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Peptide: N- glycanase (PNGase) enzyme cleaves oligosaccharides from the misfolded glycoproteins and prepares them for degradation. This enzyme plays a role in the endoplasmic reticulum associated degradation (ERAD) pathway in yeast and mice but its biological importance and role in multicellular development remain largely unknown.
In this study, the PNGase from the cellular slime mold, Dictyostelium discoideum (DdPNGase) was identified based on the presence of a common TG (transglutaminase) core domain and its sequence homology with the known PNGases. The domain architecture and the sequence comparison validated the presence of probable functional domains in DdPNGase. The tertiary structure matched with the mouse PNGase. Here we show that DdPNGase is an essential protein, required for aggregation during multicellular development and a knockout strain of it results in small sized aggregates, all of which did not form fruiting bodies. The in situ hybridization and RT-PCR results show higher level of expression during the aggregate stage. The expression gets restricted to the prestalk region during later developmental stages. DdPNGase is a functional peptide:N-glycanase enzyme possessing deglycosylation activity, but does not possess any significant transamidation activity.
We have identified and characterized a novel PNGase from D. discoideum and confirmed its deglycosylation activity. The results emphasize the importance of PNGase in aggregation during multicellular development of this organism.
Peptide: N-glycanase (PNGase; EC 184.108.40.206) is a member of transglutaminase (TG) -like superfamily and is characterized by TG -like core domain (called PNGase core domain) with the conserved cysteine (C), histidine (H) and aspartate (D) core residues, similar to the TG enzymes . PNGase catalyzes a deglycosylation reaction and cleaves at β-aspartyl glucosylamine bond and removes complete glycan moiety from the glycoprotein substrate. Its reaction is different from TG catalyzed transamidating or amide bond formation reaction . Mutagenesis studies have confirmed that the catalytic triad residues (C, H, and D) of PNGase are essential for its deglycosylation activity .
PNGases are ubiquitously present from prokaryotes to eukaryotes and from lower to higher metazoans. The PNGase activity was firstly identified and characterized in almond [4,5] and was called PNGaseA. PNGase from bacteria Flavobacterium meningosepticum (PNGaseF) was characterized and found to be similar to PNGaseA as both could deglycosylate high mannose and complex type native glycoproteins  but were later reported to be kinetically different in substrate specificity . The first evidence of PNGase in animal was obtained from medaka fish (Oryzias latipes) embryo . Two PNGaseMs were characterized having different optimum pH for activity- acidic PNGaseM (3.5–4 pH) and neutral PNGaseM (neutral pH). The expression of these two PNGases was developmentally regulated with neutral PNGase expressing at 4–8 cells stage and early gastrula while acidic PNGaseM expressing after gastrulation . These are responsible for the deglycosylation of various yolk glycoproteins leading to accumulation of N- glycans. Subsequently, PNGases were reported in the cytoplasm of mammalian cells , hen oviduct , S. cerevisiae and Drosophila. The cytoplasmic PNGases are very different from those found in bacteria and acidic PNGases, as the former require a thiol reactive group, a neutral pH, reducing environment (DTT) for optimum activity and possess unique carbohydrate binding properties . Unlike bacterial PNGase, cytoplasmic PNGase cannot act on native glycoproteins and selectively deglycosylate denatured (non-native) glycoproteins . Subcellular localization studies demonstrated that PNGases are mainly present in the cytoplasm, but there are reports of its membrane association, especially with the endoplasmic reticulum membrane  and its presence in nucleus, in case of S. cerevisiae  has been confirmed. PNGase activity was found to be growth phase dependent in S. cerevisiae with no activity in logarithmic phase cells and high activity during stationary phase cells . S. cerevisiae png1p- strain is not affected in growth rate and viability, so it does not seem to be an essential gene in S. cerevisiae, but it leads to the accumulation of misfolded glycoprotein in cytosol and a delay in its degradation . The C. elegans png1p- mutants are defective in axon development and branching . Recently, Maerz et al  have shown that the PNGase from filamentous ascomycete, Neurospora crassa, lack deglycosylation activity but is essential for cell polarity as well as for cell wall integrity and DNA repair.
Despite accumulating knowledge about PNGases from yeast to mammals, there is not much knowledge about the biological significance of this protein during development and differentiation of organisms. In the present study we have identified and characterized the PNGase from Dictyostelium discoideum, a model system having great significance due to the phylogenetic position occupied by it. In the present work, we identified a novel PNGase from D. discoideum genome using in silico analyses and characterized its role in growth, development and differentiation. The domain architecture and the sequence comparison validated the presence of probable functional domains in DdPNGase. The tertiary structure matched most with the mouse PNGase.
DdPNGase is a functional peptide:N-glycanase enzyme possessing deglycosylation activity, but does not possess transamidation activity. RT-PCR data revealed almost 3–4 fold increase of PNGase transcript during aggregation stage after which they declined suggesting its importance during the process of aggregation. In situ hybridization studies revealed the abundance of png transcript in the prestalk region, specifically in the pstB and pstAB regions. Our observations suggest that PNGase plays a role in regulating the number of aggregates that develop to form multicellular structures. The png- cells make smaller aggregates upon starvation but only few of them proceeded with further development. One could say that DdPNGase is required for the signaling taking place during aggregation whose consequences are required for cell type differentiation mainly of the prestalk cells.
D. discoideum, Ax2 (axenic strain) cells (unicellular) were maintained in liquid suspension in standard HL-5 medium (pH 6.5) at 22°C with 200rpm shaking. The medium was supplemented with antibiotics as indicated. Log phase cells at a density of ~2.5–3.5 x 106 cells/ml was used for all the experiments.
Cells were grown at a density of 0.5–1.0 x 106 cells/ml with indicated antibiotics in a flask under shaken conditions and growth was monitored at the indicated times as shown.
To induce multicellular development, cells were harvested from exponentially growing cultures, washed twice in ice cold KK2 buffer (16 mMKH2PO4, 4mM K2HPO4.3H2O, pH 6.2) and plated at a density of 1.0x107 cells/cm2 on non-nutrient agar (1.5% in KK2 buffer) plates.
Development was synchronized by incubating the plates with the cells at 4°C for 4–5 hours and then transferring them to 22°C for further development .
The genomic DNA, cDNA and protein sequences of the putative PNGase were obtained from dictybase online resource (http://www.dictybase.org). The protein sequences of known PNGase were obtained from UniProt KB database (http://www.uniprot.org). The domain architectures of the proteins were deduced by Simple Modular Architecture Research Tool, SMART (http://SMART.embl-heidelberg.de). PNGase orthologues were searched by Basic Local Alignment Search Tool (BLASTp) at NCBI (http://blast.ncbi.nlm.nih.gov/Blast.cgi), UniProt and dictybase. Multiple alignments were performed using ClustalW2 at EBI server (http://www.ebi.ac.uk/Tools/clustalw2/). PHYLIP package (Phylogeny Inference Package, version 3.68), was used to construct Neighbor joining (NJ) phylogenetic trees with 1000 bootstrap replicates to create a consensus tree.
Secondary structure of the candidate protein was predicted by Jpred3 (http://www.compbio.dundee.ac.uk/www-jpred/). The protein sequence of putative DdPNGase was used as query in Robetta server (http://robetta.bakerlab.org) for domain prediction which identified proteins of known tertiary structures having significant homology to the primary sequence of the query domains. The best homologous mouse PNGase protein structure (PDB- 2f4mA) was used as a template for comparative modeling of the tertiary structure of the query protein domain using SWISS MODEL server (http://swissmodel.expasy.org/) in alignment mode . The 3D model for DdPNGase was analyzed based upon the crystal structures of ScPNGase  and mouse PNGase . The stereochemical quality of the protein model was analyzed through residue-by-residue geometry and overall structure geometry in Ramachandran plot that was obtained with PROCHECK tool at Structure Analysis and VErification Server, SAVES (http://nihserver.mbi.ucla.edu/SAVES/). The superimposed images of the template (mouse PNGase) and DdPNGase tertiary structure was obtained from SuperPose, Version 1.0 (http://wishart.biology.ualberta.ca/SuperPose/) to mark the differences between the two structures.
Cells were incubated at 0.5–1.0 x 107 cells/cm2 on dialysis membrane, supported by KK2 agar, until the desired developmental stages were attained. In situ hybridization with 200ng/ml of digoxigenin (DIG) labeled pngase RNA was carried as described earlier by Escalante and Sastre . A sense pngase probe was used as an internal control. The spatial expression pattern of the transcript of Ddpngase was investigated using probes obtained by in vitro transcription of the exonic region after cloning in commercially available pBSII SK+(pBluescript II phagemid) vector. RNA of 1.2Kb (705 to 1955 nucleotides) was synthesized from 1.2 Kb exonic region amplified by PCR using the primers FP (BamHI): 5′- GATGCGGATCCCTACTATCAACTAAATGTGGAAGATGTGGT-3′ and RP (XhoI): 5′ ACTACTCGAGAATAACCAATTGAAAAACCTGAAATTATATGAG-3′ and digested with BamHI/XhoI and cloned directly into BamHI/XhoI site of pBSII SK+. The construct pBSII SK+(pngase probe) was digested with BamHI to yield template for antisense probe synthesis by T7 RNA polymerase, while digestion with XhoI yielded template for sense probe synthesis by T3 RNA polymerase. Sense and antisense probes were processed for hydrolysis due to their larger size (1.2 Kb) using 1x carbonate buffer and incubated at 65°C for 15min.
For semi-quantitative detection of the transcript, RNA was isolated from cells collected at two hour time intervals from cells developing synchronously on a non- nutrient agar plate using the Trizol reagent (Sigma, USA). RNA was treated with RNase-free DNase and purified using the RNeasy minikit. cDNA was synthesized from 1μg of total RNA with Thermo script RT-PCR system from Invitrogen using oligo dT primers. RT-PCR reactions were performed using specific primer sets as shown below and rnlA was used as an internal control. The cycle numbers used for amplification were within the linear range of amplification. Primer set for the amplification of pngase was FP-5′- AATCAATCTAAAACTATAAATTTAATATATAATG-3′ and RP-5′-ATTCTTAAACCAATCCAATAACAT-3′. The primer set used for rnlA was FP-5′- GGATTCTGCAAAATGGCAAC-3′ and RP- 5′-GTCCTCTCGTACTAAAGGAAGG-3′.
The Ddpngase gene identified by in silico analyses was PCR amplified using FP: (BamHI):5′- ACGCGGATCCAATCAATCTAAAACTATAAATTTAATATATAATG-3′and RP: (XhoI):5′- ACTACTCGAGAATAACCAATTGAAAAACCTGAAATTATATGAG-3′ from the genomic DNA and expressed as a fusion protein with the enhanced yellow fluorescent protein (EYFP) at the C-terminal . The expression was driven by the constitutive promoter, actin 15. The construct was introduced into wild type Ax2 cells by electroporation and the transformants were selected with 100μg/mlG418 and was called act15/png-eyfp/Ax2 strain.
To prepare a pngase gene disruption construct, two DNA fragments of the png gene comprising nucleotides from 4–518 and from 705–1493 were amplified by PCR from the vector pact15/png- eyfp using oligonucleotides (first fragment, FP- BamHI: 5′-GACGCGGATCCAATCAATCTAAAACTATAAATTTAATATATAATG-3′ and RP-EcoRI: 5′- CTAGGAATTCATTCTTAAACCAATCCAATAACAT-3′; second fragment, FP-BamHI: 5′-GATGCGGATCCCTACTATCAACTAAATGTGGAAGATGTGGT-3′ and RP-XbaI:5′- CTATCTAGAGCCATACCATCAGCACCATTAGT-3′) that add a 5’-BamHI and 3’-EcoRI site to the first fragment and a 5’- XbaI and 3’-BamHI site to the second fragment. These fragments were three-point ligated with XbaI and EcoRI digested pBsrΔBamH1 vector . The construct was linearized with BamHI which yielded a pBsrΔBamHI plasmid flanked with a 515 and 531bp of 5’ and 3’ pngase sequence respectively and introduced into wild type Ax2 cells. Transformed cells were selected for growth at 10μg/ml blasticidin and selected clones were screened for homologous recombination by two separate PCR reactions and confirmed by sequencing. The knock outs were called png-/Ax2 strain.
Lysates prepared from act15/png-eyfp/Ax2 and png-/Ax2 strains and the commercially available PNGase F (Sigma Aldrich) were used for comparing the capability to deglycosylate native and denatured form of chicken ovalbumin as per the protocol of Joshi et al with minor modifications. Briefly, the lysates (prepared from 1x105 cells) of the different strains were incubated with 80μg ovalbumin (native or denatured) in 1000μl reaction containing 5mM DTT in 20mM Na2HPO4 and 0.5M NaCl at pH 7.2 at 22°C for different time points (0h-overnight). The reaction was stopped by boiling in SDS sample buffer at 100°C for 5min and analyzed by Western hybridization. Samples (10μl) of deglycosylated reaction was resolved on 10% SDS- PAGE and transferred to the nitrocellulose membrane and blocked with 4% non-fat dry milk. The membrane was treated with 1:4000 diluted rabbit polyclonal anti- chicken egg albumin antibody (Sigma Aldrich) in blocking solution, followed by washing with 1x TBST buffer, followed by treatment with 1:6000 diluted goat anti- rabbit IgG-HRP (Bangalore Genei, India) conjugated, in blocking solution. The blot was treated with SuperSignal West Pico chemiluminiscent substrate (Thermo Scientific) and exposed to X-ray film. Film was developed and fixed, and the ovalbumin bands were visualized.
Freshly grown log phase cultures of the transformants and the wild type strain were taken for the experiments. The assays were performed using TG assay kit (CS1070, Sigma-Aldrich) according to the manufacturer’s instructions. Briefly, 1.5–2 x 107 cells were lysed to prepare a crude protein extract. Around 10μg total protein extract was added to each poly-L-lysine coated microplate wells. 0.1mU pure guinea pig liver TG2 was used as a positive control while the negative control wells did not contain any protein. Assay buffer containing biotin labeled TBQQEL-OH glutamine substrate and DTT was added in equal volumes to the proteins and the reaction was allowed to proceed at 22°C for 60min. The wells were washed 3 times with MQ water and incubated with 0.1μg Streptavidin-Peroxidase in 100μl PBS-T for 20min at 22°C. The wells were washed thrice with 200μl PBS-T without incubation. 200μl 3,3’,5,5’-tetramethylbenzidine (TMB) liquid substrate was added to each well for 3min. 100μl stop solution was added to stop the color development. The absorption was measured at 450nm. The protein content of each sample was measured by Bradford method using BSA for standards . The results were expressed as percent activity, taking wild type activity as 100%. A minimum of 4–5 independent experiments in triplicates was carried out.
Recent evidences in various organisms have established the role of PNGase in ERAD related events but its biological significance has just begun to be revealed. In the present study, we have identified the PNGase ortholog from Dictyostelium discoideum using in silico analyses and describe its functional characterization. The major function of this protein is in degradation of misfolded glycosylated proteins; however we also show here its requirement during multicellular development.
The putative PNGase protein of D. discoideum shows maximum homology to an uncharacterized protein from another cellular slime mold, Polyspondylium pallidum. It also shows significant homology with PNGase core and β-lectin legume domains of PNGase of Naegleria gruberi (amoeba). PNGase core domains of Phylophthora infestans (fungus) and Ostreococcus tauri (green alga) also show high homology to the putative DdPNGase. Domain architecture analyses of known PNGases (Figure (Figure1A)1A) show the presence of PNGase core domain. PNGases possess a carbohydrate binding domain (PAW) at the C-terminus which probably assists in binding to the glycan of the misfolded proteins. ScPNGase lacks both N and C terminal domains and possess only a functional core domain. DdPNGase possess a catalytic core domain (54 aa) and a C- terminal β-lectin legume (β-LL) domain (223 aa) for binding to glycan moiety. β-LL domain is originally present in lectins of legumes and requires tightly bound calcium and manganese ions for their interaction with carbohydrate. Naegleria gruberi PNGase also possess a highly homologous PNGase core and β-LL domains. The N-terminal region (1–117 aa) of putative DdPNGase does not show high homology to any characterized protein at NCBI. BLASTP2 results at EMBL show its low homology (Score 36 bits, 31% identity, 58% positives) with UBQ (ubiquitin homolog) domain of ubiquitin carboxy terminal hydrolase of fungus Neurospora crassa, which is a de-ubiquitinating enzyme. It shows the presence of a deglycosylating core domain, glycan binding β-LL domain and probable de-ubiquitinating UBQ domain.
We observe diverse structural organization between species which may reflect on its diverse functions. For example, the CePNGase has a thioredoxin domain having an oxidoreductive activity apart from being a functional PNGase. Similarly, the PUB domain in Drosophila and mouse may also serve in protein-protein interactions.
The analysed PNGases were phylogenetically separated into three clades. DdPNGase is closer to the PNGase of Naegleria gruberi (NgPNGase). The putative DdPNGase and NgPNGase belong to one clade while the HsPNGase, MmPNGase, DmPNGase and CePNGase grouped together in another clade. ScPNGase and AtPNGase are grouped together (Figure (Figure11B).
Sequence alignment (Figure (Figure2A)2A) shows that DdPNGase possess the catalytic triad residues Cys210, His237 and Asp252, corresponding to the conserved core residues of other PNGases. DdPNGase also possess the corresponding tryptophan (W239 and W248), arginine (R229) and glutamate (E241) conserved residues which could possibly be essential for catalysis. Two CXXC motifs are present in D. discoideum but the second cystine of each motif is absent which probably may affect the Zn binding in this putative PNGase. The exact role of Zn binding is not understood but it has been suggested to modulate the enzyme tertiary structure in other systems. The cysteine residues of CXXC motif are essential for S. cerevisiae PNGase activity . Studies on C. elegans N-glycanase (NGLY1) revealed that it contains two Zn binding motifs - C191PKC194 and C225DGC228, but it did not get activated by Zn binding. It suggests that all PNGase may not require Zn ion for their deglycosylation activity. In contrast to ScPNGase, CePNGase activity was inhibited by Zn2+ and other metal ions such as Cu2+ and Co2+ . Although the mechanism of inhibition of PNGase activity by Zn2+ in C. elegans and activation in S. cerevisiae is not clearly understood but it may be due to changes in tertiary structure of the enzyme which could modulate the accessibility of the catalytic cleft to the substrate glycoprotein.
DdPNGase is a single copy gene encoding a protein of 618 amino acids. In most cases, prediction of tertiary structure can validate the function of a novel protein. To model the 3D structure of an unknown protein, tertiary structures of the proteins which show significant sequence homology to the query protein are identified. These known structures are then used as a template for comparative homology modeling of the unknown protein tertiary structure. Prior to tertiary structure prediction, the 87–340 aa region around the Zn binding domain and core domain of DdPNGase was submitted at the Jpred3 for secondary structure prediction. This confirmed the secondary structure around the core and Zn binding domains. We identified some known 3D structures of PNGases showing high homology to the primary sequence of our query protein (putative DdPNGase) sequence while doing secondary structure prediction at Jpred3 server. The putative DdPNGase primary sequence show maximum homology (41% identity, 55% positives) to the M. musculus PNGase core sequence. Its tertiary structure is available in the structural database as PDB entries 2f4m-A chain and 2f4o-A chain. PDB 2f4m is the tertiary structure of MmPNGase complexed with HR23B and PDB 2f4o is MmPNGase complexed with HR23B and a synthetic peptide inhibitor. High percent homology suggests that our query protein is probably a PNGase.
To create a tertiary structure of the DdPNGase core region, mouse PNGase core tertiary structure (2f4m-A) was chosen as a template for homology modeling. Structural homologues of the three different domains of DdPNGase, the N-terminal (1–84), core domain (85–376) and the C-terminal (377–618) depict a near perfect match with the template. Figure Figure2A2A shows the multiple alignment of the highly conserved region of the core domain from both D. discoideum and Mus musculus.
The core domain sequence of putative DdPNGase was submitted to the SWISS MODEL (Version 8.05) server for modeling of tertiary structure based on alignment with the template protein (MmPNGase core- 2f4mA). The model thus created by SWISS MODEL as viewed under the MOLMOL software is shown in Figure Figure2B.2B. The DdPNGase core region consists of six stranded antiparallel β-sheet (S6–S11) surrounded by eight α-helices (H3 to H9 and H11) on one side and four α-helices (H9, H10, H10’ and H12) on the other side of the sheet. The numbering of secondary structure elements has been done according to MmPNGase tertiary structure as done by Zhao et al , with the N-terminal helix labeled as H3, as the first two helices of ScPNGase are not present in the M. musculus and D. discoideum PNGases. The zinc binding domain contains a three-stranded β-sheet (S2–S4). A small β-sheet (S1 and S5) is located between the zinc binding and catalytic domains. Similar to MmPNGase, C-terminal α-helices H11 and H12 of DdPNGase may probably interact with Rad23. H5 α-helix and the loop following it are comparatively longer in MmPNGase with 5 extra amino acids in each of them. H6 α-helix is half the size in DdPNGase as compared to MmPNGase (14 aa). A helical region of 5 amino acids in the Zn binding region between S2 and S3 as shown in the tertiary structure model of MmPNGase (2f4mA) is also not mentioned in literature . Even with the existing differences, we found that the cleft composed of H8 helix and six antiparallel β-strands to be completely superimposed. The position of catalytic triad residues is also conserved in both the PNGases. The α-helix H8 possess the catalytic Cys residue (Dd C210MmC306), strand S7 possess catalytic His (Dd H237MmH333) at the N-terminal end and strand S8 possess triad Asp residue (Dd D252Mm D350) at the C3-terminal end. Thus, the core domains of both the PNGases consist of six antiparallel β- strands (S6–S11) with helices around the sheet. The C-terminal H11 and H12 α-helices of mouse PNGase interact with the HR23 protein , and may be involved in the same interaction of DdPNGase with HR23 or Rad23 homologue in D. discoideum. The stereochemistry of the model prepared for the core domain region of the putative DdPNGase is good with 98% of the residues located in the most favoured and additionally allowed regions of the Ramachandran plot. 1% of the residues are located in generously allowed regions in the Ramachandran plot. Merely 1% residues could not be obtained in the allowed regions, as checked by Structure Analysis and VErification Server (SAVES) online resource. These residues are present in loop, bend and coil regions of the tertiary structure.
The Eyfp (green) tagged DdPNGase from the act15/png-eyfp/Ax2] overexpressing strain colocalized in the nucleus along with DAPI blue stained DNA. It was also present to a lower extent in the cytosol (Figure (Figure3A).3A). The PNGases are generally localized in close proximity to the proteasomal machinery as they are proposed to participate in the proteasome dependent glycoprotein degradation pathway. The S. cerevisiae PNGase is reported mostly in the nucleus  where its proteasomes reside. In D. discoideum, the proteasomes are reported to be present in cytosol but in higher concentrations in the nucleus . A part of it may also be localized on the ER membrane as in the case of mouse PNGase ortholog, Ngly1  which was reported to be associated with the ER resident proteins such as gp78  or Derlin .
Temporal expression pattern of the Ddpngase transcript during development was carried out by a semi- quantitative RT-PCR using intron spanning primers and was normalized against the constitutively expressed rnlA transcript. RNA was collected from different specific stages of development and also from isolated prestalk and prespore cells. Relative abundance of the transcript of Ddpngase with respect to the transcript of rnlA was plotted in Figure Figure3B.3B. The RNA derived product with a predicted size of approximately 400bp was amplified from all the developmental stages (from vegetative to fruiting body stages) taken but showed highest expression at the time of aggregation (both loose and tight aggregates appearing at t6 and t8 hours) and declined thereafter. There was slight increase at the fruiting body stage at t24 hours. There was more than 2.0 folds increased expression in the isolated prestalk cells as compared to the isolated prespore cells (Figure (Figure3C).3C). The absence of a 500bp band that is expected from amplification of the genomic DNA confirmed the purity of the RNA (data not shown). These data confirm that pngase is transcribed throughout development.
To examine the spatio- temporal expression pattern of Ddpngase during development, RNA in situ hybridization was carried in various multicellular stages of development (Figure (Figure4).4). A strong hybridization signal was observed both in the loose (Figure (Figure4a)4a) and tight aggregates (Figure (Figure4b)4b) and by the first finger stage the expression got restricted largely to the prestalk region with very low levels in the prespore region (Figure (Figure4c).4c). By the time migrating slugs were formed, the expression further got restricted to the pstB cells in the prestalk region and the rear-guard cells (RGC) (Figure (Figure4d).4d). During early culmination the expression was found in the pstAB and RGC (Figure (Figure4e).4e). During mid-culmination (Figure (Figure4f)4f) the expression was seen in the upper and the lower cup region and also in the basal disc (BD). In the fruiting body stage (Figure (Figure4g)4g) the basal disc and the tip region showed higher expression while low expression was also seen in the sorus. PstA cells express extracellular matrix protein A (EcmA), pstB cells express extracellular matrix protein B (EcmB) and pstAB cells express both EcmA and EcmB proteins. The ecmA is strongly expressed in the anterior 10% of the slug (pstA region). The ecmB gene is expressed in the central core region of slug tip. The collar region which forms the border between the prestalk and prespore cells in the slug express low level of EcmA protein and are called as pstO cells. As culmination proceeds, pstA cells follow the pstB cells into the stalk tube and initiate the expression of ecmB gene and become pstAB cells. The pstAB cells form the basal disc along with the anterior-like cells (ALC). The ALC comprise approximately 15% of the posterior prespore zone. ALCs also migrate upward and downward to form part of upper and lower cup of the culminant. PstO cells also contribute to the upper cup formation.
The expression detected with pngase antisense probe is specific as no signal was detected using DIG labeled RNA probe prepared against the sense strand of cDNA. These results suggest that pngase transcript is present throughout development and they may play a critical role during the aggregate formation. Their presence also suggests their role in prestalk/stalk differentiation or patterning.
To provide more insight into the biological significance of the PNGase ortholog in D. discoideum we generated and characterized both the overexpressing [act15/png-eyfp/Ax2] and knockout (png-/Ax2) mutant strains of the pngase gene. The knockout mutants were made by gene disruption followed by homologous recombination. The deletions were molecularly characterized by PCR with DNA primers flanking the deletion points and sequencing the resulting PCR products (data not shown). On the other hand, no transcripts could be detected from the knock out strains while the wild type and the Bsr integrant strain (RI) showed the transcript (data not shown). This result indicates that png-/Ax2 is a bonafide null allele of the pngase.
Having established mutant strains for pngase (both [act15/png-eyfp]/Ax2 and [png-/Ax2]), we then compared their growths and phenotypes with the wild type strain transformed with an empty vector ([act15/eyfp]/Ax2). Figure Figure5A5A shows the growth profiles of the wild type, knockouts, overexpressers and the random integrants (comparable to the wild type). The knockout mutant, [png-/Ax2], were found to be slow growers with a doubling time of 10.3± 0.6 hours, while the overexpressers, [act15/png-eyfp]/Ax2, were slightly fast growers with a doubling time 7.21±0.34 hours as compared to the wild type and the random integrants which had a doubling time of 8.24±0.41 hours.
The knockout strain, [png-/Ax2], developed slower, taking 2–3 hours more as compared to the wild type to form fruiting bodies (Figure (Figure5B).5B). They formed numerous small aggregates by approximately 12 hours of starvation as compared to the wild type which took almost 8 hours. The formation of the mound from the aggregate was faster as it took almost 2 hours while the wild type took almost 4 hours. Very few aggregates formed slugs which were medium sized. The transition from the migrating slug stage to the early culminant took only 2 hours as compared to the wild type which took 3–4 hours. The [act15/png-eyfp]/Ax2 cells showed normal development with timings similar to that of the wild type cells. Nevertheless, the size and morphology of different developmental stages formed were smaller than the wild type but appeared normal, though the number of aggregates culminating into fruiting bodies were lesser as compared to wild type cells. The fruiting bodies formed by the [act15/png-eyfp]/Ax2 cells were the smallest in size showing small sturdy stalks with enlarged basal disc and slightly larger sorus, while that formed by the [png-/Ax2] cells had slightly thinner stalk with sorus slightly bigger than that formed by the Ax2 cells but smaller than the knock out cells (Figure (Figure5B5B vii–ix). As per our observations, many cells did not participate in development and very few aggregates were formed which finally culminated into fruiting bodies. From the observed transcript levels, one could speculate that the pngase may be required by the prestalk cells, and overexpression of this maybe biasing many cells towards the prestalk pathway as a result of which they die prematurely before they can take part in the development. We speculate that the lack of PNGase in D. discoideum probably inhibits the cell to cell signaling events responsible for the process of aggregation. There are chances that either cAMP signaling or cell polarity gets inhibited as a result of which the amoebae could not aggregate and only few such aggregates which could come in the near vicinity finally coalesce to form the multicellular structures. Transformation of the png- cells with the plasmid containing the wild type PNGase expression driven under actin15 promoter could rescue the phenotype (data not shown).
Loss of function mutations has been carried out in different systems like Arabidopsis , C. elegans  and yeast. The plant did not show any change in its phenotype as well as in growth and development but it was found to limit axon branching during organ formation in C. elegans. Loss of function in D. discoideum brought about changes in growth, development as well as cell differentiation. Its loss slowed down the growth of the cells by nearly 2hrs. Our observations suggest that PNGase plays a role in regulating the number of aggregates which would develop to form multicellular structures. The png- cells do make small aggregates upon starvation but only few of them proceeded with further development. This suggests that PNGase may be involved in cell to cell signaling required for aggregation with a possibility of defects in cAMP signaling or in cell polarity as seen in case of Neurospora . Since the png- cells later went on to develop normal sized fruiting body with slightly longer stalks, one could say that PNGase may be required for the signaling taking place during aggregation whose consequences are required for cell type differentiation mainly of the prestalk cells.
Our search for the gene having transglutaminase activity in D. discoideum resulted in the identification of few transglutaminase-like superfamily members, of which one of them was identified as a peptide: N-glycanase during further in silico analyses of the protein sequence. We found a small but statistically insignificant increase in TG activity in the act15/png-eyfp/Ax2 cells over the wild type Ax2 cells (Figure (Figure6A).6A). The png null strain did not show any reduction in the TG activity suggesting that DdPNGase does not have TG activity. Della Mea and group  had also found transglutaminase activity in the recombinant AtPNGase1 but could not detect its loss in the knockout strain.
We analyzed the capability of DdPNGase to deglycosylate the native and denatured ovalbumin substrates. Crude extracts of [act15/png-eyfp]/Ax2 and [png-/Ax2] strains, were incubated with either native or denatured ovalbumin in appropriate buffer conditions and the reaction was stopped at varying time points. The activity was compared with that obtained with the commercially available purified PNGase F (Figure (Figure6B).6B). In each case, a glycosylated (+CHO) band comparable to that seen with ovalbumin (Ov) after overnight incubation without the enzyme was observed. When pure enzyme was used, we saw a time dependent increase in the intensity of the lower deglycosylated band (−CHO) (Figure (Figure6B,6B, lanes 12–16). When we measured the deglycosylating activity present in the lysate of the DdPNGase overexpressing strain, we found similar results showing a time dependent increase in the intensity of the -CHO band (Figure (Figure6B6B lanes 2–6). A time dependent study using the knockout strain showed the lower deglycosylated band (Figure (Figure6B,6B, lanes 8–11), comparable to that observed with only ovalbumin (Figure (Figure6B,6B, lane 7) confirming the loss of PNGase activity in them.
Figure Figure6B6B shows the results obtained using denatured ovalbumin as substrate. The native ovalbumin did not show any deglycosylation activity and thus are not shown here. Joshi et al had utilized the two glycoprotein substrates namely, yeast carboxypeptidase and chicken egg albumin (ovalbumin) to study the deglycosylation activity of yeast PNGase and its mutants and showed that misfolding of the glycoproteins was a prerequisite for PNGase mediated deglycosylation. Funakoshi et al have provided evidence of an essential deglycosylation independent activity for DmPNGase. A mutation in the gene led to the failure in proper multicellular development demonstrating the functional importance of the PNGase apart from its deglycosylation activity in D. discoideum. What is interesting is that the modulation of the level of PNGase in D. discoideum did not affect drastically the overall developmental patterns even when the transcript levels showed cell type biasness.
In summary, we have identified and characterized a novel PNGase from D. discoideum. The DdPNGase is a functional peptide:N-glycanase enzyme possessing deglycosylation activity, but does not possess transamidation activity. DdPNGase was identified based on the presence of a common TG core domain and its sequence homology with the known PNGases. The domain architecture and the sequence comparison validated the presence of probable functional domains in DdPNGase. The tertiary structure matched with the mouse PNGase the most. RT-PCR data revealed almost 3.0 folds increase in pngase transcript during aggregation stage after which they decline suggesting its importance during the process of aggregation. The pngase transcript is abundant in the prestalk regions, specifically in the pstB and pstAB regions. This needs to be further studied to find out the role in differentiation. PNGase showed nuclear localization. Unlike yeast, mutation in the DdPNGase caused developmental aberrations indicating its importance in multicellular development. Apart from having deglycosylation activity and a role in development it requires further characterization to find its precise role in differentiation.
There is no conflict of interest with the authors.
AG and RL contributed equally to the work. The concept and manuscript was mostly written by SS and partly by AS. The manuscript in the present form has the consent of all the four authors. All authors read and approved the final manuscript.
Infrastructure facilities provided by the School of Life Sciences, Jawaharlal Nehru University are gratefully acknowledged. The confocal pictures were taken at the advanced infrastructure and research facility of JNU. SS thanks the Department of Biotechnology, New Delhi for research support (BT/PR5157/BRB/10/372/2004). AG and RL thank Council of Scientific and Industrial Research (New Delhi) for awarding fellowship.