Multiple Wnts Redundantly Control Polarity Orientation in Caenorhabditis elegans Epithelial Stem Cells

During development, cell polarization is often coordinated to harmonize tissue patterning and morphogenesis. However, how extrinsic signals synchronize cell polarization is not understood. In Caenorhabditis elegans, most mitotic cells are polarized along the anterior-posterior axis and divide asymmetrically. Although this process is regulated by a Wnt-signaling pathway, Wnts functioning in cell polarity have been demonstrated in only a few cells. We analyzed how Wnts control cell polarity, using compound Wnt mutants, including animals with mutations in all five Wnt genes. We found that somatic gonadal precursor cells (SGPs) are properly polarized and oriented in quintuple Wnt mutants, suggesting Wnts are dispensable for the SGPs' polarity, which instead requires signals from the germ cells. Thus, signals from the germ cells organize the C. elegans somatic gonad. In contrast, in compound but not single Wnt mutants, most of the six seam cells, V1–V6 (which are epithelial stem cells), retain their polarization, but their polar orientation becomes random, indicating that it is redundantly regulated by multiple Wnt genes. In contrast, in animals in which the functions of three Wnt receptors (LIN-17, MOM-5, and CAM-1) are disrupted—the stem cells are not polarized and divide symmetrically—suggesting that the Wnt receptors are essential for generating polarity and that they function even in the absence of Wnts. All the seam cells except V5 were polarized properly by a single Wnt gene expressed at the cell's anterior or posterior. The ectopic expression of posteriorly expressed Wnts in an anterior region and vice versa rescued polarity defects in compound Wnt mutants, raising two possibilities: one, Wnts permissively control the orientation of polarity; or two, Wnt functions are instructive, but which orientation they specify is determined by the cells that express them. Our results provide a paradigm for understanding how cell polarity is coordinated by extrinsic signals.


Introduction
For tissues and organs to be properly organized, it is often essential that cell polarity be coordinated among cell groups. In the Drosophila wing, for example, cells are polarized in the same proximal-to-distal orientation to produce hairs pointing distally [1]. Similarly, in the mammalian cochlea, stereociliary bundles form at the outer edge of all hair-producing cells [2]. Such coordinated polarizations are often controlled by the Wnt/PCP (planar cell polarity) pathway, which involves the polarized localization of signaling molecules such as Frizzled, Dvl/ Dishevelled, and Van Gogh proteins [3][4][5]. One plausible model for cell polarity coordination is that individual cells recognize extrinsic cues that orient their polarity. Although Wnt proteins have been considered candidates for orienting molecules, their functions in regulating cell polarity are not well understood.
In Drosophila, where PCP phenotypes are lacking in some Wnt mutants, including wingless, Wnt proteins are not believed to be required for regulating PCP. Instead, PCP is coordinated by communication between neighboring cells, although the presence of extrinsic cues is still anticipated. In the mammalian cochlea, Wnt7a has been suggested as a cue to instruct cell polarity orientation, based on overexpression and inhibitor studies in organ cultures [6]. However, there is no PCP phenotype in the cochlea of Wnt7a null mice [6], suggesting that other Wnt proteins function redundantly with Wnt7a. In Xenopus and zebrafish, Wnt11 and Wnt5 are required for convergent extension movements during gastrulation, which is also regulated by the PCP pathway [7,8]. However, these Wnts are thought to function permissively in cell polarization, rather than providing a directional cue. The presence of global extrinsic cues that orchestrate polarity orientations has not been shown in any organism.
In C. elegans, the Wnt/ß-catenin asymmetry pathway controls asymmetry in most somatic cell divisions occurring along the anterior-posterior axis [9]. In this regulation, Wnt pathway components localize asymmetrically. For example, after asymmetric divisions, the ß-catenin homologs WRM-1 and SYS-1 accumulate in the posterior daughter nuclei, while POP-1/TCF localizes more to the anterior than posterior nuclei [10]. Such localization has been observed in most cell divisions, during which cells are accordingly polarized in the anterior-posterior orientation. But how the polarity orientation is determined is not known, except in a few cases. We have shown that Wnts instructively orient the polarity of the EMS blastomere in embryos and of the T cell in larvae [11]. It has also been suggested that MOM-2/Wnt and LIN-44/Wnt expressed in the anchor cell orient the polarity of the P7.p cell, while EGL-20/Wnt expressed near the anus antagonizes these Wnts to orient the P7.p polarity in the opposite orientation [12]. However, it is not known whether or how Wnts globally regulate the polarity of many other cells.
To elucidate the mechanisms of polarity coordination, we focused on a population of epithelial stem cells called seam cells (V cells). At the L1 stage, the six seam cells V1-V6 are positioned on each lateral side of the animals, and repeatedly undergo selfrenewing asymmetric cell divisions in each larval stage to produce anterior daughters that fuse with the hypodermal syncytium (hyp7) and posterior daughters that remain as seam cells ( Figure 1A) [13]. As with many other cells, the polarity of seam cells is controlled by the Wnt/ß-catenin asymmetry pathway [14,15], which determines the polarized localization of WRM-1/ß-catenin to the posterior daughter nuclei. Among seam cells, the polarity of the V5 cell reverses fairly frequently in egl-20/Wnt mutants [16]. However, Wnt gene regulation of the polarity of other seam cells has not been reported.
By analyzing various compound Wnt mutants, including quintuple Wnt mutants, we found that the Wnt genes lin-44, cwn-1, egl-20, and cwn-2 are redundantly required to coordinate the orientation of seam cell polarity at the L1 stage, but three of their receptors are essential for generating the cells' polarity in the first place. The Wnt genes are expressed either anterior or posterior to the seam cells, and each one alone can determine the polarity orientation. Our results provide an important basis for elucidating undiscovered mechanisms in the coordination of cell polarity by Wnt genes.

Multiple Wnts control seam cell polarity
To analyze the polarity of the seam cell divisions, we used elt-3::GFP, which is expressed in hyp7 but not in seam cells [17,18] ( Figure 1A, 1D). About 1 hour after the division of seam cells (V1-V6) at the L1 stage in wild-type animals, the anterior daughters fuse with hyp7; their nuclei immediately begin fluorescing like those of hyp7 cells, because they incorporate GFP from the hyp7 cell. Therefore, we can unambiguously determine the daughter cell fates, from which we can deduce the division polarity type (normal, reverse, or loss of polarity) ( Figure 1B). (In Figure 1C and the figures presented below, the proportions of the polarity types of individual seam cells were mathematically converted to RGB colors as described in the figure legend.) The C. elegans genome contains five Wnt genes, lin-44, cwn-1, cwn-2, egl-20, and mom-2. To understand how seam cell polarity is regulated, we first analyzed the phenotypes of animals with mutations in one of the five Wnt genes. Except for egl-20, in which the V5 polarity was reversed [16], the Wnt mutants showed weak phenotypes, if any (Figure 2), raising the possibility that multiple Wnt genes redundantly regulate seam cell polarity.
We found that the polarity of all the seam cell divisions was abnormal in the quintuple Wnt mutants ( Figure 1E and Figure 2, p,0.01 in V1-V6 by Fisher's exact test), indicating that multiple Wnts are redundantly required for appropriately oriented seam cell polarity. Although the phenotypes varied among the cells, the polarity tended to be either normal or reversed, and symmetric division was less frequent (represented by the absence of yellowish colors in Figure 2). Although we cannot exclude residual mom-2 activity in quintuple mutants with the mom-2(ts) allele, the results suggest that seam cells are mostly polarized even in the absence of Wnt functions.

Most seam cells can be properly polarized by a single Wnt gene
To determine which combinations of Wnt genes are required for the properly oriented polarity of individual seam cells, we analyzed them in double, triple, or quadruple Wnt mutants. The phenotype of quadruple Wnt mutants (lin-44; cwn-1; egl-20 cwn-2) was quite similar to that of quintuple mutants (Figure 2; p.0.1 in V1-V6 for the abnormalities), suggesting that mom-2 has only minor functions, if any, in seam cell polarity. Next, we constructed triple Wnt mutants from these four Wnt mutations. Through these analyses, we found three distinct regulations that depended on cell type, grouped into V1-V4, V5, and V6.
V1-V4. The phenotypes of V1-V4 Wnt triple mutants (cwn-1; egl-20 cwn-2) were similar to those of Wnt quadruple (p.0.1 in V1-V4 for the abnormalities) and quintuple mutants (p.0.1 in V1, V2 and V4; p.0.05 in V3) (Figure 2), suggesting that the polarity in these cells are regulated primarily by these three Wnt genes. In any double combination of these three Wnt mutations, the polarity of the divisions was almost normal, although V4 was weakly affected by cwn-1; egl-20 ( Figure 2) (p,0.01). The results indicate that functions of these three Wnts are redundant in all four of these cells.
V6. The most posterior seam cell, V6, was affected in quadruple Wnt mutants (p,0.01), but not in any triple or

Author Summary
Proper functions and development of organs often require the synchronized polarization of entire cell groups. How cells coordinate their polarity is poorly understood. One plausible model is that individual cells recognize extrinsic signal gradients that orient their polarity, although this has not been shown in any organism. In particular, although Wnt signaling is important for cell polarization, and Wnt signal gradients are important for the coordinated specification of cell fates, the Wnts' involvement in orienting cell polarity is unclear. In the nematode Caenorhabditis elegans, most asymmetrically dividing mitotic cells are polarized in the same anterior-posterior orientation. Here we show that multiple Wnt proteins redundantly control the proper orientation of cell polarity, but not for polarization per se, in a group of epithelial stem cells. In contrast, Wnt receptors are indispensable for cells to adopt a polarized phenotype. Most stem cells are properly oriented by Wnt genes that are expressed either at their anterior or posterior side. Surprisingly, Wnt signals can properly orient stem cell polarity, even when their source is changed from anterior to posterior or vice versa. Our results suggest the presence of novel mechanisms by which Wnt genes orient cell polarity.
double combination analyzed ( Figure 2). Therefore, the V6 cell polarity is redundantly regulated by the four Wnts.
V5. In contrast to V1-V4 and V6, one Wnt, egl-20, is essential for V5 polarity, as reported previously [16]. In egl-20 mutants, the polarity of the division was reversed in 38% of the V5 cells ( Figure 2). This phenotype was strongly enhanced to nearly complete reversal (98%) in cwn-1; egl-20, suggesting that functions of cwn-1 and egl-20 are partially redundant. Although the cwn-2 mutation slightly enhanced polarity reversal in the egl-20 background (p,0.01), it instead suppressed the phenotype in the cwn-1 egl-20 background (p,0.01) (Figure 2), suggesting that cwn-2's functions in the V5 cell polarity are complex. One possibility for the unique regulation of V5 might be its distinct cell lineage compared to the other seam cells. Only the V5 cell produces neurons at the L2 stage. To test this possibility, we analyzed lin-22 mutants, in which not only V5, but also the V1-V4 cells produce neurons [21]. However, even in lin-22 egl-20 double mutants, polarity reversal was observed mostly in the V5 cell (data not shown). Therefore, V5's neuron production is unlikely to be the reason for its unique regulation.
Wnt genes control seam cell polarity through the Wnt/ß-catenin asymmetry pathway To confirm that Wnt genes regulate the Wnt/ß-catenin asymmetry pathway, we analyzed POP-1/TCF localization in triple Wnt mutants (cwn-1; egl-20 cwn-2), in which the polarity of V1-V5 is disrupted. We found that POP-1 asymmetry was   Figure 1C. The symbol (+M) indicates maternal contributions. In most cases, ''loss of polarity'' indicates divisions in which both daughter cells adopted the hyp7 fate, except for some divisions (indicated by asterisks in this and the following Figures; in all cases, one sample per cell) in which both daughters adopted the seam cell fate. Random asymmetry of the V1-V5 divisions in the cwn-1; egl-20 cwn-2 mutants was also observed using scm::GFP ( Figure S1). doi:10.1371/journal.pgen.1002308.g002 abnormal in V1-V5 cells in the triple Wnt mutants ( Figure 3A, 3D, 3E; p,0.01 in V1-V5). As judged by elt-3::GFP expression ( Figure 2), polarity reversal is more frequent than loss of polarity (represented by purplish colors in Figure 3A). Therefore, these Wnt genes control seam cell polarity via the Wnt/ß-catenin asymmetry pathway.
Since seam cells are polarized in a planar (anterior-posterior) orientation in contact with each other before division, interactions between neighboring cells might coordinate their polarity, as with PCP regulation in the Drosophila wing. However, in triple Wnt mutants (cwn-1; egl-20 cwn-2), we did not observe any significant correlation of polarity reversal between neighboring seam cell pairs (data not shown). In addition, the polarity of the V5 cell division is not affected by laser ablation of the V6 cell [16]. Furthermore, we found that the polarity of the seam cell divisions was normal in mutants of the putative PCP components vang-1/ Van Gogh(tm1422) (n = 20) and prkl-1/Prickle(ok3182) (n = 20) (the phenotype of vang-1 was analyzed using scm::GFP, as described in Materials and Methods). Therefore, it is likely that the polarity of each seam cell is independently controlled by Wnt genes.

Three Wnt receptors are required for seam cell polarization
To understand how Wnts control polarity, it is important to identify their receptors. The C. elegans genome contains six Wnt receptors, four Frizzled (MIG-1, LIN-17, CFZ-2, and MOM-5), one Ror (CAM-1) [22], and one Derailed (LIN-18) family members. Among these, it has been reported that cam-1/Ror mutations reverse the polarity of the V1 and V2 cell divisions at a low frequency [23] and that lin-17/Frizzled mutants cause mostly symmetric divisions of a tail seam cell called a T cell [24].
First, we analyzed single mutants of each receptor gene. Similar to cam-1, the mom-5 mutation weakly affected the polarity of the V1 and V2 divisions (p,0.01 in V1 and V2). V1-V2 defects were enhanced in mom-5 cam-1 (RNAi) animals (p,0.01 in V1 and V2 by the comparison with mom-5 mutants or cam-1(RNAi) animals), indicating that MOM-5 and CAM-1 redundantly control V1-V2 polarity ( Figure 4). Single mutants for the other receptors showed only minor defects, if any, in the polarity of seam cell divisions, suggesting that their functions are redundant for V3-V6. Since lin-17 and mom-5 show a strong genetic interaction in gonad development [19], we next analyzed lin-17 mom-5 double Frizzled mutants and found that the polarity of all the seam cell divisions was abnormal (p,0.01 in V1-V6) ( Figure 4). The mig-1, cfz-2, or lin-18/Derailed mutations slightly modified the phenotype of the lin-17 mom-5 mutants. However, since the mig-1; cfz-2; lin-18 triple mutants showed nearly normal polarity (Figure 4), these receptors are not essential and are likely to function redundantly with other receptors.
Next, we constructed lin-17 mom-5; cam-1 triple mutants, and found that this combination was embryonically lethal. Therefore, we inhibited cam-1 by RNAi in lin-17 mom-5, and found that all seam cell divisions were symmetric at high penetrance ( Figure 1F) (p,0.01 in V1-V6 and p,0.01 in V1-V4, p,0.05 in V5, p.0.1 in V6 for symmetric division by the comparison with wild type and lin-17 mom-5, respectively; represented by yellowish colors in Figure 4). These results indicate that LIN-17, MOM-5, and CAM-1 are the main receptors that redundantly regulate seam cell polarity, whereas the receptors MIG-1, CFZ-2, and LIN-18 weakly affect polarity in the absence of the main receptors. Most importantly, the phenotype of lin-17 mom-5; cam-1 is clearly distinct from that of quintuple Wnt mutants in which polarity orientation is randomized (p,0.01 in V1-V6 for symmetric division). These results suggest that Wnt receptors can function even in the absence of Wnts to generate polarity, while Wnts are required to orient polarity.
It was previously suggested that CAM-1 functions as a receptor for CWN-2 [25,26]. If this is the case for seam cell polarity, the cwn-2 mutation should have the same or stronger effects than the cam-1 mutation. However, as described above, the cwn-2 mutation alone did not affect the V1 cell, which was affected in cam-1 mutants. Furthermore, the lin-17 mom-5; cwn-2 mutants had a weaker phenotype than lin-17 mom-5 cam-1(RNAi) (p,0.05 in V2 and V3, p = 0.066 in V4) ( Figure 4). Therefore, it is unlikely that CAM-1 is a specific receptor for CWN-2 for seam cell polarity.

Ectopically expressed Wnts rescued Wnt triple mutants
Our results indicate that each seam cell except V5 can be polarized by a single Wnt gene expressed either anterior or posterior to the cells. For example, V1 is properly polarized merely by cwn-2 expressed nearby and at its anterior, or by egl-20 expressed posterior to and far from V1. To determine whether the position of Wnt expression is important in regulating polarity, we expressed Wnt genes ectopically. If Wnts function permissively, abnormal polarity in Wnt compound mutants should probably be rescued irrespective of the location of Wnt expression. If the Wnts were instructive, we expected that ectopic Wnt expression opposite to its normal location would enhance polarity reversals.
As reported previously, EGL-20 expressed in the pharynx by the myo-2 promoter can rescue V5 polarity defects in egl-20 mutants [16]. However, since the myo-2 promoter is also weakly active in the posterior region [11], the appropriate interpretation of these results was uncertain. We first used the hlh-8 promoter to express egl-20 in the M cell, a mesodermal blast cell positioned between the V4 and V5 cells on the right side, in egl-20 mutants [31]. We found that this had no significant effect on V5 cell polarity ( Figure 5F), suggesting that egl-20 does not function (i.e., it is not produced, secreted, or modified) in polarization when it is expressed in the M cell.
We then expressed cwn-1 or cwn-2 ectopically in the anterior (using the ceh-22 promoter) [32,33] posterior (using the egl-20 promoter) [29] regions in Wnt triple mutants (cwn-1; egl-20 cwn-2). Surprisingly, the posterior expression of CWN-2, which is normally expressed in the pharynx, efficiently rescued the triple mutant phenotype (Figure 5H, p,0.01 in V1-V5). Similarly, the anterior expression of CWN-1, which is normally expressed in the posterior region, appeared to rescue the polarity defects of the V1-V3 divisions ( Figure 5H, V1 p = 0.1076, V2 p,0.01, V3 p,0.05). The effect of ceh-22p::CWN-1::Venus was comparable to that of ceh-22p::CWN-2::Venus. These results seem to suggest that the position of Wnt expression is not important and that Wnt functions are not instructive, even though Wnts are required for correct polarity orientation. However, the results can also be explained by assuming that functions of Wnts are determined by the cells that express them (see Discussion).

Wnt-independent regulation of somatic gonad precursor polarity
Similar to seam cells, the Wnts regulating the polarity of Z1 and Z4 cells, which are somatic gonad precursors (SGPs), have not been identified. The SGPs have a mirror-symmetric polarity, which is important for producing the mirror symmetry of the C. elegans gonad [34]. POP-1 asymmetry in the Z1 daughters is reversed compared to other cells, including Z4. POP-1 is higher in the posterior and anterior daughters of Z1 and Z4, respectively ( Figure 6A, 6G) [35]. SGP polarity is also regulated by the Wnt/ßcatenin asymmetry pathway [35], although the involvement of Wnt genes has not been demonstrated. We found that the SGP polarity was not affected in quintuple Wnt mutants from mothers heterozygous for cwn-2, egl-20 and mom-2, as judged by the normal POP-1 localization (Figure 6B, 6G) and the presence of distal tip cells (DTCs; data not shown). Although we could not analyze the POP-1 asymmetry in the quintuple Wnt mutants from homozygous mothers, all such animals we examined (n = 85) had two gonad arms as in wild type, indicating that normal numbers of DTCs were produced from SGPs. These results suggest that the polarity of SGPs is regulated by Wnt-independent mechanisms.
To explore the polarity-regulating mechanisms in SGPs, we used mes-1 mutants, which frequently lack germ cells [36], to analyze the roles of the germ cells Z2 and Z3, which are positioned between Z1 and Z4. In mes-1 mutants lacking germ cells, the polarity of both Z1 and Z4 was abnormal, although the defect in Z4 was weaker than that in Z1 (Z1 p,0.01, Z4 p,0.05) ( Figure 6E, 6F, 6G). Such defects were not observed in mes-1 mutants that had germ cells ( Figure 6C, 6D, 6G). These results suggest that non-Wnt signals from germ cells control SGP polarity and hence regulate the proper organization of the somatic gonad. near the pharynx. White arrow heads, blue arrows and the orange arrow indicate GFP puncta, hypodermal cells expressing the elt-3::GFP marker, and neuronal processes expressing the mec-4::GFP marker, respectively. (F-H) Each colored box represents the polarity of individual seam cell divisions, as in Figure 1C. (F) The egl-20 phenotype was not affected by EGL-20 expression in the M cell (hlh-8p::EGL-20). Since the M cell is on the right side of the animals, we scored seam cells only on the right side. (G) cwn-1p::CWN-1::Venus rescued the defect of the cwn-1 mutation in cwn-1; egl-20. (H) The phenotype of cwn-1; egl-20 cwn-2 was rescued by cwn-2p::CWN-2::Venus, by CWN-2 expressed in the pharynx (ceh-22p::CWN-2::Venus) or in the cells near the anus (egl-20p::CWN-2::Venus#1 and #2 with mec-4::GFP and egl-5::GFP as coinjection markers, respectively), or by CWN-1 expressed in the pharynx (ceh-22p::CWN-1::Venus). doi:10.1371/journal.pgen.1002308.g005 We also examined the possibility that these germ cell signals function redundantly with Wnts. In quadruple Wnt mutants (lin-44; cwn-1; egl-20 cwn-2) lacking germ cells due to the mes-1 mutation, polarity defects appear to be enhanced in Z4 but not Z1 as compared to mes-1 mutants, although the difference did not reach significance ( Figure 6G) (Z1: p = 1.0, Z4: p = 0.11), raising the possibility that Z4 polarity is redundantly controlled by Wnts and signals from germ cells. In contrast, the polarity of the Z1 cell appeared not to be affected by the Wnt mutations, and Z1, in wild type, exhibits a reversed orientation compared with Z4 and the seam cells (i.e., POP-1 is higher in the posterior daughter). Z1 may therefore be regulated by signals from germ cells but may be insensitive to Wnt signals.

Redundant regulation by multiple Wnts
We have shown that seam cell polarity is redundantly regulated by multiple Wnt genes. The V1-V4 and V6 cells are affected only by combinations of three and four Wnt mutations, respectively. Such redundancy has been reported in other organisms [37]. For example, double knockout of Wnt1 and Wnt3a in mice causes much stronger CNS developmental abnormalities than the single knockouts [38]. Because all metazoan species have multiple Wnt genes (e.g., 19 in humans), our results suggest that Wnt genes in any organism may have undiscovered functions that can not be identified by the inhibition of one or a few of them.

Distinct regulation of polarity orientation and polarity generation
The defects observed in Wnt mutations in any combination were mostly randomized (normal or reverse) polarity, and less frequently, loss of polarity. Similar observations were reported in a mutant lacking mig-14/Wntless function, which is required for Wnt secretion [39]. Our observations are consistent with a recent report that seam cell numbers are not significantly altered in lin-44; cwn-1; egl-20 cwn-2 animals [15], since the cell numbers were not affected by random orientations of their asymmetry. Even though quintuple Wnt mutants may contain residual mom-2 activity from the ts allele, our results strongly suggest that functions of at least four Wnts (lin-44, cwn-1, cwn-2, and egl-20) determine the polarity orientation of seam cells. In contrast, cell polarization itself appeared to be Wnt-independent, although we cannot eliminate the possibility that cells were not polarized in the complete absence of Wnt functions.
In contrast to the randomized polarity found in compound Wnt mutants, triple receptor mutants (lin-17 mom-5; cam-1) showed a severe loss of polarity. These three receptors are likely to function in the polarity generation that occurs even in the absence of Wnts. Even though the other three receptors (MIG-1, CFZ-2, and LIN-18) appear to be involved in regulating polarity, based on genetic interactions with lin-17 mom-5 mutations, their triple mutants showed nearly normal polarity. Therefore, it is likely that LIN-17, MOM-5, and CAM-1 function in the regulation of polarity orientation as Wnt receptors in addition to having a role in the polarity generation that occurs even in the absence of Wnts, although their activities may be modified by the other three receptors (MIG-1, CFZ-2, and LIN-18). Consistent with this interpretation, strains with mutations in these three receptors showed polarity reversal: V1 and V2 in cam-1 or mom-5 single mutants, and V6 in lin-17 cam-1 double mutants. Our results strongly suggest the presence of distinct mechanisms for polarity orientation, which is Wnt-dependent, and polarity generation, which can occur independently of Wnts. Do Wnts permissively control polarity orientation?
Our ectopic expression experiments appear to indicate that although Wnt functions are required to correctly orient polarity, those functions are permissive. Assuming Wnts are permissive, how do they control polarity orientation in seam cells? One model is that Wnts act indirectly through other cells that produce real polarity cues in response to Wnts ( Figure 7A). In this case, the same Wnt receptors should function in other cells to produce the cues, and in seam cells to generate polarity. For this model, it is strange that, even though Wnts are apparently present near the seam cells, the Wnt receptor activity to polarize seam cells appears not to be affected by Wnts. Together with our finding that LIN-17 functions in seam cells, this model appears unlikely.
A second model is that Wnt receptors function only in seam cells. They have two distinct functions: one to generate polarity via the Wnt/ß-catenin asymmetry pathway, and the other to interpret intrinsic polarity cues (which might be determined by extrinsic cues) through an unknown pathway (orientation pathway) to generate polarity orientation-but only when they are activated by Wnts ( Figure 7B). In the absence of Wnts, the receptors still function to polarize cells, but the intrinsic cues cannot be used, resulting in randomly oriented polarity. Although BAR-1/ßcatenin, which functions downstream of LIN-17 in the migration of the Q neuroblast [40], appears to be a good candidate for mediating the orientation pathway, bar-1 single mutants have normal seam cell divisions (H.S. unpublished observation). Whatever the mechanism of the orientation pathway is, the key question regarding this model is how Wnts elicit the function of the receptors to activate the orientation pathway without affecting the receptors' function in the Wnt/ß-catenin asymmetry pathway, which generates polarity even in the absence of Wnts.

Possible Wnt instructive functions in polarity orientation
Because Wnts instruct the polarity of some cells (EMS, T, and P7.p) [11,12], it is reasonable to imagine that Wnts also instruct seam cells. Assuming that Wnts are instructive, how are the results of ectopic expression explained? One model would be that Wnts' functions depend on the cells that express them. For instance, CWN-2, which is expressed in the pharynx, might receive some specific modification, say, ''anterior modification,'' whereas CWN- 1, which is expressed in the posterior region, might receive a different modification, say, ''posterior modification'' ( Figure 7C). When cells receive CWN-2 with the anterior modification from their anterior side, they recognize the direction of the Wnt source as ''anterior'' and localize their signaling components accordingly (e.g. POP-1 in the anterior daughter nuclei). When CWN-1 is ectopically expressed in the pharynx, it may receive anterior modification, like CWN-2, and function like CWN-2 to instruct normal seam cell polarity, rather than functioning like CWN-1 with posterior modification.
This model can explain EGL-20's lack of function when expressed in the M cell-assuming that the M cell cannot modify EGL-20. In addition, we have reported that LIN-44 expressed by the egl-5 promoter (egl-5::LIN-44) anterior to a T cell can efficiently reverse T cell polarity in the absence of endogenous LIN-44 expressed at the posterior of the T cell [11]. However, in the presence of endogenous LIN-44 (LIN-44 is expressed in both sides of the T cell), the effect of egl-5::LIN-44 is quite weak despite egl-5's promoter activity being stronger, as judged by egl-5::GFP, than that of the lin-44 promoter, as judged by lin-44::GFP. This observation is also consistent with the model that Wnt functions depend on the cells that express it. Another possibility for cellspecific Wnt functions is that Wnt-expressing cells or their neighbors express specific cofactors of Wnts that bind tightly to Wnts and determine their functions.
Even though there is no direct evidence for the above models, and other explanations may be possible, our results suggest the presence of novel mechanisms that control the orientation of cell polarity. Such mechanisms, as well as the redundancy of Wnt proteins, may also explain Wnt functions that control cell polarity in other organisms.