AKAP200 is a Drosophila melanogaster member of the “A Kinase Associated Protein” family of scaffolding proteins, known for their role in the spatial and temporal regulation of Protein Kinase A (PKA) in multiple signaling contexts. Here, we demonstrate an unexpected function of AKAP200 in promoting Notch protein stability. In Drosophila, AKAP200 loss-of-function (LOF) mutants show phenotypes that resemble Notch LOF defects, including eye patterning and sensory organ specification defects. Through genetic interactions, we demonstrate that AKAP200 interacts positively with Notch in both the eye and the thorax. We further show that AKAP200 is part of a physical complex with Notch. Biochemical studies reveal that AKAP200 stabilizes endogenous Notch protein, and that it limits ubiquitination of Notch. Specifically, our genetic and biochemical evidence indicates that AKAP200 protects Notch from the E3-ubiquitin ligase Cbl, which targets Notch to the lysosomal pathway. Indeed, we demonstrate that the effect of AKAP200 on Notch levels depends on the lysosome. Interestingly, this function of AKAP200 is fully independent of its role in PKA signaling and independent of its ability to bind PKA. Taken together, our data indicate that AKAP200 is a novel tissue specific posttranslational regulator of Notch, maintaining high Notch protein levels and thus promoting Notch signaling.
AKAP200 belongs to a family of scaffolding proteins best known for their regulation of PKA localization. In this study, we have identified a novel role of AKAP200 in Notch protein stability and signaling. In Drosophila melanogaster, AKAP200’s loss and gain-of-function (LOF/GOF) phenotypes are characteristic of Notch signaling defects. Furthermore, we demonstrated genetic interactions between AKAP200 and Notch. Consistent with this, AKAP200 stabilizes the endogenous Notch protein and limits its ubiquitination. AKAP200 exerts its effects on Notch by antagonizing Cbl-mediated ubiquitination and thus lysosome targeting of Notch. Based on these data, we postulate a novel PKA independent mechanism of AKAP200 to achieve optimal Notch protein levels, with AKAP200 preventing Cbl-mediated lysosomal degradation of Notch.
Citation: Bala Tannan N, Collu G, Humphries AC, Serysheva E, Weber U, Mlodzik M (2018) AKAP200 promotes Notch stability by protecting it from Cbl/lysosome-mediated degradation in Drosophila melanogaster. PLoS Genet 14(1): e1007153. https://doi.org/10.1371/journal.pgen.1007153
Editor: Norbert Perrimon, Harvard Medical School, Howard Hughes Medical Institute, UNITED STATES
Received: August 8, 2017; Accepted: December 13, 2017; Published: January 8, 2018
Copyright: © 2018 Bala Tannan et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was supported by grants from the National Institutes of Health to MM, grant numbers EY013256 and GM102811. Confocal microscopy was performed at the Tisch Cancer Institute Microscopy Core, supported by grant P30 CA196521 from the NCI. Fly strains and antibodies were provided by the Bloomington Stock Center, Vienna Drosophila RNAi Center, Drosophila Genomics Resource Center (DGRC, supported by NIH grant 2P40OD010949-10A1) and Developmental Studies Hybridoma Bank (DSHB, supported by the NICHD of the NIH and maintained at the University of Iowa). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Signaling pathways are critically involved throughout embryonic development, as well as adult tissue function and homeostasis. Many of these pathways are highly conserved from invertebrates to humans, and were first discovered in Drosophila melanogaster, making it an ideal model system for identification and analysis of new pathway components. Notch signaling, is one such pathway, and is required for fundamental developmental processes including polarity, cell fate specification, tissue growth, stem cell maintenance, and organ patterning [1–5]. Moreover, misregulation of Notch signaling underlies several human diseases including various cancers highlighting the importance of Notch pathway regulation [1, 3, 6–8].
In Drosophila, Notch signaling is activated by the interaction of the ligands Delta and Serrate with the extracellular domains of the Notch receptor . Ligand binding activates extracellular cleavage of Notch by ADAM/TACE metalloproteases , followed by γ-secretase mediated cleavage , which releases the Notch intracellular domain (NICD) . The NICD, which is the signal transducing end of the protein, enters the nucleus, forms a complex with the transcription factor Suppressor of Hairless [Su(H)]/CSL and activates target genes [5, 13–15]. The same fundamental elements/mechanisms of the pathway are conserved in mammals [16, 17]. Notch signaling is tempered by endocytosis of the receptor and degradation of NICD and these processes are essential to avoid hyperactivity [18, 19]. Several studies have demonstrated proteasomal degradation of Notch. For example, dominant negative mutations of proteasomal subunits enhance Notch signaling in Drosophila . Initial evidence for lysosomal degradation of Notch came from a study in skeletal myoblasts, the C2C12 cell line, where a role was demonstrated for c-Cbl (Casitas B-lineage lymphoma, a proto-oncogene and E3 ubiquitin ligase) in mono-ubiquitinating the endogenous transmembrane Notch1 and targeting it for lysosomal degradation . Suppressor of Deltex [Su(dx)]/Itch (Drosophila/mouse) and Sel10 have been shown to decrease Notch signaling in this context [22–25].
Mutations in Notch affect many developmental decisions in various Drosophila tissues [26, 27]. For example, Notch signaling instructs specification of the eye field and initiation of eye development, as well as controlling growth and cell fate [28–31]. The interplay between Notch and Frizzled (Fz)/Planar Cell Polarity (PCP) signaling is critical for induction of specific photoreceptor (PR) subtypes [29, 30, 32–34]. In the developing eye disc, there is a Frizzled/PCP activity gradient that is highest at the dorso-ventral midline, termed the equator, and lowest at each pole [30, 35, 36]. Within each developing PR cluster, there are pairs of cells that are initially equivalent that then develop into photoreceptor 3 and 4 (R3 and R4). Within each pair, the cell that is closest to the midline adopts the R3 fate and upregulates the Notch ligand Delta, and neuralized and signals via Notch to its polar neighbor to adopt the R4 fate [30, 36–38].
In a screen for novel regulators of PCP signaling in the Drosophila eye, we identified a scaffolding protein, A Kinase Anchoring Protein 200 (AKAP200) . AKAPs are a family of proteins responsible for the subcellular compartmentalization of Protein Kinase A (PKA), which facilitate the spatial and temporal regulation of signaling [40–42]. Despite being structurally and sequentially diverse, the AKAP family of proteins show functional conservation amongst species . AKAP200 is one member of the AKAP family of proteins and is expressed throughout all stages of Drosophila development. Alternative splicing produces two isoforms of AKAP200—the full length AKAP200-Long (AKAP200-L), and the short isoform, AKAP200-Short (AKAP200-S). AKAP200-S lacks the PKA-interaction domain and may therefore be limited to PKA- independent functions [44, 45].
Here we provide evidence that AKAP200 is required for the regulation of Notch protein levels, via the lysosomal degradation pathway. AKAP200’s loss and gain-of-function (LOF/GOF) phenotypes are characteristic of misregulation of the Notch signaling pathway. AKAP200 LOF mutants display defects in cell fate specification manifested as loss of PRs in the eye and extra sensory bristles in the thorax, while AKAP200 overexpression causes wing vein defects and tissue overgrowth in the wing. Genetic interaction studies revealed that AKAP200 acts as a positive regulator of Notch signaling, as loss of AKAP200 suppresses Notch overexpression phenotypes in the eye and thorax. Consistent with this, we observe a decrease in overall Notch protein levels and increased ubiquitination in the AKAP200 mutant relative to wild type (WT). Importantly, AKAP200’s effects on Notch are independent of PKA. However, we find that the suppression of Notch hyperactivity in AKAP200 mutant tissues is instead dependent on the E3 ubiquitin ligase Cbl and the lysosomal degradation pathway. Based on these data, we postulate a novel mechanism for the regulation of Notch levels, with AKAP200 preventing Cbl-mediated lysosomal degradation of Notch.
AKAP200 mutants display Notch like phenotypes
To identify novel genes involved in PCP-mediated photoreceptor specification, we performed a genetic screen for dominant modifiers of a gain-of-function (GOF) of the core PCP factors dgo and pk . Overlapping deficiencies narrowed down a region on chromosome 2L that enhanced the dgo GOF PCP eye phenotypes (S1A Fig). Further analysis using RNA interference (IR) against specific genes in this interval revealed that A Kinase Anchoring Protein 200 (AKAP200) reproduced the interaction, implicating it as the gene responsible (S1A and S1B Fig).
To investigate AKAP200 functions, we first generated mutant alleles by excising the coding sequence of AKAP200 using flanking piggyBac/FRT insertions (S1C Fig). This led to the isolation of two null alleles, AKAP200M30 and AKAP200M24 that were confirmed by PCR characterization (S1D Fig; see  for method). These were lethal homozygous, or transheterozygous over a deficiency chromosome, with rare escapers (S1G–S1J Fig). To analyze the loss-of-function (LOF) phenotypes we generated mutant clones via the Flp-FRT system . In the eye, AKAP200M30 mutant clones displayed loss of or misspecification of photoreceptors (PRs) (Fig 1B, 1C and 1F). These phenotypes were also consistently seen in escapers from different AKAP200 transheterozygous LOF genetic backgrounds and also mimicked the phenotypes seen with AKAP200-IR knock-downs (S1G and S1H Fig; these were often quantitatively weaker than the null clones). A frequent defect was loss of R7 in mutant ommatidia (Fig 1B, 1C and 1F), with R7 specification requiring both Notch and RTK (Sev and Egfr) signaling. To confirm this we analyzed developing eye discs with molecular markers (Elav to stain all R-cells and Pros labeling R7), which revealed partial photoreceptor specific loss of Pros staining in mutant eye discs (S1I and S1I’ Fig). Together with the identification in the PCP screen, the observed eye phenotype was suggestive of a possible link to Notch function, with similarities to aspects of Notch LOF phenotypes [28, 48–50]. Also as an interplay between Notch and Fz/PCP signaling is critical for R3/R4 specification and PCP patterning in the eye, regulators of either pathway were expected to be and were identified in the screen .
(A-C) Tangential adult eye sections with anterior left and dorsal up. (A) Example of wild type (WT) eye tissue identified by presence of pigment granules (shaded grey, also in B and C, in schematics). (B-C) AKAP200 mutant tissue, lacking pigment (clonal marker used was w+, small wt areas shaded grey). (B) Dorsal and (C) ventral eye regions, with AKAP200M30 tissue displaying frequent loss of photoreceptors (schematized in lower panels); see panel (F) for key and quantification. (D-E) Thorax of indicated genotypes, anterior is up. (D) WT control showing normal sensory bristle pattern. (E) AKAP200 mutant clones (marked by absence of y+, some wt patches outlined with yellow line) display defects in SOP specification, resembling Notch signaling defects, as evident by bald spots (white arrow) and supernumerary scutellar bristles (example highlighted by red arrow). (F) Schematic of different ommatidial phenotypes observed in (B-C). Blue box/dots depict loss of one or several outer photoreceptors and green boxes/dots depict loss of R7, with or without simultaneous loss of outer photoreceptors. Graph: quantification of distribution of phenotypes in AKAP200M30 (n = 666 from 8 eyes).
The AKAP200 LOF thorax phenotype [generated using ubx-Flp inducing clones in all imaginal discs at early larval stages ] revealed supernumerary scutellar bristles, and loss of or mispositioned microchaetae (Fig 1E, red arrow marks supernumerary bristles and white arrow a bald patch representing loss of bristles, compare to wild-type area with evenly spaced and regular positioning of microchaetae bristles). Strikingly, the supernumerary scutellar bristles (macrochaetae; Fig 1E, red arrow) are a hallmark Notch-/+ haploinsufficiency phenotype, and this resembled Notch signaling defects. Notch is required at multiple steps in the process specifying SOPs (sensory organ precursors) and the different cell types originating from them, including the positioning and spacing of SOPs and asymmetric activation of Notch during their multiple asymmetric divisions. Based on at what time point in this process Notch signaling is disrupted, a variety of phenotypes can be expected [52–58]. When analyzed in pupal thorax clones, relative to neighboring wild type (WT), AKAP200 mutant tissue displayed loss of SOPs and SOP mispositioning (S1E and S1F Fig), as well as rare SOP lineage defects (Fig 1E and S1F and S1F’ Fig, arrowheads).
In the wing, AKAP200 mutant wings appeared blistered as did mutant clones, but we did not observe defects to the margin (S1J Fig). Interestingly, the blistered wing phenotype suggested a PKA related function of AKAP200 [59, 60], whereas the eye and thorax phenotypes resembled a subset of Notch LOF defects with no obvious link to PKA signaling. Taken together, these phenotypic defects suggest that AKAP200 might affect Notch signaling in the eye and thorax, whereas it seems to act ‘canonically’ via PKA in wings.
AKAP200 promotes Notch signaling
The AKAP200 mutant phenotypes resembled that of Notch LOF in eyes and the thorax, suggesting a novel function for AKAP200. To gain further insight into its potential involvement in the Notch pathway, we tested for genetic interactions between AKAP200 and Notch-associated genotypes (LOF and GOF) in the eye and thorax.
The Drosophila eye is a compound eye with a mirror symmetric organization of ommatidia across the dorso-ventral midline  (Fig 2A and 2B). Perturbation of Notch signaling during ommatidial assembly can lead to a variety of phenotypes [28, 31, 33, 50]. These can be classified into ommatidia with the WT complement of photoreceptors, PRs (6 outer photoreceptors and single R7/R8) and include altered ommatidial orientation, flips, or clusters with a symmetrical appearance; and ommatidia with PR number defects (for example loss or gain of R7; Fig 2A).
(A) Schematic of eye phenotypes. Ommatidia with 6 outer PRs and 1 R7 are classified as WT complement of PRs: WT PR clusters are represented by flagged-arrows, black and red respectively for dorsal and ventral chiral forms, intermixing of these indicates flips. Blue arrows represent symmetrical clusters with two R4s. Loss of any PR is indicated with a black dot, black and blue semi-circles represent 5 outer PRs and 2 R7s, and 4 outer PRs and 3 R7s, respectively. Any ommatidia lacking a PR (outer or R7) are classified as PR number defects in quantifications, unless otherwise indicated. (B-F) Tangential adult eye sections of indicated genotypes; anterior is left and dorsal up in all panels with schematics in lower panels. (B) WT control, note regular arrangement of chiral forms in a mirror symmetric manner across the equator. (C-D) The heterozygous AKAP200 null mutant markedly suppresses the phenotype of the membrane tethered activated sev-NΔECD, which is ligand independent, quantified in (H). (E-F) sep-Gal4, UAS-N flies raised at 18°C show chirality flips and R4/R4 symmetrical clusters (E). Note that AKAP200M30/+ suppresses sep-Gal4, UAS-N induced R4/R4 symmetrical clusters. Quantified in (I). (G) Confocal images of third instar eye discs of indicated genotypes stained for neuronal marker Elav (red, labeling all PR cells) and Pros (green, labeling R7). One R7/ommatidium is observed in WT (top row). Activation of Notch signaling by sev-NΔECD increases R7s/ommatidium (middle row), which is suppressed with simultaneous reduction of AKAP200 (bottom row; quantified in J). (H) AKAP200 mutants suppress Notch PR number defects (including loss, transformation of outer PRs to 2 or 3 R7s). Quantification of genotypes of sev-NΔECD related to (C-D) as indicated. sev-NΔECD causes PR number defects which were reduced in sev-NΔECD/+, AKAP200M30/+ and reproducible in heterozygous and homozygous AKAP200 null mutants (M30 and M24) and deficiency. ***p<0.0001 by chi square test (against sev-NΔECD/+), n = 320–569 from 3–4 independent eyes. (I) Quantification of genetic interactions in (E-F). sep>N caused R4 symmetrical clusters (27% ± 1%). In sep>N, AKAP200M30/+ these were reduced to (9% ± 3%) (***p<0.0001 by chi square test, from 3–4 independent eyes). (J) Quantification of (G), n = 163–234 ommatidia from 7 independent eyes; ***p<0.0001 by chi square test.
To probe the relationship of AKAP200 and the Notch pathway, we asked whether AKAP200 mutants influenced Notch signaling in the eye. NΔECD, a membrane-tethered deletion of the extracellular domain that renders Notch active in a ligand-independent manner , was expressed under the control of the sevenless (sev) promoter [which is initially expressed in R3-R4, and later in R1,6 and 7 and cone cells ]. sev-NΔECD causes the formation of R4 symmetrical clusters and chirality flips besides frequent defects in PR number and supernumerary R7s (Fig 2C and 2H). Reducing the copy number of AKAP200 in the sev-NΔECD background markedly reduced these defects. Whereas PR cell loss was reduced, a proportional increase was seen in less severe Notch GOF phenotypes, including R4 symmetrical clusters and chirality flips (Fig 2D and 2H). The suppression of Notch overactivation by AKAP200M30 was comparable to reducing Notch protein levels, e.g. Notch-/+ (Fig 2H). These interactions were reproducible with all AKAP200 alleles and deficiencies tested, and was strongest upon homozygous removal of AKAP200 (AKAP200M30/M24) in rare escapers (Fig 2H), altogether suggesting that AKAP200 promotes Notch signaling. To confirm this assessment, we tested additional phenotypes associated with the activated Notch pathway. A milder Notch GOF background, using a weaker sev-Gal4 driver (sev-enhancer with sev promoter: “sep>”) resulted in chirality defects with flips and R4 symmetrical clusters (Fig 2E and 2I). Upon removing one copy of AKAP200 in this background, the number of R4 symmetrical clusters was markedly reduced (Fig 2F and 2I), again consistent with the notion that AKAP200 promotes Notch signaling.
To confirm these interactions, we next analyzed larval eye discs for the expression of Prospero (Pros), a molecular marker for R7 (and also later in cones cells) (Fig 2G; Elav, was used as a pan-neuronal marker to stain all PRs). In contrast to WT, where each ommatidium has a single Pros positive R7, in sev-NΔECD most ommatidia had 2 or 3 Pros positive R7s. Removing a copy of AKAP200 suppressed this phenotype, with an appearance closer to WT (Fig 2G and 2J). These observations are consistent with the interactions above and correlate with phenotypes seen in adult eyes (Fig 2C, 2D and 2H). We next performed the equivalent experiment using a Notch signaling reporter, mδ0.5-lacZ, a 500 bp fragment of the E(spl)mδ promoter , which serves as a molecular readout of Notch signaling specifically in R4 (it is initially expressed at low levels in the R3/R4 pair, and following Notch activation it is upregulated in R4). In WT, each ommatidium displayed a single mδ-lacZ positive cell, whereas, in contrast, sev-NΔECD eye discs displayed generally 2 mδ-lacZ positive cells per ommatidium. Consistent with the effects in adult eyes, removing one copy of AKAP200 in the sev-NΔECD background suppressed this phenotype, with most ommatidia displaying only one mδ-lacZ positive cell (S2K and S2L Fig).
In order to solidify the notion that AKAP200’s eye phenotypes are directly related to Notch signaling or whether other pathways are involved, we also tested for a potential AKAP200 involvement with Egfr signaling, which has similar phenotypes [64, 65]. To do this, we performed genetic interactions with Egfr GOF by using the EgfrElp1/+ allele (S2M Fig) and saw no significant difference in its PR number defect phenotype when one copy of AKAP200 was removed. Furthermore, we performed this interaction in the wing. Again, AKAP200M30/+ (S2O Fig) was unable to modify the ectopic vein phenotypes of EgfrElp1/+ (S2N Fig).
We next wished to confirm the link between Notch and AKAP200 in the thorax, as AKAP200 LOF displayed supernumerary scutellar macrochaetae defects (Fig 1E, red arrow), which highly resemble the Notch haploinsufficiency phenotype. Strikingly, an increase in Notch copy number (3 copies) suppressed the macrochaetae defects of AKAP200 LOF mutants (S3N and S3O Fig). In contrast, removing one copy of AKAP200 enhanced the Notch haploinsufficiency (N55e11/+) thorax phenotype (quantified in S2F Fig, depicted in S2G–S2J Fig). These data confirmed a positive requirement for AKAP200 in Notch signaling and suggested that AKAP200 might affect Notch levels (see below). Since the N null alleles do not display haploinsufficient phenotypic defects in the eye, analogous eye experiments could not be tested.
To further corroborate the link between AKAP200 and Notch signaling, we tested Notch GOF genotypes in the thorax. Overactivation of Notch signaling in the thorax can be achieved via the haploinsufficient Hairless (H) mutant. H is a nuclear antagonist of Notch signaling and represses Notch target genes by assembling a transcriptional repressor complex . H is involved in neuronal fate specification, and the mutant thorax phenotype reflects overactivated Notch signaling during SOP specification, resulting in reduction of bristles (quantified in S2A Fig, depicted in S2B and S2C Fig). Su(H) is the DNA-binding transcription factor that is directly bound by NICD. H antagonizes Su(H)’s ability to bind to NICD and thereby activate transcription , consistent with known interactions between Su(H) and H/+ (quantified in S2A Fig, depicted in S2D Fig). Similarly, N55e11/+ suppressed H/+ albeit to a lesser degree (S2A Fig). Supporting the interactions in the eye, AKAP200M30 and AKAP200M24, as well as the AKAP200 deficiency suppressed the H/+ phenotype (S2A Fig, depicted in S2E Fig). Taken together, the data from the eye and thorax are consistent with AKAP200 promoting Notch signaling activity.
AKAP200 promotes Notch signaling in a PKA-independent manner
Since AKAP200 is known to interact with and confine the cellular localization of PKA, we next determined whether AKAP200’s effects on Notch signaling required PKA. We tested the ability to rescue the AKAP200 LOF phenotype of AKAP200-L, which binds PKA, and AKAP200-S, which does not as it lacks the PKA interaction domain (Fig 3A). Strikingly, ubiquitous expression of each isoform (under tubulin-Gal4 control; Fig 3D and 3E) rescued the AKAP200 photoreceptor number defects (Fig 3C). This suggests that eye phenotypes are not related to PKA (quantified in Fig 3B; this also confirmed that the mutants are clean AKAP200 alleles; see also S3 Fig). Similarly, both isoforms were capable of rescuing the AKAP200 bristle defects (S3K, S3M and S3O Fig). To lend further support to the hypothesis that AKAP200’s supernumerary bristle phenotype can be attributed to Notch signaling, we added an extra copy of Notch using N-GFP,Cherry flies  in an AKAP200 mutant background. Here as well we observed a rescue of the AKAP200 bristle defects (S3N and S3O Fig).
(A) AKAP200 has 2 splice variants. AKAP200-L, which can interact with the regulatory subunits of PKA via a tethering site coded for by exon 5 (blue). This exon is spliced out in AKAP200-S, eliminating its ability to interact with PKA. (B-E) Both AKAP200 isoforms can rescue PR number defects in the eye and lethality. Note in schematic of eye phenotypes, loss is indicated by a solid black dot and loss specifically of R7 is indicated by a hollow dot (B) Quantification of genotypes shown in (C-E) ***p<0.0001 by chi square test (against AKAP200M30, n = 514–726, from 3 independent eyes). (C-E) Tangential adult eye sections of indicated genotypes (C) Homozygous AKAP200M30 escaper displays PR number defects. Expression of AKAP200-L (D) and -S (E) via tubulin-Gal4 rescues the AKAP200 phenotype, suggesting that this phenotype is PKA independent. (F-J) PKA-independent effects of AKAP200 on N signaling. (F) Quantification of genotypes shown in (G-J), ***p<0.0001, by chi square test (n = 320–573 from 3–4 independent eyes). (G-J) Tangential adult eye sections of indicated genotypes. PR number defects caused by sev-NΔECD (G) is not modified by PKA-/+ (H), but is suppressed by AKAP200 mutant (I), or both together (J). There is no statistical difference in the effect on sev-NΔECD of removing either one copy of AKAP200 alone or together with PKA, suggesting that PKA may not be required for AKAP200’s effect on Notch signaling.
We also assessed the potential direct involvement of PKA in promoting Notch signaling, and asked whether sev-NΔECD (Fig 3G) is sensitive to PKA levels. Removing one genomic copy of PKA did not modify the sev-NΔECD phenotype (Fig 3H). Moreover, simultaneous removal of one copy each of AKAP200 and PKA (Fig 3J) had the same effect on sev-NΔECD as removing only AKAP200 (Fig 3I; quantified in Fig 3F). To lend further support to this hypothesis, we tested for potential effects of AKAP200-L and AKAP200-S on the sev-NΔECD/+ eye phenotypes (S3C Fig); sev-Gal4 driven overexpression of either AKAP200-L (S3D Fig) and AKAP200-S (S3E Fig) both enhanced sev-NΔECD to comparable extents (quantified in S3F Fig); as overexpressing AKAP200-L or S alone caused no defects in the eye (although each of them did in the wing, S3A and S3B Fig), this indicated that in the eye the enhancement is not an additive effect of unrelated phenotypes. Finally, overexpression of either Notch itself (S3H Fig), AKAP200-L (S3I Fig) or AKAP200-S (S3J Fig) in the entire wing blade (nubbin-Gal4 control) produced similar phenotypes of expanded wing veins.
Taken together, these data are consistent with the notion that AKAP200’s positive role on regulation of Notch signaling is PKA independent.
AKAP200 stabilizes Notch protein
Next, we investigated whether AKAP200 and Notch can be present in the same protein complex. Since both AKAP200 isoforms are equivalent with respect to modulating Notch function, we performed our analyses with AKAP200-S only. A Notch encoding plasmid was transfected into S2 cells with either AKAP200-S-Flag or Flag alone. Immunoprecipitation with the Flag antibody led to the co-immunoprecipitation (co-IP) of the NICD fragment in the AKAP200-S-Flag sample but not the control (Fig 4A, schematic of Notch protein in S4B Fig). Long exposure revealed also co-immunoprecipitation of the NEXT with AKAP200-S, but we did not detect immunoprecipitation of full length Notch (S4A Fig). In an inverse experiment, an AKAP200-S-Flag encoding plasmid was transfected into S2 cells with either Notch-GFP or GFP alone. Immunoprecipitation with the GFP antibody led to the co-immunoprecipitation (co-IP) of AKAP200-S-Flag in the Notch-GFP sample but not the control (Fig 4B).
(A) Notch is co-immunoprecipitated by AKAP200-S: immunoblot from S2 cell whole cell lysates expressing Notch either in combination with Flag-control or AKAP200-S-Flag. Cell lysates were immunoprecipitated with anti-Flag antibody (IP-Flag) and blots were probed with anti-NICD antibody, revealing specific co-IP of Notch with AKAP200-S-Flag with no binding to Flag (right panel-10% input, bottom panel- blots probed with anti-Flag antibody). The specific interaction of AKAP200 and the NICD could be because of the experimental conditions; full length Notch is a large membrane bound protein (270 KDa) it may not be as easily accessible to AKAP200 as the NICD. Given the large size of full length Notch, one cannot exclude the possibility that the physical conformation of the interaction prevents co-immunoprecipitation; for example, AKAP200 maybe buried inside full length Notch. (B) AKAP200-S is coimmunoprecipitated by Notch: immunoblot from S2 cell whole cell lysates expressing AKAP200-S-Flag in combination with GFP-control or Notch-GFP. Cell lysates were immunoprecipitated with anti-GFP antibody (IP-GFP) and blots were probed with anti-Flag antibody, revealing specific co-IP of AKAP200-S-Flag with Notch with no binding to GFP (right panel-10% input, bottom panel- blots probed with anti-GFP antibody). (C) Confocal eye sections from third larval instar eye discs of tub>AKAP200-S-Flag depicting localization AKAP200-S, Notch, and PatJ (marking cellular outlines at junctional level and highlighting developing PR clusters, with strongest staining observed in R2/R5). Note co-localization between anti-NICD punctae and AKAP200-S-Flag (example marked by white arrow), Pearson co-efficient R = 0.67.
To confirm the physiological relevance of these results, we examined the localization of AKAP200-S-Flag and endogenous Notch in third instar eye and wing imaginal discs. We observed co-localization of AKAP200 and Notch (Fig 4C, co-stained with PatJ, R = 0.67, S4C Fig, co-stained with E-Cad). Similarly, we observed colocalization of the two proteins in the portion of the wing imaginal discs from which the thorax arises (S4D Fig, R = 0.4).
To dissect the mechanism(s) underlying the genetic interactions between AKAP200 and Notch and as AKAP200 promotes Notch signaling, we tested whether AKAP200 could regulate Notch protein cleavage or levels. We did not observe any reproducible changes to the Notch cleavage patterns (examples in Fig 5A and S5A Fig). However, strikingly, total endogenous Notch levels were markedly reduced in homozygous AKAP200 mutant backgrounds as compared to WT (Fig 5A and 5C; total Notch levels are the sum of full length Notch, transmembrane Notch/NEXT, and NICD, S5A Fig). Conversely, overexpression of AKAP200-S caused an increase in Notch levels (Fig 5B and 5C). Furthermore, RT-PCR amplification of Notch showed no significant gene expression differences in AKAP200M30 eye disc lysate relative to WT (S5B Fig). Several studies have demonstrated both lysosomal and proteosomal degradation of Notch [20–24]. Thus, we postulated that AKAP200 might regulate Notch turnover. To test this hypothesis, we asked if there is differential ubiquitination of Notch in AKAP200 mutants relative to WT. We performed immunoprecipitations of Notch-Flag from eye disc lysates of WT and AKAP200M30/+ larvae. Upon immunoprecipitation with Flag (and thus Notch) and probing for ubiquitin, there was an increase in ubiquitinated Notch-fl, NEXT and NICD fragments in AKAP200M30/+ backgrounds (Fig 5D). These observations suggest that AKAP200 promotes Notch signaling by stabilizing Notch protein levels and are consistent with the genetic interaction data and corroborated by the observation that 3 genomic copies of Notch rescue AKAP200 LOF defects.
(A-B) Western blots of third instar larval eye disc extracts using NICD and gamma tubulin antibodies [blue arrow: full length Notch; black arrow: membrane bound NEXT; red arrow: NICD, ]. (A) In AKAP200M30 samples, note a decrease in Notch protein levels compared to WT (loading control:©-Tubulin [Y-Tub], bottom here and all other panels). (B) Over-expression of AKAP200-S (by sev-Gal4) leads to an increase in Notch levels, compared to WT. (C) Quantification of Notch protein levels in (A-B) (n = 3, ***p<0.0001, *p = 0.01 by student’s t test; error bar = standard deviation). (D) Increased ubiquitination of Notch is observed in AKAP200M30 mutant. Eye disc lysates from Notch-Flag/+ or Notch-Flag/+, AKAP200M30/+ were immunoprecipitated with anti-Flag and probed with anti-Flag and anti-Ubiquitin. Leupeptin and protease inhibitors were added to the lysis buffer. Blotting with anti-Ubiquitin revealed an increase of ubiquitinated full length Notch, NEXT and NICD in the AKAP200 mutant.
AKAP200 negatively regulates Cbl-mediated lysosomal degradation of Notch
In C2C12 myoblasts, Notch has been shown previously to be targeted for lysosomal degradation as a consequence of mono-ubiquitination by the E3 ubiquitin ligase, Cbl . We thus hypothesized that the reduction of Notch levels and its increased ubiquitination in AKAP200 mutants could involve Cbl.
To explore a role for cbl in the interplay between AKAP200 and Notch, we first tested whether they interacted genetically. Removing one genomic copy of cbl (Fig 6B) did not modify the sev-NΔECD/+ phenotype (Fig 6A). However, the AKAP200M30/+ suppression of sev-NΔECD/+ (Fig 6C) was dependent on Cbl levels, with the suppression effect being markedly reduced upon simultaneous removal of one copy of both AKAP200 and cbl (Fig 6D, quantified in Fig 6E). This suggests that the positive effect of AKAP200 on Notch levels and signaling activity is through antagonizing the negative function of Cbl.
(A-D) Tangential adult eye sections of indicated genotypes, with schematics in lower panels (see Fig 2A for key). (A) PR number defects induced by sev-NΔECD are not modified by the heterozygous cbl mutant alone (B), but are suppressed by heterozygous AKAP200 mutant (C). (D) Simultaneous reduction of one genomic copy of both cbl and AKAP200 reduces the effect of AKAP200 suppression of Notch activation. (E) Quantification of genetic interactions of genotypes in (A-D): ***p<0.0001 from chi square tests (n = 320–686 from 3–4 independent eyes). (F-G) Western blot (F) of third instar larval eye disc lysate showing Notch protein expression (blue arrow: full length Notch, black arrow: membrane bound NEXT, red arrow: NICD). Relative to WT (left lane), a reduction in total endogenous Notch protein is observed in AKAP200M30/+ (middle lane), which is partially suppressed in lysates from AKAP200M30/+; cbl/+ (©-Tub [Y-Tub], bottom, serves as loading control). (G) Quantification of Western blot lanes from (F); n = 3, **p = 0.003, p = 0.01 from student’s t test (error bars represent standard deviations).
To confirm this, we examined the interaction between AKAP200, cbl and Notch in SOP specification, activating the pathway with the H1 allele and using bristle loss as the GOF assay (quantified in S6A Fig, depicted in S6B Fig). Consistent with the eye data, AKAP200M30/+ suppressed the H/+ phenotype (S6D Fig, quantified in S6A Fig). Simultaneously removing one copy of both AKAP200 and cbl (S6E Fig) dampened the effect of AKAP200’s loss on the H/+ phenotype (S6D Fig, quantified in S6A Fig; note that cbl/+ alone as a control has no effect on H1/+, S6C Fig). As previously observed (S2F and S2I Fig), AKAP200M30/+ enhanced the N55e11/+ scutellar phenotype (S6I Fig), and consistently with the above interactions, simultaneous removal of a genomic copy of both AKAP200 and cbl limited the effect of AKAP200M30/+ on N55e11/+ (S6J Fig; note that N55e11/+; cbl/+ alone as a control has no effect S6G Fig). Taken together, these data are consistent with the notion that AKAP200 antagonizes Cbl to promote Notch stability and hence promote signaling.
The Cbl docking consensus site has been mapped to the vicinity of Notch’s PEST domain (S4B Fig). We thus expressed a Notch isoform truncated at amino acid 2155  and thereby deleting the PEST domain (under sev-Gal4 control) either in WT or in the AKAP200M30 background. Unlike with full-length Notch, we detected no significant difference in the phenotypic effect between the two genotypes (S6K and S6L Fig, quantified in S6M Fig). This suggests that the role of AKAP200 in promoting Notch function depends on the presence of the PEST domain, consistent with the hypothesis that AKAP200 protects Notch from Cbl-mediated ubiquitination.
We next assessed the effects of AKAP200 on Cbl-mediated Notch level reduction. We compared Notch protein levels from WT eye discs to AKAP200M30/+ and AKAP200M30/+; cbl/+ discs. While reducing the copy number of AKAP200 resulted in a decrease of Notch levels, concurrent reduction in copy number of both AKAP200 and cbl largely abolished this effect (Fig 6F, quantified in Fig 6G). In line with this observation, Cbl/+ suppresses the AKAP200M30 PR number defect phenotype (S6N Fig).
To confirm specificity of the AKAP200 effect on Cbl, we tested other E3-ubiquitin ligases for an interaction with AKAP200. The Drosophila homolog of Sel10/Fbw7 E3-ligase, archipelago (ago), is an E3 ligase that also has been shown to ubiquitinate NICD and target it for proteosomal degradation . Since ago is also a transcriptional target of Notch , the effect of removing one copy of ago likely affects feedback loops, and thus was not included in our analyses. Instead, we tested if the AKAP200 effect on Notch can be altered if a copy of ago is also removed together with AKAP200. Simultaneous removal of one copy of both, ago and AKAP200, affects the sev-NΔECD/+ phenotype to the same extent as removing only a copy of AKAP200, implying that AKAP200 and ago act via unrelated mechanisms (S6M Fig). This suggests that AKAP200’s effect is specific to Cbl’s ubiquitination of Notch.
Since AKAP200 appeared to protect Notch against the effects of Cbl, which targets Notch to the lysosome, we wanted to investigate the requirement of the lysosome in AKAP200’s action on Notch. We thus analyzed the effect of AKAP200 on sev-NΔECD in the presence of the lysosomal inhibitor chloroquine, which is a lysosomotropic agent acting by increasing lysosomal pH thus inhibiting lysosomal hydrolases as well as fusion of endosomes and lysosomes and thereby impairing degradation [71–74]. The effect of AKAP200M30/+ on sev-NΔECD/+ under control conditions (Fig 7A and 7B, quantified in Fig 7E) was lost when larvae were raised on 1mg/ml chloroquine (Fig 7C and 7D, quantified in Fig 7E). At this dosage, chloroquine by itself had negligible effects on normal development and cell viability, and PR number (quantified in Fig 7E, S7F Fig). Also, the average lifespan of both sev-NΔECD/+ and sev-NΔECD/+, AKAP200M30/+ were comparable at increasing exposures to chloroquine; survival of both genotypes dropped only at chloroquine concentrations significantly greater than 1mg/ml (S7F Fig; confirming a specific effect at 1mg/ml chloroquine and not a general interference). Immunofluorescence analyses in the larval eye disc showed minimal, if any, colocalization of AKAP200 and the lysosome (S7G Fig). This is consistent with the notion that AKAP200 acts on Notch to prevent its targeting to the lysosome by antagonizing Cbl-mediated ubiquitination of Notch which occurs before Notch is targeted to the lysosome.
(A-D) Tangential adult eye sections of indicated genotypes and conditions, and (E) quantification of indicated genotypes/conditions; suppression of PR number defects of sev-NΔECD/+ by AKAP200 is lost in the presence of 1mg/ml of lysosomal inhibitor, chloroquine (***p<0.0001 from chi square tests, n = 378–644 from 3–4 independent eyes). (F) Quantification (**p = 0.005, *p = 0.02, n = 4) and (G) western blot of third instar larval eye discs showing Notch protein levels in indicated genotypes. Relative to WT, heterozygous AKAP200 mutant decreases Notch levels (under control condition, H20 treatment), this effect is lost in the presence of 1 mg/ml chloroquine (Y-Tub, bottom, serves as loading control).
Importantly, reduction of Notch protein levels in the heterozygous AKAP200 mutant background, relative to WT, was lost upon chloroquine treatment (Fig 7G, quantified in Fig 7F). This highlights AKAP200’s dependence on the lysosome to promote Notch signaling and is consistent with its antagonistic effect on Cbl-mediated ubiquitination of Notch.
To confirm these results, we conducted analogous experiments in the context of SOP specification. AKAP200/+ suppression of the H/+ bristle phenotype observed under control conditions (quantified in S7A Fig, depicted in S7B and S7C Fig), was largely lost upon chloroquine treatment (S7D and S7E Fig, quantified in S7A Fig).
Taken together, our data indicate that the mechanism by which AKAP200 promotes Notch signaling, is by protecting Notch protein from the action of Cbl, which targets Notch for lysosomal degradation.
In this study, we have identified AKAP200 as a positive regulator of the Notch signaling pathway, and carried out a detailed analysis of its LOF phenotypes in eyes and wings using null alleles. We demonstrate that AKAP200 promotes Notch signaling, and that the two proteins co-localize and coexist in a complex. AKAP200 exerts its effects on the Notch protein by protecting it from Cbl/lysosome-mediated degradation in specific contexts, in particular during photoreceptor neuron and sensory bristle specification.
AKAP200, Notch, and signaling pathway contexts
AKAP200 was identified in a PCP-signaling mediated screen performed in the Drosophila eye . However, AKAP200 LOF phenotypes resemble Notch LOF. As PCP is instructive to Notch signaling in the R3/R4 specification context in the Drosophila eye, the identification of novel Notch pathway regulators was expected and in line with previous experiments; for example, the Notch ligand Dl was identified in the screen as well . Furthermore, AKAP200’s strong and specific interaction with sev-NΔECD, which is a membrane tethered, ligand-independent activated Notch, indicates that it acts on Notch itself.
Due to AKAP200’s ‘canonical’ role in PKA regulation, we tested how AKAP200 acts in Notch signaling. Analyses of the two isoforms of AKAP200, which differ in their ability to bind PKA, revealed that AKAP200’s Notch associated function is PKA independent, which was corroborated by functional rescue assays with both isoforms rescuing the AKAP200 eye phenotypes indistinguishably. The AKAP200 LOF mutants display other defects, which in some tissues are PKA associated phenotypes: for example AKAP200 mutant wings have a penetrant wing blistering phenotype, which has been observed upon disruption of the PKA pathway [59, 60] and, similarly, AKAP200 mutant ovaries have developmental defects, which have been linked to PKA signaling .
Our work identifies AKAP200 as a regulator of Notch protein levels (also below). However, it does not affect Notch in all tissues, and even in tissues where it is required, it is specific to a subset of Notch signaling contexts. In the eye for example, it affects Notch signaling during photoreceptor specification but not during lateral inhibition in the furrow. Strikingly, there are no effects of AKAP200 on Notch signaling mediated wing margin development, which is even a haplo-insufficient Notch phenotype [76, 77]. Likely, the Notch signaling feedback loops at the wing margin, which also includes Wingless (Wg) expression [78–80], are not sensitive to AKAP200 mediated input. However, overexpression of AKAP200 in the wing led to expansion of wing veins, a phenotype linked to Notch GOF [81, 82], and thus consistent with the Notch GOF effects in photoreceptor specification in the eye. Taken together, our data suggest that AKAP200 affects Notch levels in a tissue and context specific manner, rather than being a general Notch protein level regulator.
AKAP200 promotes a subset of Notch signaling events
How do the AKAP200 Notch signaling requirements relate to each other? In the eye, AKAP200 LOF defects correlate with photoreceptor specification, particularly with R7 and R4 induction, and associated steps. Specification of R7 and R4 both require Notch signaling activation from neighboring R-cells, R1/6 and R8 induce R7 and R3 activates the pathway in R4, and interestingly in both contexts Egfr/RTK signaling is also required for the specific R-cell fate [30, 33, 36–38, 83]. We did not detect an interaction between AKAP200 and the GOF EgfrEllipse alleles, however, suggesting that AKAP200 does not act via Egfr.
Can this correlation be related to other AKAP200 requirement contexts? In the wing, although there is no AKAP200 effect on the margin, both overexpression and LOFs of AKAP200 affect wing vein development. Establishment of wing veins is a multi-step, multi-pathway process, involving coordination of Notch signaling and other pathways, which also include Egfr/RTK signaling [84–88]. Notch signaling causes restriction of cell fate and width of the vein [4, 66, 89–92]. Consistent with the defects in the eye, LOF or GOF of AKAP200 correlates with vein development or vein widening, respectively.
In the thorax, Notch is required at different stages of SOP specification and AKAP200 LOF phenotypes resemble several of these. Can this be linked to Egfr signaling as well? Previous reports have shown an involvement of Egfr/RTK signaling in promoting bristle development, where Egfr hypomorphs developed fewer bristles [93, 94]. The Egfr requirement has been attributed to SOPs requiring Egfr-signaling to maintain wild-type levels of ac-sc expression .
In summary, it appears that AKAP200 affects Notch activity/levels in specific contexts and that these involve Egfr signaling in some capacity.
AKAP200 prevents Cbl-mediated ubiquitination and degradation of Notch
The role of AKAP200 appears to be in stabilization of the Notch protein: there is a decrease of endogenous Notch in the AKAP200 LOF vs. an increase of Notch in AKAP200 GOF backgrounds. We also observed increased ubiquitination of Notch in AKAP200 null mutant backgrounds. Ubiquitination and subsequent degradation of cellular proteins serves as a key mechanism to regulate their activity and disruption in this process often lead to overactivation of signaling. Both AKAP200 and Notch have previously been associated with the E3 ubiquitin ligase, Cbl [21, 96], and strikingly Cbl has also been linked to the regulation of Egfr [97, 98]. Thus, we explored a role for Cbl in AKAP200’s regulation of Notch. Strikingly, suppression of Notch hyperactivation by AKAP200 depends on the presence of wild-type levels of Cbl. Our studies thus suggest that AKAP200’s function is to antagonize Cbl effects on Notch ubiquitination and protein levels. Of note, it is also possible that AKAP200 modulates Notch or other components of the signaling pathway via other mechanisms.
One hypothesis that leads from our work is that AKAP200 could maintain the balance between Cbl’s effects on Notch and Egfr. Since AKAP200 is a scaffolding protein, it may affect both pathways, and only processes that require balanced effects of Notch and Egfr signaling may be impacted. AKAP200 was previously identified as a positive regulator of Ras signaling . However, we did not pursue AKAP200’s role in this context as we did not detect interactions with the EgfrElp allele.
In conclusion, we postulate a novel mechanism of regulation of Notch signaling by AKAP200 antagonizing Cbl-mediated lysosomal degradation of Notch. This study advances our understanding of the tight regulation of Notch protein levels, which is fundamental to numerous key developmental processes and diseases.
Materials and methods
Drosophila strains and genetics
Flies were raised on standard medium and maintained at 25°C unless otherwise indicated. All WT experiments were performed in w1118 backgrounds.
The following stocks lines were used and their sources are indicated:
- Df(2L)Ed623 (stock #8930), Df(2L)N22-14(stock #2892), w1118, N55e11 (stock #28813), PKA-C1H2 (stock #4101), UAS-Notch (stock #26820), cblF165 (stock #9676), Notch-GFP,Flag (stock #BL38665), agoEY01092 (stock #20064)—Bloomington stock collection
- UAS-AKAP200-IR (stocks- 1- #5647, 2- #102374)–VDRC
- Elp–gift from Dr. Ross Cagan, sev-NΔECD–gift from Dr. Mark Fortini, mδlacZ , UAS-NotchΔTAD,PEST- gift from Dr. Edward Giniger, H1 , Su(H)Δ47 , UAS-Dgo;sev-Gal4 , Actin-Gal4;UAS-GFP-huLamp–gift From Dr. Andreas Jenny, N-GFP,Cherry–gift from Dr. Francois Schweisguth .
sev-gal4 (sev-enhancer with heat-shock promoter) initially drives expression in the R3/R4 precursor and later in R1/6 and R7 (note, there is basal expression in other tissues due to the presence of the heat shock promoter from hsp70). sep-gal4 which has the sev-enhancer with sev promoter, results in weaker expression levels than sev-gal4.
AKAP200M30 clones were produced by mitotic recombination via the FLP/FRT system  with eyFLP in an AKAP200M30 FRT40A/ w armlacz FRT40A background and ubxFLP in AKAP200M30FRT40A/ y FRT40A background.
AKAP200M30 and AKAP200M24 were generated using a FLP-recombinase-mediated excision of two piggybac/FRT insertions grkf07069 and AKAP200d03938 and characterized by PCR as previously described . To generate UAS-AKAP200-Flag transgenic flies, the Flag tag was added to the C-term of AKAP200 sequence by PCR amplification using DGRC LD42903 and RE01501 cDNA clones for AKAP200-L and AKAP200-S respectively. The PCR amplified products were cloned into pUASt-attB vector using EcoRI and XhoI sites.
The following primers were used: 5’-CCGGAATTCATGGGTAAAGCTCAGAGCAA-3’and 5-CCGCTCGAGCTTGTCGTCGTCGTCCTTGTA-3’
Transgenic injections were performed by BestGene Inc. where the constructs were targeted to predetermined genomic sites on chromosome 3R using the phiC31 integrase (strain 9744).
For drug treatments, crosses were setup on instant food (Carolina Biological Supply Company) to which chloroquine diphosphate salt (Sigma) or water was added at the indicated concentrations.
To compare relative amount of Notch mRNA, RNA was extracted from eye disc lysates from WT or AKAP200M30 flies using RNeasy Mini Kit as per manufacturer’s protocol (Qiagen). 1 ng of RNA was reverse transcribed (50°- 30’ and 94°- 2’) and real-time PCR was performed using SYBR Green I Master (Roche) on LightCycler 480 (Roche). Quantification was performed using the 2-ΔΔCT method and Gapdh transcript as a reference. Measurements were performed in duplicate. The following primers were used:
- rp49–5’-GACAGTATCTGATGCC-3’ and 5’- TTCCGACCACGTTACAAGAAC-3’
- Notch- 5’-GAGTGGAGCCGGCAATGGAAAT-3’ and 5’-TTCAAAACCTACAGAACTACGA-3’
The amplified products are expected to be ~300 bp for rp49 and ~1600 bp for Notch. As control for DNA contamination in eye disc lysates, a reaction was run using Notch primers excluding reverse transcriptase (rxn mixture).
Immunofluorescence and histology
Third larval instar eye discs were dissected in ice cold PBS and fixed in PBS-4% paraformaldehyde for 20 minutes at room temperature. After three washes in PBT (PBS + 0.1% Triton-X), discs were incubated in primary antibody overnight at 4°C. After three PBT washes, secondary antibody incubation for 2 hours at room temperature and three more PBT washes, the discs were mounted in Vectashield (Vector Laboratories). For immunofluorescence, the following antibodies were used- mouse anti-Prospero (#MR1A, 1:10, Developmental Studies Hybridoma Bank-DSHB), rat anti-Elav (#9F8A9, 1:20, DSHB), mouse anti-NotchICD (#C17.9C6, 1:10, DSHB), rabbit anti-Flag (#637301, 1:100, Biolegend), mouse anti-Flag (#F1804, 1:1000, Sigma), rat anti-DE Cadherin (#5D3, 1:20, DSHB), rabbit anti-Patj (1:500), rabbit anti-GFP (#1828014, 1:1000, invitrogen), rabbit anti-β-gal (1:1000, Molecular probes). Fluorescent secondary antibodies came from Jackson Laboratories. Eye disc and thorax images were acquired at room temperature using a Zeiss LSM 880 or Leica SP5 DMI confocal microscopes Subsequent image processing was performed on ImageJ (National Institute of Health). For colocalization analyses, the JaCoP plugin was used in ImageJ to calculate the Pearson’s coefficient (R).
Eye sections were prepared as previously described . All eyes were sectioned near the equatorial region. For analysis of adult thoraces, whole flies were incubated in 70% ethanol and mounted on gelatin plates. Imaging was done using a stereomicroscope and acquired using Zeiss Axioplan color type 412–312 (Carl Zeiss) camera and Zen Blue software. For analysis of adult wings, wings were removed and incubated in PBT, mounted on a slide in 80% glycerol and imaged using a Zeiss Axioplan microscope (Carl Zeiss).
Western blotting and co-immunoprecipitation
For analysis of Notch protein levels, 10–15 pairs of larval eye discs were lysed in ice cold lysis buffer (50mM Tris HCl pH 7.5, 150mM NaCl, 1mM EDTA and 1% Triton-X). Supernatant from these extracts were resolved and subjected to standard western blotting procedures using mouse anti-NotchICD (#C17.9C6, 1:500, DSHB) and mouse anti-Y-Tubulin (Sigma Aldrich, 1:1000) antibodies.
For co-immunoprecipitation assays, S2 cells were transfected with pmt-Notchfull length (#1022 from DGRC) with pAC-Flag control or pac-AKAP200-S-Flag, or pac-AKAP-200-S-Flag with pUAST-GFP or pUAST-Notch-GFP (gift from Dr. Shigeo Hayashi), both with Actin-Gal4. Transfections were performed using Effectence (QIAGEN, Hilden, Germany) in accordance with manufacturer’s instructions. For pmt-Notch, Notch was induced using 600 μM CuSO4 24 hours after transfection for 24 hours .
For Flag IPs and ubiquitin assays, cells were harvested, washed and lysed in ice-cold lysis buffer (50mM Tris HCl pH 7.5, 150mM NaCl, 1mM EDTA and 1% Triton-X). For ubiquitin assays, the lysis buffer was supplemented with 100 μg/mL leupeptin (Roche 1017101) and protease inhibitor cocktail tablets (Roche, 14268500).
For Flag IPs, lysed samples were incubated overnight at 4°C using anti-Flag M2 agarose beads (Sigma, A2220). Beads were washed three times and protein was eluted by boiling in Laemmli buffer.
For GFP IPs, cells were harvested, washed and lysed in ice-cold lysis buffer (0mM TrisHCl pH7.5, 150mM NaCl, 0.5mM EDTA, 1% TritonX). Following this, we used the GFP-Trap A from Chromotek as per manufacturers protocol (wash buffer: 10mM TrisHCl pH7.5, 150mM NaCl, 0.5mM EDTA).
Western blots were carried out with the immunoprecipitated samples using mouse anti-NotchICD (#C17.9C6, 1:500, DSHB), mouse anti-Flag (#F1804, 1:1000, Sigma), mouse anti-Ubiquitin (#MA1-10035, 1:5000, Thermofisher) and rabbit anti-GFP (#1828014, 1:1000, Invitrogen). HRP coupled secondary antibodies were obtained from Jackson laboratories.
S1 Fig. AKAP200 shows N-signaling like phenotypes in the Drosophila eye and thorax.
(A-B) AKAP200 was identified in a dominant modifier screen. (A) Table shown summarizes modifications of the core PCP factor dgo by AKAP200 deficiencies and IR (dgo was overexpressed by sev-Gal4 which has the sev enhancer and hs promoter leading to strong expression in R3, 4, 1, 6, 7 and cone cells, and basal expression in other tissues including the wing). (B) Quantification of genetic interactions in adult eyes: AKAP200IR enhances rotation defects from dgo overexpression (***p<0.001 from chi square test; n = 536–754, 3–4 independent eyes). (C-D) AKAP200 mutant generation and characterization: schematic of locus (C), grey bars represent coding exons of the gene. Transposable elements used to generate null mutants, P(AKAP200d03938) and Pbac(grkf07069) hereafter called XP5 and WH5 respectively, are indicated in orange and green, and flank the gene. Precise excision results in fusion of the elements and elimination of AKAP200 coding sequences. For PCR characterization, a primer pair was used that sits on elements XP5 and WH5 (depicted by black arrows), or directly outside XP5 and WH5 (depicted by blue arrows). Due to the genomic distance between the primers, in both cases, PCR amplification is only possible if the excision event happened. The expected band size for amplified band when primer combination sitting on XP5 and WH5 is used is ~1.5 Kb and for the primers outside these elements is ~1.7 Kb. (D) PCR characterization of AKAP200 null mutants from genomic DNA extracted from adult escaper flies of indicated genotypes. For lanes labeled in black, primers used sit within the transposable elements XP5 and WH5; for lanes labeled in blue, primers used sit directly outside XP5 and WH5. XP5 and WH5 are absent in WT DNA resulting in no PCR amplification, and the primers outside these elements are too far to result in PCR amplification in WT DNA. Genomic DNA from two null mutants AKAP200M30 and AKAP200M24 give a band at the expected sizes of ~1.5–1.7 Kb upon PCR amplification. (E-F) Pupal thorax clones stained for Elav (white) and Cut (red); mutant tissue marked by absence of green marker. Note irregular spacing of SOPs and “bald” patches (yellow arrows) as evident by Elav staining in (E-E’). Higher magnifications (F-F”) reveal defects in SOP lineages with clusters containing two Elav positive cells (yellow arrowheads) or reduced Elav staining (blue arrowhead). (G) Quantification of distribution of eye phenotypes upon AKAP200 knockdown by two independent IRs or from transheterozygous AKAP200 null mutant/AKAP200 deficiency. White indicates WT, blue indicates loss of one or more outer PRs, green indicates loss of R7 with or without simultaneous loss of outer PRs. Of note, AKAP200 null mutant/AKAP200 deficiency have highy reduced viability (<5%). In contrast, overexpression of AKAP200 caused minimal defects. (H) Tangential adult eye sections from example escaper transheterozygous AKAP200 mutants (genotype as indicated). (I-I’) AKAP200 defects in developing eye discs as revelaed by Elav staining (green) and Pros staining (red). Note defects in Elav positive cells and (I’) loss of Pros+ (R7) cells (examples marked by yellow arrowheads; note that Pros staining in cone cells [blue arrowhead is present and serves as control]). A wt looking example is marked by white asterisks. (J) Homozygous AKAP200M30 escaper showing penetrant blistered wing phenotype.
S2 Fig. AKAP200 promotes Notch signaling.
(A) Quantification of genetic interactions in adult nota by assessing bristle number in indicated genotypes. Activation of the Notch pathway using the Hairless (H) mutant, the co-repressor that keeps Notch target genes off in the absence of signal, results in decreased number of bristles compared to WT. This phenotype is dominantly rescued by removal of one copy of Su(H)[Su(H)Δ47, null allele] or Notch (N55e11, null allele). Similar suppression is observed with AKAP200 mutants (M30 and M24) and deficiency, note AKAP200M30/+ has no phenotype (***p<0.0001, *p = 0.02 by Mann Whitney test against H1/+ from 5–20 flies). (B-E) Examples of adult heads as representations of total bristles of indicated genotypes, loss of bristles is indicated by blue asterisk. (B) WT head showing normal bristle arrangement. (C) H1/+ head showing loss of bristles. (D) H1/+, Su(H)/+ and (E) AKAP200M30/+; H1/+ showing strong and moderate suppression of H1/+ loss of bristles phenotype respectively. (F) Quantification of genetic interactions in adult scutellum by assessing supernumerary bristles in indicated genotypes. Reduction of Notch signaling in N55e11 null mutant causes increase in number of bristles, which is enhanced by loss of AKAP200 mutants or deficiency, note AKAP200M30/+ has no phenotype (***p<0.0001, **p = 0.0016, *p = 0.04 by Mann Whitney test against N55e11/+ from 9–35 flies). (G-J) Examples of adult scutellar bristles of indicated genotypes, red arrow indicates supernumerary bristles. (G) WT scutellum showing normal bristle arrangement. (H) N55e11/+ showing supernumerary bristles. (I) N55e11/+; AKAP200M30/+ and (J) N55e11/+; AKAP200M24/+ show significant enhancement of N55e11/+ phenotype. (K) Confocal images of third instar eye discs of indicated genotypes stained for neuronal marker Elav (red, labeling all PR cells) and LacZ which stains mδ (Green, initially expressed at low levels in R3 and R4, following Notch activation it is upregulated in R4). One R4/ommatidium is observed in WT (top row). Activation of Notch signaling by sev-NΔECD increases R4s/ommatidium (middle row), which is suppressed with simultaneous reduction of AKAP200 (bottom row). (L) Quantification of (K), n = 91–125 ommatidia from 4 independent eyes; ***p<0.0001 by chi square test. (M) Removal of one genomic copy of AKAP200 has no effect on the PR number defects of EGFR GOF allele Elp (chi square tests, n = 547–683 from 4 independent eyes) (N-O) Examples of adult wings of indicated genotypes (N) Elp/+ displays wing vein overgrowth defect and (O) taking away one copy of AKAP200 in this background does not this dominant phenotype.
S3 Fig. AKAP200 promotes Notch signaling in a PKA independent manner.
(A-E) Tangential adult eye sections of indicated genotypes (A) AKAP200-L and (B) AKAP200-S overexpression under sev-Gal4 results in <1% defects. sev-Gal4 driven overexpression produces stronger phenotypes than tub-Gal4; both isoforms of AKAP200 produced a negligible effect upon overexpression by sev-Gal4. This indicates that AKAP200 overexpression rescues the mutant with no additive effects of its own phenotype (cf. to Fig 3A). (C-E) The PR number defects induced by sev-NΔECD (C) are enhanced by co-expression of AKAP200-L (D) and AKAP200-S (E) under sev promoter, further implying that AKAP200’s effects on Notch is unrelated to its ability to bind PKA. (F) Quantification of genotypes in (A-E) (***p = 0.0003, <0.0001 from chi square test, n = 543–746 from 3 independent eyes). (G-J) Adult wings: (G) WT wing. (H) Notch overexpression under nubbin-Gal4 (expressed throughout wing) causes vein expansion and deltas, which is also observed by AKAP200-L (I) and AKAP200-S overexpression (J). (K-N) Examples of adult thoraces of indicated genotypes, red asterix indicates supernumerary bristles; (K-M) both isoforms of AKAP200 rescue its mutant phenotype (N) N-GFP,Cherry flies express an extra copy of WT Notch which also rescues the AKAP200 mutant phenotype. (O) Quantification of genotypes in (K-N) (***p<0.0001 by Mann Whitney test against AKAP200M30 from 10–16 flies).
S4 Fig. AKAP200 and Notch co-localize.
(A) Longer exposure of Notch co-immunoprecipitation by AKAP200-S: immunoblot from S2 cell whole cell lysates expressing Notch either in combination with Flag-control or AKAP200-S-Flag. Cell lysates were immunoprecipitated with anti-Flag antibody (IP-Flag) and blots were probed with anti-NICD antibody, revealing specific co-IP of Notch with AKAP200-S-Flag with no binding to Flag (right panel-10% input, bottom panel- blots probed with anti-Flag antibody). Upon longer exposure, there is specific binding of NEXT and NICD, but not full length Notch. (B) Schematic representation of the structure of the Notch protein. Notch receptors are type I transmembrane proteins. The extracellular domain is largely comprised of 36 EGF repeats. Egfr 8 is involved in ligand selectivity, Egfrs 11 and 12 are required for ligand binding. Following the Egfrs is the NRR, negative regulatory region, whose function is to prevent ligand independent Notch activation by concealing the S2 cleavage site. The NRR is comprised of 3 Lin-12-Notch repeats (LNR) and a hydrophobic region responsible for mediating heterodimerization (HD). The S1 and S2 cleavage sites are present here and the S3 cleavage site is present in the TM domain. NICD is composed of a RAM domain involved in CSL interaction, two NLS’s responsible for nuclear translocation, Ankyrin repeats needed for interaction with Mam, a TAD domain that recruits further coactivators needed for maximally efficient signaling, and a PEST domain targeting NICD for degradation and essential for signal termination. NEXT is comprised of the TM domain and the NICD . (C) Confocal eye sections of third larval instar eye discs of tub>AKAP200-S-Flag, depicting localization of AKAP200-S-Flag (green), NICD (red), and E-Cad (blue, marking cellular outlines at junctional level and highlighting developing PR clusters, most strongly expressed in R2/R5, and R8, and R3/R4 also visible). Co-localization is observed between NICD punctae and AKAP200-S-Flag highlighted by white arrow (D) Confocal sections of third larval instar wing discs of tub>AKAP200-S-Flag, depicting the cells that give rise to the thorax. AKAP200-S-Flag (green) and NICD (red) colocalize (examples are marked by yellow arrowheads; Pearson co-efficient R = 0.4); Patj (blue) marks cellular outlines.
S5 Fig. Quantification of Notch protein levels.
(A) Western blot of third instar larval eye discs showing endogenous Notch protein; blue arrow indicates full length Notch (~290 KDa), black arrow indicates membrane bound NEXT (~120 KDa), red arrow indicates NICD (~110 KDa), all highlighted by green boxes . Quantification of total Notch protein was the sum of pixel intensity of full length Notch, NEXT and NICD. See S4B Fig for schematic of Notch, highlighting the position of each Notch band/cleavage form. (B) Agarose gel electrophoresis of RNA extracted from eye disc lysate in WT and AKAP200M30 which shows no significant difference in Notch gene expression. 1 ng of RNA was used. Lanes 1,3 and 5 are RNA from eye disc lysates from WT flies, lanes 2,4 and 6 are RNA from eye disc lysates from AKAP200M30 flies. Lanes 1 and 2 were amplified with rp49 specific primers as a positive control for the RT-PCR. Lanes 3 and 4 were amplified with Notch specific primers, lanes 5 and 6 used the same primers without reverse transcriptase.
S6 Fig. AKAP200’s effect on Notch signaling is dependent on Cbl.
(A) Quantification of genetic interactions shown in (B-E) of adult heads by assessing bristle number in indicated genotypes (**p = 0.001, 0.004, 0.008 from Mann Whitney tests, n = 9–24). Note, AKAP200M30/+ has no phenotype- see S2A and S2F Fig. (B-E) Adult heads as representations of total bristles of indicated genotypes, loss is indicated by blue asterisks. (B) H1/+ exhibits decreased bristle number. (C) Removing one genomic copy of cbl does not modify the H1/+ phenotype. (D) Removing one genomic copy of AKAP200M30 suppressed H1/+. (E) Reduced suppression of H1/+ phenotype, when one genomic copy of both AKAP200M30 and cbl are removed. (F) Quantification of genetic interactions shown in (G-J) of adult nota by assessing supernumerary scutellar bristle number in indicated genotypes (**p = 0.001, from Mann Whitney tests, n = 7–35). Note AKAP200M30/+ has no phenotype, see S2A and S2F Fig. (G-J) Adult scutellar bristle of indicated genotypes, red arrow indicates supernumerary bristles (G) N55e11/+ shows supernumerary bristles. (H) N55e11/+; cbl/+ does not vary from (G). (I) N55e11/+; AKAP200M30/+ shows enhancement of N55e11/+ phenotype. (J) N55e11/+; AKAP200M30/+; cbl/+ does not vary from (G): when both AKAP200 and cbl are reduced by one gene copy, the enhancement of the Notch mutant phenotype by AKAP200 is lost. (K-L) Tangential adult eye sections of indicated genotypes. (K) PR number defects induced by sev>NΔ2155/+ is not modified by the AKAP200M30/+ (L). (M and N) Quantifications of the respective genotypes. (M) 1–2 are sev>NΔ2155/+ and sev>NΔ2155/+, AKAP200M30/+; no significant change in phenotype is observed (chi square tests, n = 290–512 from 3–4 independent eyes). 3–5 are quantifications of genetic interaction of sev-NΔECD/+ along with the removal of one genomic copy of AKAP200M30 alone or both, ago and AKAP200M30. The AKAP200M30 mediated suppression of sev-NΔECD/+ is not affected by ago/+ (chi square tests, n = 614–677 from 4 independent eyes). (N) Removal of one genomic copy of Cbl suppresses the PR number defects of AKAP200M30 (*** p<0.001, chi square tests, n = 387–504 from 3–4 independent eyes).
S7 Fig. AKAP200 effect on Notch levels is dependent on lysosomal function.
(A) Quantification of genetic interactions in adult nota by assessing bristle number in indicated genotypes (***p<0.0001, **p = 0.0012 from Mann Whitney’s tests, n = 11–20). (B-E) Adult heads as representations of total bristles of indicated genotypes, loss is marked by blue asterisks. (B) H1/+ exhibits decreased bristle number. (C) AKAP200M30 suppresses the H1 phenotype under control condition (H20 treatment) (D-E) but is unable to do so in the presence of 1 mg/ml chloroquine. Subtle deviation from the expected number of bristles (40) in WT upon exposure to 1 mg/ml of chloroquine suggests that lysosomal dysfunction has a phenotype on its own. (F) Survival rate of flies of indicated genotypes (blue and grey lines, see panel) after exposure to increasing doses of chloroquine (indicated on x-axis). (G) Confocal eye sections of third larval instar eye discs of Ac>AKAP200-S-Flag,UAS-huLamp-GFP depicting localization of AKAP200-S-Flag (red), lysosome (green), and E-Cad (blue, marking cellular outlines at junctional level and highlighting developing PR clusters, with strongest staining observed in R2/R5, and R8, and R3/R4 also visible). Minimal co-localization is observed between lysosomes and AKAP200-S-Flag. Bottom panel is a zoom of highlighted area of the top panel (R = 0.03).
We thank the Bloomington Drosophila Stock Center, Vienna Drosophila RNAi Center, Drosophila Genomics Resource Center (DGRC), Ross Cagan, Francois Schweisguth, Ed Giniger, Shigeo Hayashi, Andreas Jenny, and Hugo Bellen for fly strains and reagents. We thank Nabila Founounou for help with the thorax clones, all Mlodzik lab members for helpful input and discussions; and R. Krauss, C. Pfleger, and M. O’Connell for helpful comments on the manuscript.
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