Cells use phagocytosis and macropinocytosis to internalise bulk material, which in phagotrophic organisms supplies the nutrients necessary for growth. Wildtype Dictyostelium amoebae feed on bacteria, but for decades laboratory work has relied on axenic mutants that can also grow on liquid media. We used forward genetics to identify the causative gene underlying this phenotype. This gene encodes the RasGAP Neurofibromin (NF1). Loss of NF1 enables axenic growth by increasing fluid uptake. Mutants form outsized macropinosomes which are promoted by greater Ras and PI3K activity at sites of endocytosis. Relatedly, NF1 mutants can ingest larger-than-normal particles using phagocytosis. An NF1 reporter is recruited to nascent macropinosomes, suggesting that NF1 limits their size by locally inhibiting Ras signalling. Our results link NF1 with macropinocytosis and phagocytosis for the first time, and we propose that NF1 evolved in early phagotrophs to spatially modulate Ras activity, thereby constraining and shaping their feeding structures.https://doi.org/10.7554/eLife.04940.001
Dictyostelium amoebae are microbes that feed on bacteria living in the soil. They are unusual in that the amoebae can survive and grow in a single-celled form, but when food is scarce, many individual cells can gather together to form a simple multicellular organism.
To feed on bacteria, the amoebae use a process called phagocytosis, which starts with the membrane that surrounds the cell growing outwards to completely surround the bacteria. This leads to the bacteria entering the amoeba within a membrane compartment called a vesicle, where they are broken down into small molecules by enzymes. The cells can also take up fluids and dissolved molecules using a similar process called macropinocytosis.
With its short and relatively simple lifestyle, Dictyostelium is often used in research to study phagocytosis, cell movement and other processes that are also found in larger organisms. For example, some immune cells in animals use phagocytosis to capture and destroy invading microbes. Most studies using Dictyostelium as a model have used amoebae with genetic mutations that allow them to be grown in liquid cultures in the laboratory without needing to feed on bacteria. The mutations allow the ‘mutant’ amoebae to take up more liquid and dissolved nutrients by macropinocytosis, but it is not known where in the genome these mutations are.
Here, Bloomfield et al. used genome sequencing to reveal that these mutations alter a gene that encodes a protein called Neurofibromin. The experiments show that the loss of Neurofibromin increases the amount of fluid taken up by the amoebae through macropinocytosis, and also enables the amoebae to take up larger-than-normal particles during phagocytosis.
The experiments suggest that Neurofibromin controls both phagocytosis and macropinocytosis by inhibiting the activity of another protein called Ras. Neurofibromin is found in animals and many other organisms so Bloomfield et al. propose that it is an ancient protein that evolved in early single-celled organisms to control the size and shape of their feeding structures.
In humans, mutations in the gene that encodes the Neurofibromin protein can lead to the development of a severe disorder—called Neurofibromatosis type 1—in which tumours form in the nervous system. Given that tumour cells can use phagocytosis and macropinocytosis to gain nutrients as they grow, understanding how this protein works in the Dictyostelium amoebae may help to inform future efforts to develop treatments for this human disease.https://doi.org/10.7554/eLife.04940.002
Phagotrophic cells feed by performing large-scale endocytosis. A wide range of unicellular eukaryotes grow in this way, suggesting that it is extremely old in evolutionary terms (Stanier, 1970; Cavalier-Smith, 2002; Yutin et al., 2009). Typically phagocytosis is used by these organisms to engulf solid particles (Metchnikoff, 1892), and nutrients are then extracted from them by lysosomal degradation (De Duve and Wattiaux, 1966). Animal cells and amoebae ingest solid material using F-actin driven projections of their plasma membrane, forming pseudopodia and ultimately cup- or crown-shaped ruffles that enclose adhered particles. These cells can also internalise bulk fluid without the guidance of a particle using a closely related process, macropinocytosis (Swanson, 2008).
Phagocytosis and macropinocytosis are controlled using a large set of cytoskeletal and membrane-associated regulators, notably a variety of small G proteins (Bar-Sagi and Feramisco, 1986; Ridley et al., 1992; Peters et al., 1995; Cox et al., 1997; Martínez-Martín et al., 2011). Oncogenes such as Src and phosphatidylinositide 3′-kinase (PI3K) have also been linked with regulation of these processes (Araki et al., 1996; Veithen et al., 1996; Buczynski et al., 1997; Amyere et al., 2000). In amoebae, growth and endocytosis have obvious connections since phagocytosed material supplies essentially all their nutrients; in contrast vertebrates are specialised to digest food extracellularly in the gut, and so links are less apparent. However, large-scale endocytosis is extremely important in immune cells (Metchnikoff, 1892; Norbury et al., 1995; Sallusto et al., 1995), while tumour cells, released from the normal constraints on growth and proliferation, can display pronounced macropinocytotic or phagocytotic uptake (Lewis, 1937; Montcourrier et al., 1994), and can feed by ingesting extracellular protein (Commisso et al., 2013). While there are clear similarities between large-scale endocytosis in animal cells and amoebae, neither the regulatory architecture nor evolutionary contexts are adequately understood.
Phagotrophic microorganisms can be difficult to study in the laboratory because of their requirement for other organisms as food. This can be overcome if cells can be cultured axenically (‘a-xenic’ indicating the absence of organisms of another species): in some cases, such as the social amoeba Dictyostelium, which feeds primarily on bacteria in the wild (Vuillemin, 1903), strains were gradually adapted to growth in complex liquid broth, and ultimately in chemically defined media (Sussman and Sussman, 1967; Watts and Ashworth, 1970; Franke and Kessin, 1977; Watts, 1977). This process involved the selection of mutants that display increased rates of macropinocytosis (Watts and Ashworth, 1970; Loomis, 1971; Hacker et al., 1997). Two important mutations, axeA and axeB, were identified by linkage analysis as being necessary for robust axenic growth (Williams et al., 1974a, 1974b), but only the latter is strictly required (Clarke and Kayman, 1987). Although these axenic mutant strains have been very widely used for over 40 years, the genetic basis of their growth has remained mysterious, since the mutations could not be precisely mapped. We used a forward genetic approach to identify mutations that promote axenic growth in Dictyostelium discoideum using whole genome sequencing. We found that the Dictyostelium orthologue of the Ras GTPase activating protein (RasGAP) Neurofibromin (NF1), a tumour suppressor that is mutated in the genetic disorder Neurofibromatosis type 1 (Xu et al., 1990), is a key regulator of both macropinocytosis and phagocytosis.
To generate fresh axenic strains for sequencing, we cultured wildtype D. discoideum cells in HL5 growth medium after washing them free of food bacteria. This medium supports the growth of axenic strains such as Ax2 and AX4, but wildtype cells arrest their growth and ultimately die. In order to minimize the number of irrelevant background mutations we avoided mutagenesis and found that spontaneous mutants that are able to grow and proliferate arise frequently among these growth-arrested populations. We selected several independent mutants and sequenced the genomes of three after clonal isolation, along with that of the parental DdB strain, which was chosen because it was also parent to the established axenic laboratory strains (Bloomfield et al., 2008).
At first, other than two large duplications that do not correlate with axenicity (Figure 1—figure supplement 1), we could only identify one mutation affecting coding sequence in any of these strains relative to their parent, a seven basepair deletion in strain HM559 (Table 1). We noted that the reference genome sequence (Eichinger et al., 2005), derived from the axenic mutant strain AX4, also differs from its parent DdB in the same gene model (annotated as DDB_G0279251). Further analysis demonstrated that AX4 has lost almost nine kilobases of this region on chromosome 3, resulting in the deletion of most of the coding sequence of a large gene encoding a homologue of the Ras GTPase-activating protein (RasGAP) Neurofibromin (NF1), as well as part of the upstream gene (Figure 1A), with a short segment of extraneous sequence inserted. The 7 bp deletion mutation in HM559 lies within the C-terminal region of this NF1 homologue, and we found that another established axenic mutant, Ax2, has exactly the same deletion-insertion mutation as AX4 (Figure 1—figure supplement 2; Table 1).
Reanalysis of our sequencing data aligned against an amended reference containing this deleted region revealed that both of the other two new mutants also possess mutations in this gene: HM557 has a short frameshifting deletion, while HM558 has undergone an inversion leading to a substitution of eight consecutive amino acids in the predicted protein (Table 1). To examine how frequently this gene is mutated in axenic mutants, we amplified and sequenced it from six further strains: five more new mutants selected from the same parental DdB strain, and one from the V12 genetic background (strains used in this study are listed in Table 2). All possess mutations in the NF1 homologue (Table 1): four have frameshifting deletions, one a nonsense mutation, and one has a substitution of a conserved lysine to asparagine.
The ubiquity of mutations in the NF1 gene in the axenic strains tested suggested that they must underlie the phenotype we selected for, and the gene's location on chromosome 3 accords with the mapping of the classically defined axeB gene (Williams et al., 1974a, 1974b). To test whether inactivation of NF1 promotes axenic growth, we engineered a deletion at the locus in a wildtype strain, DdB, and found that the resulting mutant is able to grow axenically in HL5 medium (Figure 1B). However, it grows more slowly than the established Ax2 strain (Figure 1B), and does not grow well in suspension in this medium (see below), confirming earlier findings that additional mutations are necessary to potentiate the basal axenic phenotype (Williams et al., 1974a, 1974b). Together, the identification of mutations in the original axenic strains on chromosome 3 and demonstration that inactivation of the affected gene results in a phenotype closely resembling axeB single mutants derived parasexually (Clarke and Kayman, 1987) gives adequate reason to believe that we have identified the original causative mutation. We therefore formally retain the name axeB for the locus, while naming the encoded protein NF1.
The Dictyostelium NF1 gene encodes a protein with the same domain organisation as the human version, with CRAL/TRIO and PH-like domains at the C-terminal side of the catalytic RasGAP domain (Figure 2A). It is also of a similar size, with homology extending across most of the two proteins' lengths (Figure 2B). The D. discoideum NF1 orthologue is about as similar to the human protein as are those from the basal metazoa and choanoflagellates (Figure 2C). NF1 is an ancient protein, conserved considerably beyond the metazoan and fungal lineages in which it has been studied to date, with homologues in a variety of unicellular eukaryotes including the excavates Naegleria and Trichomonas as well as other amoebae (Figure 2C,D and Figure 2—figure supplement 1; Carlton et al., 2007; Fritz-Laylin et al., 2010; Clarke et al., 2013). RasGAPs are more broadly distributed than NF1, being present in further excavates as well as in certain ciliates, oomycetes, and the foraminiferan Reticulomyxa (Figure 2—figure supplement 2 and Figure 2—source data 1; van Dam et al., 2011; Glöckner et al., 2014). The dictyostelids, Entamoeba, Thecamonas, and Naegleria all possess separate smaller homologues with a similar domain organisation to NF1 but lacking homology outside of the central region; we term these proteins ‘MNF’ (for ‘miniature neurofibromin’). The D. discoideum NfaA protein (Zhang et al., 2008) falls into this class (Figure 2A,D and Figure 2—figure supplement 1), and is discussed further below.
The lysine to asparagine substitution occurring in one of our new axenic mutants (see above) has also been found in human cancer and Neurofibromatosis type 1 patients (Li et al., 1992), and affects a lysine residue (numbered 1423 in the human polypeptide) that is located on the surface of the GAP domain where it contacts Ras, and that is essential for GAP activity (Poullet et al., 1994). This strikingly underscores the homology inferred from sequence analysis, and furthermore suggests that overactivation of Ras subfamily small G proteins causes the axenic mutant phenotype.
Established axenic mutants have very high rates of macropinocytosis (Hacker et al., 1997). To examine fluid uptake in our NF1 knockout mutant, we incubated amoebae with fluorescent dextran and compared them with both the wildtype DdB strain and the established axenic mutant Ax2. When they are harvested directly from bacterial growth plates, NF1 mutants ingest fluid at about the same rate as an established axenic strain, Ax2, and more than four times more rapidly than wildtype cells (Figure 3A). After prolonged incubation in HL5 medium without bacteria, Ax2 cells and NF1 mutants increase their uptake further while wildtype cells decrease it, such that after 24 hr mutants take in fluid at a rate more than twenty times higher than the wildtype (Figure 3A). Fluid uptake is linear at the earliest times measured with no evidence for rapid recycling of fluid in any of these strains (Figure 3—figure supplement 1), in agreement with earlier studies of axenic mutants (Aubry et al., 1993; Padh et al., 1993). Membrane uptake measured using the accumulation of FM1-43 dye was not increased in NF1 mutants (Figure 3—figure supplement 2), consistent with an earlier comparison of Ax2 with wildtype cells (Aguado-Velasco and Bretscher, 1999). Since this assay predominantly measures uptake into small vesicles or tubules with a high surface to volume ratio, we conclude that clathrin-dependent and -independent micropinocytotic processes in these cells (Neuhaus et al., 2002; Hirst et al., 2014), are unaffected by NF1 loss.
Confocal microscopy reveals striking differences between the NF1 knockout mutant and wildtype cells. When bathed in fluorescent dextran, NF1 mutants accumulate large dextran-filled endosomes more prominently than wildtypes (Figure 3B), consistent with the fluorimetry of cell populations. NF1 mutants attached to glass coverslips also tend to flatten periodically, a phenotype often observed in established axenic strains such as Ax2 but not in wildtype cells (Figure 3B). In four-dimensional timelapse imaging, when freshly harvested from bacteria mutants and wildtype cells can be observed to enclose large macropinosomes after projecting cup- or crown-shaped ruffles, with the mutant performing macropinocytosis in this way four times as frequently as wildtype cells (Figure 3C). The NF1 mutation therefore accounts for the increased macropinocytotic fluid uptake of axenic strains.
Despite taking in a similar amount of fluid, the NF1 knockout mutant grows more slowly than Ax2 (see above). We examined whether the mutant processes ingested medium effectively by incubating cells with BODIPY-labelled bovine serum albumin (DQ-BSA), which becomes fluorescent only after lysosomal degradation releases fluorophores that previously quenched each other. Ax2 and the NF1 null strain rapidly and comparably degrade protein after internalization by macropinocytosis and maturation of endosomes, (Figure 3—figure supplement 3). Wildtype DdB cells effectively degrade DQ-BSA when taken freshly from bacterial growth but not after overnight incubation in axenic conditions (Figure 3—figure supplement 3), again suggesting that they shut down endocytic feeding as part of a starvation response.
Given the known function of NF1 in regulating Ras, and the conserved mutation affecting the RasGAP domain in one of our mutants, we examined the involvement of Ras signalling in macropinocytosis, and the specificity of individual RasGAPs in controlling it. First, we deleted the closely related MNF RasGAP, nfaA, from wildtype cells, and found that this does not confer the ability to grow axenically (Figure 4—figure supplement 1), suggesting that NF1 has specific functions not shared by other GAPs. This corroborates earlier findings that NfaA has a distinct function regulating pseudopodium formation during chemotaxis (Zhang et al., 2008).
We then asked whether inactivation of NF1 results in a global increase in Ras activity. Pulldowns of Ras-GTP using the Raf1 Ras-binding domain (RBD) from growing cells indicated no increase in Ras activity in mutants compared to wildtype cells (Figure 4—figure supplement 2). Similarly, confocal microscopy of cells expressing the GFP-RBD reporter revealed no difference between mutant and wildtypes in overall Ras activity estimated by determining the proportion the cell periphery labelled with the RBD (Figure 4—figure supplement 3). This is not surprising, since NF1 is only one of twelve putative RasGAPs encoded in the D. discoideum genome (not including IQ-GAPs, which generally act as small G protein effectors and scaffolds and do not stimulate Ras GTPase activity [Shannon, 2012]).
Having ruled out a global increase in Ras activity resulting from NF1 inactivation, we examined activity at sites of macropinocytosis. In wildtypes, as well as weak localisation at the leading edge of the cell, the GFP-RBD reporter is recruited intensely to small ruffles as they become concave and close into macropinosomes (Figure 4A). In NF1 mutants, these specifically macropinocytotic ruffles tend to be larger (Figure 4A), 50% of them being greater than 2 µm across upon closure, compared to less than 10% in wildtype cells (Figure 4B).
To examine the role of NF1 in regulating macropinocytosis more directly, we expressed full-length constructs of the D. discoideum orthologue tagged with GFP. A construct using the native polypeptide sequence reduced axenic growth of the NF1 null mutant considerably (Figure 4C), almost completely suppressing macropinosome formation as assessed by confocal microscopy (Figure 4D) and displayed an evenly cytosolic distribution (Figure 4E). In contrast, a version in which two consecutive arginine residues were mutated in the ‘arginine finger’ motif required for GAP activity (Ahmadian et al., 1997) (NF1-AS) did not retard growth (Figure 4C) nor affect macropinosome formation (Figure 4D), and localised transiently to membrane ruffles and macropinosomes (Figure 4E). This further supports a role for NF1 GAP activity in limiting macropinocytosis. A full length construct expressing the human NF1 protein also adversely affected growth of mutant cells, but a version with the critical arginine residue mutated to alanine reduced growth by a similar amount, suggesting non-specific effects (unpublished data). Since the spontaneous inversion mutation we identified (Table 1) affects the C-terminal region of the protein, we also tested whether the core RasGAP-Sec14-PH region of the D. discoideum NF1 protein could rescue the NF1 mutant; like the NF-AS version this did not suppress axenic growth (Figure 4C), and displayed an evenly cytosolic distribution (Figure 4E), suggesting that other regions of the protein are required for its correct localisation. The inactive NF1-AS form of the protein is presumably recruited by strong Ras activity at macropinocytotic crowns that it is then unable to attenuate. This localisation implies that the NF1 protein directly regulates signalling at the plasma membrane during ruffling, and together with the more extensive Ras signalling during macropinocytosis, suggests that this RasGAP regulates a pool of Ras responsible for this feeding process.
Two Dictyostelium Ras proteins have been linked to endocytic functions (Chubb et al., 2000; Hoeller et al., 2013); to examine their involvement in NF1-controlled events we expressed GFP-tagged versions of each in NF1 mutant and wildtype cells. All tested GFP-tagged Ras constructs localised to the plasma membrane, except for dominant negative (S17N mutant) RasG and RasS, expression of which was apparently poorly tolerated in these strains (Figure 4—figure supplement 4). None of the Dictyostelium Ras expression constructs phenocopied the loss of NF1; constitutively active RasG was deleterious to growth, as was expression of wildtype or constitutively active RasS (Figure 4—figure supplement 5), suggesting that improper activation of these isoforms interferes with endocytosis or other Ras-influenced processes leading to detrimental effects on cell growth.
Active Ras at the plasma membrane recruits class 1 phosphoinositide 3′-kinases (PI3Ks; Rodriguez-Viciana et al., 1997), allowing the spatially restricted formation of phosphatidylinositol trisphosphate (PIP3) and other inositol phospholipids that occurs during macropinocytosis (Araki et al., 1996; Buczynski et al., 1997; Hoeller et al., 2013). Confirming that the macropinosomes observed in NF1 mutants are mechanistically similar to those previously documented, we find that Ras activity at membrane ruffles in NF1 mutants is accompanied by recruitment of PH-domain reporters that bind the plasmanyl inositides produced by Dictyostelium class 1 PI3Ks (Figure 5A; Clark et al., 2014), as well as by actin polymerisation (Figure 5B). PH domains are also prominently recruited during macropinocytosis in wildtype cells; regions of recruitment tend to be larger in mutants reflecting the increased Ras signalling that results from the absence of NF1 (Figure 5C). This pattern of Ras activity and PIP3 formation is invariably observed in every instance of macropinocytosis in Dictyostelium. The contributions of other Ras effectors remain unclear; for example no increase in ERK activity is observed in NF1 mutants compared to wildtype cells (Figure 5—figure supplement 1).
The observations described above indicate that wildtype cells perform qualitatively similar macropinocytosis to NF1 mutants, but on a smaller scale. This results in a markedly different outcome when the cells are incubated in HL5 medium: mutants can grow but the wildtype cannot. One possible explanation is that nutrient-uptake below a certain threshold leads to a growth arrest. To test this idea, we asked whether wildtype cells can maintain growth in an enriched axenic medium, as suggested by earlier work (Sussman and Sussman, 1967). Wildtype cells incubated in stationary cultures in HL5 supplemented with foetal bovine serum (or bovine serum albumin, data not shown) were able to grow, albeit still much more slowly than NF1 mutants cultured in the same medium (Figure 6A,B). The morphology of wildtype cells was not appreciably altered after several days of axenic growth, while NF1 mutants remained consistently more flattened and extensively ruffled than wildtype cells in the same conditions (Figure 6C). Wildtype cells were also found to degrade DQ-BSA efficiently after axenic growth in the presence of serum (Figure 6—figure supplement 1). Serum addition also stimulated the growth of NF1 mutants in shaking suspension (Figure 6—figure supplement 2). These findings suggest that the additional nutrients in the richer broth allow these cells to avoid the starvation-triggered growth arrest that can occur in axenic media.
Finally, since macropinocytosis and phagocytosis are closely related processes we compared phagocytosis in NF1 mutants and wildtype cells. Mutant and wildtype strains grow well on bacteria (Figure 7—figure supplements 1, 2) and take up bacterium-sized polystyrene microspheres (1 μm and 1.8 μm diameter) at very similar rates (Figure 7A), although the standard strain Ax2 is marginally but consistently less effective at internalising smaller beads than the other strains (Figure 7B). Against expectation, we found that wildtype cells cannot efficiently ingest yeast or beads greater than 3 μm in diameter (Figure 7A,C), whereas NF1 mutant cells can ingest beads larger than 4 μm in diameter (Figure 7A) or yeast cells very readily (Figure 7C). In line with earlier findings in Ax2 cells (Clarke et al., 2010), RBD and PH domain reporters localised to phagosomes as they formed, essentially identically to their behaviour during macropinocytosis (Figure 7—figure supplement 3). We conclude that, as well as controlling macropinocytosis, NF1 limits the size of nascent phagosomes, supporting the idea that these large-scale endocytic processes share regulatory as well as structural features. The striking improvement in phagocytosis of larger cells after NF1 deletion also suggests that variation in or loss of this gene can have important ecological and evolutionary consequences by enabling predators to target additional prey species (Porter, 2011).
We set out to explain the genetic basis of the axenic growth phenotype of standard laboratory D. discoideum strains, which has remained mysterious for decades despite the widespread use of these cells. In freshly selected mutants, we discovered coding sequence mutations only in the Dictyostelium orthologue of the tumour suppressor NF1. Importantly, all axenic mutants, across two distinct genetic backgrounds, bear mutations in this gene. While it is possible that mutations in other genes will result in similar phenotypes, it is clear that NF1 mutations must be the most frequent by far that cause axenic growth. The further mutations enabling faster growth in the established axenic strains remain to be identified, and their precise effect is still unclear. Our identification of the axeB gene as NF1 will provide a route towards creating new axenic strains from wild isolates, thus giving strains with minimal background mutations.
Vegetative wildtype cells perform macropinocytosis in a qualitatively similar way as axenic mutants but to a lesser extent, and accordingly they can grow axenically when the standard medium is supplemented with bovine serum. NF1 mutants retain a large growth advantage in the more complex medium, and so will still be selected during prolonged culture. Nevertheless, this protocol should be of use for short-term axenic culture of wildtype strains; standard defined medium supplemented with bovine serum albumin also enables slow growth of wildtype strains (unpublished data) suggesting that fully synthetic defined media should be attainable. This further supports the idea that the important effect of serum is the provision of bulk nutrients, preventing the nitrogen starvation that initiates Dictyostelium development (Marin, 1976).
One important focus of Dictyostelium research is chemotaxis, and key roles for Ras and PIP3 in steering migrating cells have been proposed (Kay et al., 2008; Artemenko et al., 2014). Although axenic cells chemotax very well to the best-studied chemoattractant, cyclic-AMP, they are much less efficient than wildtype cells in chemotaxis to folic acid, due to interference from large, PIP3-rich, macropinosomes (Veltman et al., 2014). It is now apparent that the reason for this poor chemotaxis is likely to be the inactivation of NF1 in axenic cells, leading to Ras and PI3K hyperactivity. Macropinosomes and intense patches of Ras activity and PIP3 also appear in cells chemotaxing to cyclic-AMP (Parent et al., 1998) and it will be important to disentangle their contribution to chemotaxis by comparative studies of axenic and wildtype cells.
Several lines of evidence emphasize the importance of Ras in the feeding process used by Dictyostelium cells. Previous studies in Dictyostelium showed defects in macropinocytosis and phagocytosis after disruption of Ras genes (Chubb et al., 2000; Hoeller et al., 2013), and Ras activates PI3K during macropinocytosis (Hoeller et al., 2013). Further, Ras activity reporters localise strongly to membrane ruffles during macropinocytosis as well as to nascent phagosomes (Sasaki et al., 2007; Clarke et al., 2010), and we found that the size of these sites of Ras activity is increased in NF1 mutants. The well-studied NF1 orthologues in mammals and yeast are specific to Ras subfamily small G proteins (Tanaka et al., 1990; Zhang et al., 1991), and one of mutations we found in Dictyostelium corresponds exactly to one that abolishes the GAP activity of the human orthologue by altering the Ras-binding interface of the protein (Poullet et al., 1994). These data, along with the effect of mutating the ‘arginine finger’ critical for RasGAP activity, suggest that Dictyostelium NF1 is most likely Ras-specific, but this remains to be demonstrated biochemically. The specificity of Dictyostelium NF1 towards different Ras isoforms remains unclear. Since the rasG and rasS null mutants have defective endocytic feeding but are still viable (Chubb et al., 2000; Hoeller et al., 2013) it is likely that multiple Ras isoforms are involved, possibly including other less well-characterised genes.
The biochemical functions of NF1 beyond its GAP activity remain poorly understood. A module comprising a CRAL/TRIO and a PH-like domain is conserved and likely mediates an interaction with lipids within cells (D'angelo et al., 2006), but has not been tied to any function of consequence. Regions of conserved sequence to either side of the relatively well-characterised core of the protein are even more mysterious, but may be important for its function in Dictyostelium, perhaps by mediating its dynamic localisation. We find that GFP-tagged full length Dictyostelium NF1 localises transiently to macropinocytotic ruffles. This translocation has only been visualised in a mutant form of the protein with the ‘arginine finger’ motif mutated, because over-expression of the active protein almost completely inhibits macropinocytosis. It will be important to identify structural determinants of this localisation as a route towards a better understanding of the cell-biological function of NF1.
Both macropinosomes and phagosomes are significantly larger in NF1 mutants than in wildtypes, suggesting that NF1 stimulates Ras GTPase activity as endocytic ruffles form and spread, thereby limiting their size (Figure 8). The control of NF1 function is not well understood, but our results suggest that it might be locally inactivated during macropinocytosis and phagocytosis. In an intriguing parallel, growth factor treatment of mammalian cells leads to rapid degradation of NF1 by the proteasome (Cichowski et al., 2003) and also triggers membrane ruffling and macropinocytosis with similar kinetics (Brunk et al., 1976; Mellström et al., 1983). However, we could find no obvious fluid-uptake phenotype in NF1 null mouse embryonic fibroblasts, suggesting that NF1 inactivation is not sufficient for stimulation of macropinocytosis in these cells (unpublished data). Given the known involvement of Ras signalling in promoting ruffling and macropinocytosis the possibility remains that NF1 function is conserved in metazoa, but in a context in which Ras activity is more heavily regulated, with additional layers of control not present in amoebae (Casci et al., 1999; Johnson et al., 2005).
The set of species possessing NF1 homologues indicates the extreme antiquity of this protein: NF1 is present in the excavates Naegleria and Trichomonas as well as the amoebae, animals, and fungi. Recent placements of the root of the eukaryotes within the excavate group (He et al., 2014; Derelle et al., 2015) suggest that NF1 evolved very early in the history of eukaryotes, and may have been present in the last eukaryotic common ancestor (LECA), along with the related protein MNF. The presence of these RasGAPs in organisms that display strikingly similar forms of circular ruffling suggests the hypothesis that NF1 and MNF evolved together to control the movements of the exploratory cell projections used in very early eukaryotes during feeding (Boschek et al., 1981; John et al., 1984; Hacker et al., 1997; Cavalier-Smith, 2013).
Macropinocytosis and phagocytosis occur in a well-defined series of stages that are shared between amoebae and vertebrate cells (Swanson, 2008). The actin cytoskeleton is used to project membrane ruffles outwards to enclose either a bound particle or extracellular fluid, inositol phospholipids accumulate and are then dephosphorylated in a well-defined sequence (Dormann et al., 2004; Egami et al., 2014). The role of Ras is less well understood, but has previously been implicated in macropinocytosis and phagocytosis in Dictyostelium (Chubb et al., 2000; Hoeller et al., 2013), and in circular ruffle formation, macropinocytosis, and trogocytosis in vertebrate cells (Bar-Sagi and Feramisco, 1986; Martínez-Martín et al., 2011; Welliver and Swanson, 2012). Our unbiased forward genetic analysis suggests that NF1 has a fundamental role in governing the feeding processes used by amoebae. The mechanistic parallels between large-scale endocytosis in metazoa and amoebae, as well as their shared history, raise the possibility that this function is conserved. The role of Schwann cells, the cell-type of origin of neurofibromas, as non-professional phagocytes during the repair of nerve damage (Stoll et al., 1989) is striking in this regard. Although the consequences of NF1 mutation are well understood in humans, its cell-biological function is still not well understood (Stephen et al., 2014). Our results, for the first time linking NF1 to macropinocytosis and phagocytosis, may provide an important clue.
D. discoideum strains (listed in Table 2) were cultivated in association with Klebsiella pneumoniae on SM agar plates at 22°C, harvested and prepared for experiments by removing the bacteria by differential centrifugation in KK2 buffer (16.5 mM KH2PO4, 3.9 mM K2HPO4, 2 mM MgSO4). For axenic growth, cells were grown in autoclaved HL5 medium (Formedium, Hunstanton, UK) on tissue-culture treated plastic dishes, or shaken at 180 rpm in 250 ml flasks, in both cases at 22°C. To prepare serum-supplemented medium foetal bovine serum (Hyclone/GE Healthcare, South Logan, Utah) was either added directly to filter sterilised HL5 medium supplemented with vitamins and microelements (HL5VME, Formedium), or first diluted to 10% vol/vol in Milli-Q water then used to dissolve powdered HL5VME before 0.2 μm filter sterilisation. Variable amounts of precipitated material are visible in filtered serum-supplemented HL5VME during incubation with cells at 22°C; these solids may help to stimulate growth (Watts, 1977). To measure growth rates on bacteria, cells were shaken in a suspension of heat-killed Escherichia coli B/r (at an OD600 of 10) in KK2. Cells were transformed according to the method of (Pang et al., 1999), except that selection was carried out growing cells on bacteria in order to avoid selection for axenic growth: for the axeB gene disruption cells were plated in 2.5 ml KK2 buffer containing a suspension of heat-killed K. pneumoniae at an OD600 of 5 and 50 μg/ml tetracycline, 100 μg/ml dihydrostreptomycin, and 40 μg/ml G418 in 6-well tissue culture dishes. Once wells became confluent, cells were passaged again in the same conditions to kill non-transformed cells before being cloned on SM agar plates and screened for the disruption by polymerase chain reaction and sequencing. Later transformations, to introduce expression constructs and to disrupt nfaA, used an improved selection protocol as follows: Klebsiella pneumoniae was grown overnight in a standing bottle of SM/5 broth (Formedium SM broth diluted fivefold in Milli-Q water) to stationary phase, then diluted fourfold in fresh SM/5 broth containing 100 μg/ml dihydrostreptomycin and 60 μg/ml hygromycin, giving a final OD600 of approximately 0.1–0.2. A total of 2.5 ml of bacterial suspension was added per well of a 6-well cluster dish, or 10 ml per 100 mm dish. The bacteria and antibiotics were replenished at least every 2 days until amoebae grew to their maximum density (typically 3–4 days after the initiation of selection). Putative nfaA disruptants were again cloned on SM agar plates before screening as above.
DdB cells were grown on mass culture SM agar plates before being washed free of bacteria and resuspended in HL5 medium. Selection was carried out without mutagenesis by incubation in HL5 medium either under shaking suspension from a starting density of 106 cells per ml (strains HM557, HM558, and HM559) or in 100 mm tissue-culture treated plastic dishes at a starting density of 107 cells per dish (subsequent mutants), at 22°C. Mutants accumulated over the course of 3–5 weeks, and were cloned on SM agar and axenic growth was retested before genome resequencing or targeted sequencing of the axeB locus.
Genomic DNA was extracted from cells starved overnight that were resuspended in lysis buffer (20 mM Tris-HCl, 5 mM MgCl2, 0.32 M sucrose, 0.02% sodium azide, 1% Triton X-100, pH 7.4) at 4°C, vortexed and incubated at 4°C for 15 min. Nuclei were pelleted at 3000×g for 10 min, resuspended in lysis buffer and pelleted again, before freezing the pellets on dry ice. Proteinase K (100 μl of a 20 mg/ml stock in water) was added, followed immediately by 10 ml digestion buffer (10 mM Tris-HCl, 5 mM EDTA, 0.7% SDS, pH 7.5), and the pellet resuspended by gentle pipetting. The lysate was incubated for 1 hr at 60°C and the DNA finally phenol-chloroform extracted using Phase Lock Gel tubes (5 Prime, Hilden, Germany). Single end Illumina sequencing libraries were constructed according to the manufacturer's instructions. Sequencing was carried out on an Illumina GAII instrument, producing reads of 36 and 45 basepairs across different runs, to a depth of approximately 17–20× after removing of potential PCR and optical duplicates. Reads were aligned against the dictyBase AX4 assembly using Stampy (Lunter and Goodson, 2010), and duplicates removed and variants called using samtools and bcftools (Li et al., 2009). Candidate variants in each strain were pre-filtered (depth greater than 3, mapping quality greater than 20, SNP quality greater than 20, ‘heterozygous’ calls excluded) to remove misalignments, then putative variants common to all four resequenced strains, representing real differences between DdB and the reference sequence, were excluded.
To display homology across the length of the NF1 protein, the Homo sapiens isoform 2 polypeptide sequence (NP_000258.1) was split into segments using a sliding window of 200 residues. These were then aligned using the EMBOSS ‘water’ local alignment software (Rice et al., 2000) to the D. discoideum, Drosophila melanogaster (AAB58975.1), and Takifugu rubripes (AAD15839.1) NF1 orthologues and the Saccharomyces cerevisiae Ira1p protein (NP_009698.1). Alignment scores were normalised to the Hs–Hs comparison such that the self-comparison gives a value of one, and plotted sequentially along the sequence length for each comparison. To display global similarity and identity percentages, the same H. sapiens polypeptide sequence was aligned to the T. rugripes, D. melanogaster, Trichinella spiralis (XP_003376664.1), Trichoplax adhaerens (XP_002115170.1), Salpingoeca rosetta (EGD75509.1), Capsaspora owczarzaki (EFW43762.1), and Batrachochytrium dendrobatidis (EGF81694.1) NF1 proteins, S. cerevisiae Ira1p and Ira2p (NP_014560.1), and D. discoideum NF1 and NfaA (XP_645456.1). The EMBOSS ‘needle’ software was used to generate global alignments in order that indels count against overall homology.
The axeB disruption plasmid was constructed by inserting the V18-tn5 cassette into the BamHI and HindIII sites of pBluescript2 KS+, then amplifying 5′ and 3′ flanking regions of the axeB gene from strain DdB using the primers KOKpnI (5′-GGTACCAAATGTATACTTGTATATGATG-3′) with KOHindIII (5′-AAGCTTGAGCTCTTCACCACCATTAAGT-3′), and KOBamHI (5′-GGATCCATTGGGTAGTTATCGATC-3′), with KOEagI (5′-CGGCCGTGCACAGTCTTTAGAAAATTTTG-3′), and inserting them either side of it. The nfaA disruption plasmid was also based on pBluescript2 KS+ using, between BamHI and XhoI sites, the hygromycin resistance gene driven by the act14 promoter; and the following primer pairs were used to amplify flanking segments: nfa2kpn (5′-GGTACCTAATGGTGTAACTCAAGTTTTCG-3′) with nfa2xho (5′-CTCGAGTGGTAATGTTTTATTTGCTGTTG-3′), and nfa2bam (5′-GGATCCAGATATTCATTGTACATCCATCAG-3′) with nfa2spe (5′-ACTAGTATACTTATAAGAAACCTTCTTCAG-3′). Expression constructs used the act14 or coaA promoter to drive the resistance gene and the act15 promoter to drive the gene fragment of interest, using the vector pDM1005 as backbone, a derivative of previously described extrachromosomal vectors (Veltman et al., 2009). The GFP-Raf1-RBD included amino acids 1–134 of the H. sapiens Raf1 polypeptide, with a short linker (TTSRT) between GFP and its N-terminal methionine. PH-CRAC-GFP contains residues 1–126 of the D. discoideum CRAC protein. GFP-PH10 contains amino acids 1–103 of D. discoideum PkgE (Ruchira et al., 2004); this fragment is longer than the previously published version, but gives a similar localisation. The GFP-Ras constructs included an RS(GGS)4RS linker between the C-terminus of GFP and N-terminus of each Ras. During the construction of the full length NF1 expression construct, in the same vector backbone including an N-terminal GFP, silent mutations were incorporated at positions 409 and 813 of the D. discoideum axeB cDNA sequence to introduce a XhoI and a XmaI site, respectively. The consecutive arginine codons in the ‘arginine finger’ region were mutated by introducing changes in overlapping PCR primers during cloning. The NF1ΔNΔC construct uses the same vector backbone and tag, and includes amino acids 1189 to 1779, with the wildtype arginine finger motif. Dual-colour experiments used plasmids containing both protein constructs as previously described (Veltman et al., 2009).
Since axeB knock-out mutants are unable to grow well under shaking suspension, growth was measured by accumulation of crystal-violet staining. Cells were pregrown on bacteria, washed, and plated at a density of 105 cells per well of 24-well tissue culture plates in 1 ml of HL5 medium; for the experiments to test the effect of serum on cell growth the initial density was 5 × 104 cells per well. At each timepoint the medium was removed, the cells washed once in KK2 buffer, then incubated for 20 min in 0.5 ml of 0.1% crystal violet (in 10% ethanol). Each well was then carefully washed three times with water, then incubated for a further 20 min in 10% acetic acid. After brief agitation, the absorbance of each well was measured at 590 nm. To measure growth on bacteria, cells were grown overnight in heat-killed E. coli B/r (OD600 of 10 in KK2 buffer) to logarithmic phase then diluted to a density of 5 × 105 per ml of fresh bacterial suspension; cells were counted using a haemocytometer every 2 hr for 8 hr.
Bacterially grown amoebae were assayed either directly or after adaptation in HL5 medium for 24 hr shaken at 180 rpm from a starting density of 2 × 105 cells per ml. Cells were resuspended at 1 × 107 per ml in KK2C (KK2 plus 0.1 mM CaCl2) and the assay initiated by adding FITC dextran (average MW 70,000) to 2 mg/ml final with 8 × 105 cells being removed (in duplicate) for each data point and mixed with 0.75 ml of ice-cold wash buffer (KK2C plus 0.5 mg/ml BSA). The cells were pelleted by centrifugation (20,000×g) for 12 s, the supernatant removed and the cells resuspended in 1.5 ml ice-cold wash buffer. The cells were pelleted and washed once more before 1 ml of lysis buffer (0.1 M Tris-Cl pH 8.6, 0.2% Triton X-100) was added. The fluorescent intensity was measured by excitement at 490 nm and emission at 520 nm (PerkinElemer LS50B Luminescence Spectrometer).
Bacterially grown cells were shaken at 180 rpm for 15 min. Then 0.1 ml was added to a stirred fluorimeter cuvette containing 0.9 ml 11 μM FM1-43 (Life Technologies, Paisley, UK) in KK2C and data collected every 1.2 s at an excitation of 470 nm and emission of 570 nm for approximately 5 min using a PerkinElmer LS50B fluorimeter.
TRITC labelled yeast was made as described by (Rivero and Maniak, 2006) and the assay itself was based on that described in the same paper. Bacterially grown amoebae were resuspended at 2 × 106 cells/ml in KK2C and the assay initiated by the addition of TRITC labelled yeast cells to approximately 1 × 107 per ml final. For each data point, 2 × 105 cells were removed and the uningested fluorescent yeast quenched by the addition of 0.1 ml of trypan blue solution (20 mM sodium citrate, 150 mM NaCl, 2 mg/ml trypan blue). The cell suspension was shaken for 3 min at 2000 rpm (Eppendorf MixMate) and then pelleted by centrifugation (4000×g) for 2.5 min. The cell pellet was resuspended in 1.5 ml of KK2C and pelleted as before. Finally, the cell pellet was resuspended in 1 ml of KK2C and the fluorescent intensity measured by excitement at 544 nm and emission at 574 nm (PerkinElemer LS50B Luminescence Spectrometer). For bead uptake experiments Fluoresbrite Bright Blue carboxylate microspheres (Polysciences, Eppelheim, Germany) were used. Bacterially grown cells were resuspended at 107 per ml in KK2C containing 0.2% (wt/vol) BSA (KK2CB) (to reduce non-specific binding) and 20 beads added per amoebae. Uptake was stopped by adding 0.5 ml of the cell suspension to an equal volume of ice-cold KK2CB containing 10 mM NaN3 (KK2CBA). The cells were pelleted at 300×g for 2 min. The pellet was then washed twice more in 1 ml of ice-cold KK2CBA and finally resuspended in 1 ml of ice-cold KK2CBA. 100 μl of this cell suspension was added to 200 μl of KK2CBA containing 40 μg/ml TRITC dextran (as a cell counterstain) in a chamber of a 8-well LabTek chambered coverslip and image stacks taken of several fields of cells for analysis. This procedure removes most non-phagocytosed beads up to 3 μm. For 3.1, and 4.4 μm beads the cells can be directly scored by phase contrast microscopy without counterstain.
Cells were imaged either directly from growth plates in SM/5 medium or after incubation overnight in Loflo medium, as indicated. To image lysosomal degradation of endocytosed protein, cells were incubated in Loflo medium (Formedium) plus 20 μg/ml DQ green BSA (Life Technologies). Images were acquired using a Zeiss 780 LSM microscope, with laser power and gain set identically for all strains and the brightness and contrast of images adjusted later identically. For DIC images, brightness and contrast was adjusted for visual clarity using ImageJ. To measure the frequency of macropinosome internalization, cells were harvested from mass-inoculation SM agar growth plates, washed three times in Loflo medium, then 1 × 105 cells plated per chamber of a Lab-Tek II 8-well chambered coverglass (Thermo, Waltham, MA) and allowed to settle for 10–15 min. Within 30 min of removal from bacteria, 0.4 mg/ml FITC- and 2 mg/ml TRITC-dextran were added, and movies recorded taking 5 Z-sections (1 μm apart) every 5 s. Pinosomes were counted if they appeared adjacent to ruffled cell projections and cups, and if they retained FITC fluorescence (FITC is rapidly bleached as endosomes that are acidified). To enable estimation of the rate of uptake, cells were tracked and included in the analysis only if they remained within the field for at least 5 min; these cells were tracked as long as they remained in the field to at most 10 min. To measure the extent of Ras signalling at the membrane of random growing cells, strains expressing the GFP-Raf1-RBD reporter were harvested during exponential growth in tissue culture dishes containing K. aerogenes in SM/5 broth, washed and plated in fresh SM/5 in Lab-Tek chambers as above. Tile scans were acquired of 25 fields, and cells were outlined manually using a custom built MatLab script (Source code 1). Normals of 3 pixels long were drawn at equidistant points along the perimeter spaced 2 pixels apart and the highest intensity value along this normal was determined. The patch threshold was set as all membrane values that were more than 3 standard deviations above the mean intensity of the cytosol. Over 100 cells from two independent experiments were analysed for each strain. To measure the extent of Ras signalling during pinocytosis, the same Ras-activity reporter strains were plated in Lab-Tek chambers in SM/5 as above, and movies of a single confocal section through the cells recorded with a 2.5 s interval. The maximum extent of GFP-RBD fluorescence across enclosed ruffles was measured in the first frame after they closed using ImageJ. Images of tagged Ras and NF1 proteins, Raf1-RBD, PH-CRAC, and LifeAct reporters were adjusted for brightness and contrast across the whole image of each channel, and cropped, for clarity.
Cells were grown in association with K. aerogenes on mass-inoculation SM agar plates, washed three times in KK2 buffer, and 2 × 107 cells resuspended in 10 ml KK2 and shaken at 180 rpm at 22°C for 30 min. The cells were then pelleted at 4°C, and lysed in 1 ml lysis buffer (0.5% Triton X-100, 150 mM NaCl, 40 mM Tris, 20 mM MgCl2, 10% glycerol, 1 mM DTT, 1 tablet per 50 ml Complete EDTA-free protease inhibitors (Roche Lifescience, Burgess Hill, UK), pH 7.4). The lysate was cleared by centrifugation at 13,000×g for 10 min at 4°C, then the supernatant added to 33 μl GST-Raf1-RBD conjugated to agarose beads (Millipore, Watford, UK) suspended in lysis buffer, with BSA added to a final concentration of 1 mg/ml. The mixture was then shaken for 30 min at 4°C, before washing twice with lysis buffer by centrifugation at 2000×g for 1 min. The bound Ras was released by boiling the washed beads in LDS sample buffer (Life Technologies) for 5 min, before immunoblotting and detection with mouse monoclonal anti-pan-Ras antibody (clone RAS 10, Millipore) and HRP-conjugated goat anti-mouse secondary antibody using standard techniques.
Cells of each strain were harvested from mass inoculation cultures grown in association with K. pneumoniae on SM agar, washed, and resuspended in autoclaved HL5 medium at a density of 2 × 106 cells per ml in a total of 10 ml in 50 ml Erlenmeyer flasks. The flasks were then shaken at 180 rpm and 22°C and aliquots taken at the indicated timepoints. These samples were lysed in LDS sample buffer (Life Technologies) in the presence of protease and phosphatase inhibitors (Roche, as above; Sodium pyrophosphate, sodium orthovanadate, and ß-glycerophosphate), and separated on NuPAGE polyacrylamide gels and blotted onto PVDF according to standard protocols. Blots were blocked in 5% bovine serum albumin in TBS-Tween and activated ERK kinases detected using an antibody raised against phospho-ERK (anti-phospho-p44/p42 MAPK rabbit antibody from Cell Signalling Technology, cat #9101), and HRP-conjugated goat anti-mouse secondary antibody.
Sequence data have been deposited in European Nucleotide Archive under the accessions HF565448 (axeB genomic sequence) and ERP002043 (whole-genome resequencing reads).
Circulation of the plasma membrane in DictyosteliumMolecular Biology of the Cell 10:4419–4427.https://doi.org/10.1091/mbc.10.12.4419
Confirmation of the arginine-finger hypothesis for the GAP-stimulated GTP-hydrolysis reaction of RasNature Structural Biology 4:686–689.https://doi.org/10.1038/nsb0997-686
A role for phosphoinositide 3-kinase in the completion of macropinocytosis and phagocytosis by macrophagesThe Journal of Cell Biology 135:1249–1260.https://doi.org/10.1083/jcb.135.5.1249
Moving towards a paradigm: common mechanisms of chemotactic signaling in Dictyostelium and mammalian leukocytesCellular and Molecular Life Sciences 71:3711–3747.https://doi.org/10.1007/s00018-014-1638-8
Kinetics of endosomal pH evolution in Dictyostelium discoideum amoebae. Study by fluorescence spectroscopyJournal of Cell Science 105:861–866.
Inactivation of two Dictyostelium discoideum genes, DdPIK1 and DdPIK2, encoding proteins related to mammalian phosphatidylinositide 3-kinases, results in defects in endocytosis, lysosome to postlysosome transport, and actin cytoskeleton organizationThe Journal of Cell Biology 136:1271–1286.https://doi.org/10.1083/jcb.136.6.1271
The phagotrophic origin of eukaryotes and phylogenetic classification of protozoaInternational Journal of Systematic and Evolutionary Microbiology 52:297–354.
The Dictyostelium RasS protein is required for macropinocytosis, phagocytosis and the control of cell movementJournal of Cell Science 113:709–719.
Dynamic regulation of the Ras pathway via proteolysis of the NF1 tumor suppressorGenes & Development 17:449–454.https://doi.org/10.1101/gad.1054703
The axenic mutations and endocytosis in DictyosteliumMethods in cell biology 28:157–176.https://doi.org/10.1016/S0091-679X(08)61642-8
Requirements for both Rac1 and Cdc42 in membrane ruffling and phagocytosis in leukocytesThe Journal of Experimental Medicine 186:1487–1494.https://doi.org/10.1084/jem.186.9.1487
Functions of lysosomesAnnual Review of Physiology 28:435–492.https://doi.org/10.1146/annurev.ph.28.030166.002251
Bacterial proteins pinpoint a single eukaryotic rootProceedings of the National Academy of Sciences of USA 112:E693–E699.https://doi.org/10.1073/pnas.1420657112
In vivo analysis of 3-phosphoinositide dynamics during Dictyostelium phagocytosis and chemotaxisJournal of Cell Science 117:6497–6509.https://doi.org/10.1242/jcs.01579
A defined minimal medium for axenic strains of Dictyostelium discoideumProceedings of the National Academy of Sciences of USA 74:2157–2161.https://doi.org/10.1073/pnas.74.5.2157
The genome of the Foraminiferan Reticulomyxa filosaCurrent Biology 24:11–18.https://doi.org/10.1016/j.cub.2013.11.027
Fluid-phase uptake by macropinocytosis in DictyosteliumJournal of Cell Science 110:105–112.
An Alternative root for the eukaryote tree of lifeCurrent Biology 24:465–470.https://doi.org/10.1016/j.cub.2014.01.036
Two distinct functions for PI3-kinases in macropinocytosisJournal of Cell Science 126:4296–4307.https://doi.org/10.1242/jcs.134015
Sucker-like structures on the pathogenic amoeba Naegleria fowleriApplied and Environmental Microbiology 47:12–14.
Developmental regulation of Dictyostelium discoideum actin gene fusions carried on low-copy and high-copy transformation vectorsMolecular and Cellular Biology 6:3973–3983.https://doi.org/10.1128/MCB.6.11.3973
Pinocytosis by malignant cellsAmerican Journal of Cancer Research 29:666–679.
The sequence alignment/map (SAM) format and SAMtoolsBioinformatics 25:2078–2079.https://doi.org/10.1093/bioinformatics/btp352
Sensitivity of Dictyostelium discoideum to nucleic acid analoguesExperimental Cell Research 64:484–486.https://doi.org/10.1016/0014-4827(71)90107-8
The effect of platelet-derived growth factor on morphology and motility of human glial cellsJournal of Muscle Research and Cell Motility 4:589–609.https://doi.org/10.1007/BF00712117
Leçons sur la pathologie comparée de l'inflammation faites à l'Institut pasteur en avril et mai 1891Paris: Libraire de l'Académie de médecine.
Characterization of very acidic phagosomes in breast cancer cells and their association with invasionJournal of Cell Science 107:2381–2391.
Morphology and dynamics of the endocytic pathway in Dictyostelium discoideumMolecular Biology of the Cell 13:1390–1407.https://doi.org/10.1091/mbc.01-08-0392
A post-lysosomal compartment in Dictyostelium discoideumThe Journal of Biological Chemistry 268:6742–6747.
Overexpression of wild-type and mutant ARF1 and ARF6: distinct perturbations of nonoverlapping membrane compartmentsThe Journal of Cell Biology 128:1003–1017.https://doi.org/10.1083/jcb.128.6.1003
Functional significance of lysine 1423 of neurofibromin and characterization of a second site suppressor which rescues mutations at this residue and suppresses RAS2Val-19-activated phenotypesMolecular and Cellular Biology 14:815–821.
EMBOSS: the european molecular biology open software suiteTrends in Genetics 16:276–277.https://doi.org/10.1016/S0168-9525(00)02024-2
Quantitative and microscopic methods for studying the endocytic pathwayMethods in Molecular Biology 346:423–438.https://doi.org/10.1385/1-59745-144-4:423
Pleckstrin homology domain diffusion in dictyostelium cytoplasm studied using fluorescence correlation spectroscopyThe Journal of Biological Chemistry 279:10013–10019.https://doi.org/10.1074/jbc.M310039200
Dendritic cells use macropinocytosis and the mannose receptor to concentrate macromolecules in the major histocompatibility complex class II compartment: downregulation by cytokines and bacterial productsThe Journal of Experimental Medicine 182:389–400.https://doi.org/10.1084/jem.182.2.389
G protein-independent Ras/PI3K/F-actin circuit regulates basic cell motilityThe Journal of Cell Biology 178:185–191.https://doi.org/10.1083/jcb.200611138
IQGAP family members in yeast, Dictyostelium, and mammalian cellsInternational Journal of Cell Biology 2012:894817.https://doi.org/10.1155/2012/894817
Molecular cloning and characterization of a gene encoding a 13.1 kDa antigenic protein of Naegleria fowleriThe Journal of Eukaryotic Microbiology 48:713–717.https://doi.org/10.1111/j.1550-7408.2001.tb00211.x
Some aspects of the biology of cells and their possible evolutionary significanceSymposium of the Society for General Microbiology 20:1–38.
Cultivation of Dictyostelium discoideum in axenic mediumBiochemical and Biophysical Research Communications 29:53–55.https://doi.org/10.1016/0006-291X(67)90539-6
v-Src induces constitutive macropinocytosis in rat fibroblastsJournal of Cell Science 109:2005–2012.
PIP3-dependent macropinocytosis is incompatible with chemotaxisThe Journal of Cell Biology 204:497–505.https://doi.org/10.1083/jcb.201309081
Une Acrasiée bacteriophageComptes rendus des séances de l'Académie des sciences de Paris 137:387–389.
Vitamin requirements for growth of Myxamoebae of Dictyostelium discoideum in a defined mediumJournal of General Microbiology 98:355–361.https://doi.org/10.1099/00221287-98-2-355
Growth of myxameobae of the cellular slime mould Dictyostelium discoideum in axenic cultureThe Biochemical Journal 119:171–174.
Isolation of strains of the cellular slime mold Dictyostelium discoideum capable of growing after a single passage in axenic mediumApplied and Environmental Microbiology 32:635–637.
Parasexual genetics in Dictyostelium discoideum: Mitotic analysis of Acriflavin resistance and growth in axenic mediumJournal of General Microbiology 84:59–69.https://doi.org/10.1099/00221287-84-1-59
Spatiotemporal regulation of Ras activity provides directional sensingCurrent Biology 18:1587–1593.https://doi.org/10.1016/j.cub.2008.08.069
W James NelsonReviewing Editor; Stanford University, United States
eLife posts the editorial decision letter and author response on a selection of the published articles (subject to the approval of the authors). An edited version of the letter sent to the authors after peer review is shown, indicating the substantive concerns or comments; minor concerns are not usually shown. Reviewers have the opportunity to discuss the decision before the letter is sent (see review process). Similarly, the author response typically shows only responses to the major concerns raised by the reviewers.
Thank you for sending your work entitled “Neurofibromin controls macropinocytosis and phagocytosis in Dictyostelium” for consideration at eLife. Your article has been favorably evaluated by Randy Schekman (Senior editor), a Reviewing editor, and three reviewers.
The Reviewing editor and the reviewers discussed their comments before we reached this decision, and the Reviewing editor has assembled the following comments to help you prepare a revised submission.
The manuscript describes the identification of the major genetic switch that prevents natural isolates of Dictyostelium (i.e. wild type, WT) to survive and proliferate by drinking their environment via macropinocytosis. Mutations that incapacitate the protein encoded by the axeB gene, an evolutionarily conserved Ras-GAP that is closely related to the human tumour suppressor NF1, leads to oversized ruffles that renders the Dictyostelium strains axenic. Since axeB mutants contain exaggerated macropinosomes, as evidenced by the use by various reporters of active Ras signaling, the authors conclude that the main function of NF1 is to restrict Ras activity at the flanks of the nascent macropinosomes (and related the phagosomes).
1) It is unclear whether only mutations of NF1 that impact the Ras-GAP activity lead to the axenic phenotype, or are mutations in other domains of this complex protein that do not affect Ras-GAP activity also uncoupling feeding from phagocytosis? Moreover, the data (e.g., Figure 3) show that WT cells do not accumulate fluid phase tracers, and you conclude that the rate of uptake is reduced; is the lack of tracer accumulation in axenic mutants due to slower uptake, faster efflux, lack of concentration, or all three?
2) The substrate specificity of the NF1 Ras-GAP is not explored in vitro (and not so directly in vivo), and the experiments based on expression of various Ras mutants do not replace biochemical evidence. You could make this a strong paper by demonstrating that the Dictyostelium NF1 is a true RasGAP acting on one of the Ras proteins involved in macropinocytosis using recombinant proteins in vitro. You have all necessary genes at hand and RasGAP assays can be easily performed with available assays using radioactivity, HPLC, fluorescence or phosphate binding reporters. Alternatively, you could approach this using genetics by investigating the localization of NF1-AS in single or double mutants lacking RasS or RasG. In case the NF1 does not localize in the mutants it is likely that other, as yet uncharacterized Ras proteins are involved.
3) If dissection of the core functions of NF1 in Dictyostelium contributes to understanding of the conserved functions of the human NF1 tumor suppressor, then complementation experiments with human NF1 in Dictyostelium axenic strains is an easy way to support this claim.
4) The argument in the Discussion section explaining the lack of localization of NF1-WT in axeB mutants is difficult to understand as there is no evidence that over-expression of active NF1 leads to loss of macropinosomes. Shouldn't cells lacking macropinosomes die in liquid medium?
[Editors' note: further revisions were requested prior to acceptance, as described below.]
Thank you for resubmitting your work entitled “Neurofibromin controls macropinocytosis and phagocytosis in Dictyostelium” for further consideration at eLife. Your revised article has been favorably evaluated by Randy Schekman (Senior editor), a member of the Board of Reviewing Editors, and three reviewers. The manuscript has been improved but there are some remaining issues that need to be addressed before acceptance, as outlined below.
All reviewers agreed that you need to make a few changes to the text, but no further experiments are necessary. You were not able to assay RasGAP activity due to the inability to purify a soluble NF1 fragment. It is therefore risky to call the protein a RasGAP at this point without biochemical evidence. A reviewer noted that he/she recalled a similar scenario for the IQGAPs, which based on a similar degree of sequence similarity, were claimed to be RasGAPs. Biochemical assays however later showed that these proteins lack RasGAP activity. The reviewers therefore suggest relativizing this notion. Why not call it a putative RasGAP, or state that it most likely represents a RasGAP?
You were unable to show localization of the NF1-probe in the respective Ras-null mutants. Thus, you employed the pan Ras-probe (Raf1-GBD) to show active Ras in macropinosomes in single Ras mutants. From these results you conclude that RasS and RasG act redundantly (and most likely as substrates for NF1). The reviewers felt that you jumped to the conclusion at this point for the following reasons. We do not know whether the Raf1-GBD probe would localize in the RasS/RasG double Ras-null mutant. If this was not the case, then they are apparently right, but if it still does, then it is likely that additional Ras proteins are involved. They suggest rephrasing this part accordingly.https://doi.org/10.7554/eLife.04940.033
- Robert R Kay
- Sophia P Sander
The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
This study was supported by the Medical Research Council (MC_U105115237). SPS was the recipient of ‘Leonardo da Vinci’ funds as part of the European Commission's Lifelong Learning Programme. Sequencing was carried out at the Cancer Research UK Cambridge Institute, and we are grateful to the Genomics and Bioinformatics facilities there for their assistance. Karen Cichowski generously provided NF1 null and control MEFs. We also wish to thank David Baulcombe, Manu Hegde, Jim Haseloff, Pablo Hollstein, Krys Kelly, and Sean Munro for help and advice.
- W James Nelson, Reviewing Editor, Stanford University, United States
- Received: September 27, 2014
- Accepted: March 6, 2015
- Version of Record published: March 27, 2015 (version 1)
© 2015, Bloomfield et al.
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