Caenorhabditis elegans SEL-5/AAK1 regulates cell migration and cell outgrowth independently of its kinase activity

During Caenorhabditis elegans development, multiple cells migrate long distances or extend processes to reach their final position and/or attain proper shape. The Wnt signalling pathway stands out as one of the major coordinators of cell migration or cell outgrowth along the anterior-posterior body axis. The outcome of Wnt signalling is fine-tuned by various mechanisms including endocytosis. In this study, we show that SEL-5, the C. elegans orthologue of mammalian AP2-associated kinase AAK1, acts together with the retromer complex as a positive regulator of EGL-20/Wnt signalling during the migration of QL neuroblast daughter cells. At the same time, SEL-5 in cooperation with the retromer complex is also required during excretory canal cell outgrowth. Importantly, SEL-5 kinase activity is not required for its role in neuronal migration or excretory cell outgrowth, and neither of these processes is dependent on DPY-23/AP2M1 phosphorylation. We further establish that the Wnt proteins CWN-1 and CWN-2, together with the Frizzled receptor CFZ-2, positively regulate excretory cell outgrowth, while LIN-44/Wnt and LIN-17/Frizzled together generate a stop signal inhibiting its extension.


Introduction
During the development of Caenorhabditis elegans, several cells, both neuronal and non-neuronal, migrate in a well-defined and invariant manner along the anterior-posterior (A-P) body axis.Other cells do not migrate but rather extend their processes along the same axis.In both instances, the directionality of migration and growth is controlled by a set of guidance cues provided by the surrounding tissue and received by the corresponding signalling apparatus in the migrating or growing cell (Silhankova and Korswagen, 2007;Sundaram and Buechner, 2016;Sherwood and Plastino, 2018;Hutter, 2019).The gradients of Wnt proteins and a panel of their receptors are the key determinants of A-P guidance in C. elegans.Wnts can act either as attractants, repellents, or permissive cues for a given cell and the cell response depends on a given combination of Wnts, Frizzleds, and other components of the Wnt pathway expressed in and around that particular cell (Silhankova and Korswagen, 2007;Ackley, 2014;Middelkoop and Korswagen, 2014;Rella et al., 2016).
Endocytosis is an important regulatory mechanism for Wnt signalling applied in both Wntproducing and Wnt-receiving cells.On the way out of the producing cell, Wnts are accompanied by a Wnt sorting receptor Wntless (WLS) (Bänziger et al., 2006;Bartscherer et al., 2006;Goodman et al., 2006).Once WLS is relieved of its cargo at the plasma membrane, it is internalized by clathrinand adaptor protein complex 2 (AP2)-dependent endocytosis (Pan et al., 2008;Port et al., 2008;Yang et al., 2008).Internalized WLS is subsequently recycled by a multisubunit retromer complex to the Golgi apparatus (Belenkaya et al., 2008;Franch-Marro et al., 2008;Pan et al., 2008;Port et al., 2008;Yang et al., 2008) and further to the endoplasmic reticulum (Yu et al., 2014).Disruption of the AP2 or clathrin function results in decreased Wnt secretion due to improper WLS recycling (Pan et al., 2008;Port et al., 2008;Yang et al., 2008).In Wnt-receiving cells, the activity of the Wnt-receptor complex, the signalosome, can be promoted by endocytosis, while at the same time, endocytosis can also attenuate Wnt signalling by regulating the membrane availability of Wnt receptors (Albrecht et al., 2021;Colozza and Koo, 2021;Wu et al., 2021).
AP2-associated kinase 1 (AAK1) belongs to the Ark/Prk or Numb-associated (NAK) family of serine/ threonine protein kinases (Smythe and Ayscough, 2003;Sorrell et al., 2016).Members of this family play an important role in regulating endocytosis in yeast, Drosophila, or mammals (Smythe and Ayscough, 2003;Peng et al., 2009).Human AAK1 has been shown to phosphorylate AP2M1, the µ2 subunit of the AP2 adaptor complex (Conner and Schmid, 2002).Phosphorylation of µ2 at Thr156 by AAK1 enhances the binding affinity of AP2 to the sorting signals of endocytosed proteins (Ricotta et al., 2002).AAK1 has also been shown to phosphorylate the endocytic adaptor and negative regulator of Notch signalling Numb and affect its subcellular localization (Sorensen and Conner, 2008).AAK1 can also interact with a membrane-tethered activated form of the Notch receptor and promote its internalization (Gupta-Rossi et al., 2011).
AAK1 knock-down resulted in elevated Wnt signalling in a mouse embryonic stem cell-based kinase and phosphatase siRNA screen (Groenendyk and Michalak, 2011).A recent study in human cells confirmed this observation and offered a mechanism.By phosphorylating AP2, AAK1 promotes endocytosis of LRP6 and thus shuts down the signalling (Agajanian et al., 2019).In C. elegans, the AAK1 orthologue SEL-5 has been genetically implicated in Notch signalling as a mutation in sel-5 can suppress the constitutively active lin-12/Notch mutants.However, suppression is observed only in the lin-12 allele activating the membrane-anchored Notch and not when the pathway is activated by expression of the intracellular domain (Fares and Greenwald, 1999).This hints that SEL-5 could regulate endocytosis in a manner similar to that of its mammalian counterpart.So far, no link has been made between SEL-5 and C. elegans Wnt signalling regulation.
In this study, we set out to analyse the potential role of the SEL-5 kinase in Wnt signalling regulation and its contribution to DPY-23/AP2M1 phosphorylation in C. elegans.We show that SEL-5 acts in collaboration with the retromer complex as a positive regulator of EGL-20/Wnt signalling during the migration of QL neuroblast descendants.We further demonstrate that although SEL-5 participates in DPY-23 phosphorylation, the observed role of SEL-5 in neuroblast migration is independent of its kinase activity, and the phosphorylation of DPY-23 is dispensable for Wnt-dependent migration of QL neuroblast descendants.SEL-5, together with the retromer, is further required during the active phase of excretory cell canal extension, again independently of its kinase activity.Finally, we show that the Wnt proteins CWN-1 and CWN-2, together with CFZ-2/Frizzled, promote excretory canal outgrowth while LIN-44/Wnt and LIN-17/Frizzled together define the stopping point for canal extension.

Results
Loss of SEL-5 affects migration of QL neuroblast descendants Q cell descendants (Q.d) migration is dependent on EGL-20/Wnt signalling.While on the right side of the L1 larva QR divides and QR.d migrate in the default anterior direction, on the left side QL.d respond to the EGL-20 signal produced in several cells around the rectum by expressing the homeotic gene mab-5 and migrate to the posterior.In the absence of active EGL-20 signalling, mab-5 is not expressed and QL.d migrate to the anterior (Salser and Kenyon, 1992;Figure 1A).To visualize Q.d migration, we utilized Pmec-7::gfp expressing transgene muIs32 which is, apart from other cells,   active in AVM and PVM touch neurons, which are QR and QL descendants, respectively (Ch'ng et al., 2003).We performed RNA interference (RNAi) against sel-5 in wild type background and observed no effect on QL.d migration (Figure 1B).To increase the sensitivity of the RNAi approach, we repeated the RNAi experiment using vps-29(tm1320) mutant strain.This strain harbours a null mutation in the VPS-29 retromer subunit, displays only weakly penetrant QL.d migration defect (Coudreuse et al., 2006), and has previously been used as a sensitized background to uncover genes required for Q.d migration (Harterink et al., 2011b;Lorenowicz et al., 2014).RNAi against sel-5 significantly increased the QL.d migration defect of vps-29(tm1320) (Figure 1B, Figure 1-figure supplement 1).To verify the results obtained with RNAi, we assessed the QL.d migration in sel-5(ok363) and sel-5(ok149) mutants.Similarly to RNAi results, mutation of sel-5 alone did not affect QL.d migration while sel-5 vps-29 double mutants displayed an almost fully penetrant defect (Figure 1C and D).
The loss of vps-29 affects EGL-20/Wnt signalling at the level of Wnt production (Yang et al., 2008).We further tested whether loss of sel-5 could enhance partially penetrant defects in QL.d migration in mutants acting at a different step of the EGL-20/Wnt pathway.We tested two Frizzled mutants which both serve to receive the EGL-20 signal in the QL, albeit to a different extent (Zinovyeva et al., 2008).The loss of sel-5 strongly increased the weak QL.d migration defect of the lin-17/Frizzled mutants but did not affect the already more penetrant QL.d defect of mig-1/Frizzled mutant animals (Figure 1D).
We next asked whether loss of sel-5 in the vps-29 background affects other Wnt-dependent processes such as the polarization of the ALM and PLM neurons, CAN neuron migration, or T cell polarity.Polarization of ALM and PLM is regulated by several Wnt proteins (Pan et al., 2006;Prasad and Clark, 2006;Hilliard and Bargmann, 2006), CAN neuron migration is governed predominantly by CWN-2 with a minor contribution from CWN-1 and EGL-20 (Zinovyeva and Forrester, 2005;Zinovyeva et al., 2008) and T cell polarity depends on the LIN-44/Wnt signal (Herman et al., 1995).We observed weakly penetrant ALM polarization defects in both sel-5(ok363) vps-29 and sel-5(ok149) vps-29 double mutants, a very mild PLM polarization defect was detected in a strain carrying the ok149 allele (Table 1).In addition, mildly penetrant anterior displacement of the CAN neuron was observed in the double mutants, while approximately 17% of the double mutant animals carrying the ok149 allele did not correctly form the phasmid sensillum, which indicates defects in T cell polarization (Table 1).Apart from these Wnt-dependent phenotypes, we also observed reduced brood size in the double mutants compared to controls (Table 1), defective tail formation (Figure 1E), and a progressive egg-laying defect leading to a bag-of-worms phenotype.
The penetrance of the observed phenotypes was not the same in the two sel-5 alleles.This was unexpected as both alleles carry deletions that hit the kinase domain of SEL-5 protein.We were able to amplify shorter than wild type transcripts from both sel-5(ok363) and sel-5(ok149) animals using primers in exon 1 and exon 17 (Figure 1F, Figure 1-figure supplement 2).Sequencing of the ok363 transcript revealed that amino acids 1-243 of the wild type protein followed by additional 32 amino acids would be translated due to a frameshift and a premature stop codon.This protein encompasses a larger part of the SEL-5 kinase domain including the active site.In agreement with data published by Fares and Greenwald, 1999, sequencing of the ok149 transcript revealed that it can give rise to a protein containing the first 153 amino acids of SEL-5 followed by 21 additional amino acids and thus is devoid of the active site (Figure 1F).If such truncated proteins are present in the mutants, either one or both may possess some residual activity that is responsible for the observed phenotypic differences.full-length SEL-5 tagged with GFP at its N-terminus under the control of different tissue-specific promoters in a sel-5 vps-29 background and assayed QL.d migration.The expression of SEL-5 from the egl-20 promoter (Coudreuse et al., 2006) resulted in a significant rescue of the QL.d migration defect of sel-5 vps-29 double mutants albeit not to the level of vps-29 single mutants (Figure 2A, Figure 2-figure supplement 1).No rescue was obtained when SEL-5 was expressed from the wrt-2 promoter that is active in the seam cells and the Q cells (Aspöck et al., 1999;Middelkoop et al., 2012).These data suggest that sel-5 is required in the EGL-20/Wnt-producing cells to control QL.d migration.However, a similar level of rescue as with egl-20 promoter was obtained also when SEL-5 was expressed from hlh-1 promoter specific for the body wall muscle cells (Krause et al., 1990;Harfe et al., 1998).When SEL-5 was simultaneously expressed from the egl-20 and hlh-1 promoters, the rescue almost reached the background frequency of the QL.d defect, caused by vps-29 alone (Figures 1D and 2A, Figure 2-figure supplement 1).Apart from the rectal epithelial cells, egl-20 expression was also detected in posterior ventral body wall muscle quadrants VL23 and VR24 (Harterink et al., 2011a); therefore, it is possible that hlh-1 promoter-driven expression of SEL-5 in these muscle quadrants is responsible for the observed rescue, and only the combined expression from all EGL-20-producing cells is sufficient to drive a complete rescue.Alternatively, the observed rescue pattern could indicate that SEL-5 is required in both the Wnt-producing and in the muscle cells.

SEL
To confirm that the tissues identified above in the rescue experiments are tissues with a genuine sel-5 expression, we set to determine the endogenous sel-5 expression pattern that has not been previously analysed.The only published expression data (Fares and Greenwald, 1999) were based on the expression from sel-12 instead of sel-5 promoter.We generated GFP knock-in strains by inserting GFP into the sel-5 genomic sequence using the SEC cassette approach (Dickinson et al., 2015).We obtained two strains, one expressing a transcriptional Psel-5::gfp reporter (Figure 2B) and one, after excision of the SEC cassette, an N-terminally tagged GFP::SEL-5 under the control of its own promoter (Psel-5::gfp::sel-5) (Figure 2C).Microscopic analyses of both strains revealed that sel-5 is expressed broadly, but at a low level judged by the intensity of the GFP signal.The most prominent expression was observed in the gonad from the beginning of its development (Figure 2B).Expression was further observed in the developing oocytes, in the vulva, in epidermal cells, and most notably, in the rectal epithelial cells that are known to produce EGL-20/Wnt (Whangbo and Kenyon, 1999; Figure 2B and C).We could not detect sel-5 expression in muscles, although we cannot exclude that a low level of expression, below the detection limit using the endogenous locus-tagging approach, is present.Interestingly, oocytes and epidermal seam cells expressing the GFP::SEL-5 fusion protein revealed its distinct subcellular localization.Protein localized to punctate structures located close to the cell surface (Figure 2C).This pattern resembles the subcellular distribution of human AAK1 (Conner and Schmid, 2002), hinting that SEL-5 could be involved in regulating intracellular transport similar to AAK1.

SEL-5 does not affect MIG-14 endocytosis
The SEL-5 orthologue AAK1 has been implicated in endocytosis regulation (Conner and Schmid, 2002;Ricotta et al., 2002).The obvious candidate that could be affected by SEL-5-dependent endocytosis in Wnt-producing cells is the Wnt cargo receptor MIG-14/Wls.Human AAK1 can phosphorylate the AP2 subunit µ2 (AP2M1) (Conner and Schmid, 2002;Ricotta et al., 2002) and thus increase the affinity of AP2 to cargo molecules (Ricotta et al., 2002).It is conceivable that SEL-5 could regulate MIG-14/Wls trafficking at the level of AP2-dependent endocytosis.The C. elegans μ2 subunit of the AP2 complex, DPY-23 (also known as APM-2), has been shown to participate in the internalization of MIG-14 (Pan et al., 2008;Yang et al., 2008).We first tested whether loss of sel-5 expression has any effect on the level of phosphorylation of DPY-23.A phospho-specific antibody recognizing phosphorylated threonine T160 (T156 in mammalian AP2M1) of DPY-23 (Hollopeter et al., 2014) revealed a decrease in the level of phosphorylated endogenous DPY-23 in sel-5 mutants compared to wild type animals (Figure 3A, Figure 3-source data 1).Similarly, T160 phosphorylation was reduced on overexpressed GFP-tagged DPY-23 (Figure 3B, Figure 3-source data 1).Next, we assessed MIG-14 levels and localization in sel-5 vps-29 mutants using a transgene expressing a functional MIG-14::GFP protein (Lorenowicz et al., 2014).However, the levels of MIG-14::GFP did not change significantly in sel-5 vps-29 compared to the vps-29 single mutant (Figure 3C and D,.Levels of MIG-14::GFP in sel-5 single mutants were variable but on average comparable to the wild  type.We therefore concluded that the significant increase in QL.d migration defects in sel-5 vps-29 compared to vps-29 cannot be attributed to changes in MIG-14/Wls levels.Importantly, MIG-14::GFP did not re-localize to the plasma membrane in sel-5 or sel-5 vps-29 mutants, in striking contrast to the MIG-14::GFP behaviour in animals treated with dpy-23 RNAi (Figure 3-figure supplement 1).This excludes the possibility that the Wnt-related phenotypes in sel-5 vps-29 mutants arise from a defect in MIG-14 internalization.

SEL-5 helps shape the EGL-20 gradient
Our tissue-specific rescue experiments revealed that for a full rescue, simultaneous sel-5 expression is necessary from both egl-20 and hlh-1 promoters.SEL-5 could therefore regulate endocytosis along the EGL-20 transport route, thus shaping the EGL-20 gradient.To test this hypothesis, we endogenously tagged EGL-20 with GFP and assessed Wnt gradient formation in control and mutant backgrounds.This approach has been previously used and revealed that extracellular EGL-20 can be detected in the form of distinct puncta that most likely represent EGL-20 bound to Frizzled (Pani and Goldstein, 2018).We detected EGL-20 puncta in all strains tested, albeit with different frequencies (Figure 4A-C).While the number of EGL-20 puncta in sel-5 mutants was not significantly different from that in control animals, in sel-5 vps-29 mutants the number of puncta was substantially reduced.However, statistical evaluation did not reveal significant differences between vps-29, sel-5 vps-29, and vps-35; although a decreasing trend in puncta number was visible (Figure 4C).In vps-35, the EGL-20 gradient was shown to be highly reduced or absent (Coudreuse et al., 2006;Harterink et al., 2011b) and was used for comparison.We also compared the signal intensity in the EGL-20 spots among the different strains but no significant differences were detected (Figure 4D).Finally, we assessed the length of the gradient by measuring how far from the rectum the EGL-20 puncta can be detected.While EGL-20 gradient formation in neither sel-5 nor vps-29 was significantly affected, the EGL-20 gradient was shorter in vps-29 sel-5 double mutants than in wild type controls (Figure 4E).Our data thus support the notion that sel-5 plays a subtle role in EGL-20 gradient formation.

SEL-5-associated phenotypes are independent of DPY-23 phosphorylation
Although endocytic cargo other than MIG-14 may be affected in sel-5 vps-29 mutants, we could not exclude the possibility that the observed phenotypes are a consequence of defects in other mechanisms unrelated to DPY-23 phosphorylation.To test this hypothesis, we repeated the rescue experiment presented in Figure 2A now with SEL-5 carrying either K75A or D178A point mutations.Position D178 corresponds to D176 of human AAK1 and is part of the conserved HRD motif in the catalytic loop, K75 corresponds to K74 in AAK1 and is predicted to affect ATP binding (Figure 5-figure supplement 1).In AAK1, both mutations abolished its ability to phosphorylate AP2M1 (Conner and Schmid, 2003).When expressed under the control of the egl-20 promoter, the mutant SEL-5 proteins could still rescue the QL migration phenotype (Figure 5A, Figure 5figure supplement 2).This indicates that SEL-5 kinase activity is not responsible for the phenotypes observed in sel-5 vps-29 mutants.To test this further, we next asked whether phosphorylation at the T160 position of DPY-23 is necessary for QL.d migration.To this end, we utilized the dpy-23(mew25) allele harbouring T160A point mutation (G.Hollopeter and G. Beacham, unpublished).Characterization of dpy-23(mew25) animals revealed that homozygous mutants are viable; they are not dumpy and look superficially wild type.This indicates that the mutants do not suffer from a gross endocytosis defect, even though no DPY-23 phosphorylation was detected in dpy-23(mew25) animals (Figure 5B, Figure 5-source data 1).In compliance with previous findings using dpy-23 alleles that harbour mutations changing the T160 amino acid (Hollopeter et al., 2014;Partlow et al., 2019), mew25 is able to rescue the 'jowls' phenotype of fcho-1(ox477) mutants (Figure 5C).FCHO-1 is a member of the muniscin family of proteins and a proposed allosteric activator of   AP2 (Hollopeter et al., 2014).We then asked whether complete loss of DPY-23 phosphorylation would lead to a QL.d migration defect.Animals carrying dpy-23(mew25) alone or in combination with sel-5(ok149) did not show any defects in QL.d migration (Figure 5D).A variable increase in QL.d migration defects was observed in vps-29;dpy-23(mew25) animals, but the penetrance of the defect never reached levels comparable to those in sel-5 vps-29 mutants (Figures 1D and 5D).Furthermore, MIG-14::GFP did not re-localize to the plasma membrane in dpy-23(mew25) similar to the sel-5 mutants and unlike in dpy-23 RNAi animals (Figure 5E).Together, these observations   strongly suggest that the role of SEL-5 in the regulation of QL.d migration is not dependent on its kinase activity and, moreover, that DPY-23 phosphorylation at T160 is not a major regulatory event in this process.

The outgrowth of excretory cell canals is impaired in sel-5 vps-29 mutants
Apart from the QL.d migration defect in the sel-5 vps-29 double mutants, in some animals, we unexpectedly noticed a severe shortening of the posterior canals of the excretory cell that prompted us to analyse this phenotype in more detail.The excretory cell (also called the excretory canal cell) is a large H-shaped cell required for osmoregulation (Buechner et al., 1999;Liégeois et al., 2007).
The excretory canal cell body is located near the posterior bulb of the pharynx and four excretory canals emanate from the cell body, two short ones directed to the anterior and two posterior canals extending to the rectum (Figure 6A).To assess the morphology of the excretory cell, we expressed GFP under the control of pgp-12 promoter which is active exclusively in the excretory cell (Zhao et al., 2004) and analysed the length of the canals in late L4 or early adult animals.While the posterior canal length in sel-5 or vps-29 single mutants was indistinguishable from the wild type controls, in more than 60% of the sel-5 vps-29 mutants the posterior canals stopped at various positions anterior to the rectum (Figure 6A and B).A similar effect, albeit with lower penetrance, was observed when assessing the anterior canal length (Figure 6C).Interestingly, the posterior canal on the right side of the animal was significantly more affected than its counterpart on the left side in sel-5 vps-29 double mutants carrying the ok149 allele (Figure 6D).A similar trend was observed in sel-5(ok363) vps-29 animals, although the difference observed there did not reach statistical significance (Figure 6D).
Active growth of the canals starts during embryogenesis and continues during L1.After that the canals passively grow with the growing animal (Fujita et al., 2003).Comparison of canal lengths at several time points within a 24 hr interval after hatching revealed that in sel-5 vps-29 double mutants the posterior canals of the excretory cell are shorter already at the time of hatching and the growth defect prevails throughout larval development (Figure 6E).
Excretory canal shortening has not previously been reported for any of the retromer components.Therefore, we tested whether this phenotype is specific for the vps-29 retromer subunit or whether the whole retromer complex is required together with sel-5 for proper excretory canal extension.We performed RNAi against vps-35, vps-26, snx-1, and snx-3 in sel-5(ok149) background and assessed posterior canal length.Except for snx-1 RNAi, significant shortening was observed with RNAi against all other retromer subunits, with vps-35 showing the strongest phenotype (Figure 6F).These data confirm that the whole retromer complex acts together with sel-5 to control excretory canal outgrowth.
Next, we tested in which tissue SEL-5 activity is required for excretory cell outgrowth.We expressed SEL-5 from either pgp-12 (excretory cell), hlh-1 (body wall muscle cells), or col-10 (hypodermis) promoters in sel-5 vps-29 double mutants and checked for any rescue.As shown in Figure 6G, the expression of SEL-5 from the pgp-12 promoter almost fully rescued the excretory cell shortening while the expression of SEL-5 from the muscle-specific hlh-1 promoter did not affect the excretory cell phenotype of the sel-5 vps-29 double mutants.As in the case of the QL.d migration defect, the excretory canal length was efficiently rescued also by the SEL-5D178A variant expressed from pgp-12 promoter arguing that SEL-5 kinase activity is not required for canal extension (Figure 6G).Expression of VPS-29 in the excretory cell partially rescued canal shortening, suggesting that SEL-5 and the retromer complex act together within the same cell to regulate canal length.Interestingly, the expression of SEL-5 from the col-10 promoter, which is active in the hypodermis (Spencer et al., 2001), also resulted in a significant rescue of the excretory canal shortening.This suggests that SEL-5 activity in both the excretory cell and the hypodermis contributes to the regulation of canal outgrowth.
To support our finding that the role of SEL-5 in excretory canal outgrowth is independent of DPY-23 phosphorylation, we analysed the length of the posterior canal in dpy-23(mew25) mutant animals.No canal shortening was observed in animals carrying dpy-23(mew25) alone (Figure 6H), while only very mild shortening was occasionally observed in either sel-5; dpy-23(mew25) or vps-29; dpy-23(mew25).These observations are consistent with a role of SEL-5 in excretory canal outgrowth that is not dependent on DPY-23 phosphorylation at T160.Wnt-dependent signalling is required to establish proper excretory cell canal length We were interested to see whether the observed shortening of the excretory canals in sel-5 vps-29 mutants could be a consequence of crosstalk with the Wnt signalling pathway as in the case of QL.d migration.lin-17/Frizzled mutants have been reported to show an overgrowth of the posterior excretory cell canals past the rectum into the tip of the tail (Hedgecock et al., 1987) while loss of axl-1, one of the two C. elegans Axin orthologues, resulted in ectopic branching of the posterior excretory canal without affecting canal length.Ectopic branching in axl-1 mutants could be rescued by simultaneous loss of bar-1/β-catenin or pop-1/Tcf expression (Oosterveen et al., 2007).Wnt signalling thus seems to play a role in excretory canal growth, but so far, the other Wnt pathway components and their mechanism of action remained unknown.Therefore, we tested whether mutations in other Wnt pathway components could affect excretory cell growth.Among the four Wnts tested (EGL-20, LIN-44, CWN-1, CWN-2), only mutants in lin-44/Wnt exhibited an almost fully penetrant posterior excretory canal overgrowth phenotype, as observed in lin-17/Frizzled mutants (Figure 7A and  B).Mild canal shortening was observed in cwn-2/Wnt and cfz-2/Frizzled mutants, while a very weak overgrowth phenotype could be detected in egl-20/Wnt mutants (Figure 7B).No change in excretory canal length was displayed by cwn-1/Wnt or mig-1/Frizzled mutants.Interestingly, highly penetrant canal overgrowth was also observed in mig-14/Wls mutants, while loss of mig-5/Dishevelled or dsh-1/Dishevelled resulted in a partially penetrant overgrowth phenotype (Figure 7B).We next tested various combinations of Wnt and Frizzled mutants and found that simultaneous loss of lin-44 and cwn-1 or lin-44 and cwn-2 expression resulted in partial rescue of the canal overgrowth and the same effect was observed after simultaneous loss of lin-17 and cfz-2.Surprisingly, the loss of egl-20 and mig-1 also partially rescued the canal overgrowth in lin-17, even though neither of them displayed canal shortening on its own.In contrast, mig-1 suppressed canal shortening in cfz-2.The most prominent canal shortening was observed in cwn-1; cfz-2 or cwn-2; cfz-2 double mutants (Figure 7B).Apart from shortening, three instead of two posterior canal branches were detected in 11% of cwn-1; cfz-2 and 15% of cwn-2; cfz-2 double mutants (Figure 7C).These data suggest that at least two Wntdependent pathways are acting during the extension of the excretory canal, one involving lin-44, lin-17, dsh-1 and mig-5 that is responsible for determining the stopping point for the growing canal, and one involving cwn-1, cwn-2, and cfz-2 that contributes to the canal growth.
The most striking phenotype is the overgrowth of the posterior excretory canal in lin-17, lin-44, and mig-14 mutants.Interestingly, when we measured the length of the excretory canal within the 24 hr interval after hatching, no difference in canal length was detected between wild type controls and lin-17, lin-44, and mig-14 mutants (Figure 7D).This suggests that the initial growth is not affected in in each segment is indicated.Segment scoring 50% or higher was highlighted in dark blue, segment scoring 15-49% was highlighted in light blue for easier orientation.All strains contained the mamEx11 transgene to visualize the excretory cell.The statistical significance of differences between the strains was analysed using Fisher's exact test for a 2 × 3 table.For the test, data from segments 0-4 were pooled into one category ('shorter') and data from segments 5 and 6 were used as the two other categories ('normal' and 'longer', respectively).The comparison was made either to the control strain or to the more severe single mutant in the case of double mutant strains.Bonferroni correction for multiple testing was applied.(C) Anterior canals of the excretory cell are shortened in sel-5 vps-29 double mutants.The excretory cell was visualized by Ppgp-12::gfp expression from a mamEx29 transgene.The scale bar represents 100 μm.(D) Posterior canals on the right side of the animals are more severely affected compared to their left counterparts.The length of the posterior canal on each side of the animal was measured and normalized to the length of the whole body of the animal.Paired Student's t-test was used to assess the significance of the difference between the two sides, ***p-value<0.001,ns, not significant.(E) Posterior excretory canals are shorter already at the time of hatching in sel-5 vps-29 mutants.The dynamics of posterior canal outgrowth was assessed by measuring the canal length and normalizing it to the total body length at hatching and at three time points during early larval development.Results are presented as mean + s.d. of at least 30 canals for each condition.Unpaired two-tailed Student's t-test was performed to assess the difference between the samples, *p-value<0.05,**p-value<0.01.(F) Loss of either vps-35, vps-26, or snx-3 retromer component expression induces posterior canal shortening in sel-5 mutants.Canal outgrowth was scored as in (B).(G) Both cell-autonomous and non-autonomous expression of sel-5 rescues excretory canal shortening in sel-5 vps-29 mutants.SEL-5 was expressed from an extrachromosomal array under the control of pgp-12, hlh-1 or col-10 promoters.Canal outgrowth was scored as in (B) and a comparison was made between animals carrying the array and their siblings which have lost the transgenic array.All strains contained also the mamEx29 extrachromosomal array to visualize the excretory canal.(H) T160 phosphorylation of DPY-23 is not required for posterior excretory canal outgrowth.Canal outgrowth was scored as in (B) in strains containing dpy-23(mew25) allele carrying T160A substitution.Comparison was made between the double mutants and either sel-5 or vps-29 single mutant.For (F-H) † differences not significant, ‡ same data as in (B).

Figure 6 continued
the mutants but rather that these mutants miss a signal determining the final position of the canal in later larval stages.Simultaneous loss of lin-17 and sel-5 led to a partial rescue of the lin-17 phenotype (Figure 7B).A similar effect was observed in lin-44; sel-5 double mutants (Figure 7B).Analysis of a lin-17; sel-5 vps-29 triple mutant was not possible as this combination was lethal.These data indicate that sel-5 is required for the initial growth of the excretory canals.The LIN-44/Wnt signal acting through  6B and a comparison was made either to the control strain (sIs10089 only) or to the more severe single mutant in the case of double mutant strains.All strains contained the sIs10089 transgene to visualize excretory canals except for lin-17; sel-5 and lin-44; sel-5 which contained mamEx11, and mig-5, which contained mamEx29.† Differences not significant.‡ Full genotype was mig-5(cp385[mNG-GLO^AID::mig-5]); mamEx29; mamEx34[eft-3p::TIR::mRuby; myo2p::tdTomato] and animals were grown on NGM plates with 1 mM auxin from L1 till L4/young adult stage.Only animals containing the mamEx34 array were used for analysis.(C) Three branches of the posterior canal were detected in cwn-1; cfz-2 animals.The excretory canal was visualized by the sIs10089 transgene, the scale bar represents 200 μm.(D) Posterior excretory canals display normal length during early larval development.The dynamics of posterior canal outgrowth in lin-44, lin-17, and mig-14 mutants was assessed by measuring the canal length and normalizing it to the total body length at hatching and at three time points during early larval development.Results are presented as mean + s.d. of at least 30 measured canals.Comparison between samples assessed by unpaired two-tailed Student's t-test did not reveal any significant differences.
the LIN-17/Frizzled receptor is either required early but the phenotypic manifestation is postponed or it is required at a later stage to terminate excretory canal extension.

Discussion
The NAK family kinase AAK1 has recently been added to the long list of Wnt signalling regulators (Agajanian et al., 2019), acting at the level of LRP6 endocytosis.In the present study, we probed the role of the C. elegans AAK1 orthologue SEL-5 in Wnt signalling and uncovered its requirement for Wnt-dependent QL neuroblast daughter cell migration.We also revealed that SEL-5 is required during the outgrowth of the excretory canal cell prior to a Wnt-dependent stop signal.Importantly, in both instances the role of SEL-5 is independent of its kinase activity, defining an alternative mode of action for this kinase.
The role of SEL-5 has not been extensively studied in C. elegans; the only available reports uncovered the role of sel-5 as a genetic suppressor of a constitutively active lin-12/Notch mutation (Tax et al., 1997;Fares and Greenwald, 1999).Information about protein function was missing.SEL-5 shows the highest similarity to the mammalian Numb-associated kinase family members AAK1 and BMP2K (Shaye and Greenwald, 2011;Sorrell et al., 2016).Both AAK1 and BMP2K were shown to phosphorylate the μ2 subunit of the AP2 adaptor at position T156 and thus regulate clathrin-mediated endocytosis (Conner and Schmid, 2002;Ricotta et al., 2002;Ramesh et al., 2021).Our findings uncovered some similarities between SEL-5 and AAK1 or BMP2K.Firstly, we show that the level of DPY-23/AP2M1 phosphorylation in sel-5 mutants is decreased compared to controls.Secondly, the subcellular localization of SEL-5 to punctate structures proximal to the plasma membrane in oocytes and epidermal seam cells resembles the subcellular distribution of human AAK1 (Conner and Schmid, 2002).These data support the notion that SEL-5 has a function analogous to its mammalian counterparts.
Given the established role of AAK1 in the regulation of mammalian endocytosis (Kadlecova et al., 2017;Agajanian et al., 2019;Wrobel et al., 2019), it was striking to see that loss of sel-5 expression alone had no obvious developmental consequences.However, even in mammalian cells complete loss of AP2M1 T156 phosphorylation does not block endocytosis but only reduces its efficiency (Motley et al., 2006;Wrobel et al., 2019).We did not observe complete loss, but only a partial reduction of DPY-23 phosphorylation in sel-5 mutants.This implies that SEL-5 is not the only kinase responsible for DPY-23 phosphorylation.It also suggests that endocytosis is not inhibited but could be only partially compromised.In such case, the level of ongoing endocytosis might be sufficient to support proper developmental decisions, such as the direction of Q neuroblast migration.We argued that in combination with an additional insult to the intracellular trafficking machinery, in this case the retromer complex, the suboptimal function of endocytosis would manifest itself.Indeed, sel-5 vps-29 double mutants display two highly penetrant phenotypes, the QL.d migration defect and shortening of the excretory cell canals.Strikingly, neither of these phenotypes can be attributed to a decrease in endocytic efficiency due to a lack of DPY-23 phosphorylation.Firstly, both phenotypes can be rescued by a tissue-specific expression of a kinase-inactive SEL-5 mutant protein.Secondly, mutants expressing only non-phosphorylatable DPY-23 do not phenocopy sel-5 vps-29 mutants.Alternative mechanisms of SEL-5 function thus have to be considered.It is possible that either SEL-5 affects endocytosis by a mechanism not dependent on DPY-23 phosphorylation or that SEL-5 regulates QL.d migration and excretory cell canal extension by endocytosis-independent mechanisms.Our findings about MIG-14/Wls behaviour, the most obvious endocytic cargo candidate for QL.d migration, argue against the first possibility; most notably the fact that MIG-14 does not re-localize to the plasma membrane in the absence of SEL-5.However, the effect of SEL-5 on a different endocytic cargo cannot be excluded.We detected significant shortening of the EGL-20 gradient in the sel-5 vps-29 mutants.Given that SEL-5 is required both in the EGL-20-producing cells and in the muscle for QL.d migration, it is possible that some receptors that serve as a sink for EGL-20 are incorrectly accumulated at the plasma membrane and thus partially hinder EGL-20 spreading.In case of the excretory canal extension, SEL-5 could regulate the turnover of guidance receptors at the plasma membrane of the growing tip.In Drosophila, the loss of Numb-associated kinase (Nak) results in the absence or shortening of higher-order dendrites and Nak has been shown to promote endocytosis of Neuroglian/ L1-CAM during dendrite extension and branching (Yang et al., 2011).In the C. elegans excretory cell, PAT-3/β1-integrin is required for canal outgrowth (Hedgecock et al., 1987).Integrins constantly cycle between the plasma membrane and intracellular compartments using various trafficking routes (Moreno-Layseca et al., 2019) and could thus serve as a putative SEL-5 cargo.
Searching for a possible endocytosis-independent mechanism of SEL-5 activity is complicated by the fact that while in the case of QL.d migration SEL-5 function is cell-nonautonomous, cellautonomous expression of SEL-5 is sufficient to rescue the sel-5 vps-29 excretory canal extension defect.This suggests that more than one mechanism might exist.One possibility common to both phenotypes comes from recent studies in mammalian cells.BMP2K has been shown to localize to the early secretory compartment and to regulate COPII coat assemblies (Cendrowski et al., 2020).SEL-5 could thus affect Wnt secretion in the case of QL.d migration or new guidance receptor delivery to the plasma membrane in the case of the excretory canals.EGL-20 gradient analyses revealed gradient shortening in sel-5 vps-29 mutants.However, no significant differences in the number of EGL-20 puncta were detected between wild type and sel-5 animals, but also not between vps-29 and sel-5 vps-29, despite the almost eightfold difference in the QL.d migration phenotype penetrance between these two mutants.This would argue against a role for SEL-5 in secretion.Shorter gradient in the double mutants could thus more likely arise from a combination of partially reduced EGL-20 secretion caused by vps-29 and a partial reduction of EGL-20 spreading caused by a possible sel-5dependent membrane retention of a receptor acting as an EGL-20 sink.A direct correlation between the amount of EGL-20, the range of the EGL-20 gradient, and the QL.d phenotype would be necessary to explain the phenotypic differences between the various mutants.More experiments will thus be required to establish how SEL-5 exerts its function.The biggest question to answer will be how it does so independently of its kinase activity.
Apart from the role of SEL-5 and the retromer complex in excretory cell canal extension, we have also uncovered a significant contribution of Wnt pathway components in defining the length of the excretory canal.The role of Wnt signalling in the outgrowth of the excretory canals has been suggested (Sundaram and Buechner, 2016); however, the only evidence came from the early observation that canals overgrow in lin-17 mutants (Hedgecock et al., 1987) and that erroneous canal branching is observed in axl-1/Axin-like mutants (Oosterveen et al., 2007).More recently, it has been shown that the loss of PLR-1, a transmembrane E3 ubiquitin ligase, results in excretory canal shortening (Bhat et al., 2015).PLR-1 is responsible for internalization of Frizzled receptors from the cell surface (Moffat et al., 2014).However, a direct link between PLR-1 function in the excretory cell and Wnt signalling has not been established.Our analysis of single Wnt and Frizzled mutants revealed that while loss of cwn-2 or cfz-2 expression resulted in a very mild shortening of the excretory canal, loss of lin-44 or lin-17 led to profound canal overgrowth (summarized in Figure 8A).These findings suggested that two independent Wnt pathways could be employed to establish a proper excretory canal length -one that promotes canal extension and one that generates the stop signal for growth termination.Further analyses of double mutants and other Wnt signalling components revealed that the extension-promoting pathway includes cwn-1 in addition to cwn-2 and cfz-2, while the stop-signal pathway encompasses lin-44, lin-17, dsh-1, mig-5, and mig-14.A similar repulsive role of LIN-44/LIN-17 complex has been described in the case of a posterior axon of the C. elegans GABAergic DD6 motor neuron (Maro et al., 2009) or PLM, ALN, and PLN neurons (Zheng et al., 2015).Loss of lin-44 or lin-17 expression promoted outgrowth of the posterior neurites of these neurons, implicating that in wild type animals, LIN-44 serves as a repulsive cue.On the other hand, cwn-2 and cfz-2 were shown to positively regulate the posterior neurite outgrowth of RMED/V neurons with cwn-2 acting as an attractive cue (Song et al., 2010).The role of two other Wnt signalling components, egl-20 and mig-1, is less clear.No effect (mig-1) or only a very mild overgrowth defect (egl-20) is observed in single mutants.However, both egl-20 and mig-1 significantly rescue the overgrowth phenotype of lin-17 mutants, while at the same time, mig-1 can suppress the shortening of canals in cfz-2 mutants.EGL-20-producing cells are localized around the rectum (Whangbo and Kenyon, 1999;Harterink et al., 2011a), exactly where the excretory canals stop, while LIN-44 is expressed more posteriorly (Herman et al., 1995;Harterink et al., 2011a).A possible explanation could thus be that while LIN-44 provides a general posterior repulsive signal, EGL-20 fine-tunes the exact stopping position of the growing canal.The role of different Wnts and Frizzleds in excretory canal outgrowth is summarized in Figure 8B.Further investigation will be required to decipher the exact way how SEL-5 and the retromer crosstalk with Wnt signalling during excretory cell outgrowth.It is clear though that more than one mechanism is likely involved.First, sel-5 vps-29 mutants display canal shortening similarly to cwn-1; cfz-2 or cwn-2; cfz-2, suggesting a positive regulatory role.Mutants in lin-17 and lin-44 display canal overgrowth, yet sel-5 is partially able to suppress this phenotype.This would imply a negative regulatory role for sel-5 and be in agreement with the role of AAK1 in Wnt pathway regulation (Agajanian et al., 2019).However, sel-5 and vps-29 are required already during the initial larval outgrowth while the LIN-44/LIN-17 signal is required later.The observed rescue might thus also be explained by delayed canal growth and not by a direct impact of sel-5 and vps-29 on LIN-44 or LIN-17 levels or localization.Alternatively, sel-5 and vps-29 may regulate LIN-44 or LIN-17 earlier but the signalling outcome does not manifest itself until later in development.
Taken together, we have uncovered cooperation between the C. elegans orthologue of the AAK1 kinase, SEL-5, and the retromer complex in regulating cell migration and cell outgrowth, and we have also outlined the engagement of Wnt pathway components in defining the length of the excretory cell canals.The surprising independence of the SEL-5 function on its kinase activity opens a new path for investigation with high relevance also for mammalian biology.AAK1 has been proposed as a potential drug target for treating various neurological disorders and preventing viral entry, where kinase activity is the target of inhibition (Martinez-Gualda et al., 2022;Xin et al., 2023).In light of our findings, the non-enzymatic activities of AAK1 should also be taken into account.(Dickinson et al., 2015) was used to generate GFP-tagged endogenous sel-5 locus and performed virtually as described (Dickinson et al., 2015; http://worm-cas9hr.weebly.com/protocols.html).647 bp upstream of sel-5 ATG (5' homology arm) and 558 bp sel-5 genomic sequence starting from ATG (3' homology arm) were PCR-amplified from N2 genomic DNA with primers harbouring overhangs for Gibson assembly with the pDD282 vector (Dickinson et al., 2013; a gift from Bob Goldstein [Addgene plasmid # 66823; http://n2t.net/addgene:66823; RRID:Ad-dgene_66823]) and assembled with pDD282 digested with ClaI and SpeI.Sequence GCTG AAAA GCCC TAGA GGCA was inserted into pDD162 vector for sgRNA expression (Dickinson et al., 2013; pDD162 was a gift from Bob Goldstein [Addgene plasmid # 47549; http://n2t.net/addgene:47549; RRID:Addgene_47549]). Sequences of all primers used for gene editing vector construction are listed in Supplementary file 2. Injection was performed as described above, injection mix contained 10 ng/ μL pDD282 with homology arms, 50 ng/μL pDD162 with corresponding sgRNA sequence, and 5 ng/ μL Pmyo-2::tdTomato.Line expressing Psel-5::gfp was first established, and several L1 animals were then exposed to a heat shock for 4 hr at 34°C to excise the selection SEC cassette and create a Psel-5::gfp::sel-5 knock-in line.The EGL-20::GFP knock-in strain was generated as described (Pani and Goldstein, 2018) with one modification -the pDD282 vector was used for cloning the homology arms.

Key resources table
RNA interference experiments were conducted by feeding using bacterial strains from the Ahringer library (Kamath and Ahringer, 2003) except for dpy-23, which came from the Vidal library (Rual et al., 2004).L4 larvae were transferred to RNAi plates with the desired bacterial clones and the effect of RNAi was assessed in the next generation after 3-4 days at 20°C.

C. elegans phenotypes, microscopy, and statistical analyses
The final position of QL. paa (PVM -QL.d phenotype) and polarity of ALM and PLM neurons were assessed in L4 larvae carrying transgene muIs32 or muIs35.PVM migration was scored as defective when PVM was located anteriorly to the posterior edge of the vulva.ALM polarity was scored as defective when bipolar or reversed neurites were observed.CAN neurons were visualized with kyIs4 transgene and their position relative to V3 seam cell was scored.CAN positioned anterior to V3 was scored as displaced.For DiI staining, L3-L4 well-fed animals were washed from a plate with M9 buffer and incubated for 3 hr in 10 μg/mL DiI solution (D282, Thermo Fisher Scientific, dissolved to 2 mg/mL stock solution in dimethylformamide).Animals were then washed three times in M9 buffer and directly observed.Excretory cell canal lengths were scored in L4 or young adult animals carrying integrated Ppgp-12::gfp transgene (sIs10089) or Ppgp-12::gfp expressed from an extrachromosomal array (mamEx11 or mamEx29).Posterior canals were scored as wild type when they reached the region between the inner edge of the posterior gonadal turn and the rectum.Shortened canal phenotype was graded according to the region within the worm body the canal reached.The following landmarks were used for each category: 0 -excretory canal missing entirely or reaching the inner edge of anterior gonadal turn; 1 -canal reaching anterior spermatheca; 2 -canal reaching vulva; 3 -canal reaching posterior spermatheca; 4 -canal reaching inner edge of posterior gonadal turn; and 5 -canal reaching rectum (wild type).Canals that overgrew the rectum and reached the tail tip were scored as 6.Anterior excretory cell canals were measured and their length normalized to the measured distance between the posterior edge of the pharynx and the nose tip.For the assessment of posterior canal extension dynamics, larval excretory cell posterior canals were measured at four developmental stages (hatch, 4, 8, and 24 hr after hatching) and normalized to the animal body length.For microscopy imaging, worms were anaesthetized either with 10 mM sodium azide or 1 mM levamisol and mounted on 3% agarose pads.Images were taken on Leica DM6 upright microscope.For confocal imaging, Zeiss LSM880 confocal microscope was used.The EGL-20/Wnt gradient was visualized in L2/L3 animals using a spinning disc microscopy setup, based on a Nikon Eclipse Ti2 equipped with a Yokogawa CSU-W1 scan head, 50 um pinhole disc, 488 nm laser, Teledyne Photometrics PRIME BSI camera, ×60 W NA1.2 objective, and operated with NIS Elements.For each animal, a z-stack of 31 slices, dz = 1 μm was acquired.Imaging was done at room temperature (22-23°C).Images were processed with the Fiji image processing package (Schindelin et al., 2012).For EGL-20 gradient quantification, a maximum projection of seven consecutive z-sections where the rectal epithelial cells were visible was made for each sample.A curved line of 150 μm in length and 3.9 μm in width was fitted through the ventral side of each animal using the rectum as the starting point and the selected region was straightened using the 'Straighten' function in Fiji.To count the number of EGL-20 puncta in these selections, images were blinded and the puncta were manually counted.Counting was repeated three times and the values for each image were averaged.These averaged values were then plotted and used for statistical evaluation.For mean pixel intensity calculations, a Gaussian blur (sigma = 3) was applied to the straightened images.Subsequently, a single segmentation threshold was determined from a representative wild type image by using the 'graythresh' inbuilt function in MATLAB (which uses the Otsu method).This threshold was multiplied by 1.7 (a factor that was determined manually) to generate a mask that segments only bright EGL-20 spots.Using the derived threshold, a binary mask was made for all images.Using this mask, the mean pixel intensity of all pixels inside the segmented EGL-20 spots was computed.Statistical analyses were performed either in GraphPad Prism or in Excel equipped with the Real Statistics Resource Pack software (Release 7.6;Zaiontz, 2021).

Materials availability
Strains and plasmids generated in this study are available upon reasonable request from academic researchers.
FK, Czech Science Foundation grant 16-17966Y to MM, Lumina quaeruntur grant LQ200522301 of the Czech Academy of Sciences to TCM, and Charles University programme SVV 260559.Microscopy was performed in the Vinicna Microscopy Core Facility co-financed by the Czech-BioImaging large RI project LM2023050.The authors acknowledge the Imaging Methods Core Facility at BIOCEV, institution supported by the MEYS CR (LM2023050 Czech-BioImaging), for their support and assistance on the spinning disc imaging done in this work.Computational resources were supplied by the project 'e-Infrastruktura CZ' (e-INFRA LM2018140) provided within the program Projects of Large Research, Development and Innovations Infrastructures.The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

Figure 1 .
Figure 1.Loss of sel-5 potentiates QL migration defect in retromer and Wnt pathway mutants.(A) QL neuroblast lineage and a cartoon indicating the position of terminally differentiated neurons (depicted with empty circles).(A has been adapted from Figure 1 of Rella et al., 2016.)The aberrant position of PVM neuron, as observed in QL.d migration defect, is highlighted in magenta.(B) RNAi against sel-5 increases the penetrance of vps-29 QL.d migration defect compared to the control (L4440) RNAi.No defect is observed in wild type background.(C) PVM position in L2 larvae of control (transgene only) and sel-5 vps-29 double mutant animals.PVM position indicated with white arrowhead, neurons visualized by expression of Pmec-7::gfp transgene muIs32, scale bar represents 100 μm.(D) Mutation in sel-5 results in increased penetrance of QL.d migration defect of vps-29 and lin-17, but not mig-1 mutants.(E) Examples of mild and severe alteration of tail tip morphology in sel-5 vps-29 double mutants.(F) Shortened transcripts are produced from the sel-5 locus in both ok363 and ok149 alleles.Potential protein products resulting from these transcripts are depicted, showing the impact of the truncation on the kinase domain (dark grey box).Extra amino acids resulting from a frameshift and thus not present in the wild type protein are also depicted (light grey box).The position of the active site is indicated.For (B) and (D), results are shown as % of WT and QL.d animals.Fisher's exact test was performed to assess the difference between the samples.Bonferroni correction for multiple testing was applied.For (B), a representative RNAi experiment is shown, n > 55 per condition, *p-value<0.02,additional experiments provided in Figure 1-figure supplement 1.For (D), data combined from three independent experiments are shown, n > 150 animals in total for each strain, **p-value<0.002,***p-value<0.0002,ns, not significant.The online version of this article includes the following source data and figure supplement(s) for figure 1: Source data 1.Source gel for Figure 1.

Figure supplement 1 .
Figure supplement 1.Additional examples of RNAi against sel-5 in wild type and vps-29 background.

Figure 2 .
Figure 2. SEL-5 is expressed in multiple tissues and is required cell non-autonomously for QL.d migration.(A) Transgenic rescue of the QL.d migration defect.sel-5 was expressed under the control of various promoters from an extrachromosomal array in sel-5 vps-29; muIs32 background and the effect of such expression on QL.d migration was quantified.Comparison was made between animals carrying the transgene and their siblings which have lost the transgenic array.The expression of each transgene in the expected tissue is shown on the right.Results are shown as % of WT and QL.d animals, data are combined from three independent experiments, n > 100 animals in total for each condition.Fisher's exact test was performed to assess the difference between the samples.Bonferroni correction for multiple testing was applied, ***p-value<0.0001,ns, not significant.Results from additional independent transgenic strains are provided in Figure 2-figure supplement 1. (B) GFP expression driven by an endogenous sel-5 promoter in the gonad of L1 and adult animals.(C) Expression of GFP::SEL-5 fusion protein driven by endogenous sel-5 promoter in various larval and adult tissues.Localized GFP::SEL-5 expression is indicated by white arrowheads, white arrows point to autofluorescent signal from gut granules.The scale bar represents 20 μm in (A-C).The online version of this article includes the following figure supplement(s) for figure 2:Figure supplement 1. Transgenic rescue of the QL.d migration defect.

Figure 3 .
Figure 3. SEL-5 alters the phosphorylation status of DPY-23 but does not affect MIG-14 levels.(A) The level of DPY-23 phosphorylation at position T160 is reduced in sel-5 mutant animals.Phosphorylation was detected by western blot analysis in lysates from a population of L4/young adults of indicated strains using phospho-specific antibody against human AP2M1.Band intensities were normalized to an alpha tubulin loading control and compared to the control sample (sample/control ratio indicated below each lane).A representative Western blot example is shown on the left, relative quantification of four independent experiments is shown on the right.(B) Level of DPY-23::GFP phosphorylation is reduced in sel-5 mutants.Phosphorylation at T160 of GFP-tagged DPY-23 was detected by western blot analysis in lysates from a population of L4/young adults using phospho-specific antibody against human AP2M1.Strains expressing either no GFP fusion protein or a GFP-tagged DPY-23T160A mutant protein were included as controls.Band intensities were normalized to a GFP signal intensity and compared to the control sample (DPY-23::GFP in wild type background), sample/control ratio is indicated below each lane.A representative western blot example is shown on the left, relative quantification of three independent experiments is shown on the right.(C) L2/L3 animals expressing MIG-14::GFP from the huSi2 transgene were imaged using a confocal microscope.The posterior part of the body with Wnt-expressing cells is shown.Images are maximum projections of four consecutive z-sections taken at 0.3 μm interval.Anterior to the left, dorsal up, scale bar represents 20 μm.(D) Western blot analysis of MIG-14::GFP levels expressed from a huSi2 transgene in various mutant backgrounds.MIG-14::GFP was detected in lysates from synchronized populations of L1 larvae of the indicated strains.Band intensities were normalized to an alpha tubulin loading control and compared to the control sample (sample/control ratio indicated below each lane).A representative western blot example is shown on the left, relative quantification of five independent experiments is shown on the right.In (A, B, D), error bars represent mean ± s.d., statistical significance was assessed by unpaired two-tailed Student's t-test for samples with unequal variance, *p-value<0.05,**p-value<0.01,***p-value<0.001,ns, not significant.Source data for (A, B, D) provided in Figure 3-source data 1.

Figure 3
Figure 3 continued on next page The online version of this article includes the following source data and figure supplement(s) for figure3:Source data 1.Source blots for Figure3.

Figure 3 Figure 4 .
Figure3 continued Figure 5. SEL-5 kinase activity and DPY-23 phosphorylation are not required for QL.d migration.(A) Transgenic rescue of the QL.d migration defect with kinase-inactive SEL-5.D178A or K75A SEL-5 mutant protein was expressed from egl-20 promoter in sel-5 vps-29; muIs32 mutant background from an extrachromosomal array and the QL.d migration defect was quantified in animals carrying the transgene and their siblings which have lost the transgenic array.Results are shown as % of WT and QL.d animals, data are combined from three independent experiments, n > 100 animals in total for each condition.Fisher's exact test was performed to assess the difference between the samples.Bonferroni correction for multiple testing was applied, ***p-value<0.0001.Results from additional independent transgenic strains are provided in Figure 5-figure supplement 2. (B) DPY-23 phosphorylation at position T160 is absent in dpy-23(mew25) mutant animals.Phosphorylation was detected by western blot analysis in lysates from a population of L4/ young adults of indicated strains using phospho-specific antibody against human AP2M1.Band intensities were normalized to an alpha tubulin loading control.(C) dpy-23(mew25) rescues the 'jowls' phenotype (white arrow) of fcho-1(ox477) animals.Heads of adult animals are shown, anterior to the left, the scale bar represents 10 μm.(D) The absence of DPY-23 T160 phosphorylation does not result in QL.d migration defect.The presence of dpy-23(mew25) allele carrying T160A substitution either alone or in combination with sel-5 does not significantly contribute to the QL.d migration defect.Results are shown as % of WT and QL.d animals, data combined from at least three independent experiments are shown, n > 180 animals in total for each strain.Fisher's exact test was performed to assess the difference between the samples, **p-value<0.01.(E) MIG-14::GFP does not relocalize to the plasma membrane in dpy-23(mew25) animals.L3 animals expressing MIG-14::GFP from the huSi2 transgene were imaged using a confocal microscope.The posterior part of the body with Wnt-expressing cells is shown.Images are maximum projections of five consecutive z-sections taken at 0.3 μm interval.Anterior to the left, dorsal up, the scale bar represents 20 μm.Source data for (B) provided in Figure 5-source data 1.The online version of this article includes the following source data and figure supplement(s) for figure 5: Source data 1.Source blots for Figure 5.

Figure supplement 1 .
Figure supplement 1.Sequence alignment of the kinase domain of SEL-5 and human AAK1.

Figure 6 .
Figure 6.sel-5 cooperates with the retromer complex to regulate the length of excretory cell canals.(A) Posterior canals of the excretory cell are significantly shortened in sel-5 vps-29 mutants.The excretory cell was visualized by Ppgp-12::gfp expression from a mamEx11 transgene.The scale bar represents 200 μm.(B) Quantification of posterior canal outgrowth defects.The outgrowth of the posterior canal of the excretory cell was quantified by dividing the region between the posterior bulb of the pharynx to the tip of the tail into seven segments.The percentage of canal arms terminating Figure 6 continued on next page

Figure 7 .
Figure 7. Wnt pathway components determine the length of the posterior excretory canal.(A) Posterior canals of the excretory cell overgrow into the tip of the tail in lin-17 mutants.The excretory cell was visualized by Ppgp-12::gfp expression from the sIs10089 transgene.Boxed areas are magnified in the bottom row, scale bare represents 200 μm.(B) Quantification of posterior canal outgrowth in Wnt pathway mutants.Canal outgrowth was scored and statistically evaluated as in Figure6Band a comparison was made either to the control strain (sIs10089 only) or to the more severe single mutant in the case of double mutant strains.All strains contained the sIs10089 transgene to visualize excretory canals except for lin-17; sel-5 and lin-44; sel-5 which contained mamEx11, and mig-5, which contained mamEx29.† Differences not significant.‡ Full genotype was mig-5(cp385[mNG-GLO^AID::mig-5]); mamEx29; mamEx34[eft-3p::TIR::mRuby; myo2p::tdTomato] and animals were grown on NGM plates with 1 mM auxin from L1 till L4/young adult stage.Only animals containing the mamEx34 array were used for analysis.(C) Three branches of the posterior canal were detected in cwn-1; cfz-2 animals.The excretory canal was visualized by the sIs10089 transgene, the scale bar represents 200 μm.(D) Posterior excretory canals display normal length during early larval development.The dynamics of posterior canal outgrowth in lin-44, lin-17, and mig-14 mutants was assessed by measuring the canal length and normalizing it to the total body length at hatching and at three time points during early larval development.Results are presented as mean + s.d. of at least 30 measured canals.Comparison between samples assessed by unpaired two-tailed Student's t-test did not reveal any significant differences.

Figure 8 .
Figure 8. Model summarizing the inputs acting in the excretory cell outgrowth.(A) Three possible outcomes of the canal outgrowth depending on the genetic background.(B) Model summarizing the role of Wnt pathway components, sel-5, and the retromer in the outgrowth of the excretory cell posterior canals.Only players discussed in this work are depicted.First, the active outgrowth of the posterior canals is controlled by sel-5, retromer, and the Wnt pathway consisting of cwn-1, cwn-2, and cfz-2.It remains to be determined whether these players act sequentially, in parallel or as components of a single pathway.After reaching the proper length, further canal extension is inhibited by a second Wnt signalling pathway governed by lin-44, lin-17, dsh-1, and mig-5.Lastly, egl-20 and mig-1 might fine-tune the precise stopping position of the growing canal.

Table 1 .
Phenotypes of sel-5 and vps-29 single and double mutants.
† % of animals with axons of one or both PLM neurons reversed, n > 60. ‡ % of CAN neurons located anteriorly of V3 seam cell, n > 40.§ % of animals with one or both phasmid sensilla not dyed with DiI, n > 40.¶ Average number of progeny from five hermaphrodites,± s.d.
Addgene_19328]) as PCR templates to amplify PH domain and mCherry, respectively.Sequences of all primers used for plasmid vector construction are listed in Supplementary file 2. To create extrachromosomal arrays, constructs were microinjected into distal gonads of young adults using Leica DMi8 inverted microscope equipped with DIC filters and InjectMan 4 and FemtoJet 4i microinjection system (Eppendorf).Microinjection mixtures contained 10 ng/μL of the plasmid of interest, 5 ng/μL Pmyo-2::tdTomato as a co-injection marker, and 135 ng/μL pBluescript as a carrier DNA.CRISPR/Cas9 SEC knock-in method