Loss of Dictyostelium HSPC300 causes a scar-like phenotype and loss of SCAR protein
© Pollitt and Insall; licensee BioMed Central Ltd. 2009
Received: 09 July 2008
Accepted: 19 February 2009
Published: 19 February 2009
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© Pollitt and Insall; licensee BioMed Central Ltd. 2009
Received: 09 July 2008
Accepted: 19 February 2009
Published: 19 February 2009
SCAR/WAVE proteins couple signalling to actin polymerization, and are thus fundamental to the formation of pseudopods and lamellipods. They are controlled as part of a five-membered complex that includes the tiny HSPC300 protein. It is not known why SCAR/WAVE is found in such a large assembly, but in Dictyostelium the four larger subunits have different, clearly delineated functions.
We have generated Dictyostelium mutants in which the HSPC300 gene is disrupted. As has been seen in other regulatory complex mutants, SCAR is lost in these cells, apparently by a post-translational mechanism, though PIR121 levels do not change. HSPC300 knockouts resemble scar mutants in slow migration, roundness, and lack of large pseudopods. However hspc300-colonies on bacteria are larger and more similar to wild type, suggesting that some SCAR function can survive without HSPC300. We find no evidence for functions of HSPC300 outside the SCAR complex.
HSPC300 is essential for most SCAR complex functions. The phenotype of HSPC300 knockouts is most similar to mutants in scar, not the other members of the SCAR complex, suggesting that HSPC300 acts most directly on SCAR itself.
The WASP/SCAR family of proteins are key regulators of actin polymerisation, connecting signalling molecules to the activation of the Arp2/3 complex. SCAR/WAVE proteins, in particular, play an important role in the regulation of actin dynamics at the leading edges of moving cells. Biochemical studies in a range of organisms demonstrate that SCAR/WAVE is found in a 1:1:1:1:1 complex with four other proteins (PIR121, Nap1, Abi2 and HSPC300) [1, 2]. It is becoming clear, in particular from studies in Dictyostelium, that individual components of the complex regulate SCAR through different signalling pathways and that some may also have additional SCAR independent functions in vivo. [3–6] Most evidence now suggests that all members of the complex are needed for the correct localisation and function of SCAR [7, 8].
The smallest SCAR complex member, HSPC300, ranges from 68 to 110 amino acids in length, giving a size of between 8 and 14 kDa. Surprisingly little is known about its contribution to SCAR complex function and stability, perhaps because of the experimental difficulty associated with its smallness. Several studies investigating the function of the plant HSPC300 homologue, BRICK1, have found that is plays a crucial role in cytoskeletal remodelling. Maize BRICK1 null mutations lead to defects in the localisation of cortical actin in dividing and expanding leaf epidermal cells. These cells fail to undergo specific shape changes in preparation for asymmetric cell division . Arabidopsis HSPC300 has been shown to be needed for SCAR complex stability, yet others have demonstrated in vitro that HSPC300 is not fundamental for the formation of the complex [1, 10]. HSPC300 has also been shown to be important in the Drosophila nervous system, in which disruption of HSPC300 leads to a similar phenotype seen in other SCAR complex mutants .
In this work we characterise the Dictyostelium hspc300 gene, and assess the consequences of its disruption.
In a range of species, removal of one SCAR complex member (either genetically or by RNAi) leads to breakdown of others, apparently by posttranslational proteolysis [6, 13]. In Dictyostelium, pirA and napA mutants contain barely detectable full length SCAR protein despite normal mRNA levels . In the same fashion, disruption of hspc300 also leads to complete loss of SCAR- as shown in Figure 1B, western blots show no detectable SCAR protein. As seen in other mutants, SCAR mRNA levels in hspc300 null and wild type cells are comparable (data not shown), implying that the reduction in SCAR protein is a result of posttranslational processes such as degradation. However, PIR121 levels are insensitive to the loss of HSPC300 (Figure 1B). This insensitivity is also seen when Dictyostelium SCAR or Abi are lost [4, 5], but loss of Dictyostelium Nap1 causes an approximate halving of PIR121 levels . Taken together these results show that the mechanisms that regulate proteolytic breakdown affect different subunits of the complex independently. The PIR121 and Nap1 subunits appear to form a stable subcomplex that is preserved without SCAR, Abi or HSPC300 (see additional file 1), whereas SCAR is broken down in the absence of any other complex subunit.
As predicted from other organisms Dictyostelium HSPC300 forms part of the complete SCAR complex. A previous in vitro study  showed that in vitro translated Abi and HSPC300 bind to the N-terminus of SCAR, but did not analyze the complex from living Dictyostelium. We expressed an N-terminally Myc-tagged HSPC300 or untagged control in hspc300 null cells from an extrachromosomal plasmid, which resulted in a restoration of normal SCAR protein levels (Figure 1C). In reciprocal co-immunoprecipitation experiments using an anti-Myc antibody, Myc-tagged HSPC300 coprecipitated with endogenous PIR121 and SCAR (Figure 1D). In other Dictyostelium SCAR complex mutants (except Nap1, in which PIR121 protein is lost), PIR121 is not recruited to the leading edge of actin protrusions as it is in wild type [4, 5]. The hspc300 null cells also fail to recruit PIR121 to the edge of actin pseudopods (additional file 2), suggesting that the proposed Rac-binding site in PIR121 – which has not been verified in Dictyostelium – is not alone sufficient for localisation (data not shown).
Additional file 3: Under agar folate chemotaxis of wild type cells. Movie of wild type cells moving towards a folate gradient under agar. Cells were imaged using phase contrast microscopy. Frames were taken every 30 seconds and are played at 10 frames/second. (MOV 2 MB)
Additional file 4: Under agar folate chemotaxis of scar null mutant. Movie of scar null cells moving towards a folate gradient under agar. Cells were imaged using phase contrast microscopy. Frames were taken every 30 seconds and are played at 10 frames/second. (MOV 1 MB)
Additional file 5: Under agar folate chemotaxis of hspc300 null mutant. Movie of hspc300 null cells moving towards a folate gradient under agar. Cells were imaged using phase contrast microscopy. Frames were taken every 30 seconds and are played at 10 frames/second. (MOV 1 MB)
Additional file 7: Under agar cAMP chemotaxis of wild type cells. Movie showing wild type cells moving up a cAMP gradient under agar as described in . Cells were imaged using DIC microscopy. Frames were taken every 30 seconds and are played at 10 frames/second. (MOV 695 KB)
Additional file 8: Under agar cAMP chemotaxis of hspc300 null mutants. Movie showing hspc300 null cells moving up a cAMP gradient under agar as described in . Cells were imaged using DIC microscopy. Frames were taken every 30 seconds and are played at 10 frames/second. (MOV 618 KB)
As development was not greatly affected by the loss of HSPC300 we investigated slug behaviour in the hspc300 null cells to see if there were any subtle differences during this stage of development. Wild type slugs will phototax effectively towards a single point source of light when allowed to develop in the dark (Figure 4B). hspc300 and scar null slugs were still capable of migrating towards the light source but not to the same extent as wild type slugs. The lengths of the tracks trailing the slugs were analysed using ImageJ (Figure 4C). Although significantly shorter than wild type slug trails, hspc300 and scar null tracks were found to be very similar in length. Thus during phototaxis, as in most other conditions, HSPC300 is required for SCAR function as the loss of HSPC300 results in a scar null phenotype.
We have demonstrated that HSPC300 is a vital component of the Dictyostelium SCAR complex. Unlike Dictyostelium Abi and PIR121, HSPC300 seems to be fully required for most SCAR functions, though phagocytosis may be better in hspc300 than in scar knockouts, raising the possibility that SCAR's role in phagocytosis does not require HSPC300. We found no evidence that HSPC300 has roles outside the SCAR complex, as has been suggested in Arabidopsis. Although this small protein is vital for the stability of the SCAR complex it remains unclear what its physiological role may be, and why such a small protein is required physiologically if its only role is as a partner for SCAR.
Dictyostelium cells were grown axenically in HL-5 medium at 22°C in Petri dishes. For growth curves, cells were grown axenically in shaken flasks. For development on filters 107 axenically grown cells were washed in KK2 (16 mM potassium phosphate pH6.2) buffer and evenly distributed onto nitrocellulose filters (45 μm, Black HABP, Millipore), placed on KK2 soaked filter pads (absorbent pads, Millipore). For cloning on bacteria, serial dilutions of axenically grown Dictyostelium cells were spread onto Klebsiella aerogenes lawns on SM agar plates and incubated for 5 days to gain single colonies.
The Dictyostelium discoideum homologue of HSPC300 was identified by BLAST searches against the Dictyostelium genome http://www.dictybase.org/, using the human protein as bait. A 1.69 Kb section of the hspc300 gene and flanking DNA was amplified from genomic DNA by PCR, with a BamHI site introduced by 4-primer mutagenesis. A blasticidin resistance cassette derived from pBsr∂Bam was cloned into the BamHI site introduced into the hspc300 gene. This construct was electroporated into Dictyostelium AX3 and NC4A2 cells. NC4A2 is a line which migrates effectively and in which SCAR shows consistent phenotypes in vegetative and developed cells, originally published as being independently axenised from NC4 ; subsequent work suggests that it is an AX3 contaminant  though we have not yet squared this with its phenotypic difference from other AX3 strains. After cloning on bacterial lawns, blasticidin resistant colonies were screened for gene disruption by PCR (see additional file 9; Forward primer: ATCTTTTTGGTGTAATCATTGGTG, Reverse Primer: TAGATCAAGAAAAACTTAATGATCG), looking for replacement of the original small fragment by one 1.3 kbp larger. Two AX3 and one NC4A2 lines were isolated, with similar phenotypes. The NC4A2-derived line (IR55) was used for the work described in this paper, with the AX3-derived one (IR54) also kept for comparison.
107 washed axenically grown cells were concentrated in 50 μl KK2 buffer. Cells were placed as a droplet onto a damp nitrocellulose filter placed on KK2 soaked filter pads. Excess buffer was removed and slugs allowed to migrate towards a unidirectional light source. Images were captured after 24 hours. The length of the slug trails were analysed using ImageJ.
Extrachromosomal constructs containing either an N-terminal Myc-tagged HSPC300 or untagged HSPC300 control under the control of an Actin15 promoter were generated and electroporated into hspc300 null cells. Whole cell lysates were made in a Triton containing buffer (50 mM Tris-HCL pH7, 150 mM NaCl, 1% Triton, 1 mM EDTA). Pre-cleared lysates were subjected to immunoprecipitation with mouse monoclonal anti-Myc antibodies (9E10) for 30 mins at 4°C and captured using protein-G-coupled sepharose beads for 1 hour at 4°C. Beads were washed four times with lysis buffer and resuspended in SDS-PAGE sample buffer. Proteins were resolved on a SDS-PAGE gel and PIR121 and SCAR detected using sheep anti-PIR121 and sheep anti-SCAR antibodies [5, 23].
Cells were washed in KK2, then protein from 2 × 105 separated using Invitrogen NativePAGE™ Novex blue gels. The cells were lysed using the kit lysis buffer, centrifuged briefly in a desktop centrifuge, then run on 3–12% gradient gels using the recommended voltage and kit buffers. After separation gels were transferred to nitrocellulose then treated the same way as SDS-PAGE immunoblots.
We used the previously described method for imaging Dictyostelium cells moving towards a folate stimulus under a thin layer of agar . Time-lapse phase images were generated with frames captured every 10 seconds. Cell speeds were calculated using ImageJ.
For phalloidin staining and immunofluorescence, cells were fixed and permeabilised with picrate/formaldehyde then stained with Texas red-conjugated phalloidin as described elsewhere .
We are very grateful to Natalie Andrew for assistance with chemotaxis assays, and Laura Machesky and Charles Saxe for helpful discussions.
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