Sticky worms: adhesion complexes in C. elegans

Caenorhabditis elegans is a powerful model system for investigating the establishment, regulation and function of adhesive structures in vivo. C. elegans has several adhesion complexes related to those in vertebrates. These include: (1) epithelial apical junctions, which have features of both adherens and tight junctions; (2) dense bodies, which are muscle-attachment structures similar to focal adhesions; (3) fibrous organelles, which resemble hemidesmosomes and mediate mechanical coupling between tissues; and (4) a putative dystrophin-glycoprotein complex that has potential roles in muscle function and embryogenesis. Recent work has increased our understanding of these structures and has given new insights into the functions of their vertebrate counterparts.

embryo (reviewed by Ohno, 2001;Etienne-Manneville and Hall, 2003), its functional role in C. elegans epithelia is not known. C. elegans has one Crumbs homolog (crb-1) and a second Crumbs-like gene (crl-1 or eat-20). Loss-of-function studies indicate that neither is essential for epithelial development (Bossinger et al., 2001), although EAT-20 is necessary for proper muscle pumping in the pharynx (Shibata et al., 2000). Thus, the function of the SAR-like region remains unclear. Accordingly, we focus here on describing recent progress in understanding the adherens junctional and DLG-AJM domains.
The C. elegans HMR-HMP complex was identified through its essential role in morphogenesis of the hypodermis (Costa et al., 1998) (reviewed by Simske and Hardin, 2001), a specialized epidermis that forms the outer layer of the worm. Epidermal cells are born on the dorsal side of the embryo after gastrulation and adhere to form a cell sheet. The free edges migrate to the ventral midline, where they seal through the formation of adhesive junctions in a process called ventral enclosure ( Fig. 2B) (Williams-Masson et al., 1997). The formation of junctions is rapid (taking fewer than 15 minutes) and is mediated by contact between actin-rich protrusions (see Movie 1, http://jcs.biologists.org/supplemental/) (Raich et al., 1999). Junction formation in cultured cells occurs more slowly, but is similarly initiated by cell protrusions (reviewed by Vasioukhin and Fuchs, 2001). Circumferential actin filament bundles (CFBs) anchor to CeAJs and their contraction aids the four-fold elongation of the embryo into a worm-like shape (Fig. 2B).
Several proteins have emerged as potential regulators of the adherens junctional domain including APR-1, Rho family GTPases and semaphorins. APR-1, a homolog of the APC tumor suppressor, localizes to epidermal cell borders, and mutants exhibit Hmr-like phenotypes in addition to defects in cell fate specification, among others (Hoier et al., 2000). The potential role of APR-1 in regulating the HMR-HMP complex has not been explored. Rho-family GTPases are key regulators of adherens junctions in other systems (reviewed by Van Aelst and Symons, 2002). C. elegans homologs of Cdc42 (CeCDC-Journal of Cell Science 117 (10) elegans. In vertebrates and Drosophila, different junctions are distinguishable by electron microscopy (EM), whereas in C. elegans there is one electron-dense region called the C. elegans apical junction (CeAJ). CeAJs consist of at least three distinct domains, although how these domains correlate to the electron-dense region is currently unclear. Note that the SAR of Drosophila is concentrated at the marginal zone but extends to the apical surface (reviewed by Tepass et al., 2001). Components of the SAR-like region of C. elegans (observed in pharynx and intestine) also localize to both the marginal zone and apical surface (Bossinger et al., 2001). Despite some differences in organization, there is compositional similarity between the regions shown in green (vertebrate tight junction, Drosophila SAR, and C. elegans SAR-like domain), blue (vertebrate, Drosophila, and C. elegans adherens junctions) and red (Drosophila septate junction and the C. elegans DLG-AJM domain) (reviewed by Knust and Bossinger, 2002). (B) TEM image of a CeAJ (arrow indicates the electron-dense region). Bar, 100 nm. 42) and Rac-1 (CED-10) localize to epidermal cell borders (Chen et al., 1996), and Rho-family GTPases appear to regulate actomyosin contractility during elongation (Wissmann et al., 1997;Wissmann et al., 1999). Beyond this, the role of Rhofamily GTPases in CeAJs is not understood. Interestingly, depleting the semaphorin MAB-20/Sema2A causes formation of ectopic epidermal cell contacts during morphogenesis (Roy et al., 2000). Abnormal contacts might be an indirect consequence of increased protrusive activity, although a more direct role for MAB-20 in regulating cell contacts cannot be ruled out. Homologs of Sema1A (SMP-1) and Sema1B (SMP-2) also appear to modulate epidermal cell contacts, but the mechanisms involved are unknown (Ginzburg et al., 2002).
Cadherin-independent mechanisms for mediating cellcell adhesion Since inactivation of cadherins and catenins in mice (Larue et al., 1994;Riethmacher et al., 1995), Xenopus (Heasman et al., 1994) and Drosophila (Tepass et al., 1996;Uemura et al., 1996) disrupts early embryonic cell adhesion, it is surprising that this is not the case in C. elegans. Other putative cadherins in C. elegans (Cox et al., 2004;Hill et al., 2001) could act redundantly with HMR-1. However, the only other cadherin characterized to date is the Fat-like cadherin, CDH-3, which regulates morphogenesis of the epidermal cell (hyp10) at the During ventral enclosure (a-b), edges of the epidermal cell sheet extend around the embryo, meet at the ventral midline, and seal through the formation of cell junctions. Note that JAC-1-GFP is not present at the leading edge of migrating epidermal cells, but is rapidly recruited to the contact region between cells at the ventral midline. Other adherens junctional components show a similar localization during enclosure. After ventral enclosure, contraction of the epidermis helps to drive the four-fold elongation of the embryo (c,d). Nomarski images of similarly aged embryos are shown for comparison (e-h). A Nomarski movie (Movie 4, http://jcs.biologists.org/supplemental/) showing development of a wildtype embryo is available online. In all images, anterior is left. Bar, 10 µm.
tip of the tail (Pettitt et al., 1996). Another possibility is the L1-CAM homolog, LAD-1 (Chen et al., 2001). LAD-1 localizes to cell-cell contacts in the early embryo and epithelia. Expression of dominant-negative LAD-1 causes body-shape defects, which could reflect perturbed epithelial adhesion. Another candidate is an analog of the ponsin-nectin-afadin complex, which provides adhesive function redundantly with the cadherin-catenin system in vertebrates (reviewed by Takai and Nakanishi, 2003). C. elegans lacks a clear nectin homolog, but has homologs of afadin (W03F11.6 and C43E11.6) and ponsin (Y45F10D.13) (McMahon et al., 2001). RNA interference (RNAi) directed against these genes does not produce lethality (McMahon et al., 2001). However, RNAi directed against W03F11.6 enhances the lethality of embryos that have a weak hypomorphic mutation in hmp-1 (M. Köppen, J.H. and J. Pettitt, unpublished), indicating that it might either act in the same pathway or one parallel to that involving the HMR-HMP complex.

DLG-AJM domain
The DLG-AJM domain lies basal to the adherens junctional domain ( Fig. 1) and plays a role in adhesion and, potentially, in paracellular permeability. DLG-1 is a membrane-associated guanylate kinase (MAGUK; Fig. 3) that has homologs in Drosophila (Dlg) and vertebrates (hDlg/SAP97). Drosophila Dlg regulates formation of adherens and septate junctions (reviewed by Müller and Bossinger, 2003), and is also important for synapse formation (Budnik, 1996) and preventing follicular cell overgrowth during oogenesis (Goode and Perrimon, 1997). Like Drosophila Dlg, vertebrate SAP97 localizes to epithelial cell contacts, acts as a tumor suppressor, and aids assembly of synaptic junctions (reviewed by Fujita and Kurachi, 2000). Mice with a partial deletion of SAP97 exhibit cleft palates (Caruana and Bernstein, 2001), highlighting its importance in morphogenesis.
Loss of DLG-1 or AJM-1 causes embryonic arrest at the two-to three-fold stage of elongation, which appears to be accompanied by necrotic cell death (C. Lockwood and J.H., unpublished) (Bossinger et al., 2001;Firestein and Rongo, 2001;Köppen et al., 2001;McMahon et al., 2001). Additionally, loss of DLG-1 results in leakage of cytoplasm from the tail and ventral midline during elongation (McMahon et al., 2001) and abnormalities in actin bundles of the pharynx and epidermis ).
The precise function of the DLG-AJM domain is not known, but transmission electron microscopy (TEM) analysis has provided some insights. In ajm-1 null mutants, junctions occasionally separate, leaving paracellular gaps of 50-200 nm (Köppen et al., 2001). This is speculated to cause loss of solute gating, leading to osmotic shock (Köppen et al., 2001). By contrast, embryos subject to RNAi directed against dlg-1 exhibit loss of electron-dense material from CeAJs McMahon et al., 2001), indicating that DLG-1 might act as a scaffold for the formation of this material. Intriguingly, epithelial cell membranes nonetheless remain closely apposed. They may be held together by the HMR-HMP complex, which remains intact in dlg-1(RNAi) embryos (Bossinger et al., 2001;McMahon et al., 2001). In light of this, it is interesting that the severity of the adhesion phenotypes induced by loss of DLG-1 or AJM-1 is enhanced by RNAi directed against the adherens junctional component vab-9 (Simske et al., 2003). This suggests that the adherens junctional and DLG-AJM domains act together to promote epithelial integrity.
Recent work shows that the claudin-like protein CLC-1 colocalizes with AJM-1 in pharyngeal cell junctions, where it might regulate paracellular permeability (Asano et al., 2003). Determining whether CLC-1 or other claudin-like proteins (CLC-2, CLC-3 and CLC-4) function within the DLG-AJM domain will be an important topic for future study. Although they have not been extensively characterized, C. elegans also has several homologs of tight and septate junctional proteins (McMahon et al., 2001;Knust and Bossinger, 2002) DLG-AJM domain, and determining whether it interacts with the cytoskeleton, will help clarify its function.

Regulation of CeAJ organization and polarity
Currently, little is known about how CeAJ polarity is established and maintained. Components of the adherens junctional domain (the HMR-HMP complex and VAB-9) are not necessary for localization of the DLG-AJM complex and vice versa (Costa et al., 1998;Bossinger et al., 2001;Firestein and Rongo, 2001;Köppen et al., 2001;McMahon et al., 2001;Simske et al., 2003). Recent insights into junctional polarity in C. elegans are derived from studies of the LAP ('leucine-rich repeat and PDZ') protein LET-413 (Fig. 3). LET-413 localizes through its leucine-rich repeat region to the basolateral membrane of epithelial cells and partially overlaps the DLG-AJM domain (Legouis et al., 2000;Legouis et al., 2003). Like its homologs in Drosophila (Scribble)  and vertebrates (Erbin) (Borg et al., 2000), LET-413 has an important role in regulating junctional organization.
In C. elegans embryos lacking LET-413, the electron-dense material at CeAJs is discontinuous, extended basally, or absent entirely (Legouis et al., 2000;McMahon et al., 2001). What accounts for this phenotype is not entirely clear, but several recent studies offer clues. First, LET-413 prevents basal diffusion of some apical CeAJ proteins, including PAR-3 and PAR-6 (Bossinger et al., 2001). Second, although LET-413 is not necessary for apical targeting of adherens junctional components (Legouis et al., 2000;McMahon et al., 2001;Simske et al., 2003), it does act with DLG-1 to exclude them from the basolateral membrane (Simske et al., 2003). Third, LET-413 is important for promoting proper distribution of DLG-1 and AJM-1 and preventing them from spreading basally (Köppen et al., 2001;McMahon et al., 2001). The molecular mechanisms through which LET-413 accomplishes these functions are unknown. LET-413 could interact with a motor complex (McMahon et al., 2001) or the Rho-family GTPases (Legouis et al., 2000), although direct evidence for either possibility is lacking. Further studies on LET-413 and the identification of other regulators of CeAJ polarity are likely to clarify how epithelial cell polarity is established in vivo.
In summary, despite organizational differences between epithelial junctions in C. elegans, Drosophila and vertebrates, there are several conserved proteins that share some analogous functions (see also Müller and Bossinger, 2003). These include the HMR-HMP (cadherin-catenin) complex, DLG-1 (Dlg/SAP-97) and LET-413 (Scribble/Erbin). C. elegans also has a PAR-aPKC complex, and it will be important to determine its functional role in epithelial cell adhesion and polarity. The conservation of these proteins indicates their importance as core elements of epithelial cell junctions and indicates that C. elegans is an excellent model system for studying their functions.

Dense bodies and M-lines
C. elegans has four longitudinal muscle quadrants that underlie the epidermis (reviewed by Francis and Waterston, 1985). Muscle quadrants are first detectable just after ventral enclosure is complete and sarcomeres are evident at the twofold stage of elongation (reviewed by Moerman and Fire, 1997). Force transduction in muscle is accomplished through anchorage of actin and myosin filaments to the muscle cell membrane. In C. elegans, mutations that perturb this process cause arrest at the two-fold stage of elongation owing to muscle paralysis (Hresko et al., 1994;Williams and Waterston, 1994;Gettner et al., 1995). Characterization of 'paralyzed at twofold' (Pat) mutants has shown that integrin attachment structures are essential for sarcomere assembly in C. elegans. Similarly, integrins are also required for the formation of functional muscles in Drosophila and mammals (reviewed by Bokel and Brown, 2002).
C. elegans is a powerful model system for exploring integrin function, in part because it has just two α-integrins (PAT-2 and INA-1) and one β-integrin (PAT-3). In C. elegans, roles for integrins in cell migration (Baum and Garriga, 1997;Lee et al., 2001), neuron fasciculation (Baum and Garriga, 1997), gonadal morphogenesis (Lee et al., 2001) and muscle tissue integrity (see below) have been documented. However, the adhesive structures organized by integrins have been most extensively examined in muscle.
During sarcomere assembly in C. elegans, parallel bundles of actin (thin filaments) and myosin (thick filaments) link to the cell membrane through dense bodies (Z-disc analogs) and M-lines, respectively (Fig. 4A,B). Dense bodies are similar to vertebrate focal adhesions, which are integrin-based complexes that mediate linkage between the ECM and the actin cytoskeleton (Hynes, 1992). In addition to their structural role, focal adhesions also mediate cell signaling (reviewed by Zamir and Geiger, 2001;Hynes, 2002). M-lines are also integrin based and are compositionally similar to dense bodies; however, they are inherently different from focal adhesions since they anchor to myosin rather than actin.

Assembly of dense bodies and M-lines
The first step in dense body and M-line assembly is recruitment of integrins to the plasma membrane, where they cluster into bands, one along the longitudinal axis of each body-wall muscle quadrant. Subsequently, these initial attachment sites segregate into a highly ordered pattern of dense bodies and Mlines (Fig. 4B).
UNC-52/perlecan, a secreted heparan sulfate proteoglycan, is the only protein known to be necessary for integrin localization to the basal muscle cell membrane (Rogalski et al., 1993;Hresko et al., 1994;Williams and Waterston, 1994;Mullen et al., 1999). Whether UNC-52 is a ligand for αPAT-2-βPAT-3, or has an indirect role in integrin recruitment, is currently unknown. Recent studies indicate that the laminin αB subunit (one of two laminin α subunits), like UNC-52, localizes to the extracellular face of dense bodies and M-lines (Huang et al., 2003). However, rather than mediating assembly, laminin αB is necessary for restricting dense body formation to the basal membrane (Huang et al., 2003).
There are at least two distinct protein complexes that are recruited separately to nascent adhesion sites. One complex contains DEB-1/vinculin, which mediates actin filament attachment to dense bodies Hresko et al., 1994). Another complex, containing UNC-112, PAT-4 and PAT-6, acts as a scaffold for the development of nascent attachment sites into dense bodies and M-lines (Rogalski et al., 2000;Mackinnon et al., 2002;Lin et al., 2003). In embryos with null mutations in these genes, UNC-52 localizes normally in the basement membrane, and integrin foci form and become associated with DEB-1, but dense bodies and M-lines do not develop.
UNC-112 has a conserved sequence present in FERMdomain proteins (Rogalski et al., 2000) that might mediate attachment to the plasma membrane (Chishti et al., 1998).
Recently, Mig-2, a human homolog of UNC-112, has been shown to localize to integrin-mediated adhesions in tissue culture, where it recruits the filamin-binding protein migfilin (Tu et al., 2003). Loss of Mig-2 or migfilin impairs cell spreading and shape modulation, although cell-substratum contacts still form (Tu et al., 2003). Currently, it is unknown whether Mig-2, like UNC-112, forms a complex with ILK and actopaxin. Conversely, whether or not UNC-112, like Mig-2, provides a link to filamin is not known.
PAT-4 is the only integrin-linked kinase (ILK) homolog in C. elegans (Mackinnon et al., 2002) and participates in recruiting proteins to nascent integrin attachment sites. Surprisingly, transgenically expressed kinase-dead PAT-4 can rescue pat-4-null mutants (Mackinnon et al., 2002) and a similar result has been obtained with the Drosophila ILK homolog (Zervas et al., 2001). This suggests that ILK primarily functions as an adaptor protein rather than a kinase (Zervas and Brown, 2002). Consistent with its role as an adaptor protein in C. elegans is the observation that PAT-4/ILK binds to UNC-Journal of Cell Science 117 (10) 112/Mig-2, UNC-97/PINCH and PAT-6/actopaxin in yeasttwo-hybrid assays (Mackinnon et al., 2002;Lin et al., 2003).
PAT-6 is an actopaxin homolog that has an important role in promoting the linkage of actin and myosin filaments to dense bodies and M-lines, respectively (Lin et al., 2003). PAT-6 might directly recruit actin to dense bodies through its two tandem, unconventional calponin-homology domains and appears to recruit myosin to M-lines indirectly through binding UNC-89 (Lin et al., 2003).

Maintaining integrity of dense bodies and M-lines
Although not necessary for the formation of dense bodies and M-lines, UNC-97 is essential for their integrity (Hobert et al., 1999). UNC-97 belongs to the PINCH family of adaptor proteins, which have important roles in integrin-dependent processes in Drosophila and mammalian cells (reviewed by Wu et al., 1999). Notably, mammalian PINCH1 binds ILK, and this interaction is important for cell spreading and motility in tissue culture (Zhang et al., 2002). Similarly, UNC-97 binds PAT-4 in yeast two-hybrid assays and is recruited to dense bodies and M-lines by PAT-4 (Hobert et al., 1999). UNC-97 also interacts with UNC-98, a C2H2 Zn-finger protein that localizes to M-lines (and possibly dense bodies) and to the nucleus (Mercer et al., 2003). UNC-98 might be involved in maintaining muscle structure, although the underlying mechanisms are not understood.

Other regulators of dense bodies and M-lines
Several other less well-characterized proteins regulate dense bodies and M-lines. The single β-G spectrin in C. elegans, UNC-70, localizes to several sites on the sarcolemmal membrane, including dense bodies and M-lines (Moorthy et al., 2000). Loss of UNC-70 results in progressive muscular dystrophy, which is associated with discontinuous dense bodies and disruption of the myofilament lattice (Moorthy et al., 2000;Hammarlund et al., 2000). Spectrin similarly localizes to Zand M-lines in vertebrate skeletal muscle (Porter et al., 1992;Zhou et al., 1998). DIM-1 ('disorganized muscle 1') is a novel immunoglobulin-domain protein that localizes between and around dense bodies and stabilizes actin filament attachment (Rogalski et al., 2003).

Other integrin-mediated adhesions in C. elegans
Integrin-based adhesions can differ in morphology, composition and function (reviewed by Zamir andGeiger, 2001) (Wehrle-Haller andImhof, 2002). Some, such as focal adhesions and dense bodies, are relatively large structures that mediate stable attachment to the ECM. By contrast, the smaller focal complexes at the leading edge of migrating cells and growth cones are rapidly turned over, permitting dynamic changes in adhesion. In addition to their role in muscle, C. elegans integrins also play a role in the formation of dynamic contacts in motile cells. For instance, migration of the distal tip cells, which directs morphogenesis of the gonad arms, is integrin dependent (Lee et al., 2001) and has recently been shown to involve CeTalin (Cram et al., 2003). Additionally, αINA-1/βPAT-3 regulates neuronal cell migration and fasciculation (Baum and Garriga, 1997) and acts at least in part through the Nck-interacting kinase (NIK) homolog MIG-15 (Poinat et al., 2002).
There is evidence that phosphorylation of βPAT-3 is important for its function in motile cells. Integrin β tails have one or two NPXY motifs that can be tyrosine phosphorylated, which thereby modulates integrin function (reviewed by Calderwood, 2004). Interestingly, the muscle defects of pat-3-null mutants can be rescued by a pat-3 transgene that has tyrosine-to-phenylalanine mutations in its two NPXY motifs (Lee et al., 2001). However, these embryos have defects in distal tip cell migration. Further studies on the structure, regulation and signaling of integrin-mediated adhesions during developmental events in C. elegans are likely to increase our understanding of dynamic requirements for integrins in vivo.

Fibrous organelles
Muscle cells in C. elegans are mechanically linked to the cuticle through trans-epidermal attachment structures called fibrous organelles (FOs). FOs comprise an epidermal intermediate filament (IF) array that is anchored basally to the underlying basement membrane and associated muscle and apically to the cuticle (Fig. 4A). FOs are restricted to epidermal regions that overlie body wall muscles, and their formation occurs concurrently with development of muscle sarcomeres (Francis and Waterston, 1991;Hresko et al., 1994;Hresko et al., 1999). In adults, FOs form circumferential bands (of 0.4 µm periodicity) composed of individual attachment spots (Bercher et al., 2001) that are in register with the spacing of cuticular ridges called annuli (Fig. 4C). By contrast, there is not a strict correlation between the location of FOs and dense bodies or M-lines (Francis and Waterston, 1991). FOs also form in other areas where force is transduced to or through the epidermis, including regions of epidermal contact with intestinal, anal and vulval muscles, and mechanosensory neurons (White, 1988;Francis and Waterston, 1991).
FOs are structurally similar to vertebrate type I hemidesmosomes (Fig. 5B) (reviewed by Hahn and Labouesse, 2001), in which transmembrane receptors form a link between cytoplasmic IFs and the basement membrane (reviewed by Nievers et al., 1999). Disruption of hemidesmosomal components causes separation of the epidermis from the basal lamina, resulting in various skin-blistering diseases (Jones et al., 1998;Nievers et al., 1999). Similarly, FOs confer structural integrity to the epidermis through anchoring IFs. In vertebrate hemidesmosomes, α6β4 integrin and BPAG2 provide anchorage to the basement membrane, and plectin and BPAG1 bind IFs (reviewed by Jones et al., 1998;Nievers et al., 1999). The only conserved protein present in FOs is the plectin homolog VAB-10A (Bosher et al., 2003). FOs do not contain integrins or a BPAG2 homolog, but have other transmembrane proteins (myotactin, MUA-3 and MUP-4) that might function analogously.

Composition and assembly of FOs
The apical and basal attachment plaques of FOs have some similarities and differences in composition (Fig. 5B). VAB-10A/plectin and VAB-19/Kank appear to be present in both apical and basal attachment plaques. Apical attachments contain the transmembrane receptors MUA-3 and MUP-4, whereas basal attachments contain myotactin. This probably reflects the need to have apical receptors specific for the collagen-rich cuticle and basal receptors specific for the basement membrane and/or muscle cell surface.
In regions of muscle contact with the epidermis, underlying  (Hresko et al., 1999); however, the nature of this cue is not well understood. Candidates include collagen IV (comprising EMB-9/α1 and LET-2/α2 subunits) and laminin αB. All are produced by myoblasts, and embryos lacking these proteins exhibit phenotypes consistent with perturbed FOs, including muscle separation from the epidermis Graham et al., 1997;Huang et al., 2003). Note that, in regions of contact with non-muscle tissues, the novel ECM protein hemicentin (HIM-4) is required for FO assembly , although the mechanisms involved are not understood.

Maintaining integrity of FOs
Several proteins are important for FO maintenance, including VAB-10A, VAB-10B, VAB-19 and the transmembrane proteins MUA-3, MUP-4 and myotactin. vab-10 produces two isoforms with distinct functions (Bosher et al., 2003). As mentioned above, VAB-10A is similar to plectins, whereas VAB-10B is similar to plakins, which are actin-microtubule crosslinking proteins. VAB-10A localizes to FOs and VAB-10B localizes to bands between FOs (Bosher et al., 2003). Loss of either VAB-10 isoform results in epidermal detachment from the cuticle and muscle and perturbation of IFs and CFBs. VAB-10A mutants exhibit a Pat phenotype, whereas VAB-10B mutants typically die in the first larval stage and have elongation and body-shape defects. In VAB-10A mutants, the number of FOs is greatly reduced, indicating a potential role in FO assembly. By analogy to vertebrate plectins, VAB-10A might mediate the link between transmembrane receptors and IFs. VAB-10B appears to regulate the thickness of the epidermis and could provide resistance against tension, although the mechanisms involved remain unclear (Bosher et al., 2003).
MUA-3 and MUP-4 are single-span transmembrane proteins that maintain adhesion between the epidermis and cuticle Bercher et al., 2001;Hong et al., 2001). mua-3 was identified in a screen for fragile muscle-attachment (Mua) mutants , and mup-4 was identified on the basis of a muscle-position-defective (Mup) phenotype (Gatewood and Bucher, 1997). In mua-3 mutants, FOs form normally but the epidermis detaches from the cuticle post-embryonically (Bercher et al., 2001). mup-4-null animals exhibit a similar phenotype, but detachment occurs earlier, typically at the three-fold stage of elongation (Hong et al., 2001). MUA-3 and MUP-4 share structural similarities but do not have any clear non-nematode homologs (reviewed by Cox et al., 2004;Hahn and Labouesse, 2001). Their extracellular domains contain a von Willebrand factor type A domain, which mediates collagen binding in other proteins (Colombatti and Bonaldo, 1991), whereas their cytoplasmic domains have some sequence similarity to filaggrins, which are IF-binding proteins (reviewed by Hahn and Labouesse, 2001).
Myotactin (LET-805) is a novel transmembrane protein required for adhesion between the epidermis and muscle (Hresko et al., 1999). The longest splice form encodes a singlespan transmembrane protein with at least 32 fibronectin type III (FNIII) repeats in the extracellular domain and a novel cytoplasmic domain. VAB-19, an ankrin repeat protein with sequence similarity to the human tumor suppressor Kank, is also required for attachment between muscle and the epidermis (Ding et al., 2003). Recruitment of VAB-19 to FOs requires VAB-10A; however, myotactin and VAB-19 require each other for their proper final localization. In myotactin and VAB-19 mutants, IFs maintain their annular arrangement but are not restricted to the area mirroring muscle/epidermal cell contact (Hresko et al., 1999;Ding et al., 2003). Apparently as a result, shortly after muscle contraction begins, muscle detaches from the epidermis.
Interestingly, the mutant phenotype of animals lacking VAB-19, but not that of other FO components, can be suppressed by mutations in the actin-binding protein sma-1/β-H spectrin (Ding et al., 2003). This suggests, along with previous studies on VAB-10 (see above) (Bosher et al., 2003), that cross-talk between FOs and actin is essential for proper cytoskeletal patterning in the epidermis. Continued studies on FOs are likely to yield important insights into how IFs and their attachment structures regulate cytoskeletal architecture and provide mechanical stability to tissues.

Putative dystrophin-glycoprotein complex
In vertebrates, the dystrophin-glycoprotein complex (DGC) confers stability to the muscle cell membrane during cycles of muscle contraction (Campbell, 1995). It is centered around dystroglycan (Fig. 5C) (reviewed by Ehmsen et al., 2002), a transmembrane receptor that binds various ligands, including the ECM components laminin, perlecan and agrin. Dystroglycan associates with a membrane-embedded sarcoglycan complex, and forms a link to the actin cytoskeleton through binding dystrophin. In addition to actin, dystrophin binds dystrobrevin and syntrophins, which interact with nitric oxide synthase (nNOS). Mutations in DGC components and in proteins that affect the ligand-binding activity of dystoglycan are found in various forms of muscular dystrophy (reviewed by Cohn and Campbell, 2000) (Michele and Campbell, 2003).
The expression and subcellular localization of DGC components in C. elegans have not been extensively studied. Some DGC components are expressed in C. elegans muscle, including DYS-1 and DYB-1 (Segalat, 2002). However, DGN-1 and a second dystroglycan-like protein (F56C3.6) do not appear to be expressed in muscle, but are expressed in epithelial and neuronal tissues (R. Johnson and J. Kramer, personal communication). Consistent with this localization is the observation that embryos lacking either gene exhibit various epithelial and neural defects (R. Johnson and J. Kramer, personal communication). Similarly, dystroglycan is present in many non-muscle tissues in mammals (reviewed by Durbeej et al., 1998;Hemler, 1999). Whether or not C. elegans assembles a DGC analogously to vertebrates and, if so, where it is present, remain unclear.
In C. elegans, loss of DYS-1/dystrophin does not cause significant muscle degeneration. However, in ten-day-old dys-1-null animals, a small percentage (<1%) of body-wall muscle cells show an abnormal striation pattern, which may indicate the beginning of degeneration (Bessou et al., 1998). Loss of DYS-1 also results in movement defects consistent with increased muscle excitability (Bessou et al., 1998), and RNAi directed against dgn-1, δ/γ-sarcoglycan (F07H5.2) and syntrophin (F30A10.8) in adult worms causes a similar phenotype (Grisoni et al., 2002). Discerning the composition of dystroglycan-mediated adhesion complexes in the muscle and non-muscle tissues of C. elegans, and learning more about their precise functions, should yield important insights into the role of the DGC in development and disease.

Conclusion
Despite its small size and relative simplicity, C. elegans employs many of the same strategies for accomplishing cell adhesion as higher organisms. Most work to date has centered on defining the composition and basic roles of these structures, particularly during development. Despite this progress, there is still much to learn about how adhesion complexes in C. elegans accomplish their functions. In particular, their roles in mediating cell signaling have been largely unexamined. Since adherens junctions, focal adhesions, hemidesmosomes and the DGC all regulate cell signaling in tissue culture (reviewed by Nievers et al., 1999;Zamir and Geiger, 2001;Rando, 2001;Braga et al., 2002), it will be important to determine whether and how the analogs of these structures in C. elegans mediate signaling and how this affects in vivo events.
In the future, C. elegans might be a useful system for analyzing cross-talk between adhesion complexes. Adhesion receptor cross-talk occurs during convergent extension in Xenopus (Marsden and DeSimone, 2003) and is likely also to be important in many other in vivo events. Elongation of the C. elegans embryo, which involves the coordinated activity of adherens junctions, FOs and dense bodies, might be a useful context for studying how biochemical and physical cross-talk between adhesion receptors contributes to complex cellular events.
Additionally, C. elegans might be useful in the study of diseases involving aberrant cell adhesion, including tumor metastasis, chronic inflammatory disorders, tissue fragility disorders, muscular dystrophy, and many others. In this regard, C. elegans is beginning to be used as a model for dystrophinmediated myopathy (reviewed by Chamberlain and Benian, 2000;Culetto and Sattelle, 2000). Thus, future studies on 'sticky worms' have the potential to advance our understanding of the basic mechanisms underlying cell adhesion and might also give insights as to how their dysregulation contributes to disease.