas et al., 2009).
The cilia-related phenotypes of arl-3 and arl-13 mutants reported in this study are quite reminiscent of those in other organisms. For example, in L. donovani, a DA form of ARL-3 (LdARL-3A) caused a truncated flagellum, whereas the dominant-negative form did not affect flagellum biogenesis. Arl3(−/−) mice show apparently normal ciliary structure but abnormal ciliary protein transport in photoreceptors. Zebrafish Arl13b/scorpion mutants show abnormal cilia formation (Sun et al., 2004), and Arl13b(−/−) mice possess shortened cilia with a specific B-tubule closing defect that is similar to what we observed in arl-13 worms (Fig. 4 S; Caspary et al., 2007).
Although IFT integrity in arl-3; arl-13 mutants was restored to a similar state as that in arl-3 mutants (Fig. 5; and Fig. 7, C and D), arl-3; arl-13 mutants still display mild ciliogenesis defects. One hypothesis to explain this observation is that the effectors of ARL-13 may have two distinct functions: one related to regulating IFT integrity and the other a non-IFT–related function, such as membrane–microtubule architecture. This hypothesis is supported by the observation with TEM that arl-3; arl-13 mutants possess misplaced doublets. ARL-3 depletion indirectly restores IFT but is not able to correct other non-IFT–related ciliogenesis defects; therefore, we did not see a complete rescue effect for the arl-3; arl-13 double mutants.
The cellular effectors of ARL-3 and ARL-13 are poorly understood. However, experiments on ARL mutants with altered GTP-binding capacity indicate that normal ciliogenesis requires the GTPase activities of both ARL-3 and ARL-13 (Fig. 2 A and Fig. 3 C). Identification of the putative GTPase exchange factor and GTPase-activating protein that bind to ARL-3 and ARL-13 will be critical to fully dissect their roles in cilia biogenesis and IFT regulation. Remarkably, the proposed roles of ARL-13 and ARL-3 in IFT regulation resemble the roles proposed for the BBSome and DYF-1 in this system (Ou et al., 2005). It would be informative to study how ARLs, BBS proteins, and DYF-1 converge in the same pathway to regulate ciliogenesis and IFT.
The C-terminal PRD of ARL-13 is indispensable for its specific targeting to the doublet segment of the cilium. The PRD and its major interacting domain, SH3 (Src homology 3), have been shown to be involved in various protein–protein interactions. Interestingly, a PRD is found in many microtubule-associated proteins such as MAP2, τ, and MAP4 and is required for the activities of microtubule-associated proteins in microtubule binding and assembly (West et al., 1991; Kanai et al., 1992; Ferralli et al., 1994; Tokuraku et al., 1999). Additionally, the PRD of the GTPase dynamin regulates its effector binding and microtubule association (Gout et al., 1993; Hamao et al., 2009). In our experiments, overexpression of the ARL-13 PRD domain induced a dominant-negative effect on ciliogenesis (Fig. 2 A). Overexpression of the ARL-13 NT truncation, which lacks the PRD domain but contains the entire GTPase domain, could also cause Dyf in the phasmid cilia of wild-type animals. Similarly, the arl-13(tm2322) allele is an in-frame deletion and encodes a truncated ARL-13 protein that lacks the PRD domain but retains the intact GTPase domain (Fig. 1 A). Both arl-13(gk513) and arl-13(tm2322) animals show comparable ciliogenesis defects (unpublished data). Remarkably, contrary to our observation that none of the IFT reporters interfere with ciliogenesis in arl-13(gk513) mutants, IFT transgene overexpression can enhance the ciliogenesis defect of arl-13(tm2322) mutant cilia (Cevik et al., 2010). These findings provide support for the view that the PRD domain of ARL-13 is critical for both ciliary targeting and cilia formation, and loss of the PRD domain could result in a truncated ARL-13 protein with deregulated GTPase activity. Thus, characterization of the ciliary proteins that bind the ARL-13 PRD domain is of great interest.
We demonstrate in this study that ARL-3 acts through the deacetylase HDAC6 to regulate cilia formation in C. elegans. HDAC6 deacetylates not only histones (Grozinger et al., 1999) but also α-tubulin (Hubbert et al., 2002), Hsp90 (Kovacs et al., 2005), and cortactin (Zhang et al., 2007). Inhibition of HDAC6 enzymatic activity causes increased transport of the kinesin-1 cargo complex along microtubules in neuronal cells (Reed et al., 2006). Reminiscent of our findings, activation of HDAC6 can promote cilia disassembly, and loss of HDAC6 activity selectively stabilizes cilia in human retinal epithelial cells (Pugacheva et al., 2007).
Currently, HDAC6 is thought to regulate microtubule-dependent processes by deacetylating α-tubulin. However, this model is inaccurate for the C. elegans ciliogenesis pathway because MEC-12, the only α-tubulin capable of being acetylated, is not expressed in ciliated amphids and phasmids (Fukushige et al., 1999). Another HDAC6 substrate, Hsp90, was shown to associate with β-tubulin and may be involved in stabilizing tubulin polymerization in cilia (Takaki et al., 2007). However, worms with a null allele of daf-21, the C. elegans homologue of Hsp90, possess normal cilia in our analysis (unpublished data). These data rule out α-tubulin and Hsp90 as candidate HDAC6 substrates during ciliogenesis in C. elegans. On the basis of our model, we propose that HDAC6 deacetylates an unknown adaptor protein in IFT-B–OSM-3 subcomplexes.
ARL-3 appears to have non-IFT–related functions in cilia. Overexpression of DA ARL-3 in arl-13 mutants produces a new defect in that some cilia are missing in the TZ area (Fig. 4 L). This striking phenotype is not the result of compromised IFT in middle segments because previous TEM analyses showed that TZs can form normally in all IFT mutants examined (Perkins et al., 1986). Because C. elegans and vertebrate ARL-3s are cytosolic (Fig. 3 B; Behnia et al., 2004; Setty et al., 2004) and at least one IFT protein (IFT20) moves between the Golgi apparatus and adjacent basal body (Follit et al., 2006), the overexpression of DA ARL-3 could interfere with normal protein transport between the Golgi and TZ. When this interference is combined with the already compromised ciliogenesis of arl-13 mutants, the normal TZ formation could be disrupted. A possible ARL-3 effector in this pathway is the retinitis pigmentosa 2 (RP2) protein. In the mammalian retina, RP2 interacts with GTP-bound Arl3 and functions as a GTPase-activating protein (Grayson et al., 2002; Veltel et al., 2008). K08D12.2, the C. elegans homologue of RP2, is expressed exclusively in ciliated cells and localizes specifically around TZs but not along the axoneme (Blacque et al., 2005). It would be informative to examine whether ARL-3 and RP2 form a functional complex and play a role in the early stage of ciliogenesis.
In conclusion, our findings reveal a novel coordination mechanism for ARL-13 and ARL-3 in cilia formation. Considering the strikingly similar mutant phenotypes across different species, the ciliary roles of ARL-13 and ARL-3 identified in this study are probably evolutionarily conserved in other organisms. The next challenge is to elucidate the effectors of ARL-13 and ARL-3 and the substrates of HDAC6 involved in regulating ciliogenesis.
The stock DiI (2 mg/ml in dimethyl formamide; Invitrogen) was diluted 1:200 in M9. Worms were incubated in diluted dye for 1 h at room temperature. After incubation, the animals were washed at least three times with M9 and observed using a fluorescence microscope (M2Bio; Carl Zeiss, Inc.).
Animals were raised at 20°C and imaged using standard C. elegans slide mounts and a Plan Apochromat 60× 1.49 NA oil objective (Nikon) on an imaging microscope (TE 2000-U; Nikon).
We performed all IFT analyses in phasmids for easier observation. IFT motility was observed using a Plan Apochromat 100× 1.49 NA oil total internal reflection fluorescence objective (Nikon). In wild-type worms, the IFT velocities in phasmid cilia were identical to those reported in amphid cilia (Table S1). Motility stacks were recorded using a charge-coupled device camera (QuantEM 512SC; Roper Industries), and kymographs were produced using MetaMorph software (MDS Analytical Technologies). Worms were anesthetized in a drop of M9 containing 10 mM levamisole, transferred to an agarose mount slide, and imaged immediately.
For TEM, worms were fixed in 2.5% glutaraldehyde in cacodylate buffer on ice. Heads were cut off, moved to fresh fixative, and held overnight at 4°C. Animals were rinsed in buffer and stained with 1% osmium tetroxide in cacodylate buffer for 1 h at 4°C. After embedding small groups of worms in agarose, the specimens were dehydrated and embedded in Embed812 resin according to the general procedures described previously (Hall, 1995). Thin sections were collected on a diamond knife and poststained before viewing on an electron microscope (JEM-1400; JEOL).
Fig. S1 shows that arl-3 and arl-13 are expressed exclusively in ciliated cells. Fig. S2 shows that ARL-3 and ARL-13 show no IFT motility. Fig. S3 shows that hdac6 is expressed in ciliated cells. Fig. S4 shows that ARL-3 localizes normally in arl-13 mutants, and TZ morphology appears normal in ARL-3Q72L(Xs); arl-13 animals. Table S1 shows IFT velocities of various IFT markers in arl-3 and arl-13 single mutants and arl-3; arl-13 double mutants. Table S2 shows all of the strains used in this study. Online supplemental material is available at http://www.jcb.org/cgi/content/full/jcb.200912001/DC1.
We thank the Caenorhabditis Genetics Center, the Japanese Bioresource Project, and Drs. Jonathan Scholey, Michel Leroux, and Maureen Barr for strains. We also thank Drs. Maureen Barr, Peter Harris, Vicente Torres, Nicholas LaRusso, Jeffery Salisbury, and Ms. Natalia Morsci for helpful discussions.
This research was funded by the Polycystic Kidney Disease (PKD) Foundation Young Investigator Award (grant 04YI09a to J. Hu). J. Hu is also supported by a FULK Career Development award, the Zell PKD Disease Research Fund, and the Upjohn PKD Research Fund from Mayo Clinic.