The tiny Hairless protein from Apis mellifera: a potent antagonist of Notch signaling in Drosophila melanogaster
© Maier et al; licensee BioMed Central Ltd. 2008
Received: 06 February 2008
Accepted: 17 June 2008
Published: 17 June 2008
The Notch signaling pathway is fundamental to the regulation of many cell fate decisions in eumetazoans. Not surprisingly, members of this pathway are highly conserved even between vertebrates and invertebrates. There is one notable exception, Hairless, which acts as a general Notch antagonist in Drosophila. Hairless silences Notch target genes by assembling a repressor complex together with Suppressor of Hairless [Su(H)] and the co-repressors Groucho (Gro) and C-terminal binding protein (CtBP). Now with the availability of genomic databases, presumptive Hairless homologues are predicted, however only in insect species. To further our understanding of Hairless structure and function, we have cloned the Hairless gene from Apis mellifera (A.m.H) and characterized its functional conservation in Drosophila.
The Apis Hairless protein is only one third of the size of the Drosophila orthologue. Interestingly, the defined Suppressor of Hairless binding domain is interrupted by a nonconserved spacer sequence and the N-terminal motif is sufficient for binding. In contrast to Apis Hairless, the Drosophila orthologue contains a large acidic domain and we provide experimental evidence that this acidic domain is necessary to silence Hairless activity in vivo. Despite the dramatic size differences, Apis Hairless binds to the Drosophila Hairless interactors Su(H), Gro, CtBP and Pros26.4. Hence, Apis Hairless assembles a repressor complex with Drosophila components that may have a different topology. Nevertheless, Apis Hairless is sufficient to repress the Notch target gene vestigial in Drosophila. Moreover, it is able to rescue Hairless mutant phenotypes, providing in vivo evidence for its function as a bona fide Notch antagonist.
This is the first interspecies-complementation analysis of the Hairless gene. Guided by evolutionary comparisons, we hope to eventually identify all the relevant structural domains and cofactors of Hairless, thereby opening an avenue for further insights into the repressor-complexes that down-regulate Notch signaling also in other, higher eukaryotes.
Cell to cell communication is essential for development and cellular differentiation of metazoans. The communication is established by signaling pathways that allow information to be sent from one cell to a neighboring cell. This information enables the receiving cell to adopt a different cell fate. One of the best studied signaling pathways that coordinate developmental decisions is the Notch pathway [1–3]. It was first described in the process of lateral inhibition in Drosophila: within a cluster of equipotential cells destined to adopt the same cell fate, one cell gains the ability to inhibit adjacent cells to engage differentiation by means of activating Notch. Notch signaling also plays important roles in asymmetric cell divisions that result in differential cell fate decisions [4–6]. Moreover, local Notch activity can induce the formation of developmental boundaries as seen during wing margin formation in Drosophila [7–9].
It is not surprising that this fundamental pathway is highly conserved in eumetazoans and is crucial at many different developmental stages in a variety of different tissues [1, 2]. The pathway is initiated by the binding of the ligands, Delta or Serrate (Delta-like and Jagged in mammals), presented on one cell to the Notch receptor on the adjacent cells. As a consequence, the intracellular Notch domain is cleaved and migrates into the nucleus, where it forms a transcriptional activator complex by binding, together with co-activators, e.g. Mastermind (Mam), to the transcriptional regulator CSL (CSF or RBP-Jκ in mammals, Suppressor of Hairless (Su(H) in Drosophila and Lag-2 in Caenorhabditis) . CSL belongs to the family of rel DNA binding molecules and allows for context specific transcriptional activation of target genes of the Notch signaling pathway . In Drosophila, Hairless (H) acts as a general antagonist of this pathway. H binds to Su(H) and, by recruiting the co-repressors Groucho (Gro) and C-terminal binding protein (CtBP), converts Su(H) into a repressor of the Notch target genes [11–14]. In this complex H acts as molecular linker between Su(H) and the co-repressors. Since H retains repressor activity even in the absence of co-repressor binding, it is thought that it impedes formation of the Notch-Su(H)-Mam activator-complex on its own .
Established structural domains of H are well conserved in insect evolution
The H gene encodes a general antagonist of the Notch signaling pathway in D. melanogaster, where it plays a central role in repressing Notch target genes . There is ample genetic evidence showing that H is involved in manifold developmental processes in Drosophila. So far it remains open, whether this reflects solely its central role in Notch signaling or whether H is involved in other pathways as well. H is a novel protein that is quite large and may contain more than the already established functional domains. A comparison with the orthologues from D. hydei (D.h.H) and A. gambiae (A.g.H) identified several conserved domains of presumed functional significance [11, 16]. Experimental analysis of D. hydei showed that the D.h.H protein with 1158 residues is somewhat larger than the D.m.H orthologue that spans 1077 amino acids [16, 19, 20]. The A.g.H is even larger and comprises approximately 1300 residues based on an in silico prediction (see Additional file 1). Meanwhile several additional genome sequences have been published. The available databases show that H orthologues are present in all Drosophilids (see Additional file 1) and several other dipterans, as well as in other insect orders including Lepidoptera, Hymenoptera and Coleoptera that are considerably further diverged (see Additional file 1). However, to date we could not detect clear H orthologues in species others than insect species, even when using the most highly conserved H domains (see below). The phylogenetic distance between Nematocera dipterans, like A. gambiae and A. aegypti, and the Cyclorrapha to which Drosophilidae belong, is about 200 – 250 millions years, whereas about 250 – 300 million years are estimated between dipterans and the other insect orders  (Fig. 1A). A comparison of the presumptive H orthologues reveals a surprisingly high degree of divergence and highlights conserved domains all the more. These domains characterize the H protein and its function. They include the Su(H) binding domain (SBD), the Gro binding domain (GBD) and, at the very C-terminus a binding sequence for CtBP (CBD) that are remarkably well conserved (Fig. 1B–D). The SBD maps to D.m.H residues 232 to 337, a region that is nearly identical in all Drosophilids (Fig. 1B; see Additional file 1) . However, in further diverged insects including Anopheles the SBD is split by a less well conserved stretch (Fig. 1B; see Additional file 1). The GBD has been mapped to nine residues in D. melanogaster [11, 12]. It is extremely well conserved in the insect H orthologues (Fig. 1C). The CBD is nearly invariant (Fig. 1D).
The structure of the SBD in the further diverged insects led us to address whether the entire region is needed for Su(H) binding (Fig. 1E). In fact we found that the N-terminal portion (NT, L171 to S270) was sufficient for Su(H) binding, in agreement with earlier results  and bound as well as the entire SBD (NT-CT, L171 to H357). In contrast, the C-terminal portion (CT, R267 to H357) did not bind to Su(H) (Fig. 1E).
The H orthologue from Apis mellifera
The A.m.H cDNA spans a total of 2726 bp; it contains two introns at positions identical to D.m.H (Fig. 2C). The cDNA has an open reading frame of 392 codons, which is only ~36% of D.m.H. Accordingly, the calculated molecular weight of A.m.H protein is ~44.5 kDa, whereas that of D.m.H is ~110 kDa.
Despite its small size, A.m.H contains the characteristic H protein domains, i.e. the SBD, the GBD and the CBD, and they are well conserved (Figs 1, 2). Three nuclear localization signals are predicted in D.m.H; two are identical in A.m.H, the third is slightly variant (Fig. 2C). D.m.H is a highly basic protein with an isoelectric point (pI) of 10.4; A.m.H is likewise basic with a pI of 10.85. Both proteins contain acidic stretches, however, only the one located within the SBD is conserved (red arrow in Fig. 2B). Unlike D.m.H, the honeybee H protein does not contain the large acidic domain downstream of the SBD (Fig. 2B, asterisk). Using the standard parameters of the BESTFIT program, the two orthologues share 54% identity. Under relaxed conditions that allow an overall alignment, the two protein sequences are 70% similar and 63% identical (see Methods).
A.m.H protein recapitulates D.m.H protein-protein interactions
The three H domains SBD, GBD and CBD serve as binding sites for the proteins Su(H), Gro and CtBP, respectively. In addition, the C-terminal half of D.m.H was shown to bind to the N-terminal half of Pros26.4, which is one of six AAA-ATPases that form the base of the 19S proteasome regulatory subunit .
The GBDs of A.m.H and D.m.H are 80% identical and 90% similar (Fig. 1C). However, binding of full length A.m.H protein to D.m.Gro protein was not seen in the yeast two-hybrid assay (Fig. 3). This was unsurprising, since full length D.m.H binds rather weakly to Gro, whereas it binds very strongly to a short peptide containing the GBD . Likewise, strong binding was observed with a corresponding small peptide (S262 to P309) spanning the A.m.H GBD, as well as with the N-terminally truncated A.m.H 4-1 construct (Fig. 3). The specificity of the interaction was confirmed by a point mutation within the A.m.H GBD: an exchange of Tyrosine 264 to Alanine was sufficient to completely abrogate binding to Gro (Fig. 3), just like the corresponding mutation in D. melanogaster . The weak binding of Gro to full length H proteins from either species may perhaps result from the three dimensional structure of H which then must be likewise retained by the tiny A.m.H protein.
The CBD of honeybee and fly H orthologues are identical (Fig. 1D). Therefore, the observed strong interaction between A.m.H and D. melanogaster CtBP was expected (Fig. 3). Mutation of A.m.H CBD* completely eliminated binding to D.m.CtBP (Fig. 3) just like the respective D.m.H mutation , confirming the specificity the A.m.H CBD. Finally, we tested interaction of A.m.H with Pros26.4. As shown in Fig. 3, the full length A.m.H as well as the N-terminally truncated A.m.H 4-1 both bound to the N-terminal part of Pros26.4 (Dm-S4-1), just like D.m.H. The Pros26.4 binding domain in D.m.H maps roughly between the GBD and the CBD . Interestingly, this region of A.m.H is only 21% of the D.m.H size and contains very few similarities. This comparison will aid to identify the relevant sequences involved in this interaction.
Activity of A.m.H in Drosophila melanogaster
Rescue of H mutant phenotypes by A.m.H
n = number of analyzed flies
a) Rescue mc on head
b) Rescue mc on notum
c) Average rescue *
yw; + / H P8
n = 100
n = 24
n = 33
n = 45
Tissue specific repression of Notch signaling in Drosophila melanogasterby Apis H
Apis H represses transcription of vestigial in D. melanogaster
vestigial (vg) is one of the Notch target genes that is activated along the dorso-ventral boundary in the wing imaginal disc and that is important for boundary formation and wing growth . Notch signals activate vg expression via the vg boundary enhancer (vgBE) that contains a Su(H) binding site . The activity of this element is restricted to the dorso-ventral boundary by the Su(H)-Notch activation complex  and is repressed in adjacent cells by the Su(H)-H co-repressor complex .
Transgenic flies carrying a lacZ reporter gene under the control of vgBE (vgBE-lacZ)  were used to study the ability of A.m.H to regulate D.m.vg transcription dependent on Drosophila co-repressors Gro and CtBP (Fig. 6B). Cells overexpressing A.m.H protein were labeled with anti-A.m.H antibodies (Fig. 6B). Compared to the normal expression of the lacZ-reporter gene, beta-galactosidase was almost completely absent in areas, where full length A.m.H was overexpressed, reflecting its repressor activity on the vgBE enhancer element. At the same time, the presumptive wing blade was notably distorted (Fig. 6B), which is typical of full length D.m.H overexpression . Overexpression of AmHG*, resulted in a likewise inhibition of vgBE-lacZ expression, however, the wing disc had only little or no morphological defects (Fig. 6B). In contrast, mutation of the CBD interfered strongly with A.m.H repressor activity, since overexpression of AmHC* caused only a small gap in the vgBE-lacZ pattern (Fig. 6B). In the absence of co-repressor binding (AmHGC*), no or very little down-regulation of vgBE-lacZ was observed (Fig. 6B).
The acidic domain in DrosophilaH attenuates its repressor activity
Comparison of A.m.H and D.m.H peptide sequence
Most strikingly, A.m.H is roughly a third of the size of D.m.H. A closer look at the D.m.H sequence reveals many poly-residues stretches, notably poly-Alanine, poly-Serine and poly-Asparagine, which are absent in A.m.H, challenging their functional importance. Moreover, A.m.H lacks the large acidic domain that attenuates D.m.H repressor activity. Accordingly, overexpression of A.m.H causes more severe defects than D.m.H, most notably during wing margin formation. However, deletion of the D.m.H acidic domain results in an even more active protein (Fig. 7), demonstrating two important points: on one hand, the acidic domain is a necessary functional domain of Hairless in Drosophila that is absent in the honeybee. On the other hand, A.m.H is less active in Drosophila compared to the endogenous D.m.H protein.
We noted one additional larger conserved domain of unknown function upstream of GBD (Fig. 2C). It contains a highly conserved nuclear localization signal, which may be the primary reason for the conservation. Other than that, there are only a few very small conserved sequence stretches between the H orthologues from Apis and fly and they are not conserved between Drosophila and Tribolium or Anopheles (see Additional file 1). Hence it seems unlikely that they are of functional relevance. With respect to the phylogenetic distance and great divergence of the Apis H gene, the remaining activity of A.m.H is quite remarkable. It is able to rescue the dominant HP8 mutant phenotype and can reproduce if overexpressed largely all phenotypes that are obtained by the overexpression of D.m.H protein (Figs 4, 5, 6; Figs 8, 9). Hence, A.m.H acts as a bone fide antagonist of Notch signaling in Drosophila. Since H is a multi-functional protein, this can only be possible if A.m.H protein is able to interact genetically and physically with the components provided by Drosophila.
A.m.H assembles a functional repression complex on Notch target genes using Drosophilacomponents
Interaction of A.m.H with Drosophila proteins was tested with two powerful approaches, the yeast two-hybrid assay and even more convincingly, a direct in vivo assay in the fly. So far, we know of four direct H interaction partners in Drosophila, Su(H), Gro, CtBP and Pros26.4 [11–13, 21, 22]. Recent data provide evidence that H assembles a repressor complex on Notch target genes by linking Su(H) with the two co-repressors Gro and CtBP. Binding of H to the Pros26.4 subunit of the proteasome is unrelated to Notch signaling [11, 12]. However, it reduces H protein stability. Therefore, Pros26.4 indirectly plays a positive role in the Notch signaling pathway . Our data show that A.m.H physically interacts with any of these four Drosophila proteins in an in vitro assay. Moreover, we show that relevant mutations in the A.m.H GBD and CBD eliminate binding to the respective co-repressors. These data highlight the importance of the mutated residues for the binding to the respective partner. Interestingly, the A.m.H double mutant retains repressor activity independent of the co-repressors, suggesting that it may interfere with the assembly of the Su(H)-Notch-Mam activator complex. A similar intrinsic repressor activity was already observed for the corresponding D.m.H*GC mutant . This intrinsic repressor activity has been conserved through considerable evolutionary time and we hope to be able to localize the responsible domain by further comparison and to understand the underlying molecular mechanisms. Taken all together Apis H is a mini-gene in comparison to the Drosophila orthologue. Interestingly this small gene mimics H function in Drosophila almost completely. This was very surprising since H executes its functions solely through protein-protein interactions. From the functional complementation we conclude that A.m.H must be able to assemble an effective repressor complex together with the Drosophila proteins Su(H), Gro and CtBP. However, whereas D.m.H is rather big with roughly 120 kDa and hence provides a sufficiently large surface area for the binding of all three proteins at once, A.m.H. has a predicted size of only about 45 kDa. For example, any of its Drosophila partners has a considerably larger molecular weight . Hence, one might expect steric hindrance in a repressor complex containing A.m.H plus Drosophila components. Because A.m.H functions well in the fly, it must allow for a topology similar to D.m.H. In this case, the interaction domains SBD, GBD and CBD must be in likewise close proximity in D.m.H, whilst the intervening, non-conserved sequences loop out. A structural analysis of Hairless proteins is required to eventually resolve the conformation of the repressor complex.
Notch signaling pathway in the honeybee
In this work, we have used A.m.H for a structure-function analysis of fly Hairless. We do not know, whether A.m.H has the same antagonistic role during Notch signaling in the honeybee as in Drosophila. Since we cannot genetically manipulate the honeybee in the same way as Drosophila, we cannot address this question directly. Instead, we searched the honeybee database for other components of the Notch pathway (see Additional file 2). In fact, we found single orthologues of Notch, Su(H), Gro and CtBP that are extremely well conserved in Apis, and one reasonably well conserved Mam orthologue. Moreover, predicted Notch target genes mγ, mβ, mβ' and mα that form the honeybee E(spl)-C have been already described . We were surprised, however, by the low conservation of Apis vestigial (vg). The A.m.vg protein has a similarity of 63% and an identity of 58% to D.m.vg (see Additional file 2). This is the lowest conservation rate of any Notch pathway component we have looked for. We were curious whether the boundary enhancer, where Su(H) binds to, is present within the presumptive A.m.vg gene. In Drosophila, this enhancer is located in the first intron and contains a single Su(H) binding site on the minus-strand with the core sequence GTGAGAA . The corresponding intron in the honeybee vg gene comprises over 30 kb and more than 20 possible Su(H) target sequences (Genomatrix), three with the identical core sequence on the minus-strand. Taken together, these findings imply that the entire Notch signaling cascade is conserved in A. mellifera.
In addition, our data indicate that A.m.H antagonizes Notch signaling in the honeybee also by the assembly of a repression complex consisting of A.m.Su(H) and the co-repressors A.m.Gro and A.m.CtBP. This is based on the high conservation of the three orthologues as well as their binding sites within A.m.H and on the direct protein interactions between A.m.H and the Drosophila Su(H), Gro and CtBP proteins (Figs 1, 3; see Additional file 2). The structure of the activation complex from mammals as well as from C. elegans, comprising Notch, Mam-like protein and DNA-bound CSL has been elucidated [40, 41] and we do not expect it to be much different in fly or honeybee. Differences may arise for target genes such as E(spl) or vg, which eventually implement Notch signals. The Apis E(spl) homologues possess typical Su(H) binding sites in their enhancer-promoters, indicating their importance in the Notch signaling pathway for honeybee development as well [39, 42].
Notch antagonists in higher eukaryotes
Hairless is the general antagonist of the Notch signaling pathway in Drosophila. To date, H has no known homologue in higher eukaryotes other than insects, in contrast to the other Notch pathway members that are well conserved from worm and fly to human. Strikingly, the Su(H) protein, which directly binds to H, shares 82% amino acid identity with its mouse orthologue RBP-Jκ over large protein portions . This is surprising and leads to speculations. For example, it was postulated that H is the counterpart of the Msx2-interacting nuclear target protein (MINT) [43, 44]. However, the corresponding Drosophila protein is encoded by split ends (spen) and has been proposed to integrate information from several different signaling pathways. Recently it has been shown to function also as genetic antagonist of certain Notch dependent processes .
A vertebrate H homologue has not yet been identified based on sequence conservation, presumably due to a high degree of divergence. One experimental approach to eventually identify such a homologue is to analyze the H structure in detail and to characterize important functional domains. The H orthologue from the honeybee will help us in this process. We have shown that A.m.H functions as a bone fide Notch antagonist in the fly despite considerable divergence with regard to size and amino acid sequence.
PCR and cloning strategies
An Apis mellifera embryonic cDNA Uni-ZAP XR library  was screened with a PCR-probe (see Fig. 2A). Two positive clones were isolated and sequenced. Based on the sequence of the A.m. EST-clone # BB160014B20G05 , which covers the N-terminus of a predicted A.m.H transcript, our longest isolated cDNA clone was incomplete at its 5' end. The 22 lacking bases were extended using the ExSiteTM PCR-based Site-Directed Mutagenesis Kit (Stratagene). An additional base was added to the lower primer such that the Eco RI site provided by the pBluescript vector allowed subsequent in frame cloning in pEG- and pMAL-vectors, respectively. Primer sequences used in this study for in vitro mutagenesis and DNA amplification are available upon request, as are details on the cloning strategies.
Computer analysis of H orthologues
The Drosophila melanogaster gene and protein sequences were accessed in FlyBase . The other Drosophila sequences as well as the sequences of Anopheles gambiae, Aedes aegypti, Culex pipiens, Bombyx mori, Tribolium castaneum, Apis mellifera, Nasonia vitripennis and Pediculus humanus corporis were screened with tblastn service of Flybase. In case of A. mellifera, screening was done also with the HUSAR TBlastN2 service of the DKFZ [49, 50]. For both databases, we used the D. melanogaster protein sequence as search sequences. Similarity and identity scores were calculated using BESTFIT. Because standard conditions only align the best conserved domains, we relaxed the parameters such that the entire protein sequence was aligned (gap weight 1, length weight 1, maximum penalty length 30). Whereas these changes have little influence on identity values of closely related sequences, they give higher scores with less conserved sequences. Multi-alignments were done with PRRN with gap extension penalty 1 and the gap open penalty 9. Further analyses were performed as previously described .
Generation of A.m.H and D.m.Hwild type and mutant constructs
Full length A.m.H cDNA was cloned into pUAST  generating UAS-AmH. Likewise, hs-AmH was cloned using pCaSpeR-hs RX8 vector . Mutant constructs were generated with the Quick change XL Site directed mutagenesis kit (Stratagene) according to the manufacturer's protocol. AmHG*: Gro binding site was destroyed by mutating Y264 into A. AmHC*: CBD was modified from PLNLSKH to VIQITKR. AmHGC*: within the mutant construct AmHG*, wild type CBD was replaced by mutant CBD* (Fig. 2A). All changes were sequence verified. The mutant constructs were shuttled into pUAST and pEG vectors, respectively.
Construction of D. melanogaster Hairless C3 deletion (R355 to V564) was described earlier ; it was shuttled into pUAST to yield UAS-DmHΔC3. The AD deletion (E358 to E465) was generated by A. Bravo-Patiño. It was likewise shuttled into pUAST (UAS-DmHΔAD).
Generation and analysis of transgenic flies
All P-element constructs, hs-AmH, UAS-AmH, UAS-AmHG*, UAS-AmHC*, UAS-AmHGC*, UAS-DmHΔAD and UAS-DmHΔC3, were injected into y 1 w 1118 embryos according to standard protocols and several independent transgenic fly lines were each established; they behaved largely identical in subsequent tests. The results shown are from parallel experiments involving a minimum of three independent lines each and are representative for the respective construct. The obtained phenotypes were non-overlapping. The H P8 null mutant was described earlier [19, 51]. Heat shock was given for half hour at 39°C to third instar hs-AmH larvae and early pupae. Overexpression experiments with UAS-lines were performed at 18°C and 25°C, respectively. As driver lines, omb-Gal4, gmr-Gal4, pnr-Gal4, sca-Gal4, ap-Gal4, ey-Gal4 and ptc-Gal4 were used . The vgBE-lacZ reporter line  was combined with omb-Gal4, and males crossed to UAS-AmH wild type or UAS-AmH mutant virgins. Wing discs of female larvae with the genotype omb-Gal4/X; vgBE-lacZ/UAS-AmH* were processed for antibody staining. Control animals were omb-Gal4/X; vgBE-lacZ.
Analysis of protein-protein interactions
Yeast two-hybrid protein interaction assays were performed as previously described using VP16-dCtBP, VP16-Gro, pEG-Gro, pJG-S4-I and pJG-Su(H) [12, 22, 31]. For bait, Apis mellifera constructs pEG-AmH, pEG-AmHG*, pEG-AmHC* and pEG-AmHGC* were used. In addition, the following pEG-constructs were generated: pEG-AmHGBD containing the Gro binding domain (codons S262 to D309), pEG-AmHGBD* (Y264 to A mutation, PCR-amplified from AmHG*) and pEG-AmH4-1 (deletion of 172 N-terminal codons). AmH4-1 is an incomplete cDNA clone; it starts with L173 and contains complete C-terminal coding sequences. The D. melanogaster Su(H)-binding domain (SBD) was subdivided into DmH-NT (codons L171 to S279) and DmH-CT (codons R267 to T362) and cloned into pEG vector, respectively. pEG NT-CT (L171 to T362) spans both parts. All constructs were sequence confirmed. Expression of the various pEG-constructs was examined with Western blots using the anti LexA antibody (Invitrogen).
Immuno-histochemistry and phenotypic analyses
A PCR construct spanning A.m.H codons N137 to P348 was cloned into pMAL-C expression vector (New England Biolabs). AmH-MBP fusion protein was expressed in E. coli and affinity purified using standard protocols. Polyclonal antisera were from Pineda ABservice (Berlin). Imaginal discs were stained as described before using rat anti-AmH (1:500) and mouse anti-beta-galactosidase (1:20) (developed by J.R. Sanes; obtained from Developmental Studies Hybridoma Bank [DSHB], Department of Biological Science, University of Iowa City, IA 52242). Pupal nota were dissected as described earlier [6, 28] and stained with rat anti-elav 7E8A10 and mouse anti-pros MR1A (each 1:10) (developed by G.M. Rubin and C.Q. Doe, respectively; obtained from DSHB).
Secondary antibodies coupled to fluorescein and Cy3 were purchased from Jackson Laboratory. Samples were mounted in Vectashield (Vector Lab) and analyzed on a Zeiss Axioskop linked to a Bio-Rad MRC1024 confocal microscope. Fly body parts were dehydrated in ethanol and mounted in Euparal or Hoyer's medium. Pictures were taken on a Zeiss Axiophot with Nomarsky optics. Pictures of adult flies were taken with a Pixera camera on a Wild 5M stereo-microscope using Pixera Viewfinder 2.0. They were assembled using Corel Photo Paint and Corel Draw software.
The Apis mellifera Hairless sequence is available from the EMBL Nucleotide Sequence Database under the accession number: AM849041.
We gratefully acknowledge U. Walldorf for the A. mellifera cDNA library and A. Bravo-Patiño for creating UAS-HΔAD transgenic lines. We thank the DSHB for antibodies. We greatly acknowledge W. Ulrich and W. Staiber for scanning electron micrographs and photography, and A.C. Nagel for critically reading of the manuscript.
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