Mutations in the human N-glycanase 1 (NGLY1) cause a rare, multisystem congenital disorder with global developmental delay. However, the mechanisms by which NGLY1 and its homologs regulate embryonic development are not known. Here we show that Drosophila Pngl encodes an N-glycanase and exhibits a high degree of functional conservation with human NGLY1. Loss of Pngl results in developmental midgut defects reminiscent of midgut-specific loss of BMP signaling. Pngl mutant larvae also exhibit a severe midgut clearance defect, which cannot be fully explained by impaired BMP signaling. Genetic experiments indicate that Pngl is primarily required in the mesoderm during Drosophila development. Loss of Pngl results in a severe decrease in the level of Dpp homodimers and abolishes BMP autoregulation in the visceral mesoderm mediated by Dpp and Tkv homodimers. Thus, our studies uncover a novel mechanism for the tissue-specific regulation of an evolutionarily conserved signaling pathway by an N-glycanase enzyme.https://doi.org/10.7554/eLife.27612.001
DNA carries the information needed to build and maintain an organism, and units of DNA known as genes contain coded instructions to build other molecules, including enzymes. Sometimes, genes can become faulty and develop mutations that can affect how an embryo develops and lead to diseases. For example, people with mutations in the gene that encodes an enzyme called N-glycanase 1 experience many problems with their nervous system, gut and other organs.
Normally, N-glycanase 1 helps the body remove specific sugar molecules from some proteins in the cells, and is also thought to be important during embryonic development. As an embryo develops, its cells undergo a series of transformations, which is regulated by different molecules and signaling pathways. For example, a pathway known as BMP signaling plays an important role in many tissues. Problems with this pathway can lead to many diseases throughout the body, including the gut, where it helps cells to develop.
Previous research has shown that fruit flies lacking the gene that codes for an equivalent N-glycanase enzyme (which is called Pngl in flies) cannot develop properly into adults. However, until now it was not known what type of cells need the N-glycanase enzyme in any organism, or if NGLY1 is essential for important signaling pathways like BMP signaling. Now, Galeone et al. have used genetically modified flies to test how losing Pngl affected their development.
The results first showed that engineering Pngl-deficient fruit flies to produce the human enzyme eliminated their problems; these flies developed and survived like normal flies. This confirmed that that the human and fly enzymes can perform equivalent roles. Galeone et al. then discovered that Pngl plays two distinct roles in a group of cells that surround the fruit fly’s gut tissue and give rise to the cells that eventually form the muscle layer in the gut. In the larvae, Pngl was required to empty the gut, which is a necessary step before the larvae can develop into an adult. Moreover, Pngl is needed for BMP signaling in the gut, and when flies had the enzyme removed, some parts of their gut could not from properly.
This study will provide a framework to improve our understanding of how BMP signaling is regulated in humans. A next step will be to test if some of the symptoms experienced by patients without a working copy of the gene for N-glycanase 1 are caused by a faulty BMP-signaling system in specific tissues. If this is the case, it could provide new opportunities to treat some of these symptoms.https://doi.org/10.7554/eLife.27612.002
NGLY1 (N-glycanase 1) encodes an evolutionarily conserved enzyme that catalyzes the cleavage of N-glycans from glycoproteins (Suzuki et al., 2000). Whole-genome and -exome sequencing has recently resulted in the identification of NGLY1 mutations in patients with an autosomal recessive developmental disorder called NGLY1 deficiency (Caglayan et al., 2015; Enns et al., 2014; Heeley and Shinawi, 2015; Need et al., 2012). NGLY1-deficient patients show a host of phenotypes including global developmental delay, movement disorder, hypotonia, absent tears, peripheral neuropathy, constipation, and small feet and hands (Enns et al., 2014; Lam et al., 2017). The mechanism by which NGLY1 deficiency causes the above-mentioned clinical phenotypes is not known, and neither has NGLY1 been linked to any major developmental signaling pathway.
In yeast, N-glycanase 1 (Peptide: N-glycanase or PNGase, encoded by PNG1) has been associated with endoplasmic reticulum-associated degradation (ERAD) (Suzuki, 2007; Suzuki et al., 2016), a process that plays a crucial role in the proteasome-mediated degradation of misfolded proteins (Brodsky, 2012; Smith et al., 2011). However, null mutants for yeast PNG1 do not show apparent phenotypic abnormalities and exhibit normal growth rate and viability under a variety of experimental conditions (Suzuki et al., 2000). A recent study has provided strong evidence that in C. elegans, a transcription factor called SKN-1 (homolog to mammalian NFE2L1/2) needs to be retrotranslocated from ER to cytoplasm by ERAD machinery and deglycosylated by NGLY1 (PNG-1 in worms) to function properly (Lehrbach and Ruvkun, 2016). However, deglycosylation does not result in SKN-1 degradation, but instead promotes the activation of SKN-1 so that it can mediate the necessary transcriptional response to proteasome disruption (Lehrbach and Ruvkun, 2016). Moreover, mouse embryonic fibroblasts lacking NGLY1 did not show impairment and/or delay in the degradation of misfolded proteins, but displayed an unconventional deglycosylation reaction that may generate aggregation-prone proteins harboring N-GlcNAc and result in cell toxicity in the absence of NGLY1 (Huang et al., 2015). Therefore, although NGLY1 seems to be functionally associated with the ERAD machinery, it does not seem to directly promote the degradation of misfolded proteins in animals.
Human NGLY1 has a single Drosophila homolog called PNGase-like (Pngl), whose loss-of-function mutants result in semi-lethality and sterility (Funakoshi et al., 2010). We have used Drosophila to determine the molecular mechanisms by which Pngl regulates animal development. Our data indicate that Pngl is required in the visceral mesoderm (VM) during midgut development to regulate bone morphogenetic protein (BMP) signaling from VM to endoderm in embryonic midgut and also to ensure midgut clearance before puparium formation. BMP ligands can signal either as homodimers or as heterodimers through homodimeric or heterodimeric BMP type I receptors (Bangi and Wharton, 2006a; Ray and Wharton, 2001). Our data indicate that loss of Pngl abolishes a BMP autoregulatory loop in the VM mediated by homodimers of one ligand (Decapentaplegic; Dpp) acting through homodimers of one receptor (Thickveins; Tkv), and hence link a deglycosylation enzyme to tissue-specific regulation of BMP signaling in flies.
Based on the analysis of three Pngl alleles (Pnglex14, Pnglex18 and Pnglex20; Figure 1A), it has previously been reported that loss of Drosophila Pngl results in developmental delay and a semi-lethality phenotype, with about 1% adult escapers (Funakoshi et al., 2010). Moreover, these phenotypes were rescued by ubiquitous expression of mouse NGLY1 (Funakoshi et al., 2010), suggesting functional conservation between Pngl and its mouse homolog. To further examine the degree of conservation between fly Pngl and its mammalian homologs, we used ΦC31-mediated transgenesis (Bischof et al., 2007; Venken et al., 2006) to generate transgenic flies capable of overexpressing wild-type (WT) human NGLY1 or the NGLY1-ΔR402 mutant, a single amino acid in-frame deletion identified in an NGLY1 deficiency patient (Enns et al., 2014), and asked whether they can rescue the homozygous lethality of Pnglex14 and Pnglex18. Ubiquitous expression of WT human NGLY1, but not NGLY1-ΔR402, was able to rescue the lethality in both Pngl alleles (Figure 1B). Both male and female Pngl–/– escaper flies are sterile and short-lived (Figure 1C and D) (Funakoshi et al., 2010). However, adult Pngl–/–; Act > NGLY1 WT animals do not show these phenotypes (Figure 1C and D). Together, these results underscore the in vivo functional homology between Pngl and NGLY1.
A previous study did not detect PNGase activity in wild-type Drosophila larval extracts in an in vitro assay using 14C-labeled asialofetuin glycopeptide as a substrate and concluded that Drosophila Pngl might not possess N-glycanase activity (Funakoshi et al., 2010). To better assess whether Pngl can function as an N-glycanase, we used RTL (RTAΔ-transmembrane-Leu2) spotting assays, which provide a reproducible in vivo model to assess the level of PNGase activity in yeast (Hosomi et al., 2010). RTL undergoes ERAD in a PNGase-mediated, deglycosylation-dependent manner and therefore leucine-auxotrophic yeast cells which express functional Saccharomyces cerevisiae PNGase (Sc-Png1) are unable to grow in media lacking leucine. However, yeast cells that lack Sc-Png1 or express a catalytically-inactive version of Sc-Png1 fail to degrade RTL and can therefore grow on leucine-deficient medium (Hosomi et al., 2010). As shown in Figure 1E, png1 mutant yeast cells (png1Δ) grow well in media with or without leucine when transfected with the RTL plasmid. Expression of Sc-Png1-HA severely decreases the ability of these cells to grow in the absence of leucine, confirming that this phenotype is PNGase-dependent (Figure 1E) (Hosomi et al., 2010). An HA-tagged version of the fly Pngl suppressed the growth of the yeast cell in media without leucine to the same extent as the Sc-Png1 (Figure 1E). Meanwhile, Pngl harboring a C303A mutation in its putative catalytic domain (Pngl-HA-C303A) failed to rescue PNGase function (Figure 1E), even though WT and C303A versions are expressed at comparable levels (Figure 1F). These observations strongly suggest that Drosophila Pngl is able to deglycosylate RTL and facilitate the efficient degradation of the RTL protein. Next, we expressed a FLAG-tagged version of RTAΔ in yeast cells and asked whether Pngl can increase the level of the deglycosylated version of this protein upon inhibition of the protein biosynthesis. In png1Δ mutant yeast cells, almost all RTAΔ was found to be in the glycosylated form (g1) at three time points (Figure 1G). Expression of Sc-Png1 or fly Pngl increased the relative level of the deglycosylated form (g0) in a time-dependent manner (Figure 1G and H). However, Pngl-C303A failed to remove glycans from RTAΔ. Similar experiments indicate that human NGLY1, but not the C309A catalytic mutant NGLY1, can also compensate for the lack of Sc-Png1 in the RTL assay (Figure 1I). Of note, NGLY1-ΔR402 showed a weak rescue of the PNGase activity in this assay, suggesting that it is a hypomorphic allele. Altogether, these observations indicate that Drosophila Pngl is indeed an N-glycanase enzyme and that there is high level of functional conservation between Pngl and its yeast and human homologs.
Pngl–/– larvae did not show any gross morphological defects. However, inspection of the larval internal organs suggested defects in the mutant larval midguts. In the anterior part of the midgut, control larvae harbor four finger-like structures called gastric caeca (Figure 2A and B and Figure 2—figure supplement 1), which play key roles in the insect digestive system, including water and ion transport and secretion of enzymes (Pullikuth et al., 2006; Volkmann and Peters, 1989). Pngl–/– larvae showed a severe shortening of the gastric caeca (Figure 2C, red asterisks) compared to y w and heterozygote controls (Figure 2B and Figure 2—figure supplement 1). Control larvae harbor a specific region in the middle midgut called the ‘acid zone’, which has a luminal pH of less than 2.3 and is considered the fly stomach (Figure 2A) (Dubreuil, 2004). The acid zone can be visualized by feeding larvae with bromophenol blue (BPB), which is blue in neutral and basic pH but turns yellow as the pH is decreased from 7.0 to 1.0 (Figure 2D and Figure 2—figure supplement 1, red dotted box). Pngl–/– larvae are almost completely devoid of the yellow color in the midgut, indicating a loss of acid zone (Figure 2E). Similar to Pnglex14/ex14 larvae, Pnglex18/ex18 and Pnglex20/ex20 animals showed shortened gastric caeca and a loss of acid zone (Figure 2—figure supplement 2 and not shown). Moreover, Pnglex14 and Pnglex18 hemizygous animals (over a deficiency allele) showed semi-lethality and midgut phenotypes (Figure 2—figure supplement 2 and not shown), suggesting that ex14 and ex18 deletions are genetic null alleles. Altogether, these data indicate that loss of Pngl leads to specific midgut defects in Drosophila larvae.
In Drosophila embryos, a member of the bone morphogenetic protein (BMP) family called Decapentaplegic (Dpp) signals from VM to endoderm and is required for midgut specification (Dubreuil, 2004; Panganiban et al., 1990). Specifically, BMP signaling from VM in parasegment 3 (PS3) and PS7 is transduced by phosphorylated Mothers against dpp (pMad) (Newfeld et al., 1996) in midgut endoderm, resulting in the formation of the gastric caeca and the acid zone, respectively (Figure 2F). Given the striking similarity between Pngl midgut phenotypes and those caused by impaired BMP signaling from VM (Panganiban et al., 1990), we examined the effects of loss of Pngl on BMP signaling by staining Drosophila embryos with an antibody against human pSMAD3, which recognizes Drosophila pMad (Li et al., 2016). Control embryos (y w and Pngl+/–) showed pMad staining in areas corresponding to PS3 and PS7 (Figure 2G and G’ and Figure 2—figure supplement 1). However, Pngl–/– embryos showed a dramatic decrease in the level of pMad in PS3 and PS7 (Figure 2H and H’). Notably, pMad staining in other regions of the embryos, including the ectodermal and head regions, was not affected by the loss of Pngl (Figure 2H’, compare to Figure 2G’ and Figure 2—figure supplement 1). Loss of BMP signaling in PS7 results in lack of second midgut constriction and impairs the expression of the acid-secreting (copper) cell-specific homeodomain gene labial in PS7 endodermal cells (Immerglück et al., 1990; Nellen et al., 1994; Panganiban et al., 1990). We used anti-Labial antibody to mark the precursors of the midgut copper cells in the embryonic endoderm and anti-Fas3 (Fasciclin 3) antibody to mark VM (Weiss et al., 2001) and to visualize midgut constrictions and chambers. As reported previously (Nellen et al., 1994), at stage 15, control embryos show a prominent second midgut constriction and Labial expression anterior to it (Figure 2I and I’ and Figure 2—figure supplement 1). However, in stage 15 Pngl–/– embryos, no Labial signal was detectable in the PS7 region (Figure 2J and J’). By stage 16, all three constrictions are clearly visible in control larvae and Labial is expressed in the midgut compartment between first and second constrictions (Figure 2K and K’ and Figure 2—figure supplement 1). However, stage 16 Pngl–/– embryos lack Labial staining and second constriction (Figure 2L and L’), in agreement with impaired BMP signaling in PS7. Together, these data demonstrate that Pngl is required for mesoderm-to-endoderm BMP signaling in Drosophila embryos.
To determine which tissues or cell types require the function of Pngl, we performed RNAi-mediated knock-down (KD) and rescue experiments. When crossed to the mesodermal driver Mef2-GAL4, the PnglRNAi KK101641 strain (http://stockcenter.vdrc.at/control/main) resulted in 100% lethality at room temperature and recapitulated the gastric caeca shortening and acid zone loss phenotypes observed in Pngl mutants (Figure 3A–C). In addition, Pngl KD by another mesodermal driver called how24B-GAL4 resulted in partial lethality and acid zone defects in larvae (Figure 3A and E). Pngl KD with how24B-GAL4 did not affect gastric caeca formation (Figure 3D), likely because this driver induces transgene expression later than Mef2-GAL4 (Figure 3—figure supplement 1), after gastric caeca anlagen have already been formed. However, Pngl KD by two endodermal drivers did not result in lethality and gut phenotypes (Figure 3A and F–I). Moreover, overexpression of human NGLY1 with Mef2-GAL4 and how24B-GAL4 rescued the lethality of the Pngl alleles (Figure 3J). In agreement with the severity of their corresponding KD phenotypes and expression patterns, Mef2-GAL4 rescued the lethality more efficiently than how24B-GAL4 (Figure 3J). Together, these data indicate that during Drosophila development Pngl is primarily required in the mesoderm to ensure animal survival and to promote BMP signaling from visceral mesoderm to endoderm.
It was previously shown that a Pngl transgene harboring the C303A mutation in the catalytic domain (Figure 1E and G) is not able to rescue the lethality of Pngl mutants (Funakoshi et al., 2010). To test whether the enzymatic activity of Pngl is required for the regulation of BMP signaling in the midgut, we overexpressed Pngl-C303A by Mef2-GAL4 in Pngl mutants. As shown in Figure 3K and L, overexpression of wild-type Pngl rescues gastric caeca and acid zone defects of Pngl mutants. However, the mutant version fails to rescue Pngl midgut phenotypes (Figure 3M and N), even though Western blot shows that this mutation does not affect the expression level or stability of Pngl (Figure 3O). Together, these data indicate that the BMP signaling impairment observed in Pngl larval midguts is due to the lack of Pngl’s enzymatic activity.
Previous reports indicate that in the absence of midgut acidification, larvae are able to reach adulthood (Dubreuil et al., 2001). Moreover, regulatory mutations that result in specific loss of dpp expression in PS3 and a complete loss of gastric caeca only show a partial lethality (Masucci and Hoffmann, 1993). Accordingly, impaired Dpp signaling in the midgut is not sufficient to fully explain the lethality of Pngl mutants, especially given that gastric caeca are not completely lost. Indeed, animals undergoing dpp KD by the same mesodermal drivers showed a higher survival compared to those undergoing Pngl KD (Figure 3P, compare to 3A). Specifically, Mef2 > PnglRNAi and how24B > PnglRNAi animals showed 0% and ~28% survival rate into adulthood, but Mef2 > dppRNAi and how24B > dppRNAi animals showed ~8% and ~80% survival rate into adulthood, respectively. The weaker effects of dppRNAi are not likely to result from inefficient dpp KD, as Mef2 > dppRNAi larvae exhibited a complete loss of gastric caeca and acid zone, and how24B > dppRNAi larvae lost the acid zone but not the gastric caeca, suggesting a loss or severe impairment of mesoderm-to-endoderm BMP signaling corresponding to the spatiotemporal expression pattern of each driver (Figure 3Q–T). These observations indicate that impaired Dpp signaling in the midgut can only partially account for the lethality observed in Pngl mutants.
So far our data suggest that Pngl also plays a Dpp-independent role in the mesoderm during Drosophila development. We noticed that during the wandering phase, Pngl–/– larvae failed to empty their guts (Figure 4A and A’). To better characterize this phenotype, we carried out midgut clearance assays. When larvae are raised on regular food supplemented with bromophenol blue (BPB), they show a dark blue gut approximately 24–48 hours before puparium formation (early L3 stage). At late L3 stage, they stop eating and enter the wandering stage, during which they empty their gut and reach the stationary stage (Denton et al., 2008). Pngl+/– (control) and Pngl–/– larvae both exhibit a blue gut during early L3 stage, indicative of eating food containing BPB (Figure 4B). Once taken off the BPB food during the wandering stage, control larvae gradually lose the blue color and pupariate, but the Pngl–/– larvae fail to empty their guts and exhibit a delay in pupariation (Figure 4B). Control y w and Pngl+/– larvae typically emptied their gut in 6 hours and reached the pre-pupal stage (Figure 4C). In contrast, most Pngl–/– larvae showed a blue gut throughout the wandering stage (Figure 4C). Indeed, even 24–48 hours later, more than 50% of the Pngl+/– animals were still in the larval stage and retained the blue food in their abdomens. These data indicate that loss of Pngl causes an impairment of gut clearance at late L3 stage.
To examine whether impaired BMP signaling can also explain the food accumulation phenotype observed upon loss of Pngl, we compared the dpp and Pngl KD phenotypes by the same mesodermal drivers. BPB feeding assays showed that Mef2 > dppRNAi larvae exhibit a food accumulation phenotype milder than that observed in Pngl mutant and Mef2 > PnglRNAi larvae, and that how24B > dppRNAi larvae do not exhibit any food accumulation phenotype, in contrast to how24B > PnglRNAi animals (Figure 4D, compare to Figure 4E). These data indicate that the food accumulation phenotype observed in Pngl mutants is at least in part independent of impaired BMP signaling.
Loss of Pngl affects BMP signaling in the midgut but not in the ectodermal regions of the Drosophila embryos. To shed light on the mechanism by which Pngl regulates BMP signaling in a tissue-specific manner, we stained Pngl mutant and control embryos with a polyclonal anti-Dpp antibody raised against its prodomain (Akiyama and Gibson, 2015). In WT and Pngl+/– embryos at stage 13, the Dpp protein is expressed in ectodermal bands, several regions in the anterior part of the embryo and two rather narrow groups of cells corresponding to PS3 and PS7, where it shows a punctate pattern superimposed on a diffuse signal (Figure 5A, B, G and H). Overall, the staining is somewhat weaker in Pngl–/– embryos, but staining in PS3 and PS7 is observed, with a notable decrease in puncta (Figure 5C and I). By stage 14, a broad and strong Dpp expression domain can be observed in PS3 and PS7 in control embryos (Figure 5D, E, J and K). In contrast, Dpp expression in the VM remains weak and narrow in PS3 and PS7 of mutant embryos (Figure 5F and L). Notably, the pattern of Dpp expression in the ectoderm is similar in control and Pngl–/– embryos at both stages, even though the staining seems to be slightly weaker in mutant embryos (Figure 5A–F). These results suggest that a failure to expand the Dpp expression domain in the VM leads to impaired mesoderm-to-endoderm BMP signaling in Pngl mutants.
Given the weaker Dpp staining in stage 13 Pngl mutant embryos, we asked whether the failure to expand the Dpp expression domain and loss of BMP signaling in the embryonic midgut of Pngl mutants is simply due to reduction of dpp expression in the mesoderm. To address this point, we used the dppS2 allele, which harbors a chromosomal breakpoint in the regulatory elements that control dpp expression in digestive tract (Masucci and Hoffmann, 1993). Embryos heterozygous for this allele exhibit a decrease in Dpp expression at stage 13 in PS7, even compared to Pngl–/– embryos (Figure 5M, compare to Figure 5G, H and I). Nevertheless, these embryos show Dpp propagation at stage 14 and proper Dpp signaling from mesoderm to endoderm, as evidenced by analyzing the expression of Dpp targets in the embryonic midgut and gastric caeca and acid zone in larvae (Figure 5N and Figure 5—figure supplement 1). These data suggest that decreased Dpp expression by itself cannot explain the impaired Dpp propagation and loss of mesoderm-to-endoderm BMP signaling in Pngl mutants.
To understand how Dpp spreads in PS7 during embryonic midgut development, we expressed UAS-GFP in embryonic mesoderm by Mef2-GAL4 driver and stained embryos for pMad at stage 13 and 14. At stage 13 the majority of pMad staining is localized to the VM and only a few cells are stained in the endoderm (Figure 5O and O’). Later at stage 14, BMP signaling spreads through the endoderm and expands in PS7, as evidenced by the presence of many pMad-positive endodermal cells (Figure 5P and P’; GFP–, round nuclei). These observations are in agreement with previous reports suggesting the existence of an autoregulatory Dpp para-autocrine loop in PS7, which acts through Ultrabithorax (Ubx) expression in VM and results in maintenance and accumulation of Dpp expression in VM cells (Figure 5Q) (Bienz, 1997; Hursh et al., 1993; Staehling-Hampton and Hoffmann, 1994). To test whether Pngl affects Dpp autoactivation in VM, we used a dpp enhancer trap line and stained embryos for pMad and βGAL. In Pngl+/– embryos at stage 13, we found a row of cells co-expressing pMad and βGAL (Figure 5R–R’), suggesting para-autocrine activation. In PS7 of Pngl–/– embryos at stage 13, dpp-lacZ expression can be detected, but pMad staining is absent (Figure 5S–S’). These results indicate that in Pngl–/– PS7, the initial, Ubx-dependent dpp expression (Sun et al., 1995) occurs, but the autoactivation loop is impaired. At stage 14, the Dpp expression domain expands in Pngl+/– embryos and dpp-lacZ expressing cells can be seen in multiple layers. Most if not all dpp-lacZ expressing cells still co-express pMad, likely due to autoactivation, while endodermal cells, as receiving cells, only express pMad (Figure 5T–T’). In stage 14 Pngl–/– embryos, dpp-lacZ-expressing cells remain confined to their initial narrow domain in PS7, and pMad staining is still not detectable (Figure 5U–U’). This is in contrast to the dorsal ectodermal region, which showed a comparable expression pattern and intensity in the dorsal ectodermal bands of Pngl+/– and Pngl–/– embryos for both dpp-lacZ and pMad (Figure 5—figure supplement 2). Altogether, these data indicate that Pngl is not required for the initial expression of dpp through Ubx in Drosophila embryos but is required for the autoregulatory role of Dpp in the VM.
We next asked whether bypassing the BMP autoactivation loop by mesodermal overexpression of a GFP-tagged version of Dpp (Teleman and Cohen, 2000) can rescue Pngl phenotypes in embryos. In control animals, dpp-GFP overexpression by Mef2-GAL4 resulted in broad pMad staining in embryonic midgut and ectopic pMad expression throughout the ectoderm (Figure 6A and D). Dpp-GFP protein can be seen by GFP staining and shows a continuous pattern going through PS3 to PS7 (Figure 6D’). In Pngl–/– embryos, mesodermal expression of Dpp-GFP restored pMad expression in PS3 and PS7, indicating a rescue of BMP signaling from VM to endoderm (Figure 6B and E, compare to Figure 6C and F). Notably, in Pngl–/–; Mef2 > dpp GFP embryos, pMad staining was limited to PS3 and PS7, and ectopic pMad expression in the ectoderm was almost completely suppressed (Figure 6B and E), indicating that loss of Pngl dramatically decreases the ability of mesodermally-expressed Dpp-GFP to induce ectopic BMP signaling.
If BMP autoactivation is impaired in Pngl–/– VM, bypassing the normal autoactivation process by expressing a constitutively active form of the BMP receptor Tkv (tkvCA) in the mesoderm should restore BMP signaling in the PS3 and PS7 endoderm. Mef2 > tkvCA embryos exhibited proper pMad staining in PS3 and PS7 in a Pngl+/+ background, although some pMad staining outside of PS7 could be seen in the VM marked by Fas3 (Figure 6G and G’, arrows). When tkvCA is overexpressed in Pngl–/– embryonic mesoderm, pMad was restored in PS3 and PS7 and still some extra pMad positive cells were detected (Figure 6H and H’, arrows). Moreover, ~30% of Pngl–/–; Mef2 > tkvCA animals reach adulthood (Figure 6I). These observations further indicate that impaired BMP signaling is partially responsible for the lethality of Pngl–/– animals. This is likely due to gastric caeca shortening (Masucci and Hoffmann, 1993), although we cannot exclude that tkvCA overexpression affects unknown BMP-related defects in other parts of mesoderm in these mutants. We note that the rescued Pngl–/–; Mef2 > tkvCA adults did not show the acid zone loss and midgut shortening phenotypes observed in Pngl–/– adult escapers (Figure 6—figure supplement 1). This indicates that the BMP-related midgut phenotypes of Pngl mutants persist to adulthood. Altogether, these results support the notion that BMP signaling in VM requires an autoregulatory step to reach the required threshold for signaling to endoderm and that this is the step during midgut development that is impaired in Pngl mutants. The data also indicate that this developmental defect contributes to the semi-lethality of Pngl mutants.
BMPs can function as homodimers or heterodimers to signal through homo- and/or heterodimeric type I receptors (Hogan, 1996; O'Connor et al., 2006). To date, three BMP ligands have been identified in Drosophila: dpp, glass bottom boat (gbb) and screw (scw) (Arora et al., 1994; Doctor et al., 1992; Padgett et al., 1987; Wharton et al., 1999). scw is required in early embryogenesis, where it acts in combination with dpp to specify dorsal cells fates (Arora et al., 1994). gbb and dpp mutants have both distinct and overlapping phenotypes during and after embryonic development, suggesting that gbb and dpp are required together for proper signaling in some developmental contexts (Goold and Davis, 2007; Haerry et al., 1998; Hong et al., 2016; Khalsa et al., 1998; Wharton et al., 1999). To assess whether gbb is involved in BMP signaling and Dpp expression in embryonic midgut and the generation of Pngl–/– phenotypes, we performed Dpp and pMad staining in gbb mutant embryos at stage 14, focusing on PS3 and PS7. Unlike control embryos (Figure 7A and Figure 7—figure supplement 1), gbbD4/D20 and gbbD4/D4 embryos showed reduced pMad staining in PS3 (Figure 7C and Figure 7—figure supplement 1), in agreement with previous work indicating that gastric caeca are somewhat short in gbb mutant larvae (Wharton et al., 1999). However, in gbb–/– embryos pMad staining in PS7 is increased and shifts anteriorly towards PS3 (Figure 7C and Figure 7—figure supplement 1). In gbbD4/D20 embryos, the Dpp expression domain in PS3 is similar in size to that in control embryos (Figure 7—figure supplement 2). However, the Dpp expression domain in PS7 is broader and stronger than controls in these embryos and extends anteriorly to PS6, and additional Dpp-positive puncta can be detected outside of the acid zone region towards PS3 (Figure 7—figure supplement 2). At stage 16, gbb–/–embryos show an abnormal expansion of the second midgut compartment and a diffuse Labial staining both anteriorly and posteriorly to the second constriction (Figure 7D and D’ and Figure 7—figure supplement 1) compared to controls (Figure 7B and B’ and Figure 7—figure supplement 1). Therefore, gbb phenotypes in the midgut are quite different from dpp and Pngl loss-of-function phenotypes. The strong and broader than normal pMad expression domain in gbb–/– PS7 indicates that BMP signaling in this region is mediated by Dpp homodimers alone and Gbb likely limits the area in the VM wherein BMP autoactivation and signaling can occur.
In Drosophila, two type I receptors Tkv and Saxophone (Sax) and one type II receptor (Punt) are involved in BMP signaling (Letsou et al., 1995; Nellen et al., 1994; Nellen et al., 1996; Ruberte et al., 1995). Given the differential roles of the Dpp versus Gbb ligands in BMP autoactivation in VM, we asked whether the contribution of Tkv and Sax to this process is also different from each other. As shown in Figure 6E, mesodermal knock-down of tkv results in a severe reduction of pMad staining in PS7 and a partial loss of pMad in PS3. Similar to Pngl–/– embryos, the Dpp expression domain in PS7 fails to expand in Mef2 > tkvRNAi embryos, although tkv KD does not seem to affect the intensity of Dpp staining at stage 13 or the presence of Dpp-positive puncta (Figure 7—figure supplement 2). In Mef2 > saxRNAi embryos, pMad staining in PS3 seems to be slightly decreased compared to controls, but it looks broader in PS7 and is extended anteriorly (Figure 7G). Furthermore, Mef2 > tkvRNAi embryos show a lack of second constriction and loss of Labial in the PS7 region (Figure 7F and F’). In contrast, mesodermal knock-down of sax did not show evident midgut constriction defects, but aberrant Labial staining was detectable both anteriorly and posteriorly to the second constriction, similar to gbb–/– embryos (Figure 7H and H’). These results strongly suggest that BMP autoactivation in PS7 mesoderm is mediated by Dpp homodimers, as ligand, and Tkv homodimers, as receptor.
Similar to its vertebrate homologs, Dpp is synthetized as an inactive proprotein (Figure 7I). Following dimerization in the endoplasmic reticulum (ER), Dpp proprotein dimers traffic through the secretory pathway, where they undergo cleavages to release the active dimer (Christian, 2012; Künnapuu et al., 2009; Sopory et al., 2010). Since our results indicate a role for Pngl in Dpp autoactivation mediated by Dpp homodimers (as opposed to Dpp-Gbb heterodimers) in PS7 VM, we examined the effects of loss of Pngl on Dpp dimerization and processing by Western blotting on larval extracts using the above-mentioned anti-Dpp antibody (Akiyama and Gibson, 2015). When ran on a reducing gel, control larvae (y w and UAS-PnglRNAi without a GAL4 driver) exhibited two prominent bands: one corresponding in size to the full-length proprotein monomer and the other to the proprotein dimer, suggesting that Dpp dimers are partially resistant to the amount of reducing agents used in our assays (Figure 7J). A third band slightly bigger and much fainter than the proprotein monomer was also observed in control larvae (Figure 6J, red asterisk). Larvae homozygous for Pngl alleles and those ubiquitously expressing Pngl dsRNA showed an accumulation of a band corresponding in size to the prodomain (cleavage product) and a significant decrease in the intensity of the band corresponding to Dpp dimers, without an apparent decrease in the intensity of the proprotein monomer band (Figure 7J). Of note, although larvae heterozygous for the Pnglex14 allele did not show any midgut defects (Figure 2—figure supplement 1), they displayed an intermediate pattern in the Western blot, suggesting that Pngl plays a dosage-sensitive role in Dpp dimerization and/or processing (Figure 7J). To better assess the level of Dpp dimers in a Pngl-deficient background, we performed Western blot analysis on larval extracts ran on a non-reducing SDS gel electrophoresis (Figure 7K). Control larvae showed two rather strong bands corresponding in size to Dpp dimers and a weaker band corresponding to a proprotein monomer. This indicates that in a non-denaturing state, Dpp molecules are primarily found in association with other molecules and form Dpp-Dpp homodimers. We found a significant decrease in Dpp dimers in Pngl mutant and knock-down larvae and a corresponding increase in the level of full-length monomer and the same cleavage product observed in regular Western blots. Again, Pnglex14/+ larvae showed an intermediate band pattern, with a significant decrease in the intensity of one of the two ‘dimer’ bands and an apparent increase in the intensity of the full-length monomer (Figure 7K). Dpp dimers are not exclusively reduced in midguts of Pngl mutants but are also decreased in other parts of the larval body (Figure 7—figure supplement 3). In summary, these data provide strong evidence that Pngl is required for the formation and/or the stability of Dpp dimers.
The broad phenotypes of children affected with NGLY1 deficiency (Enns et al., 2014; Need et al., 2012) and the semi-lethality of Pngl–/– flies (Funakoshi et al., 2010) indicate that NGLY1 plays important roles during animal development. However, the N-glycanase function has not been linked to any developmental signaling pathway. Here we report that fly Pngl regulates BMP signaling during embryonic midgut development without affecting BMP signaling in ectodermal and head regions of the embryo. Our data indicate that Pngl is not required in the midgut endoderm to receive the BMP signal, but rather is required in the VM to send the BMP signal. It has previously been shown that BMP signaling uses a paracrine/autocrine loop in the VM to sustain and increase the expression of Dpp in PS3 and PS7 of embryonic VM. This loop is proposed to ensure that the level of BMP ligands in the VM is high enough to induce signaling in the endoderm and to specify gastric caeca, the second midgut constriction and the acid zone (Bienz, 1997; Hursh et al., 1993; Staehling-Hampton and Hoffmann, 1994). Several lines of evidence indicate that the BMP autoregulation mediated by the para-autocrine loop in the VM is the step which is impaired in Pngl-deficient embryos. First, Pngl is not required for the initial, Ubx-dependent expression of dpp. In fact, even a 50% decrease in the expression of dpp in the visceral mesoderm of dpps2/+ animals does not impair BMP autoactivation and midgut development. Second, despite expressing Dpp at early stages, BMP signaling is not activated in Pngl–/– VM, as evidenced by the lack of pMad staining. Third, overexpression of Dpp-GFP in the mesoderm is able to induce BMP signaling in the endoderm in Pngl–/– embryos. Lastly, bypassing the para-autocrine loop by transgenic expression of a constitutively active BMP receptor in the mesoderm results in restoration of BMP signaling in PS3 and PS7 regions of the endoderm and in partial rescue of lethality in Pngl–/– embryos.
In the BMP para-autocrine loop, VM cells both secrete the BMP ligand and respond to it. Therefore, theoretically, Pngl might play a critical role in sending the BMP signal, receiving the BMP signal, or both. Although our data do not allow us to exclude any of these possibilities, based on the following observations, we favor a scenario in which Pngl is required in VM cells to send the Dpp signal not to receive it: (1) Pngl is not required to receive the BMP signal in the endoderm; (2) Loss of Pngl and Pngl KD result in a dramatic decrease in the level of Dpp homodimers and the Dpp-positive puncta; (3) Expression of a constitutively active form of Tkv in the mesoderm is able to restore midgut pMad staining in embryos and the copper cell region in the adult midgut, and partially rescue the lethality of Pngl–/– animals; (4) Loss of Pngl almost fully suppresses the aberrant BMP signaling caused by mesodermal overexpression of Dpp-GFP.
Whole larval protein extracts from Pngl-deficient animals show an increase in the level of the monomeric forms of Dpp (full-length and a cleavage product) and a simultaneous decrease in the bands corresponding in size to Dpp dimers. Moreover, Pngl–/– embryos show a decrease in Dpp-positive puncta both in the mesoderm, where signaling is impaired, and in the ectoderm, where signaling is not impaired. Together, these observations indicate that the effect of loss of Pngl on the Dpp protein itself is not limited to the mesoderm. Indeed, protein extracts from Pngl-deficient midgut and carcass (without midgut) both show a decrease in Dpp dimer levels. This suggests that either Pngl regulates BMP signaling by affecting Dpp dimer levels in other larval tissues not identified yet, or that Dpp dimers are only important in the midgut and although they are decreased elsewhere, Dpp-Gbb heterodimers compensate for the lack of Dpp dimers in most other tissues. Regardless, we propose that loss of BMP signaling in Pngl mutant midguts results from a requirement for Dpp homodimers in the para-autocrine autoregulatory loop present in the visceral mesoderm.
BMP ligands can signal both as homodimers and as heterodimers (Bragdon et al., 2011; O'Connor et al., 2006). In vitro and in vivo studies have shown that in general, BMP heterodimers have stronger bioactivity than their homodimers counterparts (Aono et al., 1995; Butler and Dodd, 2003; Israel et al., 1996; Little and Mullins, 2009; Morimoto et al., 2015; Valera et al., 2010). In some cases, the homodimers induce weak to moderate signaling, and in other cases they either do not elicit signaling or even play an antagonistic role (Bangi and Wharton, 2006b; O'Connor et al., 2006). Stronger activity of BMP heterodimers can at least in part be explained by differential affinities of individual BMP ligands for different BMP receptors, combined with stronger signal transduction by heterodimeric type I receptors compared to homodimers of each type I receptor. For example, in Drosophila, Dpp has a higher affinity for Tkv, whereas the other two ligands–Gbb and Scw–have a higher affinity for Sax (Bangi and Wharton, 2006b; O'Connor et al., 2006; Shimmi et al., 2005). A similar receptor-ligand binding preference has been observed among the vertebrate orthologs (Aoki et al., 2001; Little and Mullins, 2009). In the embryonic dorsal midline and the wing imaginal disc, Dpp/Scw and Dpp/Gbb heterodimers induce high levels of signaling, respectively, through Tkv/Sax heterodimers (Bangi and Wharton, 2006b; O'Connor et al., 2006). Comparison of the gbb mutant phenotypes in the midgut with those caused by Pngl loss and by dpp KD indicates that Dpp homodimers are the only productive form of ligand in PS7. Moreover, mesodermal KD of tkv severely decreases BMP signaling in PS7, but mesodermal KD of sax not only does not decrease pMad staining in PS7, but also results in an expansion of pMad expression domain in the PS7 region, similar to gbb mutant embryos. Together, these observations strongly support the notion that the BMP autoregulatory loop in the VM, which is essential for the activation of BMP signaling in the endoderm, relies solely on Dpp and Tkv homodimers, and therefore is impaired in Pngl mutants due to the severe decrease in the level of Dpp homodimers in these animals.
Vertebrate and invertebrate BMP proteins and other members of the TGFβ superfamily each harbor several N-linked glycosylation sites, which have been shown to be glycosylated in many cases (Groppe et al., 1998; Miyazono and Heldin, 1989; Tauscher et al., 2016). Various functional roles have been ascribed to N-glycans on these ligands, including enhancing receptor binding of BMP6 (Saremba et al., 2008), keeping the TGFβ1 ligand in a latent state (Miyazono and Heldin, 1989), and promoting inhibin (α/β) heterodimer formation at the expense of activin (β/β) homodimer formation (Antenos et al., 2007). Accordingly, given the significant increase in Dpp monomeric forms and the simultaneous decrease in Dpp dimers upon loss of Pngl, it is possible that Pngl removes one or more N-glycans from Dpp and thereby promotes the formation or the stability of Dpp homodimers. Whether the regulation of Dpp by Pngl is direct or mediated via other proteins will remain to be explored.
In agreement with a previous report (Masucci and Hoffmann, 1993), our data suggest that the lethality of Pngl mutants cannot be fully explained by shortening of the gastric caeca and impairment of BMP signaling in midgut development. Pngl KD with mesodermal drivers leads to a higher degree of lethality compared to dpp KD with the same drivers. Moreover, how24B > PnglRNAi animals show ~70% lethality, even though they do not have gastric caeca defects. Finally, restoring BMP signaling in the midgut by expressing tkvCA only recues the lethality in ~30% of Pngl–/– animals. Phenotypic analysis of Pngl mutants combined with rescue and KD experiments suggest that a failure to properly empty the gut before puparium formation contributes to lethality in these animals. The molecular mechanisms for the food accumulation phenotype and other potential Pngl–/– phenotypes contributing to lethality are still under investigation.
In summary, our work indicates that the fly Pngl is an evolutionarily conserved N-glycanase enzyme necessary to sustain BMP autoactivation in the VM mediated by para-autocrine activity of Dpp homodimers through Tkv homodimers. Although we cannot exclude that Pngl plays important roles in other cell types as well, our data indicate that Pngl is primarily required in the mesoderm during midgut development and its loss results in Dpp-dependent and Dpp-independent midgut defects. Given the reports on potential para-autocrine functions of mammalian Dpp homologs (Grimsrud et al., 1999; Rege et al., 2015; Shukunami et al., 2000; Tokola et al., 2015) and prominent human pathologies associated with dysregulated BMP signaling in ophthalmic, gastrointestinal and musculoskeletal systems (Wang et al., 2014), tissue-specific alterations in BMP signaling might contribute to some of the NGLY1 deficiency phenotypes including retinal abnormalities, delayed bone age and osteopenia, small feet and hands, and chronic constipation (Enns et al., 2014; Lam et al., 2017). Finally, understanding the mechanisms underlying the food accumulation phenotype in Pngl–/– larvae might shed light on the pathophysiology of chronic constipation in NGLY1 deficiency patients.
Animals were grown on standard food containing cornmeal, molasses and yeast at room temperature, except for RNAi crosses, which were cultured at 30°C. The following strains were used in this study: y w, w; L/CyO, kr-GAL4 UAS-GFP (CyO-GFP), TM3, Sb1/TM6, Tb1, Act-GAL4, Mef2-GAL4, how24B-GAL4 (Brand and Perrimon, 1993; Staehling-Hampton et al., 1994), dpp10638 (dpp-lacZ) (Zecca et al., 1995), dpps2 (Masucci and Hoffmann, 1993), UAS-dpp-GFP (Teleman and Cohen, 2000), UAS-dppRNAi (Liu et al., 2010), UAS-tkvRNAi, gbbD4 and gbbD20 (Chen et al., 1998), UAS-tkvCA (Adachi-Yamada et al., 1999), Df(2R)ED1484, UAS-CD8::GFP (Bloomington Drosophila Stock Center), Pnglex14, Pnglex18, Pnglex20, UAS-Pngl and UAS-Pngl-C303A (Funakoshi et al., 2010), NP3207-GAL4 and NP3270-GAL4 (Tanaka et al., 2007) (Kyoto Drosophila Stock Center), UAS-PnglRNAi KK101641, UAS-saxRNAi (Vienna Drosophila Resource Center), UAS-attB-NGLY1-WT-VK31 and UAS-attB-NGLY1-ΔR402-VK31 (this study).
To identify homozygous animals in sibling crosses, Pngl and gbb mutants were balanced over a CyO, kr-GAL4 UAS-GFP chromosome. To examine dpp transcription in a Pngl–/– background, a dpp-lacZ Pnglex14/CyO-GFP recombinant strain was generated and crossed to Pnglex14/CyO GFP animals. To overexpress NGLY1 in Pngl–/– animals, Pngl– (ex14 or ex18)/CyO; GAL4 (Actin, Mef2 or how24B)/TM6, Tb1 animals were crossed to Pngl–/CyO; UAS-attB-NGLY1-VK31 (WT or ΔR402)/TM6, Tb1 animals. To overexpress TkvCA or Dpp-GFP in a Pngl–/– background, Pnglex14/CyO-GFP; Mef2-GAL4 animals were crossed to Pnglex14/CyO-GFP; UAS-tkvCA (or UAS-dpp-GFP) and absence of the CyO-GFP was used to select the intended genotype. To overexpress Pngl and Pngl-C303A in Pngl–/– animals, Pnglex14/CyO-GFP; Mef2-GAL4 animals were crossed to Pnglex14/CyO-GFP; UAS-Pngl and Pnglex14/CyO-GFP; UAS-Pngl-C303A animals and selected similar to the above crosses.
For survival (eclosion) tests, the expected ratio of offspring was calculated based on Mendelian inheritance for each genotypic class and the observed/expected ratio is reported as a percentage. Fertility was assessed by placing 2-day-old single male of each genotype with three 4-day-old virgin y w females or three 4-day-old virgin females of each genotype with three 4-day-old virgin y w males. Flies were transferred to fresh vials every 5 days for three times. The total number of progeny produced over 20 days by each animal was counted. Data are represented as mean ±SD of 3 independent sets of experiments. For longevity analyses, newly eclosed males of each genotype were collected and housed at a density of 5 flies per vial. Flies were transferred to fresh food every 3–4 days, and dead flies were counted every day until all died. Data are represented as mean of 3 independent sets of experiments.
Human NGLY1 cDNA in pCMV6-AC vector (clone SC320763, OriGene) was used as template for site-directed mutagenesis to introduce the c.1205_1207del clinical mutation (Enns et al., 2014), which results in the generation of NGLY1-ΔR402. Wild-type and ΔR402 cDNAs were transferred from pCMV6-AC to pUAST-attB vector by EcoRI-XhoI double digestion and ligation, verified by sequencing, and integrated into the VK31 docking site by ΦC31-mediated transgenesis (Bischof et al., 2007; Venken et al., 2006).
Larvae were raised on standard food supplemented with 0.05% bromophenol blue (BPB). Wandering larvae were collected from the side of the vial with a wet paint brush, transferred to a petri dish lined with wet Whatman paper and monitored for gut clearance until puparium formation. About 30 larvae were scored for each genotype at each time point. Each data point is from three independent experiments. For larval gut acidification studies, 72 hours after egg deposition, larvae were transferred to standard food containing 0.05% BPB and dissected after 12 hours. For examination of adult acid zones, one-day old animals were fed on food supplemented with 0.05% BPB for two days and then dissected. The images were taken by ToupCam Camera and analyzed by ToupView software.
RTL spotting assay was carried out using png1Δ cells (png1::KanMX4 Mata his3Δ1 leu2Δ0 met15Δ0 ura3Δ0) and pRS313-GAL4RTL essentially as described previously (Masahara-Negishi et al., 2012). In brief, strains harboring the RTL expression plasmid were spotted on to SC-histidine-uracil or SC-histidine-uracil-leucine medium containing 2% galactose (w/v), and plates were incubated at 30°C for 3 days. Photographs of the plates were taken using FUJIFILM LAS-3000 mini (Fujifilm Co., Tokyo, Japan).
png1Δ cells harboring the pRS315-GPDFLAG-RTAΔ (Hosomi et al., 2010) were grown at 30°C in SC-leucine liquid medium. Cycloheximide was added at t = 0 min (final concentration, 4 μg/ml), and the samples were collected at the indicated times and subjected to SDS-PAGE, followed by immunoblotting with anti-DYKDDDDK antibody 1:10,000 (Wako Cat# 018–22381, RRID:AB_10659453). Phosphoglycerate kinase (Pgk1) was used as a loading control and was probed with anti-Pgk1 antibody 1:10,000 (Molecular Probes Cat# A-6457, RRID:AB_221541).
Proteins were extracted from whole larvae in lysis buffer containing protease inhibitor cocktail (Promega). The following antibodies were used: rabbit anti-NGLY1 1:500 (Sigma-Aldrich Cat# HPA036825, RRID:AB_10672231), mouse anti-tubulin 1:1000 (Santa Cruz Biotechnology Cat# sc-8035, RRID:AB_628408), mouse anti-actin 1:1000 (DSHB Cat# 224-236-1, RRID:AB_10571933), rabbit anti-Pngl 1:250 (Funakoshi et al., 2010), rabbit anti-Dpp 1:1000 (Akiyama and Gibson, 2015), mouse anti-HA 1:20,000 (Sigma-Aldrich Cat# B9183, RRID:AB_439706), goat anti-rabbit-HRP and goat anti-mouse-HRP 1:2000 (Jackson ImmunoResearch Laboratories). Western blots were developed using Pierce ECL Western Blotting Substrates (Thermo Scientific). The bands were detected using an ImageQuant LAS 4000 system from GE Healthcare. At least three independent immunoblots were performed for each experiment.
The following antibodies were used: rabbit anti-pSMAD3 1:250 (Abcam Cat# ab52903, RRID:AB_882596), guinea pig anti-Labial 1: 1000 (Guo et al., 2013), rabbit-anti Dpp 1:100 (Akiyama and Gibson, 2015), mouse anti-βGAL 1:50 (DSHB Cat# 40-1a, RRID:AB_528100), mouse anti-Fas3 1:50 (DSHB Cat# 7G10 anti-Fasciclin III, RRID:AB_528238), mouse anti-GFP 1:500 (Thermo Fisher Scientific Cat# 33–2600, RRID:AB_2533111), goat anti-rabbit-Cy3 1:500, goat anti-mouse-Cy5 1:500 (Jackson ImmunoResearch Laboratories). Confocal images were taken with Leica TCS-SP8 microscope. All images were acquired using Leica LAS-SP software. Amira 5.2.2 and Adobe Photoshop CS6 were used for processing and Figures were assembled in Adobe Illustrator CS6.
Potent ectopic bone-inducing activity of bone morphogenetic protein-4/7 heterodimerBiochemical and Biophysical Research Communications 210:670–677.https://doi.org/10.1006/bbrc.1995.1712
Endoderm induction in Drosophila: the nuclear targets of the inducing signalsCurrent Opinion in Genetics & Development 7:683–688.https://doi.org/10.1016/S0959-437X(97)80017-2
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathyEuropean Journal of Medical Genetics 58:39–43.https://doi.org/10.1016/j.ejmg.2014.08.008
Morphogen gradients in development: from form to functionWiley Interdisciplinary Reviews: Developmental Biology 1:3–15.https://doi.org/10.1002/wdev.2
Methods and protocols for studying cell death in DrosophilaMethods in enzymology 446:17–37.https://doi.org/10.1016/S0076-6879(08)01602-9
Copper cells and stomach acid secretion in the Drosophila midgutThe International Journal of Biochemistry & Cell Biology 36:742–752.https://doi.org/10.1016/j.biocel.2003.07.004
BMP-6 is an autocrine stimulator of chondrocyte differentiationJournal of Bone and Mineral Research 14:475–482.https://doi.org/10.1359/jbmr.19188.8.131.525
Biochemical and biophysical characterization of refolded Drosophila DPP, a homolog of bone morphogenetic proteins 2 and 4Journal of Biological Chemistry 273:29052–29065.https://doi.org/10.1074/jbc.273.44.29052
Injury-induced BMP signaling negatively regulates Drosophila midgut homeostasisThe Journal of Cell Biology 201:945–961.https://doi.org/10.1083/jcb.201302049
Multi-systemic involvement in NGLY1-related disorder caused by two novel mutationsAmerican Journal of Medical Genetics Part A 167A:816–820.https://doi.org/10.1002/ajmg.a.36889
Bone morphogenetic proteins: multifunctional regulators of vertebrate developmentGenes & Development 10:1580–1594.https://doi.org/10.1101/gad.10.13.1580
Identification of an Htm1 (EDEM)-dependent, Mns1-independent Endoplasmic Reticulum-associated Degradation (ERAD) pathway in Saccharomyces cerevisiae: application of a novel assay for glycoprotein ERADThe Journal of Biological Chemistry 285:24324–24334.https://doi.org/10.1074/jbc.M109.095919
Prospective phenotyping of NGLY1-CDDG, the first congenital disorder of deglycosylationGenetics in Medicine 19:160–168.https://doi.org/10.1038/gim.2016.75
A plant peptide: N-glycanase orthologue facilitates glycoprotein ER-associated degradation in yeastBiochimica et Biophysica Acta (BBA) - General Subjects 1820:1457–1462.https://doi.org/10.1016/j.bbagen.2012.05.009
Clinical application of exome sequencing in undiagnosed genetic conditionsJournal of Medical Genetics 49:353–361.https://doi.org/10.1136/jmedgenet-2012-100819
Molecular characterization of sodium/proton exchanger 3 (NHE3) from the yellow fever vector, Aedes aegyptiJournal of Experimental Biology 209:3529–3544.https://doi.org/10.1242/jeb.02419
Specificity of bone morphogenetic protein-related factors: cell fate and gene expression changes in Drosophila embryos induced by decapentaplegic but not 60ACell Growth & Differentiation : The Molecular Biology Journal of the American Association for Cancer Research 5:585–593.
PNG1, a yeast gene encoding a highly conserved peptide:N-glycanaseThe Journal of Cell Biology 149:1039–1052.https://doi.org/10.1083/jcb.149.5.1039
Cytoplasmic peptide:N-glycanase and catabolic pathway for free N-glycans in the cytosolSeminars in Cell & Developmental Biology 18:762–769.https://doi.org/10.1016/j.semcdb.2007.09.010
K VijayRaghavanReviewing Editor; National Centre for Biological Sciences, Tata Institute of Fundamental Research, India
In the interests of transparency, eLife includes the editorial decision letter and accompanying author responses. A lightly edited version of the letter sent to the authors after peer review is shown, indicating the most substantive concerns; minor comments are not usually included.
Thank you for submitting your article "Tissue-specific regulation of BMP signaling by Drosophila N-glycanase 1" for consideration by eLife. Your article has been reviewed by two peer reviewers, and the evaluation has been overseen by K VijayRaghavan as the Senior Editor and Reviewing Editor. The reviewers have opted to remain anonymous.
The reviewers have discussed the reviews with one another and the Reviewing Editor has drafted this decision to help you prepare a revised submission.
In this manuscript, the authors investigate the role of the pngl gene (which encodes an enzyme that removes N-linked glycans) during Drosophila development. This study is highly relevant as mutations in the human ortholog of this gene (NGLY1) are responsible for a congenital disorder of glycosylation where patients present with major developmental delays. Using genetic deficiencies, deletions and RNAi interference, the authors identify a role for this gene in Dpp signaling during early development that results in phenotypic abnormalities in larvae. Specifically, they demonstrate that loss of pngl influences the extent of Dpp propagation in PS3 and PS7 of embryonic development, thereby affecting mesoderm to endoderm signaling. This study is thorough, well-controlled and will provide important insights into signaling pathways and cellular mechanisms that may be responsible for the phenotypes observed in human NGLY1 patients.
This study does represent an important step in understanding how the loss of this gene influences a particular signaling pathway during a stage of development and could be very useful in beginning to interpret some of the developmental defects occurring in the patients. It would be very informative to know if (and how) the glycosylation status of dpp is altered upon loss of pngl, but we do see that is beyond the scope of the current study.
Please use the specific comments from the reviewers, some overlapping, to submit a revised manuscript.
Comments of Reviewer #1:
The overall concerns with the manuscript at this point are some of the interpretations and lack of biochemical mechanistic insight into the link between N-glycanase activity and Dpp homodimerization.
1) Why are Pngl mutants lethal? Mutants that lead to loss of the Copper cell region do not result in lethality (Cell Tissue Res. 2001 Oct: 306(1): 167-78). how-Gal4 driven knockdown also results in lethality but does affect gastric caeca formation. This suggests that lethality is not due to loss of the caeca.
2) Mef2-Gal4 and how-Gal4 expression of human NGLY1 partially rescues Pngl lethality. Mef2-Gal4 and how-Gal4 expression of Pngl RNAi results in 0 and 28% survivability and Mef2-Gal4 and how-Gal4 expression of dpp RNAi results in loss of the acid region and caeca and 8 and 80% survivability, leading the authors to conclude that Pngl plays a dpp independent role. This may indeed be the case and should be mentioned in the Abstract. However, an alternative explanation is that dpp is required in other tissues and the knockdown by these drivers is not effective in the other tissues.
3) Subsection “Loss of BMP signaling in Pngl–/– embryonic endoderm is caused by impaired BMP autoactivation in VM”: Mef>tkvCA rescues Pngl lethality. Given the concerns that lethality is not due to caeca or acid region loss, this would argue that Pngl is required for BMP/ (maybe TGF-B) signaling elsewhere.
4) Do Mef>tkvCA Pngl minus flies that make it to adulthood have a Copper cell region. It would be interesting to know if Pngl is required for proper midgut formation during metamorphosis.
5) Mutants that make it to adulthood are sterile. Do these animals have ovaries/testis that are consistent with loss of dpp, i.e. germline stem cell loss? Knowing this might help to establish Pngl as a gene required for a subset of BMP signaling pathway events. It would especially be interesting as gbb is also required for germline stem cell maintenance.
6) From the Abstract, the authors write,"[…]without affecting BMP signaling in other contexts[…]" It's impossible to be sure it is not affecting BMP signaling in other contexts. It's just that the authors were not able to identify any others. The same concern relates to the last sentence of the subsection “BMP signaling from VM to endoderm is impaired upon loss of Pngl”. The word "specifically" should be removed.
7) Do Pngl genes harboring a C303A mutation fail to rescue the Pngl mutant fly phenotypes. This would at least genetically link the catalytic domain/activity to described phenotypes. There is no data in this paper to how Pngl affects dpp.
8) Why did the authors, in Figure 6, do Western Blots on whole larvae and not midguts versus carcass (midgut minus)? Changes in dimmer accumulation in carcass could help identify other tissues where Pngl may act.
9) "BMP ligands can signal both as homodimers and as heterodimers (Bragdon et al., 2011; 383 O'Connor et al., 2006)."
If so, have the authors examined the tissues where the ligands act as homodimers? Do they have phenotypes? Changes in accumulation on Western Blots?
Comments of Reviewer #2:
1) As the mesodermal knockdown of pngl was more severe that the knockdown of dpp, can the authors comment on reasons for this (are there other suspected targets of Pngl in the mesoderm)?
2) Clarification with regard to rescue experiments-is Dpp-GFP processed and dimerized in the same manner as endogenous Dpp? Does it have the same N-glycans? If not, could this affect your interpretation (or perhaps give clues as to what region of Dpp is affected by Pngl)?
3) In pngl mutants, can you distinguish between Dpp protein simply being produced at a lower level (due to instability, higher turnover, etc.) vs. Dpp protein not being able to mediate autoregulation? Or are these different ways of saying the same thing?
4) Can the authors comment on whether any of the major phenotypes seen in the NGLY1 patients are thought to be due to changes in BMP signaling?https://doi.org/10.7554/eLife.27612.020
- Tadashi Suzuki
- Hamed Jafar-Nejad
- Hamed Jafar-Nejad
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
We thank Huda Zoghbi for her support; Kartik Venkatachalam and Noah Shroyer for discussions; Hugo Bellen and Kevin Lee for comments on the manuscript; The Bloomington Drosophila Stock Center (NIH P40OD018537), the Developmental Studies Hybridoma Bank, Benjamin Ohlstein, Takuya Akiyama and Matthew Gibson for reagents. This work was supported by the Grace Science Foundation through Texas Children’s Hospital. Work in Jafar-Nejad laboratory is also supported by the NIH (R01GM084135 and R01DK109982). Imaging was performed at the Confocal Microscopy Core of the BCM IDDRC (U54HD083092; the Eunice Kennedy Shriver NICHD)
- K VijayRaghavan, Reviewing Editor, National Centre for Biological Sciences, Tata Institute of Fundamental Research, India
© 2017, Galeone et al.
This article is distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use and redistribution provided that the original author and source are credited.