We developed strategies to study Ci expressed at physiological levels from ‘genomic ci’ transgenes (gCi) and CRISPR-engineered ci alleles (crCi). The former strategy used a 16 kb genomic region of ci that included upstream and downstream regulatory regions (Figure 1A) previously used within a second chromosome P-element insertion to rescue ci null animals (Méthot and Basler, 1999), inserted into an att site on the third chromosome (Garcia-Garcia et al., 2017). A gCi-WT transgene was readily able to rescue homozygous ci null (ci⁹⁴) animals to adulthood, with normal morphology, and behaved almost like a normal ci allele but with marginally lower ci expression and activity in wing discs (Figure 1C,G). We created gCi variants using this strategy.

Figure 1

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We also created mutant ci alleles by using CRISPR in two rounds: in the first round, we put a mini-white marker gene in the first intron of ci (Figure 1A’); in the second round, we selected against the mini-white gene and introduced our mutation of interest, replacing the DNA between the first intron and the 3’UTR by homologous recombination (Figure 1A”). A single copy of crCi-WT in combination with ci⁹⁴ resulted in efficient development of normal adults and larval wing discs with normal patterns of En, ptc-lacZ and Ci-155 expression in the anterior compartment (Figure 1D,H).

During these studies, we also became aware of an artifact, whereby low levels of ptc-lacZ product were detected sporadically in posterior cells of wing discs when there was a single ci⁹⁴allele; this occurred in flies with a normal ci allele (on the Dp(y⁺) ‘balancer’) (Figure 1E) or with the crCi-WT allele (Figure 1D). The artifact was also seen with gCi-WT when ci⁹⁴ was heterozygous (data not shown) but not when ci⁹⁴ was homozygous (Figure 1C) or when crCi-WT was homozygous (Figure 1B). We sequenced the relevant region of the ci⁹⁴ allele and confirmed that it was the same deletion originally reported (Méthot and Basler, 1999; Slusarski et al., 1995) and in FlyBase. We also induced homozygous ci⁹⁴ clones (by FRT-mediated recombination to remove a second chromosome genomic ci transgene) and confirmed that ci⁹⁴ encoded no detectable Ci-155 protein (data not shown). Thus, despite the observed sporadic expression of ptc-lacZ in posterior cells in some genetic backgrounds, we are confident that the activity of Ci variants can be assayed in anterior wing disc cells in a null background under physiological conditions using either crCi alleles or gCi transgenes.

PKA phosphorylates Ci-155 at amino acids S838, S856, and S892 to create recognition sites for both GSK3 and CK1, which further phosphorylate Ci-155 at a consecutive series of primed phosphorylation sites (Smelkinson and Kalderon, 2006; Smelkinson et al., 2007). The phosphorylation series creates a binding site for Slimb that includes the core peptide pSpTYYGpS₈₄₉MQpS, spanning residues 844–852. Ci-S849A lacks the last CK1 target site initially primed by PKA phosphorylation of S838 and Ci-P(1-3)A has alterations to all three PKA sites (S838A, S856A, and S892A). Ci fragments with those alterations showed complete loss of Slimb binding in vitro after phosphorylation by PKA, CK1 and GSK3, while UAS-Ci transgene products with those changes showed no processing in wing discs, judged by a sensitive assay of repressor function in posterior compartment wing disc cells (Smelkinson and Kalderon, 2006; Smelkinson et al., 2007). The activity of these proteins has not previously been measured under physiological conditions. We therefore used ci alleles with those alterations to determine how loss of processing affects Ci protein levels and activity at normal physiological levels.

The wing discs of animals with crCi-S849A or crCi-P(1-3)A in combination with ci⁹⁴ had expanded anterior regions (Figure 2A–D), as expected because Ci-75 repressor, normally produced from Ci-155 processing, is required to silence dpp expression in anterior cells and ectopic anterior Dpp induces anterior growth (Méthot and Basler, 1999). We also found that these wing discs had strongly elevated Ci-155 levels throughout the anterior, indicating that full-length Ci-155 was not being processed in the absence of the Hh signal, as expected (Figure 2A–D; Figure 2—figure supplement 1A–D,G,H).

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Although normal wing discs have a clear stripe of elevated Ci-155 at the AP border relative to anterior cells (Figure 2A), Ci-155 levels actually decline over the posterior half of the AP border (Figure 2G) in a manner that depends on strong activation of the Hh pathway (Ohlmeyer and Kalderon, 1998; Strigini and Cohen, 1997). Although Ci-155 protein levels were strongly elevated compared to normal for Ci-S849A and Ci-P(1-3)A in anterior cells, there was a sharp decline toward the posterior of AP border territory (Figure 2H,I; Figure 2—figure supplement 1A–D,G,H). This profile represents the gradient of Hh-stimulated Ci-155 loss that has generally been attributed to full degradation. It has not previously been seen in isolation because it is normally super-imposed on an unknown profile due to inhibition of Ci processing for wild-type Ci (Figure 2K). Moreover, if the observed pattern of Ci-155 reduction is the same for wild-type Ci (see later), we can subtract this profile from the observed Ci-155 profile of wild-type Ci to deduce a profile of wild-type Ci-155 processing (Figure 2L). The result shows that the inhibition of Ci-155 processing is graded, with a spatial profile broadly similar to that of ptc-lacZ activation, but with a slightly higher sensitivity to low levels of Hh (Figure 2L). Thus, comparison of the Ci-155 profiles of wild-type and processing-resistant variants provided the best evidence to date of the spatial patterns of graded inhibition by Hh of Ci-155 processing (Figure 2L) and of graded, Hh-promoted Ci-155 loss at the AP border (Figure 2H,I,K).

We also created a ci allele, Ci∆1270–1370, resembling a C-terminal deletion variant that had previously been found not to undergo processing in assays using cultured cells and UAS-Ci transgenes in wing discs (Wang and Price, 2008; Zhou and Kalderon, 2010). Ci∆1270–1370 also had uniformly elevated Ci levels in anterior wing disc cells, consistent with a lack of processing (Figure 2E,J; Figure 2—figure supplement 1E). However, unlike Ci-S849A and Ci-P(1-3)A, this Ci variant induced ptc-lacZ and En only weakly at the AP border (Figure 2A–E,G–J; Figure 3A–C; Figure 2—figure supplement 1P; Figure 2—figure supplement 2E). There was also no decline of Ci-155 protein within AP territory (Figure 2J,K), consistent with prior evidence that Hh-stimulated Ci-155 reduction, visualized clearly with the other processing-resistant Ci variants, is only observed at high levels of Hh signaling.

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To study Hh-promoted Ci-155 reduction further we created an allele encoding a Ci variant with compromised Rdx/Hib binding. Rdx/Hib binds to Ci-155 through multiple sites; altering three principal binding regions (designated S3,4,5 in the cited study) through clustered point mutations rendered the altered Ci-155 (‘Ci-S3-5’) largely insensitive to Rdx/Hib in a tissue culture assay (Zhang et al., 2009). We found that animals expressing one copy of crCi-S3-5 (in combination with ci⁹⁴) developed efficiently into adults with normally patterned wings (data not shown). In larval wing discs, the peak of ptc-lacZ expression was slightly elevated at the AP border compared to normal but the domain of induction of En (a high-level Hh target) was not expanded (Figure 2F; Figure 2—figure supplement 1F,I,M–O). The Ci-155 profile included low anterior levels, suggesting normal processing, and declined in the posterior regions of the AP border much like wild-type Ci-155, showing that Hh-stimulated Ci-155 reduction remained robust (Figure 2F; Figure 2—figure supplement 1I,L). The properties of Ci-S3-5 suggest that direct action of Rdx/Hib on Ci-155 does not account for a significant fraction of the reduction of Ci-155 stimulated by the highest levels of Hh signaling. Previous studies have not specifically tested only the direct effects of Rdx/Hib on Ci-155 in wing discs; some studies found that elimination or reduction of Rdx/Hib activity increased Ci-155 levels (Kent et al., 2006; Zhang et al., 2006), while others found no change in Ci-155 levels in the posterior half of the AP border region (Seong et al., 2010; Seong and Ishii, 2013).

Suppressor of fused (Su(fu)) may participate in the Hh-stimulated reduction of Ci-155 at the AP border, potentially in more than one way. It has been found that Rdx/Hib indirectly reduces Su(fu) protein levels at the AP border (Liu et al., 2014) and it has been suggested that Su(fu) competes with Rdx/Hib for Ci-155 binding (Zhang et al., 2006). It has also been shown that loss of Su(fu) leads to greatly reduced Ci-155 levels, presumed to be due to enhanced degradation of Su(fu)-free Ci-155, throughout the wing disc (Ohlmeyer and Kalderon, 1998) and it has been conjectured that Hh may activate Ci-155 in part through Su(fu) dissociation from Ci-155, as suggested by studies of Gli activation (Humke et al., 2010; Lee et al., 2016; Tukachinsky et al., 2010).

We examined Ci-155 AP border profiles for wild-type Ci and Ci-S3-5 in the absence of Su(fu). The two profiles were extremely similar; Ci-155 levels appeared to peak at, or very close to the AP compartment boundary, suggesting little or no Hh-stimulated loss (Figure 2—figure supplement 1J–L). The results are consistent with the hypothesis that Su(fu) is a key factor in the regulation of Hh-stimulated Ci-155 reduction at the AP border. This role of Su(fu) was apparent even in the absence of normal Rdx/Hib binding to Ci-155, suggesting that Su(fu) is not acting principally by competing with Rdx/Hib for Ci-155 binding.

Remarkably, the pattern of En and ptc-lacZ induction at the AP border was normal for Ci-S849A and Ci-P(1-3)A (Figure 3A–C; Figure 2—figure supplement 1P), showing that Ci-155 processing is not essential for dose-dependent induction of these Hh target genes. The unchanged profile of pathway activity suggests that the profile of pathway-induced Ci-155 reduction is also likely to be the same for wild-type Ci and processing-resistant Ci variants, supporting the validity of using the latter profile to deduce the processing pattern of wild-type Ci-155 (Figure 2L).

Ci-S849A and Ci-P(1-3A) wing discs expressed dpp ectopically in anterior cells, as expected from the absence of Ci-75 repressor (Figure 2—figure supplement 2A,B). The expanded anterior regions of these wing discs are likely responsible for the failure to recover adults expressing only processing-resistant Ci variants, precluding analysis of adult wing patterning. The addition of a ci^Ce allele, which encodes a constitutive repressor form of Ci (and no activator) (Méthot and Basler, 1999; Slusarski et al., 1995), restored normal wing disc morphology without significantly affecting ptc-lacZ expression at the AP border (Figure 2—figure supplement 2C,D) and allowed recovery of adults.

Normal wing morphology depends on long-range patterning elicited by the central stripe of Hh-induced Dpp and on creation of a central inter-vein region between veins 3 and 4 by stronger Hh signaling, sufficient to induce the transcription factor Collier, also known as Knot (Mohler et al., 2000; Vervoort, 2000; Vervoort et al., 1999). The adult wing phenotypes of animals with one copy of gCi-WT or gCi-S849A in a ci⁹⁴/ci^Ce background were similar to each other, with a consistent moderate pinching between veins 3 and 4 (Figure 3G,H), although some animals with gCi-S849A also showed a greater narrowing of the inter-vein region (Figure 3I). We then tested the activity of a gCi transgene together with a crCi allele in trans to ci^Ce. We found that wing morphology was absolutely normal for flies with both gCi and crCi encoded wild-type Ci or when both encoded processing-resistant Ci-S849A (Figure 3J–L). Hence, we conclude that Hh can fulfill its normal morphogenetic function, culminating in a normally patterned wing in the complete absence of regulated Ci-155 processing.

Fu can be activated synthetically in the absence of Hh stimulation by overexpression of Fu variants with either a membrane-targeting tag (GAP-Fu) or acidic residue replacements of phosphorylation sites key to normal activation (Fu-EE) (Claret et al., 2007; Zhou and Kalderon, 2011). Activated Fu can partially activate Smo (Claret et al., 2007; Sanial et al., 2017) but direct downstream, Smo-independent actions can be measured by assaying responses in smo mutant anterior clones expressing Fu-EE or GAP-Fu. Previously, such experiments showed that activated Fu alone was sufficient to elicit strong Hh target gene induction, suggesting that Ci-155 activation can be effective even without the normal inhibition of processing that occurs at the AP border (Zhou and Kalderon, 2011). Fu kinase activity is not required for Hh to block Ci-155 processing at the AP border (Alves et al., 1998; Ohlmeyer and Kalderon, 1998; Zadorozny et al., 2015). Nevertheless, synthetically activated Fu was observed to increase Ci-155 levels in anterior clones and further tests suggested this likely resulted from partial inhibition of Ci-155 processing mediated by Cos2 phosphorylation (Zhou and Kalderon, 2011).

To clarify the dependence of Ci-155 activation by Fu on Ci-155 processing inhibition we compared the activities of wild-type and processing-resistant Ci variants in smo mutant clones expressing activated GAP-Fu. We found that Ci-S849A or Ci∆1270–1370, provided by a single crCi allele in trans to ci⁹⁴, mediated ptc-lacZ induction in anterior smo GAP-Fu clones to the same level as at the AP border, whereas induction mediated by a single wild-type crCi allele was much lower (about 50%) (Figure 4A–D,J). In each case, the activity in clones was compared to the AP border of the same wing discs and reflects the activity of the same source of Ci. Similar results were seen in GAP-Fu clones that retained a functional smo allele, with ptc-lacZ induction of the three processing-resistant variants (Ci-S849A, Ci-P(1-3)A, and Ci∆1270–1370) greatly exceeding that of wild-type Ci (Figure 4F–I,K). Thus, Hh target gene induction by Fu kinase alone was quite weak in the presence of a single wild-type ci allele and was substantially increased if Ci-155 processing was also inhibited. The observed increase could in principle be due to an increased supply of Ci-155 or loss of Ci-75 repressor, or both. When slightly lower levels of wild-type Ci protein were provided by a single gCi transgene instead of a cr-Ci allele, GAP-Fu induced significantly lower levels of ptc-lacZ (Figure 4J), suggesting that the supply of Ci-155 is a key factor. Thus, producing a robust supply of Ci-155 that is not substantially diminished by processing to Ci-75 is important for Fu to elicit high Ci-155 activity. This dependence was highlighted by using only a single functional ci allele and by assaying synthetically activated Fu in anterior cells.

Figure 4

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The Ci-155 levels detected within smo GAP-Fu clones were much lower than in surrounding territory in wing discs expressing processing-resistant Ci variants (Figure 4A,B,D,J). The reduction in Ci-155 was similar in magnitude to that observed in posterior regions of the AP border and presumably reflects Ci-155 reduction due to high Hh pathway activity. By contrast, wild-type Ci-155 levels were elevated in smo GAP-Fu clones relative to neighboring cells. Since ptc-lacZ in these clones was significantly lower than at the AP border (Figure 4C,J) there is likely little or no reduction in Ci-155 due to high pathway activity. The fact that Ci-155 clone levels were lower than maximal AP border Ci-155 levels for wild-type Ci (Figure 4C) therefore indicates that GAP-Fu does not inhibit processing to the same degree as Hh inhibits processing at the AP border. Thus, although the absolute steady-state levels of Ci-155 for Ci-WT and Ci-S849A in smo GAP-Fu clones were quite similar (Figure 4J), Ci-155 accumulation was limited by largely different mechanisms; significant continued processing for Ci-WT and pathway-stimulated loss for Ci-S849A.

In summary, activation of Ci-155 by Fu to produce high levels of Hh target gene expression also requires provision of high levels of primary Ci-155 translation product that is protected from processing. The elevated Ci-155 supply produced by processing-resistant Ci variants is, however, not directly evident from measurement of steady-state Ci-155 levels because of subsequent, robust Ci-155 loss in response to high pathway activity. Even though steady-state Ci-155 levels are similar for Ci-WT and Ci-S849A, the proportion of Ci-155 molecules that are active is presumably higher for Ci-S849A in GAP-Fu clones.

It was previously appreciated that Cos2, PKA and Slimb are all necessary for Ci-155 processing but that induction of Hh target genes was higher in anterior cos2 and pka mutant clones than in slimb mutant clones (Jiang and Struhl, 1998; Smelkinson et al., 2007; Wang et al., 1999). Loss of PKA also increased ptc-lacZ induction in slimb mutant clones (Smelkinson et al., 2007). These observations suggested that PKA and Cos2 inhibit Ci-155 activity in addition to promoting Ci-155 processing, with the potential reservations that the slimb alleles used in some tests may not have fully blocked Ci-155 processing or that Slimb may have additional relevant actions that reduce Ci-155 activity. The effect of PKA loss on the activity of processing-resistant UAS-Ci transgenes has also been investigated previously but the transgenes were expressed at non-physiological levels and such transgenes do not support normal Hh responses at the AP border (Smelkinson et al., 2007; Garcia-Garcia et al., 2017).

To test the effects of PKA and Cos2 on the activity of processing-resistant Ci-155 expressed at physiological levels, we induced pka or cos2 clones in wing discs expressing Ci-P(1-3A) from a single allele in combination with ci⁹⁴. We found that in both types of clone, there was a marked increase of ptc-lacZ expression compared to surrounding tissue (Figure 5B,C,I,L) and compared to clones with no change in PKA or Cos2 activities (Figure 3F). The level of ptc-lacZ induced was found to be about 75% (pka clones) or 50% (cos2 clones) of AP border levels in the same wing discs (Figure 5L). The levels of ptc-lacZ induced in equivalent clones in wing discs expressing one allele of wild-type Ci were very similar (Figure 5A,H,L), indicating that the activity of Ci-P(1-3A) reflected the normal response of wild-type Ci to loss of PKA or Cos2 and hence that the three PKA sites that are key for processing (P1-3) are not required for the regulation of Ci-155 activity by PKA or Cos2.

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Induction of ptc-lacZ was substantially lower for pka mutant clones expressing wild-type Ci from a gCi transgene rather than from a cr-Ci allele (Figure 5F,L), showing that Ci-155 activity elicited by loss of PKA depends on Ci-155 levels. This dependence was previously shown by comparing wild-type animals and ci heterozygotes, and it was further shown that Hh target gene induction depended on the relative stoichiometry of Ci-155 and Su(fu), suggesting the hypothesis that only Su(fu)-free Ci-155 is active in pka mutant clones (Ohlmeyer and Kalderon, 1998). In all cases (pka or cos2 mutant clones, Ci-WT or Ci-P(1-3A), gCi-WT or crCi-WT), the levels of Ci-155 in clones matched or exceeded the highest levels at the AP border, suggesting little or no loss of Ci-155 due to high pathway activity. Indeed, activity in pka and cos2 clones may depend on Ci-155 levels exceeding the inhibitory capacity of Su(fu). No such requirement is expected in GAP-Fu clones because Fu can relieve inhibition by Su(fu). Thus, in contrast to the situation with GAP-Fu clones, the contribution to activity of a robust supply of Ci-155 that is not processed is reflected in elevated steady-state Ci-155 levels. In summary, the results for Ci-P(1-3A) clearly indicate that PKA and Cos2 inhibit the activity of Ci-155 that is not processed in the absence of Hh stimulation. The magnitude of inhibition is substantial.

Surprisingly, ptc-lacZ induction by Ci-S849A was not clearly higher in pka or cos2 mutant clones than in surrounding cells (Figure 5D,G,J). Quantitation revealed that this was largely due to significant ptc-lacZ expression in heterozygous tissue surrounding the clones (Figure 5L). Similar, low levels of ptc-lacZ activity were observed also for Ci-S849A, but not Ci-WT or Ci-P(1-3A), in clones with normal PKA and Cos2 activity (Figure 3D–F). These results suggest that S849 is relevant to the regulation of Ci-155 activity by PKA and Cos2.

Ci∆1270–1370, which is also not subject to processing, did not induce ptc-lacZ in wild-type anterior cells (Figure 2E,J; Figure 2—figure supplement 2E) or in pka/+ or cos2/+ cells and was not strongly activated by loss of PKA or Cos2, producing ptc-lacZ expression significantly lower than Ci-WT (Figure 5E,K,L). Ci∆1270–1370 also has lower activity than Ci-WT at the AP border of wild-type discs (Figure 2E,J), but it is strongly activated by GAP-Fu (Figure 4B,I–K). Based on these observations and the hypothesis that PKA and Cos2 primarily inhibit Su(fu)-free Ci-155, we speculate that Ci∆1270–1370 may be inhibited more strongly than wild-type Ci by Su(fu), so that release from PKA and Cos2 inhibition is without effect and full relief from Su(fu) inhibition is achieved only by artificially strong GAP-Fu activation and not by normal Fu activation at the AP border.

To investigate how Cos2 silences Ci-155 activity, we further examined the interactions between these proteins. Cos2 can bind to Ci-155 through three regions defined by in vitro binding assays: the CDN region (residues 346–440), the zinc fingers (residues 506–620) and the CORD domain (residues 934–1065) (Wang and Jiang, 2004; Zhou and Kalderon, 2010). Measurement of processing through Ci-155 levels and generation of repressor activity from UAS-Ci transgenes in wing discs previously showed that processing was absent only when the zinc finger and CORD domains were both removed (Zhou and Kalderon, 2010). To test whether Cos2-binding domains might be responsible for inhibiting Ci-155 activity we generated ci alleles lacking CDN, CORD or both regions. There are no known alterations to the zinc-finger region that affect Cos2 binding without compromising DNA binding and hence transcriptional activity of Ci-155.

We induced pka and cos2 clones in wing discs expressing only Ci∆CORD, Ci∆CDN or Ci∆CDN∆CORD. The level of ptc-lacZ in pka mutant clones was similar for wild-type Ci and Ci∆CDN but it was significantly higher for Ci∆CORD and Ci∆CDN∆CORD; it was also higher for Ci∆CORD than Ci-WT expressed from a gCi transgene (Figure 6A–F,K). These results indicate that the presence of the CORD domain reduces Ci-155 activity when Ci-155 is not processed in a pka mutant clone, while the CDN domain appears to have no impact on Ci-155 activity. By contrast, ptc-lacZ levels in cos2 mutant clones were very similar for Ci∆CORD, Ci∆CDN, Ci∆CORD∆CDN, and Ci-WT (Figure 6G–K). The simplest interpretation of these results is that Cos2 inhibits Ci-155 by binding to the CORD domain and that deletion of either the CDN or CORD domain does not affect any significant Ci-155 property other than binding to Cos2. Thus, in clones where Ci-155 is not processed the activity of Ci-155 is increased by loss of either Cos2 or the CORD domain but loss of the CORD domain cannot activate Ci-155 further in a cos2 mutant clone. Moreover, the greater activity of Ci lacking the CORD domain in pka clones than in cos2 clones shows that Ci-155 activation by loss of PKA activity and loss of Cos2-CORD binding can be additive.

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In wing discs with no additional alterations, Ci∆CORD, Ci∆CDN, and Ci∆CORD∆CDN all supported a near-normal Ci-155 profile, indicating substantially normal regulation of Ci-155 processing, and strong ptc-lacZ expression confined to the AP border (Figure 7A–D). There was a slight enhancement of anterior Ci-155 levels for Ci∆CORD, which was also evident in a pka heterozygous background (Figure 6B) and in a Su(fu) mutant background (Figure 7—figure supplement 1A,C). That may indicate a mild processing deficit. However, there was a very strong contrast between low anterior and high AP border Ci-155 levels of Ci∆CORD∆CDN (Figure 6D; Figure 7D), supporting previous evidence that Ci-155 lacking both these Cos2-binding domains is processed very efficiently, perhaps even more efficiently than wild-type Ci, and that Hh blocks processing efficiently (Zhou and Kalderon, 2010). The experiments reported here, using Ci variants expressed at physiological levels, revealed a dependence on the Cos2-binding CORD domain for inhibiting Ci-155 activity that is not observed for Ci-155 processing or regulation of processing by Hh.

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The absence of ectopic anterior ptc-lacZ in wing discs expressing Ci∆CORD (Figure 7B,D) suggests that loss of Cos2-CORD association only leads to Ci-155 activity when Ci-155 processing is also inhibited. To test this hypothesis further, we created an allele expressing a processing-resistant Ci variant (S849A) that also lacked the CORD domain. We found that, unlike Ci∆CORD, Ci-S849A∆CORD in combination with ci⁹⁴ resulted in wing discs with expanded anterior compartments and ectopic ptc-lacZ throughout the anterior (Figure 7B,E). Ectopic ptc-lacZ was much stronger than observed for Ci-S849A and was also evident cell autonomously in clones lacking a wild-type Ci transgene within wing discs expressing Ci-S849A∆CORD (Figure 7K). These results confirm that the CORD domain, which is only known to interact with Cos2, reduces Ci-155 activity when Ci-155 is not processed. Moreover, the observations that induction of ptc-lacZ in response to loss of PKA, Cos2 or the CORD domain depends on the dose of ci and protecting Ci-155 from processing are consistent with the idea that only Su(fu)-free Ci-155 is subject to inhibition by PKA and by Cos2 binding to the CORD domain.

If the CORD domain serves only to permit Ci-155 inhibition by binding to Cos2, it might be expected that Ci∆CORD either has the same activity at the AP border as wild-type Ci, or perhaps greater activity if Hh does not normally fully oppose Cos2-CORD interactions at the AP border. In fact, Ci∆CORD (and Ci∆CDN∆CORD) supported normal levels of ptc-lacZ but reduced En induction (Figure 7A,B,D,F,G,I). Loss of Su(fu) did not restore robust En expression (Figure 7—figure supplement 1B,D) and induction of ptc-lacZ was much reduced by loss of Fu kinase, just as for Ci-WT (Figure 7—figure supplement 1E,F). Wing discs lacking both Fu kinase and Su(fu) had strong ptc-lacZ but no En induction at the AP border for both Ci∆CORD and Ci-WT (Figure 7—figure supplement 1G,H), consistent with an earlier report that Ci-155 activation by Fu operates substantially, but not entirely by antagonizing inhibition by Su(fu) (Zhou and Kalderon, 2011). We also found that Ci∆CORD responded to activated GAP-Fu similarly to Ci-WT (Figure 7—figure supplement 1I–L,N). From these results, we speculate that the CORD domain may facilitate a facet of activation of Ci-155 by Fu that does not involve countering Su(fu) inhibition. For example, Fu activated by Hh at the AP border may not engage efficiently with Ci-155 complexes in the absence of the CORD domain, leading to a deficit in En induction, but excess GAP-Fu may largely compensate for that deficiency to produce similar activation of Ci-WT and Ci∆CORD.

Surprisingly, despite its high constitutive activity, Ci-S849A∆CORD showed markedly lower induction of En at the AP border than Ci∆CORD (Figure 7J), even though Ci-S849A induced En normally (Figure 3B). Since Ci-S849A∆CORD is neither processed nor inhibited by Cos2, it is presumably incompletely activated by Fu kinase activity, as hypothesized for Ci∆CORD. The lesser induction of En when processing is fully inhibited suggests the possibility that those Ci-155 molecules spared from processing but failing to engage with activated Fu might compete with activated Ci-155 and thereby limit Hh target gene induction.

Processing of Ci-155 is initiated by phosphorylation of three PKA sites (‘P1-3’) and involves the creation of a Slimb-SCF complex binding site that includes phosphorylated S849. It has previously been shown that alteration of the PKA sites (P1-3A) or S849 (S849A) abrogates Slimb binding in vitro, Ci-75 production detected by Western blot of embryo extracts expressing HA-tagged transgenes and all Ci-75 repressor activity, assayed by hh-lacZ repression in smo mutant clones expressing ci transgenes in the posterior compartment of wing discs (Méthot and Basler, 2000; Price and Kalderon, 1999; Price and Kalderon, 2002; Smelkinson and Kalderon, 2006; Smelkinson et al., 2007). Moreover, we found here that Ci-P(1-3)A and Ci-S849A expressed at physiological levels produced high levels of Ci-155 throughout the anterior with no elevation at the AP border, and that dpp-lacZ was ectopically expressed in anterior cells, as expected if no Ci repressor is present (Méthot and Basler, 1999). Thus, the absence of processing for Ci-P(1-3)A and Ci-S849A has been firmly established.

We found that normal patterns of induction of the Hh target genes ptc-lacZ and En at the AP border were supported by a Ci variant that cannot be processed. We tested only one copy of the ci-S849A and ci-P(1-3)A alleles, so it remains possible that two copies might impair patterning. We also found that one crCi-S849A allele together with a genomic gCi-S849A transgene and the constitutive repressor allele ci^Ce produced adults with normally patterned wings. The result shows that wing patterning by Hh does not require regulation of the level of either repressor or full-length Ci protein by processing.

Animals lacking both Fu kinase and Su(fu) also develop normal wings, although late third instar wing discs do lack anterior En induction (Ohlmeyer and Kalderon, 1998; Préat, 1992; Zhou and Kalderon, 2011). Thus, regulation of Ci-155 processing and the most prominent regulator of Ci-155 activation, Fu kinase activity, are each largely dispensable for Hh morphogen action, suggesting that each graded patterning mechanism can suffice in the absence of the other. The spatial morphogen action of Hh is aided by the negative feedback loop of ptc transcriptional induction leading to increased Hh sequestration by Ptc protein (Chen and Struhl, 1996). That feature diminishes Hh spread through cells with hyper-sensitive signal transduction and increases spread through cells of reduced sensitivity, potentially accommodating limited deficiencies in signal transduction due to the loss of one major mode of Ci activity regulation.

The profile of Hh inhibition of Ci-155 processing had not previously been observed or deduced because wild-type Ci-155 is also subject to Hh-stimulated degradation and potentially other changes that also affect Ci-155 levels. Here, we have derived a clear profile of Hh-stimulated processes that lead to reduced Ci-155 by examining Ci variants that are not subject to processing. The Hh-stimulated decline in Ci-155 levels begins at a location where ptc-lacZ induction is roughly half-maximal and is roughly linear, resulting in a reduction of over twofold by the compartment boundary (Figure 2H”, I”, K; Figure 8). Although the mechanisms contributing to Hh-stimulated reduction in Ci-155 are not fully understood (see below), they appear always to be in proportion to pathway activity. Since both Ci-P(1-3A) and Ci-S849A have the same pathway activity profiles as Ci-WT, measured by ptc-lacZ and En, we assume that the Ci-155 reduction profile observed directly for the processing-resistant variants is very similar for wild-type Ci. We therefore added the observed value of Ci-155 loss at each AP location to the observed Ci-155 profile of wild-type Ci to deduce the normal Ci-155 profile due to processing alone (Figure 2L; Figure 8). The inhibition of Ci-155 processing extended from a location slightly anterior to the edge of ptc-lacZ induction to the AP border in a clearly graded manner that, in isolation, would alter Ci-155 levels more than two-fold. Thus, we have derived the first clear visualization of graded inhibition of Ci-155 processing and of graded, pathway-stimulated, Ci-155 loss.

Both the mechanism and the purpose of Hh-stimulated Ci-155 reduction at the AP border remain uncertain. It was initially suggested that Hh-stimulated Ci-155 reduction was due to the transcriptional induction of Rdx/Hib, which bound activated Ci-155 directly to promote its degradation and limit the magnitude of Hh target gene induction by the highest levels of Hh (Kent et al., 2006; Zhang et al., 2009; Zhang et al., 2006). However, other studies found that Ci-155 levels remained low in high Hh signaling territory even when Rdx/Hib activity was eliminated and that Rdx/Hib might influence Ci-155 indirectly via modulation of Su(fu) protein levels (Liu et al., 2014; Seong et al., 2010; Seong and Ishii, 2013).

Here, we specifically tested the contribution of direct targeting of Ci by Rdx/Hib for the first time in a physiological setting by using a Ci variant with multiple alterations to sites of Rdx/Hib association; those alterations had been shown to nearly eradicate direct down-regulation of Ci-155 by Hib E3 ligase complexes under synthetic conditions (Zhang et al., 2009). This Ci variant (Ci-S3-5) supported a normal pattern of Hh target gene induction in wing discs and the development of adults with normal wings. The Ci-155 profile was also very similar to wild-type Ci with robust Hh-stimulated Ci-155 reduction in the posterior part of the AP border. While the Ci variant may retain some residual Hib binding, our results suggest that the majority of Hh-promoted Ci-155 reduction is through mechanisms other than degradation due to direct binding of Rdx/Hib.

The complete absence of Su(fu) greatly reduces Ci-155 levels but not ci RNA levels throughout wing discs (Ohlmeyer and Kalderon, 1998), leading to the hypothesis that direct binding of Su(fu) to Ci-155 protects Ci-155 from degradation. It is also commonly speculated that pathway activation elicits Ci-Su(fu) dissociation, as suggested by studies of mammalian Hh signaling (Humke et al., 2010; Tukachinsky et al., 2010). Such dissociation, if stimulated in proportion to Fu activation, would promote Ci-155 degradation in proportion to Ci-155 activation without the necessary participation of a transcriptionally induced intermediate, such as Rdx/Hib (Figure 8). Consistent with this hypothesis, no reduction of Ci-155 levels close to the source of Hh was apparent in wing discs lacking Su(fu). The sensitivity of those measurements was, however, limited by the low Ci-155 levels throughout such wing discs. Whether Ci-155 activation by Fu does involve dissociation of Su(fu) and whether that contributes significantly to pathway-stimulated Ci-155 degradation remain to be thoroughly investigated.

Although the Rdx/Hib and Su(fu)-dependent proteolytic mechanisms outlined above are prominent candidates for mediating Hh-stimulated reduction of Ci-155 at the AP border, it is possible that transcriptional, RNA processing, or translational mechanisms are also involved. Initial studies of ci RNA and a lacZ enhancer trap of the ci locus (ci-lacZ) suggested that third instar larvae have spatially uniform anterior ci transcription and RNA (Eaton and Kornberg, 1990; Ohlmeyer and Kalderon, 1998). ci-lacZ was, however, seen to be markedly lower in AP border regions 30 hr after pupariation, possibly resulting from transcriptional repression of ci by En, which is itself induced in anterior cells only in late third instar larvae (Blair, 1992). Other studies have shown that the pattern of ci RNA splicing and overall RNA levels can be selectively altered by reduced activity of the exon-junction complex or the splicing factor, Srp54, suggesting the potential to regulate ci RNA processing (Garcia-Garcia et al., 2017).

We found that artificially activated Fu (GAP-Fu) can activate processing-resistant Ci in anterior, Hh-free territory as effectively as normal Fu activity at the AP border. Wild-type Ci activated by GAP-Fu induced roughly two-fold lower levels of ptc-lacZ, and barely induced ptc-lacZ at all if it was produced at slightly lower levels by a gCi transgene rather than a ci allele. These results are consistent with the simple idea that more activated Ci-155 molecules collectively induce transcription more strongly. However, the steady-state level of Ci-155 in cells with synthetically activated Fu was not significantly higher for processing-resistant variants than for wild-type Ci, presumably because of robust Ci-155 degradation in response to high pathway activity. An analogous circumstance is apparent in posterior regions of the AP border: Ci-155 processing is largely inhibited, Fu kinase and Ci-155 are strongly activated but Ci-155 levels are similar to those in anterior cells because of robust Hh-stimulated Ci-155 reduction. The GAP-Fu experiment reports that high pathway activity causes a high rate of Ci-155 loss and that high pathway activity can only be maintained if there is an adequate, constant supply of fresh Ci-155 protected from processing. This imposed requirement might be the major purpose of Hh-promoted Ci-155 reduction at the AP border, rather than modulating the profile of the Hh signaling gradient. Under this arrangement, cells will continue to express high-level Hh target genes only when constantly stimulated. The arrangement also allows for the possibility of modulating pathway activity through both the degree of Fu activation and the rate of supply of Ci-155 that is protected from processing.

We used the processing-deficient variant Ci-P(1-3A) to show that genetic removal of PKA or Cos2 substantially increased Ci-155 activity in the absence of Hh, providing evidence that both PKA and Cos2 inhibit Ci-155 activation in addition to their well-established roles of promoting Ci-155 processing (Figure 8). Earlier tests concerning the role of PKA generally reached the same conclusion but were subject to a number of caveats (Smelkinson et al., 2007; Wang et al., 1999). The findings reported here supersede those conclusions because physiological expression of Ci-155 variants was assayed in normal locations. They also showed that the magnitude of inhibition by Cos2 and PKA was substantial and allowed some exploration of the mechanisms involved.

We found that removal of the CORD domain of Ci conferred significantly higher activity on a processing-resistant Ci variant and increased the response of otherwise normal Ci to loss of PKA, but not to loss of Cos2. These observations are consistent with the hypothesis that the CORD domain is the major mediator of the inhibitory action of Cos2. By contrast, deletion of the CDN Cos2-binding domain did not alter the activity of processing-resistant Ci. Ci-155 processing remained efficient in the absence of both CDN and CORD domains, confirming a previous deduction from UAS-Ci transgenes that Cos2 binding to the zinc finger domain of Ci can suffice to promote processing (Zhou and Kalderon, 2011). Removal of the CORD domain reduced En induction at the AP border and we hypothesize that this might result from a deficiency in targeting activated Fu to Ci. Thus, although Ci-155 has three domains that can bind to Cos2, it appears that they do not contribute equally to regulate Ci-155 processing, inhibition and activation.

We did not resolve how PKA inhibits Ci-155. The finding that loss of PKA increased the activity of Ci-P(1-3A) shows that the PKA sites used to direct processing (P1-3) are not essential targets for PKA to inhibit Ci-155. Ci-155 includes two additional consensus sites at residues 962 and 1006. In earlier studies using multiple UAS-Ci transgenes at a variety of genomic locations, Ci variants lacking all five PKA sites (P1-5A) were found to be more active than those lacking just sites P1-3 (Price and Kalderon, 1999). However, the relative levels of ci transgene expression were not measured in that study and all were likely higher than physiological levels. In mouse studies, evidence was provided, albeit with non-physiological expression levels, that alteration of PKA sites in Gli2 analogous to residues 962 and 1006 in Ci-155 increased Gli2 activity (Niewiadomski et al., 2014). We were unable to recover a crCi allele encoding a variant with all five PKA sites altered. We were similarly unable to recover variants with processing-resistant alterations together with Su(fu)-binding site alterations, and the processing- resistant variant with a CORD domain deletion was also difficult to recover and propagate. We speculate that these difficulties may all derive from a shared characteristic of constitutively high activity, providing a hint that PKA sites 962 and 1006 might be important to restrain Ci-155 activity. However, both these sites are within the CORD domain and Ci lacking the CORD domain is more strongly activated by loss of PKA than by loss of Cos2, indicating that PKA inhibition does not require PKA sites 4 and 5. There may, of course, be more than one target through which PKA inhibits Ci-155 activation, including the possibility that PKA acts separately through sites 1–3 and 4–5.

Another unresolved issue is to what extent Hh signaling at the AP border antagonizes the inhibitory influences of Cos2 and PKA. When Hh signals, Ci-155 processing is reduced primarily through partial dissociation of Cos2-Ci complexes (Li et al., 2014; Ranieri et al., 2014) and this processing inhibition occurs even in the absence of Fu kinase activity (Ohlmeyer and Kalderon, 1998; Smelkinson and Kalderon, 2006). It is not clear what degree of dissociation is elicited at the AP border or whether Cos2-CORD interactions might be altered within intact Cos2-Ci complexes to relieve Cos2 inhibition. Ci-P(1-3)A induced no ptc-lacZ in anterior cells, low ptc-lacZ levels at the AP border of Fu-kinase deficient discs and significantly higher ptc-lacZ levels in cos2 and pka mutant clones. We can therefore deduce that in the absence of Fu kinase there may be some reduction of inhibition by Cos2 and PKA at the AP border, leading to low ptc-lacZ induction, but the reduction is much less than from complete elimination of Cos2 or PKA activities. It is possible that Hh additionally counters inhibition by Cos2 or PKA through Fu activation. Indeed, anterior En induction at the AP border requires Fu activity even in the complete absence of Su(fu), showing that Fu opposes Ci-155 inhibition by factors other than Su(fu) (Zhou and Kalderon, 2011). Cos2 and PKA are the only other known inhibitory factors.

In summary, at the AP border of wing discs, Hh inhibits Ci-155 processing, activates full-length Ci-155 and promotes reduction of Ci-155, most likely substantially through proteolytic degradation (Figure 8). Processing-resistant Ci variants revealed the profiles of Hh-promoted Ci-155 reduction and Ci-155 processing inhibition (Figure 2K,L and Figure 8), and showed that Hh can pattern wing discs and wings normally in the absence of regulated processing. Ci variants lacking Rdx/Hib-binding sites showed that Ci-155 reduction likely depends on Hh-stimulated processes other than direct binding to the transcriptionally induced component of an E3 ubiquitin ligase, plausibly involving protection from degradation by Su(fu) association (Figure 8). We also found that Ci-155 that is not subject to processing is substantially inhibited by PKA and by association with Cos2 through the CORD domain in addition to Su(fu), and that activation by Fu only elicits strong induction of Hh target genes if there is a continued ample supply of Ci-155 protected from processing.

Genomic transgenes were created by cloning the entire 16 kb genomic ci region from a Bluescript-SK (BSK) vector (provided by Dr. K. Basler; Méthot and Basler, 1999) into an att-Pacman Expression vector (DGRC). To facilitate mutagenesis, the 16 kb fragment was first separated into two parts. The region including the promoter, first exon and part of the first intron (‘Ci fragment 2’) was cloned as a BamHI-NheI fragment into BSK cut with BamHI and XbaI to create BSK-CiF2. The complementary NheI-KpnI fragment containing all other exons and the 3’ UTR (‘Ci Fragment 1’) was cloned into BSK cut with SpeI and KpnI to create BSK-CiF1. BSK-CiF2 was cut with NotI and Bsp1201 to clone the whole CiF2 fragment into the P[acman]-CmR vector cut with NotI, so that RsrII and PmeI vector sites were downstream of ci first intron sequences in RP-CiF2. CiF1 was amplified from BSK-CiF1 by long-range PCR using PfuUltraII Fusion HS DNA polymerase (Agilent Technologies), adding RsrII and PmeI at either end and cloning the product into a Zero Blunt Topo cloning vector (Invitrogen). The RsrII-PmeI fragment was then cloned into RP-CiF2 cut with the same enzyme to create the final Pacman vector containing the entire 16 kb genomic ci DNA. The 28 kb gCi attPacman transgene was then inserted at the att ZH-86Fb landing site at cytological location 86F8 (Rainbow Transgenic Services).

For crCi-WT, ∆CORD, P(1-3)A, S849A, S849A∆CORD, ∆1270–1370, ∆CDN, ∆CDN∆CORD plasmid design was developed using APE software. Overlapping primer PCR reactions were used to add, mutate, and delete regions on Ci with PfuUltraII Fusion HS DNA polymerase (Agilent Technologies). PCR products were introduced into the Zero Blunt Topo cloning vector (Invitrogen). The alterations in Ci were then re-introduced from the Zero Blunt Topo cloning Vector into the BSK-F1 Donor construct using compatible enzymes or Gibson Assembly (New England Biolabs). The final constructs were fully sequenced (Genewiz).

Drosophila stocks were maintained on standard cornmeal/molasses/agar medium at room temperature.

Females of the genotype yw hs-flp; ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to yw hs-flp; Sp/Cyo; gCi-WT/∆CORD/S849A; ci⁹⁴/Dp[y⁺] males, selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with third chromosome transgenes as the only source of Ci.

Females of the genotype yw hs-flp; ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to yw hs-flp; Sp/Cyo; crCi-X/Dp[y⁺] males, selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci.

Females of the genotype yw hs-flp; Su(fu)^LP ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to yw hs-flp; Sp/Cyo; Su(fu)^LP/TM6B, Tb; crCi-X/Dp[y⁺] males, selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci in a Su(fu) null background.

Females of the genotype (‘2L’) yw hs-flp UAS-GFP; tub-Gal80 FRT40A/Cyo; C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; pka-C1^H2 FRT40A/Cyo; gCi-WT/∆CORD/S849A/TM6B, Tb; ci⁹⁴/Dp[y⁺] or yw hs-flp; pka-C1^H2 FRT40A/Cyo; crCi-X/Dp[y⁺], selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci and GFP-marked pka mutant clones.

Females of the genotype (‘2b’) yw hs-flp UAS-GFP; FRT42D P[Ci⁺] tub-Gal80/Cyo; C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; FRT42D/Cyo; crCi-X/Dp[y⁺], selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci in GFP-marked clones lacking P[Ci⁺] with neighboring cells including P[Ci⁺].

Females of the genotype (‘2b’) yw hs-flp UAS-GFP; FRT42D P[Ci⁺] tub-Gal80/Cyo; C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; FRT42D cos2²/Cyo; gCi-WT/∆CORD/S849A/TM6B, Tb; ci⁹⁴/Dp[y⁺] or yw hs-flp; FRT42D cos2²/Cyo; crCi-X/Dp[y⁺], selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci in GFP-marked clones lacking cos2 activity and P[Ci⁺] with neighboring cells expressing P[Ci⁺].

Females of the genotype (‘2b’) yw hs-flp UAS-GFP; FRT42D P[Ci⁺] tub-Gal80/Cyo; C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; smo² FRT42D UAS-GAP-Fu/Cyo; crCi-X/Dp[y⁺], selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci in GFP-marked clones expressing GAP-Fu and lacking P[Ci⁺] with neighboring cells expressing P[Ci⁺].

Females of the genotype (‘2R’) yw hs-flp UAS-GFP; smo² FRT42D P[Smo⁺] tub-Gal80/Cyo; C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; FRT42D cos2²/Cyo; crCi-X/Dp[y⁺], selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci and GFP-marked clones lacking cos2 activity.

Females of the genotype (‘2R’) yw hs-flp UAS-GFP; smo² FRT42D P[Smo⁺] tub-Gal80/Cyo; C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; smo² FRT42D UAS-GAP-Fu/Cyo; crCi-X/Dp[y⁺], selecting third instar larval progeny lacking y⁺ and Tb to obtain wing discs with a single constructed crCi allele as the only source of Ci in GFP-marked clones expressing GAP-Fu and lacking smo activity.

Females of the genotype yw hs-flp fu^mH63; FRT42D P[y⁺] P[Fu+]/Cyo; (Su(fu)^LP) C765-GAL4 ptc-lacZ/TM6B, Tb; ci⁹⁴/Dp[y⁺] were crossed to males of the genotype yw hs-flp; Sp/Cyo; (Su(fu)^LP/TM6B); crCi-X/Dp[y⁺], selecting male third instar larval progeny lacking y⁺ and Tb to obtain wing discs lacking Fu kinase activity (with or without functional Su(fu)) and a single constructed crCi allele as the only source of Ci.

Wing disc clones were generated by heat-shocking late first or early second instar larvae for 1 hr at 37°C and dissections took place 3.5 to 4 days later in wandering third instar larvae. Wing discs were dissected from late third instar larvae in PBS and fixed in 4% paraformaldehyde (in PBS) for 30 min, rinsed 3X with PBS, blocked with 10% normal goat serum (Jackson ImmunoResearch Laboratories, Inc) in PBS-T (0.1% Triton) for 1 hr, and stained with the following primary antibodies: rabbit anti–β-galactosidase (1:10,000; MP Biomedicals), mouse 4D9 anti-Engrailed (1:5 Developmental Studies Hybridoma Bank), Rat 2A1 anti-Ci (1:3 Developmental Studies Hybridoma Bank), overnight at 4°. Inverted Larvae were then washed three times in PBST for 10 min each and incubated with Alexa Fluor 488, 546, 594, or 647 secondary antibodies (1:1000; Molecular Probes) for 1 hr at room temperature. Larvae were washed twice in PBST for 20 min each, once in PBS for 10 min and mounted in Aqua/Poly mount (Polysciences).

Fluorescence images were captured using 20x, 63x, or 40x (discs with far anterior clones) objectives using 1.4 NA oil immersion lenses on a confocal microscope (LSM 700 and LSM800; Carl Zeiss). The range indicator was used to set the appropriate laser intensity per experiment for each fluorophore such that the signal was in the linear range.

Intensity Profiles: To measure intensity profiles along the AP axis, an elongated rectangle was drawn on a central region of the wing pouch, avoiding the D/V border. The y-axis shows the average fluorescence intensity over the height of the rectangle at each point on the x-axis (AP axis) for ptc-lacZ expression or Ci-155 protein, measured using Image J software (NIH, Bethesda, Maryland). In general, three wings discs per condition were measured and averaged for each plot, using the posterior edge of ptc-lacZ expression as a reference point for the AP border.

Clone Measurements: The average fluorescent intensity of ptc-lacZ or Ci-155 over specific regions was measured using Image J. Multiple clones or clone regions (for large clones), anterior regions (most commonly three per disc), AP border sections (three per disc), posterior regions (three per disc), were analyzed for each disc. To make sure the best region was acquired for measurements in clones, the region was selected using the GFP marker in the central part of the clone and confirmed to not be on a fold or shadowed region. For the AP border, regions were measured avoiding the DV boundary and abnormal folds. For Figures 4 and 6, ptc-lacZ clone intensity was calculated relative to AP border levels after subtracting anterior cell intensity values from each because ptc-lacZ is sometimes expressed artifactually in posterior cells: (clone-averaged anterior)/(averaged AP border-averaged anterior). In Figure 5 ptc-lacZ intensity in clones and anterior cells outside clones was in each case divided by AP border intensity without any subtractions. Ci-155 clone intensity and intensity in anterior cells outside clones (Figure 4) were calculated relative to AP border levels after subtracting posterior cell intensity values from each: (clone-averaged posterior)/(averaged AP border-averaged posterior) and (anterior-averaged posterior)/(averaged AP border-averaged posterior). For Figure 5, ptc-lacZ intensity measurements in clones and anterior regions were divided by the AP-Border.

Adult wings were pulled off anaesthetized flies and placed in 70% ethanol for 5 min, transferred to 100% ethanol, and then mounted in Aqua/Poly Mount (Polysciences). They were imaged with Transmitted Light on a Nikon Diaphot 300 microscope using a 10x objective.

All images shown are representative of at least five examples. No statistical method was used to predetermine sample size but we used prior experience to establish sufficient sample sizes. No samples were excluded from analysis, provided staining was of high quality. The experiments were not randomized; samples presented as groups in the results were often all part of the same experiment and were always treated in exactly analogous ways without regard to the identity of the sample. Investigators were not blinded during outcome assessment, but had no pre-conception of what the outcomes might be. For comparisons between the measured levels of ptc-lacZ product or Ci-155 a t-test was used to determine significance between pairs of genotypes (generally Ci variant versus wild-type Ci), and the errors for individual values determined from multiple samples was reported as the standard error of the mean.

The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.

This work was supported by NIH RO1 GM041815 awarded to DK. We thank Aaron Choi, Jason Li and Sarah Finkelstein for research assistance, Hoyon Kim and other lab members for continued discussions and input, Rebecca Delker and Dr. Richard Mann for advice on CRISPR engineering, the Bloomington stock center for provision of genetic reagents, the Developmental Studies Hybridoma Bank (DSHB) for antibodies, FlyBase as an information resource, and the confocal microscope resource provided by the Dept. of Biological Sciences, Columbia University.

© 2020, Little et al.

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