Two isoforms of Serpent containing either one or two GATA zinc fingers have different roles in Drosophila haematopoiesis
2002; Springer Nature; Volume: 21; Issue: 20 Linguagem: Inglês
10.1093/emboj/cdf545
ISSN1460-2075
Autores Tópico(s)Invertebrate Immune Response Mechanisms
ResumoArticle15 October 2002free access Two isoforms of Serpent containing either one or two GATA zinc fingers have different roles in Drosophila haematopoiesis Lucas Waltzer Lucas Waltzer Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Laetitia Bataillé Laetitia Bataillé Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Sandrine Peyrefitte Sandrine Peyrefitte Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Marc Haenlin Corresponding Author Marc Haenlin Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Lucas Waltzer Lucas Waltzer Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Laetitia Bataillé Laetitia Bataillé Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Sandrine Peyrefitte Sandrine Peyrefitte Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Marc Haenlin Corresponding Author Marc Haenlin Centre de Biologie du Développement-CNRS, 31062 Toulouse, France Search for more papers by this author Author Information Lucas Waltzer1, Laetitia Bataillé1, Sandrine Peyrefitte1 and Marc Haenlin 1 1Centre de Biologie du Développement-CNRS, 31062 Toulouse, France *Corresponding author. E-mail: [email protected] The EMBO Journal (2002)21:5477-5486https://doi.org/10.1093/emboj/cdf545 Correction(s) for this article Two isoforms of Serpent containing either one or two GATA zinc fingers have different roles in Drosophila haematopoiesis01 March 2016 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info serpent (srp) encodes a GATA transcription factor essential for haematopoiesis in Drosophila. Previously, Srp was shown to contain a single GATA zinc finger of C-terminal type. Here we show that srp encodes different isoforms, generated by alternative splicing, that contain either only a C-finger (SrpC) or both a C- and an N-finger (SrpNC). The presence of the N-finger stabilizes the interaction of Srp with palindromic GATA sites and allows interaction with the Friend of GATA factor U-shaped (Ush). We have examined the respective functions of SrpC and SrpNC during embryonic haematopoiesis. Both isoforms individually rescue blood cell formation that is lacking in an srp null mutation. Interestingly, while SrpC and SrpNC activate some genes in a similar manner, they regulate others differently. Interaction between SrpNC and Ush is responsible for some but not all aspects of the distinct activities of SrpC and SrpNC. Our results suggest that the inclusion or exclusion of the N-finger in the naturally occurring isoforms of Srp can provide an effective means of extending the versatility of srp function during development. Introduction Members of the GATA family are zinc finger transcription factors, conserved from yeast to vertebrates, that regulate a variety of developmental processes (Patient and McGhee, 2002). These factors bind to the consensus WGATAR DNA site (Martin and Orkin, 1990; Merika and Orkin, 1993) and contain one or two conserved zinc fingers with the characteristic Cys-X2-Cys-X17-Cys-X2-Cys spacing. In vertebrates, all GATA factors contain two distinctive zinc fingers separated by 29 amino acids and referred to as the N-finger (for N-terminal zinc finger) and C-finger (for C-terminal zinc finger), respectively. However, a number of invertebrate GATA factors, including the Drosophila GATA factor Serpent/dGATAb (Srp) (Abel et al., 1993; Rehorn et al., 1996), contain only a C-finger (Lowry and Atchley, 2000). The C-finger is responsible for DNA binding (Martin and Orkin, 1990) and for interaction with other transcription factors (Merika and Orkin, 1995; Rekhtman et al., 1999). In vertebrates, the GATA N-finger can modulate the binding of the C-finger to specific GATA sites (Trainor et al., 1996, 2000). Moreover, studies in mice have revealed a specific requirement for the GATA-1 N-finger for erythroid differentiation (Weiss et al., 1997) and for full rescue of GATA-1 loss of function (Shimizu et al., 2001). Similarly, specific mutations in the N-finger of the Drosophila GATA factor Pannier/dGATAa (Pnr) produce dominant effects on the formation of sensory bristles (Ramain et al., 1993). Among others, these data suggested that the N-finger could act as a binding domain for a cofactor regulating GATA activity. Most notably, it was shown in vertebrates and in flies that GATA N-finger mediates the interaction with transcriptional coregulators of the Friend of GATA (FOG)/U-shaped (Ush) family (Haenlin et al., 1997; Tsang et al., 1997). FOG genes, described in mammals, Xenopus and Drosophila, code for structurally related proteins with multiple C2H2 and C2HC zinc fingers (Cubadda et al., 1997; Tsang et al., 1997; Tevosian et al., 1999; Deconinck et al., 2000). They specifically recognize the GATA N-finger through some of their C2HC fingers (Fox et al., 1998, 1999). Initially, FOG-1 was identified in mammals by a two-hybrid screen for factors that interact with the GATA-1 N-finger domain (Tsang et al., 1997). The interaction between GATA-1 and FOG-1 is necessary for erythroid and megakaryocytic differentiation (Tsang et al., 1998). Recently, human familial dyserythropoietic anaemia and thrombocytopenia has been associated with mis-sense mutations in the GATA-1 N-finger that diminish or abrogate GATA-1–FOG-1 interaction, thereby highlighting the importance of this interaction in vivo (Nichols et al., 2000; Mehaffey et al., 2001). Concomitantly with the cloning of FOG-1, we identified the Drosophila FOG homologue Ush by virtue of its antagonism of Pnr during adult neurogenesis (Cubadda et al., 1997; Haenlin et al., 1997). In addition, Drosophila Ush and vertebrate FOG-2 were shown to participate in cardiogenesis in flies and in vertebrates, inhibiting Pnr and GATA-4 functions, respectively (Fossett et al., 2000; Tevosian et al., 2000). However, the precise mode of action of the GATA–FOG complex remains unclear. In fact, FOG can either repress or enhance GATA-mediated transactivation, depending on the cell and promoter context (Tsang et al., 1997; Fox et al., 1999; Holmes et al., 1999). Recent evidence suggests that blood cell differentiation in vertebrates and in Drosophila shares a common molecular basis (Fossett and Schulz, 2001). During Drosophila embryogenesis, blood cells (haemocytes) originate from the procephalic mesoderm and differentiate into two known lineages: plasmatocytes and crystal cells (Tepass et al., 1994; Lebestky et al., 2000). The plasmatocytes migrate throughout the embryo along several invariant paths and act as macrophages (Cho et al., 2002). They contribute to host defence by phagocyting microbes, and they play a crucial role in normal development by eliminating apoptotic bodies. This activity is largely dependent on the expression of croquemort, a member of the CD36 receptor family (Franc et al., 1999). They also participate in the synthesis of extracellular matrix components such as peroxidasin (Nelson et al., 1994). Crystal cells remain located around the proventriculus during embryogenesis and play a role in melanization, a defence-related process, during larval stages (Rizki et al., 1980). Several genes that control blood cell formation and differentiation in Drosophila have been identified. Expression of the GATA transcription factor Srp in the procephalic mesoderm is required for the formation and differentiation of both classes of haemocytes (Rehorn et al., 1996). The transcription factor encoded by glial cell missing (gcm) is involved in plasmatocyte formation (Bernardoni et al., 1997), whereas the Runt factor Lozenge (Lz) is absolutely required for crystal cell formation (Lebestky et al., 2000). Finally, the Drosophila FOG protein, Ush, appears to repress crystal cell production (Fossett et al., 2001). All these three genes require the activity of srp since in its absence none of them is expressed in the haematopoietic anlage. Yet it is still not understood how these genes control blood cell formation at the molecular level. Of particular interest is the case of Srp and Ush. So far, all known functions of FOG proteins seem to be mediated by GATA factors (see for example Chang et al., 2002). Since Srp contains only a C-finger, it should be unable to interact with Ush. This suggests either that Ush has a GATA-independent function in haematopoiesis or that Ush acts via an uncharacterized GATA protein containing an N-finger. In order to gain insight into the molecular mechanisms controlling blood cell formation, we sought new potential GATA protein-encoding genes in the Drosophila genome. We found that the srp locus contains an N-finger-coding exon that is alternatively spliced to give rise to proteins that contain either a C-finger (SrpC) only or both an N-finger and a C-finger (SrpNC). We have characterized these two isoforms in vitro and in vivo during haematopoieisis. Interestingly, we show that SrpC and SrpNC have both common and distinct activities. Finally, we provide evidence that Ush interacts with SrpNC and regulates its activity with respect to specific target genes. We propose that the co-expression of Srp proteins containing either one or two zinc fingers provides an extension of the regulatory properties of srp, consistent with its broad range of functions during development. Results serpent encodes isoforms including N and C zinc fingers In a systematic search for GATA zinc finger-coding sequences in the Drosophila genome, we found five genes (see Materials and methods for details): dGATA-E (CG10278), dGATA-D (CG5034), pnr, grain and srp. dGATA-E and dGATA-D appear to include only a C-finger, while Pnr and Grain have already been shown to contain both an N- and a C-finger (Ramain et al., 1993; Lin et al., 1995). Interestingly, while Srp was reported previously to contain a single C-finger, our search revealed the presence of a putative exon (E4A) coding for an N-finger motif in srp. Using RT–PCR assays with various combinations of oligonucleotides (see Materials and methods and Figure 1A), we showed that E4A is expressed and that E4A and E4B are alternatively spliced to exon 5 (data not shown). In the course of these experiments, we also identified an additional splice acceptor site within E7 (Figure 1A). This downstream acceptor site in E7 is out-of-frame and leads to the deletion of the Srp glutamine-rich C-terminal region. Our data indicate that four alternatively spliced mRNAs are transcribed from srp, two encoding products with a single C-finger (SrpC and SrpCδ) and two encoding products with both N- and C-fingers (SrpNC and SrpNCδ) (Figure 1A). Interestingly, in SrpNC and SrpNCδ, the two fingers present the same conserved organization as in other GATA factors (Figure 1B). Notably, they are separated by 29 amino acids, as in all vertebrate GATA. In the following experiments, we used the two isoforms that contain the full-length exon 7, i.e. srpC and srpNC, to address the functional consequences of the alternative splicing of E4A and E4B. Figure 1.(A) Schematic representation of the srp locus and alternatively spliced transcripts. The location and orientation of the primers used for RT–PCR analysis are indicated. The non-coding regions in srp transcripts are indicated as open boxes. Exons 4A and 5, coding for the N- and the C-finger, respectively, are indicated as grey boxes. Exon 4A starts at position 121 031 and ends at 121 202 with reference to Drosophila scaffold region AE003711 (Flybase). Similarly, the internal splice acceptor site in exon 7 is located at position 123 288. (B) Alignment of the GATA zinc finger domains of SerpentNC with Pannier, Grain, mouse GATA-1, -2, -3 and -4 and Caenorhabditis elegans Elt-1. Arrows above the SrpNC sequence delineate the region coded by exon 4A. Conserved residues in each column are coloured according to the consensus character assigned to that column; brown, R and K; green, N, T, Q and S; purple, E and D; blue, I, F, L, A, V and M; red, H and Y; orange, G; light green, P; and yellow, C. (C) Semi-quantitative RT–PCR analysis of srp transcripts containing either exon 4A or exon 4B. RT–PCR was performed with E3 and E5 primers on RNA extracted from stage 5–14 embryos. Aliquots of the PCR were taken after different numbers of cycles. Products containing exon 4A or 4B were resolved on acrylamide gel, and their relative amount was quantified. Download figure Download PowerPoint SrpNC shows specific features of a two-fingered GATA factor We first determined whether SrpC and SrpNC displayed different properties in vitro. While the C-finger is necessary and sufficient for specific DNA binding, it has also been shown in vertebrates that the N-finger can stabilize the binding to particular double GATA sites (Trainor et al., 1996). We tested, by electophoretic mobility shift assays (EMSAs), whether SrpNC and SrpC had similar DNA-binding properties. As shown in Figure 2A (lanes 2 and 9), both in vitro translated SrpC and SrpNC proteins bound to an oligonucleotide containing a consensus GATA site. The binding was specific, since it could be competed out efficiently by an excess of cold GATA oligonucleotide (Figure 2A, lanes 3–5 and 10–12), but not by an excess of the GATC oligonucleotide (Figure 2A, lanes 6–8 and 13–15). The stability of the SrpN and SrpNC complex on a single or on a palindromic GATA site was assessed by dissociation experiments. While the rate of dissociation was similar for SrpC and SrpNC on a single GATA probe (Figure 2B), SrpNC bound more stably than SrpC to the palindromic GATA sites (Figure 2C). Figure 2.(A–C) EMSAs using in vitro translated SrpC or SrpNC proteins. (A) SrpC and SrpNC both specifically bind a consensus GATA probe. Increasing concentrations (5- to 500-fold excess) of unlabelled wild-type (GATA) or mutant (GATC) competitors were added to the reaction as indicated in the upper part of the panel. No GATA-binding activity was observed with unprogrammed reticulocyte lysate (lane 1). (B and C) SrpC and SrpNC have distinct site-dependent binding properties as revealed by dissociation rate assays. After formation of the complexes between SrpC (upper panel) or SrpNC (lower panel) with either a single GATA site (B) or a palindromic double GATA site (C), an excess of the corresponding unlabelled oligonucleotides was added to the reaction mix and samples were loaded on the gel at various times, as indicated. (D) Only SrpNC interacts with Ush in vitro. Equivalent molar amounts of the GST fusion proteins were tested for their interaction with in vitro translated 35S-labelled Ush as indicated in the upper part of the panel. Download figure Download PowerPoint The GATA N-finger allows interaction with cofactors of the FOG family (Fox et al., 1998). Key residues that are required for the interaction between GATA and FOG are conserved in the Srp N-finger. In order to test the binding between Ush and srp products, we performed pull-down assays in vitro. We found that in vitro translated [35S]methionine-labelled Ush bound to GST–SrpNC, but not to GST alone nor to GST–SrpC (Figure 2D). Thus, Ush specifically interacts with Srp isoforms that contain the N-finger. In addition, like its vertebrate homologues (Fox et al., 1999), Ush interacted with the transcriptional corepressor dCtBP in this assay (Figure 2D). Taken together, our results indicate that SrpNC displays features characteristic of two-fingered GATA factors. The two types of naturally occurring isoforms encoded by srp (with or without the N-finger) have different DNA-binding properties, and only the isoforms including an N-finger can interact with Ush. srpC and srpNC transcripts have identical expression patterns In order to determine whether a spatial regulation of the alternative splicing leading to SrpC and SrpNC occurs during embryonic development, we assessed the distribution of the corresponding srp transcripts by in situ hybridization using specific probes for exon 4A or 4B. At the blastoderm stage and during gastrulation, srpC and srpNC show the same expression pattern (Figure 3A, B, E and F). They are expressed in the procephalic mesoderm, the haemocyte primordium (arrows in Figure 3), at the anterior and posterior pole, in the primordium of the anterior and posterior midgut as well as in the amnioserosa and in the yolk cells. Later, during germ band extension, and after germ band retraction, srpC and srpNC are expressed identically in the developing fat body (Figure 3C, D, G and H) (for a full description of srp expression see Rehorn et al., 1996). Thus, srpC and srpNC transcripts are not differentially regulated spatially during embryonic development. However, the level of the transcripts is not identical. Indeed, by means of semi-quantitative RT–PCR, we determined that exon 4B-containing mRNA is five times more abundant than exon 4A-containing mRNA (Figure 1C), suggesting that two-fingered isoforms of Srp are less abundant than single-fingered isoforms. Figure 3.The transcripts containing either exon 4A (srpNC and srpNCδ) or exon 4B (srpC and srpCδ) have similar expression patterns during embryogenesis. Side views of stage 5 (A and E), stage 8 (B and F), stage 11 (C and G) or stage 14 (D and H) embryos hybridized with an RNA probe directed against either exon 4A (A–D) or exon 4B (E–H). Arrows indicate the expression of srp in the haemocyte primordium. Download figure Download PowerPoint SrpC and SrpNC differ in their capacity to activate certain target genes in vivo In order to analyse SrpC and SrpNC activities, we tested their capacities to activate gene expression in vivo during Drosophila embryonic haematopoiesis. Using the UAS-GAL4 system, we ectopically expressed them in the mesoderm and we then assessed the expression pattern of various haematopoietic markers. The two genes ush and gcm play critical roles in embryonic haematopoiesis. Their expression in the haematopoietic primordium occurs early and appears to depend on srp activity (Bernardoni et al., 1997; Fossett et al., 2001). Therefore, we decided to determine whether they are transcriptional targets of SrpC and/or SrpNC. We found that, whereas in a wild-type early embryo, ush expression is restricted to the anterior mesoderm, twist-driven expression of SrpC (twist-SrpC) or SrpNC (twist-SrpNC) induced strong expression of ush throughout the mesoderm (Figure 4, compare A with B and C). In contrast, twist-SrpC induced gcm expression poorly and in a limited number of mesodermal cells of stage 5 embryos (arrow in Figure 5B), whereas twist-SrpNC strongly activated gcm expression segmentally from stage 5 to 9 (Figure 5C and F). Figure 4.SrpC and SrpNC have a similar capacity to activate ectopically the expression of ush, pxn and pro-PO. (A–C) Side views of ush mRNA expression in stage 10 embryos. (D–F) Side views of pxn mRNA expression in stage 11 embryos. (G–I) Dorsal views of pro-PO mRNA expression in stage 11 embryos. (A, D and G) Wild type, (B, E and H) twist-Gal4; UAS-SrpC and (C, F and I) twist-Gal4; UAS-SrpNC. Download figure Download PowerPoint Figure 5.SrpC and SrpNC differentially activate gcm and crq expression. (A–F) Side views of gcm mRNA expression in stage 5 (A–C) or stage 9 (D–F) embryos. (G–I) Side views of crq mRNA expression in stage 10 embryos. (A, D and G) Wild type, (B, E and H) twist-Gal4; UAS-SrpC and (C, F and I) twist-Gal4; UAS-SrpNC. The arrow in (B) points to the few cells that express gcm ectopically in response to SrpC. Download figure Download PowerPoint Next we looked at the expression of haematopoietic lineage-specific markers. As plasmatocyte markers, we used peroxidasin (pxn) and croquemort (crq). Since, Rizki et al. (1980) suggested that crystal cells are the only source of prophenoloxidase (pro-PO) in Drosophila, we used expression of this gene to monitor crystal cell formation. pro-PO transcripts were indeed detected in these cells from early stage 11 to the end of embryogenesis. We confirmed that pro-PO expression is specific to the crystal cells since it was not detected in lz mutant embryos (data not shown). Analysing these markers, we again observed two situations. On the one hand, twist-SrpC and twist- SrpNC had similar abilities to induce expression of the plasmatocyte marker pxn and of the crystal cell marker pro-PO (Figure 4E and F, and H and I, respectively). On the other hand, expression of crq was induced by twist-SrpC but not by twist-SrpNC (Figure 5, compare H with I). Note that pxn and crq were induced through most of the mesoderm, while pro-PO activation was restricted to the head region. Taken together, our data show that SrpC and SrpNC have both common and different activities during haematopoiesis. Indeed, both isoforms activated the expression of ush, pxn and pro-PO in a similar manner. However, SrpC and SrpNC differentially stimulate the expression of crq and gcm, respectively, in the mesoderm. SrpC and SrpNC both induce the crystal cell and plasmatocyte lineages in an srp null embryo srp is absolutely required for determination of all haematopoietic lineages (Rehorn et al., 1996; Lebestky et al., 2000). However, the relative contributions of SrpC and SrpNC to this process are unknown, since there is no known mutation in srp that affects only one of the two classes of isoforms. To address this question, we asked whether SrpC and SrpNC individually could rescue the plasmatocyte and/or crystal cell lineages in an srp mutant background. During haematopoiesis, srp expression is first detected at the blastoderm stage in a patch of cells within the mesoderm. Therefore, we used the twist-Gal4 driver to express UAS-SrpC or UAS-SrpNC in the mesoderm of srp mutant embryos. To monitor crystal cell formation and plasmatocyte formation, we assessed the expression of pro-PO and pxn, respectively. Whereas no pro-PO expression was detected in srp mutant embryos, pro-PO expression was restored around the proventriculus and in an additional patch of cells located above the pharynx upon expression of twist-SrpC or twist-SrpNC (Figure 6, compare B with C and D). This phenotype is equivalent to that which we observed previously in wild-type embryos expressing twist-SrpC or twist-SrpNC. Higher magnification views showed that the pro-PO-expressing cells had the typical morphology of crystal cells. Similarly, no expression of pxn was detected in srp mutant embryos, while scattered pxn-positive cells were observed in srp− embryos expressing twist-SrpC or twist-SrpNC (Figure 6, compare F with G and H). Morphological analysis confirmed that these cells were genuine plasmatocytes (Tepass et al., 1994). Thus our results suggest that SrpC and SrpNC are each able to induce the formation of both lineages. Figure 6.SrpC and SrpNC individually can rescue the lack of crystal cells and plasmatocytes due to an srp null mutation. In situ hybridization revealing pro-PO (A–D) or pxn (E–H) expression in stage 13–14 embryos. (A and E) Wild type, (B and F) srp6G/srp6G, (C and G) twist-Gal4/+; UAS-SrpC; srp6G/srp6G and (D and H) twist-Gal4/UAS-SrpNC; srp6G/srp6G. Ten-fold higher magnifications of labelled cells are shown to the right of the wild-type and rescued embryo panels. Download figure Download PowerPoint Misexpression of SrpC or SrpNC controls crystal cell formation independently of Ush Previous studies have shown that ush acts to repress crystal cell formation. Notably, Fossett et al. (2001) showed that lz-Gal4-driven expression of UAS-Ush led to a variable decrease in the number of crystal cells, as monitored by the expression of a Uas-lacZ reporter gene driven by lz-Gal4. However, the molecular mechanism of action of ush in this process remained largely unknown. The expression of SrpNC during haematopoiesis suggested that it might act with Ush. Thus we decided to analyse the consequences of misexpressing either SrpC or SrpNC in the crystal cells. Because only SrpNC can interact with Ush, we surmised that SrpNC, but not SrpC, would repress crystal cell formation. We used the lz-Gal4 driver to express UAS-SrpC, UAS-SrpNC or UAS-Ush in the crystal cells. Misexpression of each transgene was visualized by in situ hybridization with a probe against srp or ush, respectively, and differentiation of the crystal cells was monitored by analysing pro-PO expression. As expected, UAS-Ush induced a reduction in the number of crystal cells in stage 13–16 embryos (Figure 7, compare A with D). Surprisingly, both UAS-SrpC and UAS-SrpNC also reduced the number of crystal cells (Figure 7B and C). Note that the reduction induced by SrpC or SrpNC was greater than that observed with Ush, although, as for Ush, we observed considerable variations of phenotype within the population of embryos. Most interestingly, we observed strong expression of UAS-SrpC or UAS-SrpNC driven by lz-Gal4 and no expression of pro-PO in the same cells in stage 13–16 embryos (arrows in Figure 7B and C). In contrast, lz-Gal4-driven expression of UAS-Ush did not prevent pro-PO expression in these cells (Figure 7D). This suggests that SrpC and SrpNC can control both the number and the differentiation of the crystal cells, while Ush only affects their number. Figure 7.Forced expression of SrpC or SrpNC in the crystal cells represses their formation independently of ush. Side views (A–G) or dorsal view (H) of stage 13 embryos processed to reveal pro-PO mRNA expression (black staining) and either srp mRNA expression (blue staining in B, C, F, G and H) or ush mRNA expression (blue staining in D). (A) Wild type, (B) lz-Gal4/+; UAS-SrpC, (C) lz-Gal4/+; UAS-SrpNC, (D) lz-Gal4/+; UAS-Ush, (E) ush1/ush1, (F) lz-Gal4/+; ush1/ush1; UAS-SrpNC and (G and H) lz-Gal4/+; ush1/ush1; UAS-SrpNC. Arrows indicate crystal cells expressing srp but not pro-PO. Download figure Download PowerPoint However, it still remained possible that SrpNC was acting in a complex with Ush to prevent crystal cell formation and differentiation. Additionally, the effect of SrpC and SrpNC on crystal cell number could be related to Ush activity, since SrpC and SrpNC can induce its expression (at least in the mesoderm, see above). In order to test this hypothesis, we misexpressed UAS-SrpC or UAS-SrpNC under the control of lz-Gal4 in an ush null mutant background. As shown in Figure 7F, G and H, even under these conditions, SrpC and SrpNC reduced the number of crystal cells and repressed pro-PO expression. Therefore, SrpC and SrpNC can both inhibit crystal cell formation and differentiation independently of ush activity. The SrpNC–Ush complex represses crq expression We have shown that the misexpression of SrpC, but not SrpNC, activates ectopic expression of crq. Conversely, SrpNC is a much stronger activator of gcm expression than SrpC. These differences in activity on particular target genes could be due to the capacity of SrpNC, unlike SrpC, to form a complex with Ush. Given that twist-SrpNC induces ush expression in the mesoderm, it is possible that Ush exerts a feedback action on SrpNC, preventing it from activating crq expression and/or enhancing its capacity to activate gcm. We decided to check this possibility by assaying the expression of crq and gcm in an ush mutant embryo expressing twist-SrpNC. The absence of ush had no detectable effect on the activation of gcm by twist-SrpNC, showing that ush is not involved in this specific activity of SrpNC (data not shown). On the contrary, we observed ectopic expression of crq by twist-SrpNC in the absence of ush function (Figure 8, compare A and B with C). Note that twist-SrpC-mediated activation of crq was similar in a wild-type and ush mutant embryo (Figure 8, compare D with E). These data strongly suggest that Ush can form a complex with SrpNC, thereby modulating the transactivation of crq. Figure 8.ush inhibits SrpNC-mediated activation of crq. Side views of crq mRNA expression in stage 10 embryos. (A) Wild type, (B) twist-Gal4/+; UAS-SrpNC, (C) twist-Gal4/+; ush1/ush1; UAS-SrpNC, (D) twist-Gal4/+; UAS-SrpC and (E) twist-Gal4/+; ush1/ush1; UAS-SrpC. Download figure Download PowerPoint This also led us to consider that ush might repress the expression of crq in the wild-type embryo. We thus assayed crq expression in an ush mutant. In wild-type stage 11 embryos, the expression of crq was barely detectable in migrating plasmatocytes, especially those localized beyond the head (Figure 9A). However, the level of expression of crq was increased in ush mutants, and crq-positive plasmatocytes were clearly visible in the trunk region (Figure 9B). Moreover, in ush embryos, the expression of crq persisted longer than in wild type (Figure 9, compare C with D). Note that this effect was specific to crq, as the expression of pxn in the plasmatocytes appeared normal in ush mutant embryos (data not shown). These observations are consistent with a role for Ush in the control of crq expression in association with SrpNC. In conclusion, these results support the idea that some, but not all, of the differential activities of SrpC and SrpNC in vivo depend on a physical interaction between SrpNC and Ush. Figure 9.ush downregulates crq expression. Side views of crq mRNA expression in stage 11 (A and B) or 14 (C and D) embryos. (A and C) Wild type, (B and D) ush1/ush1. Download figure Download
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