Portal de Periódicos da CAPES

Brinker requires two corepressors for maximal and versatile repression in Dpp signalling

2001; Springer Nature; Volume: 20; Issue: 20 Linguagem: Inglês

10.1093/emboj/20.20.5725

1460-2075

Peleg Hasson,

Kruppel-like factors research

Article15 October 2001free access Brinker requires two corepressors for maximal and versatile repression in Dpp signalling Peleg Hasson Peleg Hasson Department of Biochemistry, The Hebrew University–Hadassah Medical School, PO Box 12272, Jerusalem, 91120 Israel Search for more papers by this author Bruno Müller Bruno Müller Institut für Molekularbiologie, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland Search for more papers by this author Konrad Basler Konrad Basler Institut für Molekularbiologie, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland Search for more papers by this author Ze'ev Paroush Corresponding Author Ze'ev Paroush Department of Biochemistry, The Hebrew University–Hadassah Medical School, PO Box 12272, Jerusalem, 91120 Israel Search for more papers by this author Peleg Hasson Peleg Hasson Department of Biochemistry, The Hebrew University–Hadassah Medical School, PO Box 12272, Jerusalem, 91120 Israel Search for more papers by this author Bruno Müller Bruno Müller Institut für Molekularbiologie, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland Search for more papers by this author Konrad Basler Konrad Basler Institut für Molekularbiologie, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland Search for more papers by this author Ze'ev Paroush Corresponding Author Ze'ev Paroush Department of Biochemistry, The Hebrew University–Hadassah Medical School, PO Box 12272, Jerusalem, 91120 Israel Search for more papers by this author Author Information Peleg Hasson1, Bruno Müller2, Konrad Basler2 and Ze'ev Paroush 1 1Department of Biochemistry, The Hebrew University–Hadassah Medical School, PO Box 12272, Jerusalem, 91120 Israel 2Institut für Molekularbiologie, Universität Zürich, Winterthurerstrasse 190, CH-8057 Zürich, Switzerland *Corresponding author. E-mail: [email protected] The EMBO Journal (2001)20:5725-5736https://doi.org/10.1093/emboj/20.20.5725 PDFDownload PDF of article text and main figures. ToolsAdd to favoritesDownload CitationsTrack CitationsPermissions ShareFacebookTwitterLinked InMendeleyWechatReddit Figures & Info decapentaplegic (dpp) encodes a Drosophila transforming growth factor-β homologue that functions as a morphogen in the developing embryo and in adult appendage formation. In the wing imaginal disc, a Dpp gradient governs patterning along the anteroposterior axis by inducing regional expression of diverse genes in a concentration-dependent manner. Recent studies show that responses to graded Dpp activity also require an input from a complementary and opposing gradient of Brinker (Brk), a transcriptional repressor protein encoded by a Dpp target gene. Here we show that Brk harbours a functional and transferable repression domain, through which it recruits the corepressors Groucho and CtBP. By analysing transcriptional outcomes arising from the genetic removal of these corepressors, and by ectopically expressing Brk variants in the embryo, we demonstrate that these corepressors are alternatively used by Brk for repressing some Dpp-responsive genes, whereas for repressing other distinct target genes they are not required. Our results show that Brk utilizes multiple means to repress its endogenous target genes, allowing repression of a multitude of complex Dpp target promoters. Introduction In multicellular organisms, the patterning of tissues depends on the intracellular integration and fine-tuning of multiple external signals, which evoke an assortment of cellular responses. Extrinsic cues are transduced by cytoplasmic effectors and, ultimately, information is relayed to the nucleus, where transcription factors are stimulated to either activate or repress target gene transcription. The transforming growth factor-β (TGF-β) superfamily members, which dictate a wide range of cellular outcomes such as proliferation, alteration of cell shape, apoptosis and cell fate specification, exemplify such signalling molecules (Raftery and Sutherland, 1999). One key Drosophila TGF-β homologue, encoded by the decapentaplegic (dpp) gene, has been shown to function as a long-range morphogen, specifying varied cell fates in a concentration-dependent manner (Lecuit et al., 1996; Nellen et al., 1996). In both embryonic and post-embryonic development, Dpp governs multiple patterning events, including the specification of cells along the dorsoventral (D/V) axis in the embryo and the patterning of the adult appendages (Podos and Ferguson, 1999). Thus, in the developing wing imaginal disc, dpp is expressed in a central narrow stripe of cells along the anteroposterior (A/P) compartment boundary, from where Dpp spreads towards the periphery, mediating both cell proliferation and A/P patterning (Burke and Basler, 1996; Lecuit et al., 1996; Nellen et al., 1996; Entchev et al., 2000; Teleman and Cohen, 2000). A seemingly simple model provides a coherent framework for explaining how the external Dpp signal is transmitted by cytoplasmic components and how it brings about nuclear transcriptional outcomes: Dpp binds to a heteromeric type II/type I transmembrane serine/threonine kinase receptor complex, encoded by thickveins and punt, triggering the phosphorylation of Mad, the Drosophila receptor-specific Smad. Subsequently, phosphorylated Mad (pMad) associates with Medea, and the pMad–Medea complex enters the nucleus to activate Dpp-responsive genes (Raftery and Sutherland, 1999). The recent cloning and characterization of brinker (brk), a resident Dpp target gene encoding a repressor protein that antagonizes Dpp-mediated activation (Campbell and Tomlinson, 1999; Jazwinska et al., 1999a,b; Minami et al., 1999), has enhanced our understanding of how Dpp is able to trigger specific target gene expression programs. Where Dpp signalling is active, the transcriptional regulator Schnurri (Shn) switches off brk expression, thus relieving a subset of Dpp-responsive genes from Brk repression (Marty et al., 2000). Consequently, brk is expressed in the ventrolateral regions of the embryo, abutting the dorsal dpp expression domain, whereas in the wing imaginal disc, brk is expressed at high levels only in the periphery of the disc, with its transcription diminishing towards the centre. Thus, two opposing and complementary gradients, i.e. activation mediated by Smads and repression by Brk, ensure that discrete thresholds for Dpp activity are attained. In this paper we explore the molecular basis underlying Brk repression. Transcription factors negate gene expression in diverse manners (Mannervik et al., 1999). Some do so 'passively', by competing with, and occluding activators from binding to coincident cis-acting DNA elements. For other repressors, DNA binding is not sufficient. Rather, these repressors are fully reliant on tethered corepressors and act more instructively, by local 'quenching' of proximally-bound activators, interference at a distance with the basal transcription machinery or altering chromatin structure and organization (Johnson, 1995; Cai et al., 1996; Gray and Levine, 1996). To date, two prototypic Drosophila corepressors have been characterized that seem to be markedly distinct from each other, i.e. where tested, one assists negative transcriptional regulators acting at short-range while the other supports long-range repressors (Zhang and Levine, 1999). Thus, the C-terminal binding protein (CtBP; Nibu et al., 1998a,b; Poortinga et al., 1998) is a corepressor that acts in conjunction with repressors obstructing the function of activators bound up to 150 base pairs away (e.g. Gray et al., 1994; Arnosti et al., 1996). In addition, the corepressor Groucho (Gro; Fisher and Caudy, 1998; Parkhurst, 1998; Chen and Courey, 2000) is required by repressors capable of hindering promoter function at long-range, shutting off transcription even over distances of up to several thousand base pairs (Paroush et al., 1994; Cai et al., 1996; Barolo and Levine, 1997; Dubnicoff et al., 1997). In this study we show that Brk contains a functional repression domain that accommodates Gro and CtBP recruitment motifs, and that Brk interacts physically with these cofactors. Although other Drosophila repressors are known to possess more than one repressor domain (e.g. Arnosti et al., 1996; Keller et al., 2000; Kobayashi et al., 2001), the biological relevance of this feature has not yet been genetically addressed. Here we investigate the functionality of Brk's association with two corepressors and demonstrate that the mechanism of repression by Brk is dependent on promoter context. We show that Brk requires either or both Gro and CtBP for switching off some target genes, whereas for the silencing of others, it requires neither of these cofactors, presumably relying on its reported ability to outcompete activators from binding DNA. We surmise that the combinatorial use by Brk of these two corepressors provides a versatility that allows it to silence a variety of composite promoters in response to graded morphogenetic activity of Dpp. Results Dpp target genes are specifically repressed by overexpression of gro Gro is ubiquitously expressed in the adult wing (Tata and Hartley, 1993) and mutations in gro have been identified in genetic screens for modifiers of various wing and eye phenotypes (e.g. Heitzler et al., 1996; Chanut et al., 2000), implicating Gro in advanced developmental stages. Indeed, Gro has been ascribed at least one specific role in the establishment of wing configuration, as a corepressor for the Enhancer of split basic-helix–loop–helix proteins acting downstream of Notch signalling in D/V wing patterning (Heitzler et al., 1996). To assess whether Gro also contributes in hitherto unrecognized ways to wing A/P axis formation, we analysed the expression of wing-patterning genes in marked clones of cells that either ectopically overexpress, or are mutant for, gro (Xu and Rubin, 1993; Pignoni and Zipursky, 1997; see Materials and methods). Overexpression of gro should enhance the silencing of genes normally repressed by Gro-dependent transcriptional regulators while, reciprocally, the loss of gro should result in derepression, and therefore in the ectopic induction of these genes. In the wing imaginal disc, cells in the posterior compartment are programmed by the engrailed selector gene product to secrete Hedgehog (Hh), which induces dpp in a stripe of anterior cells along the A/P boundary. Dpp then acts as a long-range morphogen that governs patterning across the entire imaginal disc field (Podos and Ferguson, 1999). To determine whether Gro participates in the implementation of Hh signalling, we stained clones overexpressing gro, or clones that are homozygous for the strong groE48 allele, for dpp-lacZ expression. In all clones, even those overlapping with the Hh activity domain, there are no noticeable alterations in the dpp expression pattern (Figure 1A; data not shown), indicating that Gro is not required downstream of Hh for dpp transcriptional regulation. In striking contrast, however, three distinct targets of the Dpp pathway, expressed either in the wing pouch (optomotor-blind; omb and vestigial; vg) or in the periphery of the wing disc (brk), are repressed in clones overexpressing gro (Figure 1B–D). Expression of omb-lacZ (Figure 1B), as well as that of a lacZ reporter driven by vg's Dpp-responsive enhancer (vgQ-lacZ; Figure 1C), is completely abrogated in these clones, whereas expression of brk-lacZ is only reduced (Figure 1D; see below). All three Dpp targets are repressed in a cell autonomous manner, i.e. only in the clones but never in adjacent cells. These results, together with an extensive gro loss-of-function clonal analysis detailed below, implicate Gro specifically as a downstream effector of Dpp signalling. Figure 1.Overexpression of gro does not affect dpp expression, but brings about repression of Dpp target genes. (A–D) Third instar larval imaginal wing discs, stained for the πMyc or CD2 markers (left) and for β-galactosidase (centre); merge, right. In these, and subsequent figures, anterior is to the left and dorsal up. (A) dpp-lacZ expression (centre, red) is unaffected by groE48 mutant clones, marked by loss of the πMyc marker (left, green), or by gro overexpression (data not shown). In contrast, gro overexpression, in clones marked by loss of CD2 (left, green), leads to the complete repression of omb-lacZ (B) and vgQ-lacZ (C), and to a reduction in brk-lacZ (D) expression levels, in a cell-autonomous manner. Download figure Download PowerPoint Brk interacts physically with two corepressors, Gro and CtBP Recent genetic and molecular studies have shown that brk encodes a repressor acting downstream of the Dpp pathway, which helps define the low end of the Dpp gradient (Campbell and Tomlinson, 1999; Jazwinska et al., 1999a; Minami et al., 1999). In particular, the Dpp targets omb and vgQ are both derepressed in brk− mutant clones and in brk− wing imaginal discs, suggesting that they are normally subjected to Brk repression (Campbell and Tomlinson, 1999; Jazwinska et al., 1999a; Minami et al., 1999). More directly, Brk binds to specific sequences within defined omb and vgQ enhancer elements, bringing about their silencing by outcompeting the Mad–Medea complex, or some other activator, from binding to overlapping DNA sites (Sivasankaran et al., 2000; Kirkpatrick et al., 2001). That putative Brk target genes are repressed in clones of cells with increased gro dosage strongly suggests that Brk is a Gro-dependent repressor. Accordingly, Brk's proposed repression domain (RD) (Campbell and Tomlinson, 1999) harbours a potential Gro recruitment motif (FKPY), similar to the Gro-binding domains defined in the repressors Hairy (WRPW), Runt (WRPY) and Huckebein (FRPW), and identical to that in Even-skipped (Eve) (Paroush et al., 1994; Aronson et al., 1997; Goldstein et al., 1999; Kobayashi et al., 2001). It has been noted previously by others that Brk also contains a CtBP-binding domain (PMDLSLG; Jazwinska et al., 1999a). Below we show that Brk is in fact able to interact physically with both Gro and CtBP, and address the functional relevance of these associations to Brk's in vivo repressor capacity. To demonstrate Brk's ability to associate with the two corepressors in vitro, we fused the protein's putative RD (amino acids 369–541) to glutathione S-transferase (GST), and incubated it with radioactively labelled Gro or CtBP (Figure 2; see Materials and methods). In GST pull-down assays, Brk's RD (BrkRD), but not GST alone, readily retains [35S]methionine-labelled Gro (Figure 2A). To test further the specificity of this interaction, three mutant derivatives of the BrkRD, fused to the GST moiety, were generated in which the Gro recruitment domain (BrkRDmutG; FKPY to FEAY; Goldstein et al., 1999), the core of the CtBP-binding motif (BrkRDmutC; DLS to AAA; Zhang and Levine, 1999) or both (BrkRDmutC/G) were altered (Figure 2D). As shown in Figure 2A, Brk's binding to Gro is impaired by the modifications in the FKPY motif. Significantly, however, Gro associates with the GST–BrkRDmutC construct as strongly as it does with the native GST–BrkRD fusion. GST–BrkRD also binds labelled CtBP in vitro (Figure 2B) and, although the binding of Brk to CtBP is weak in this assay, the specificity of the interaction is clearly evident: the association between the two proteins is abolished by mutations in the CtBP recruitment domain but is unaffected by alterations in the Gro recruitment motif (Figure 2B). Figure 2.Brk interacts physically with Gro and CtBP. (A and B) In vitro pull-down assays. 35S-labelled Gro (A) or dCtBP (B) were incubated with GST–BrkRD derivatives immobilized on glutathione–agarose beads and, following washing, retained 35S-labelled protein was subjected to SDS–PAGE (not shown) and autoradiography. (A) Gro binds specifically to GST–BrkRD (lane 5) and to GST–BrkRDmutC (lane 7), but not to GST–Brk variants in which Brk's FKPY motif is mutated (lanes 6 and 8). GST–Hairy (lane 3) serves as a positive control, whereas Hairy lacking its C-terminal Gro-binding domain (HairyΔNotI, lane 4) and GST alone (lane 2) are negative controls. (B) CtBP binds specifically to GST–BrkRD (lane 3) and BrkRDmutG (lane 4), although to a lesser extent than to GST–Snail (lane 2), an established CtBP partner (Nibu et al., 1998a). Mutating Brk's CtBP recruitment core motif abolishes CtBP binding (lanes 5 and 6). GST alone, lane 7. (A and B) 10% of input-labelled protein was run in lane 1. Arrows indicate positions of full-length Gro (A) and CtBP (B). (C) Yeast two-hybrid assay. Full-length Brk, or just its RD, interacts strongly in yeast with full-length Gro (not shown), with pZP54 (Gro251–719) and with CtBP (white colonies indicate lack of interactions). Mutating either the Gro or CtBP recruitment motif in Brk's RD results in loss of interactions between Brk and the corresponding corepressor. (D) A schematic representation of Brk's RD (residues 369–541) and derived constructs. The Brk corepressor recruitment motifs, and respective mutant versions, are indicated. Download figure Download PowerPoint We confirmed Brk's ability to interact with Gro and CtBP, particularly the specificity of the associations, using the yeast two-hybrid system (Figure 2C; see Materials and methods). The full-length Brk, or only its RD portion, interacts strongly with Gro and pZP54 (Gro251–719; Paroush et al., 1994), as with CtBP (Figure 2C; data not shown). Here too, mutations in one recruitment motif selectively obliterate the binding of Brk to only the single respective corepressor but not to the other. Brk contains a functional repression domain that depends on corepressors Brk has been reported to negate transcription by competing with activators, such as Mad/Medea, for overlapping DNA target sites, thereby preventing them access to target promoters (Sivasankaran et al., 2000; Kirkpatrick et al., 2001; Rushlow et al., 2001). Its direct interactions with Gro and CtBP, however, suggest that Brk acts in a more instructive manner. While in the former 'passive' mechanism Brk is expected to rely solely on its competitive DNA-binding activity, the latter 'active' mechanism predicts that it accommodates an innate RD that depends on the recruitment of corepressors. To establish whether Brk contains a functional RD that can silence gene expression, separable from its DNA-binding domain, we employed an in vivo assay that relies on repression of the sex-determining Sex-lethal (Sxl) gene by ectopic expression of the pair-rule gene hairy (Parkhurst et al., 1990; Jiménez et al., 1997). Sxl is normally expressed only in female embryos whereas, in males, it is repressed by Deadpan (Dpn), an autosomally encoded Hairy-related repressor protein. When Hairy is expressed prematurely, under the hunchback (hb) promoter, it mimics Dpn's repressor function and eradicates Sxl transcription in the anterior of syncytial blastoderm female embryos. Because Sxl is essential for dosage compensation in females, this repression subsequently leads to female-specific lethality (Parkhurst et al., 1990). A form of Hairy, lacking its own RD, is inert in this assay. However, fusion of heterologous RDs to the truncated Hairy protein restores its ability to repress Sxl (Jiménez et al., 1997; Goldstein et al., 1999). Indeed, the equivalent expression of a hb-Hairy-BrkRD transgene results in an effective repression of Sxl in the anterior halves of female embryos (Figure 3A) and female-specific lethality ensues (Figure 3F; see Materials and methods). Thus, the region in Brk spanning the Gro- and CtBP-binding domains promotes potent repression in embryos. Figure 3.Brk requires both Gro and CtBP for full repression of Sxl. (A) Expression of Hairy-BrkRD blocks Sxl expression in the anterior halves of female embryos and, consequently, strong female-specific lethality ensues (F). The ability of the BrkRD to repress Sxl in female embryos is compromised when the CtBP-binding motif is mutated (B) and is completely abolished by mutations in the Gro recruitment domain (C and D). Female-specific lethality is, correspondingly, affected (F). (E) Wild-type expression of Sxl. (A–E) Early Sxl expression was monitored using the Sxl-Pe:lacZ reporter strain (Estes et al., 1995). Equivalent results were obtained by staining embryos with a monoclonal antibody specific to the active form of Sxl. (F) The proportional number of transgenic (black) and non-transgenic (white) females of representative lines indicates the magnitude of female-specific lethality (see Materials and methods). Download figure Download PowerPoint The ability to selectively disrupt Brk binding to each individual corepressor allowed us to start exploring the dependence of its repressor potential on Gro and/or CtBP in vivo. As both Gro- and CtBP-mediated repression can be detected in the Sxl-repression assay (Jiménez et al., 1997), we fused truncated Hairy to the three derivatives of the Brk RD, mutated in the Gro, CtBP or both recruitment motifs (see Figure 2D) and placed them under hb promoter regulation. In female embryos expressing Hairy-BrkRDmutC, Sxl is substantially repressed, although not as effectively as by Hairy-BrkRD (Figure 3B). Furthermore, this repression still leads to statistically significant female-specific lethality (Figure 3F; p = 0.001; see Materials and methods). Thus, blocking CtBP binding does not completely abolish activity of the Brk RD. In comparison, mutating the Gro recruitment domain causes only residual Sxl repression (Figure 3C) and no apparent female-specific lethality (Figure 3F). Finally, Sxl expression is seen throughout female embryos expressing hb-Hairy-BrkRDmutC/G (Figure 3D), and no female-specific lethality is observed (Figure 3F). Thus, Brk relies mainly on Gro for repressing Sxl. Nevertheless, since mutating the CtBP recruitment motif in Brk's RD attenuates Sxl repression (Figure 3B and F), we conclude that, for full potency as a negative transcriptional regulator, Brk requires both corepressors. omb and spalt are repressed by Brk independently of Gro and CtBP The above data indicate that the interactions between Brk and the corepressors Gro and CtBP are indispensable for maximal repression of Sxl in vivo. We next sought to establish whether Brk requires both cofactors for repression of its endogenous target genes. Below (Figures 4, 5, 6, 7) we show that, for repression of distinct target genes, Brk requires Gro and/or CtBP differentially, presumably as a function of specific promoter topology and architecture (see Discussion). Figure 4.Brk represses omb independently of Gro and CtBP. Wing imaginal discs, bearing gro− single (A) or CtBP−, gro− double mutant (B) clones, discernible by loss of the πMyc marker and by the appearance of a nearby twin-spot (left, green), do not show elevation of omb-lacZ expression (centre, red; arrows); merge, right. Download figure Download PowerPoint Figure 5.Brk requires Gro, but not CtBP, for repressing vgQ. (A) Clones of cells mutant for gro and marked by the loss of πMyc (left, green) show ectopic vgQ expression (centre, red). In contrast, CtBP− clones show a reduction in levels of vgQ expression (B). Note that gro− clones show a phenotype only when in the periphery of the disc, as seen in brk mutant clones (Campbell and Tomlinson, 1999), while the downregulation of vgQ in CtBP− clones is observed regardless of their position, indicating that these effects are Brk independent. (C) A composite phenotype in CtBP−, gro− double mutant clones resembles that of gro− in peripheral clones (arrow) and that of CtBP− in central clones (arrowhead). Download figure Download PowerPoint Figure 6.Negative autoregulation of brk requires either Gro or CtBP. Single gro− (A) or CtBP− (B) clones do not affect brk expression whereas CtBP−, gro− double mutant clones show ectopic brk expression (C). The phenotype in (C) is seen only in the periphery of the disc, suggesting that it is Brk dependent and Schnurri independent. Download figure Download PowerPoint Figure 7.Brk requires corepressors for its repressor function in the embryo. (A) Transgenic embryos overexpressing full-length Brk (from UAS-brk transgenes, driven by maternal Gal4VP16), either in its native form or with its corepressor-binding domains mutated, were stained for the expression of zen (right), tld (centre) and dpp (left) during mid- to late-cellularization. The Y-axis designates the percentage of embryos expressing a given target gene, calculated relative to the number of expressing wild-type embryos, referred to as 100%. n = number of embryos, at the appropriate stage, that were scored. (B–G) Representative embryos. (B) UAS-BrkmutC/G, stained for zen; (C) UAS-BrkmutC, stained for tld; (D) UAS-BrkmutG, stained for tld; (E) UAS-BrkmutC, stained for dpp; (F) UAS-BrkmutG, stained for dpp; (G) UAS-BrkmutC/G, stained for dpp. Repression of zen is independent of corepressors (A and B) whereas that of tld is strictly Gro dependent (A, C and D). As for the silencing of dpp, Brk relies mainly on Gro (A and E–G). Nevertheless, since the level of dpp expression is significantly lower in BrkmutG-expressing embryos (A, marked by '**'; F) when compared with wild-type embryos or with embryos expressing the BrkmutC/G transgene (G), CtBP must also be contributing to maximal Brk repressor ability. Download figure Download PowerPoint Brk competes with an activator for binding to an omb wing enhancer (Sivasankaran et al., 2000), suggesting that, for this promoter, Brk should act independently of corepressors. Consistent with this, we find that omb-lacZ is not ectopically expressed in cells homozygous for groE48 (hereafter referred to as gro− clones) (Figure 4A), nor is it affected by CtBP loss-of-function clones, generated using the l(3)87De-10 allele (CtBP−; data not shown), or by CtBP−, gro− double mutant clones (Figure 4B). Thus, single and double mutant clones for gro and CtBP do not phenocopy the omb derepression seen in brk− clones (Campbell and Tomlinson, 1999; Jazwinska et al., 1999a; Minami et al., 1999), implying that Brk can repress omb even in the absence of these corepressors. Repression of the Dpp target gene spalt (sal; Nellen et al., 1996) is also independent of Gro and CtBP (data not shown). Nonetheless, in gro overexpression clones, omb is repressed (Figure 1B), suggesting that, even for the omb promoter, Gro reinforces Brk repressor function (see Discussion). Brk requires Gro, but not CtBP, for repressing vgQ To establish whether Brk represses vgQ via Gro, CtBP or both, we monitored vgQ-lacZ expression in gro− and CtBP− single, and CtBP−, gro− double mutant clones. In this instance, we find a mandatory requirement for Gro, but not for CtBP; in gro− clones, vgQ is upregulated (Figure 5A). Importantly, as is the case for brk− clones (data not shown; Campbell and Tomlinson, 1999), the cell-autonomous upregulation of vgQ is seen only in gro− clones close to the periphery of the disc, suggesting that the observed effects are Brk dependent. In contrast, in CtBP− mutant clones vgQ expression is downregulated, in the Brk territory but also outside it, at the centre of the disc (Figure 5B), indicating that these effects are Brk independent and that CtBP is positively required for vg expression (see Discussion). CtBP−, gro− double mutant clones show a composite effect: ectopic expression and upregulation of vgQ in clones in the brk expression domain, and a phenotype resembling that of CtBP− clones at the middle of the disc, where brk is not expressed (Figure 5C). Thus, Brk repression of vgQ is Gro- but not CtBP-dependent. Negative autoregulation of brk requires either Gro or CtBP omb and vgQ expression is completely shut off in clones of cells overexpressing gro, whereas that of brk is only reduced (Figure 1), suggesting that Brk might be repressing its own transcription via a negative autoregulatory loop (B.Müller and K.Basler, unpublished results). To establish whether, in negating its own expression, Brk is assisted by Gro and/or CtBP, we stained gro− and CtBP− single (Figure 6A and B), or CtBP−, gro− double (Figure 6C) mutant clones for brk-lacZ expression. Figure 6A and B shows that brk is never ectopically expressed in any of the single mutant clones, whereas ectopic brk expression is clearly observable in double mutant clones (Figure 6C). Thus, in the absence of one corepressor, repression is adequately mediated by the other, suggesting that negative autoregulation by Brk is robust, relying on either Gro or CtBP. Strikingly, the effects on brk expression are seen only in double mutant clones found at the periphery of the disc, but not at the centre where Shn is active (Figure 6C; Marty et al., 2000), supporting the notion that the effects are, indeed, Brk- but not Shn-dependent. Furthermore, the fact that double mutant clones at the middle of the disc do not ectopically express brk suggests that Shn-mediated repression of brk transcription must be taking place even in the absence of both corepressors. Corepressors are required for Brk repression in the embryo In embryogenesis, Brk plays a comparable role to that in the wing disc, i.e. it blocks low- and intermediate-level Dpp target gene expression (Jazwinska et al., 1999b; Ashe et al., 2000; Rushlow et al., 2001; Zhang et al., 2001). We next wanted to establish whether, in the developing embryo, Brk is also reliant on corepressors for the silencing of its downstream targets. A direct assessment of Brk's dependence on Gro using germ-line clones devoid of maternal gro is hindered, however, by the pri