TnaA, a trithorax group protein, modulates wingless expression in different regions of the Drosophila wing imaginal disc

wingless expression is exquisitely regulated by different factors and enhancers in the imaginal wing discs of Drosophila melanogaster in four domains: the dorsal band, the dorso-ventral boundary, and the inner and outer ring domains. tonalli is a trithorax group gene that encodes a putative SUMO E3 ligase that binds to chromatin to regulate the expression of its targets, including the Hox genes. However, its role in modulating gene expression is barely known. Here, we show that TnaA modulates the wingless expression at two domains of the wing disc, the dorso-ventral boundary and the inner ring. At first, tonalli interacts genetically with Notch to form the wing margin. In the inner ring domain, TnaA modulates wingless transcription. When the dosage of TnaA increases in or near the inner ring since early larval stages, this domain expands with a rapid increase in wingless expression. TnaA occupies the wingless Inner Ring Enhancer at the wing disc, meanwhile it does not affect wingless expression directed by the Ventral Disc Enhancer in leg discs, suggesting that TnaA acts as a wingless enhancer-specific factor. We describe for the first time the presence of TnaA at the Inner Ring Enhancer as a specific regulator of wingless in the development of wing boundaries.


Results
tonalli genetically interacts with Notch at the D/V boundary wing disc to form the wing margin.The wing disc is divided into different regions according to complex gene expression patterns.One of the genes that is expressed in these regions is wg (Fig. 1A).
In previous work, we identified modifiers of the BRAHMA complex that include tna 12 .Individuals with mutations in some of these BRAHMA modifiers, which did not include tna at that time, have notched wings among other phenotypes 15 .This notched wing phenotype resembles that exhibited by individuals with defects in the Notch signaling pathway at the D/V boundary of the wing disc (Fig. 1B).
To investigate whether tna is related to Notch signaling, we assayed the genetic interaction of N with tna, looking for the notched-wing phenotype in flies carrying the null N allele, N 55e11 , in combination with different tna alleles that include tna 1 , tna 5 , tna EY22929 and tna MI01482 (Fig. 1B, and Table 1, for location and description of the alleles, see Sup.Fig. 1A, and "Methods").Female heterozygote individuals carrying any of the tested tna alleles have normal wings (e. g. tna 1 /+, Fig. 1B, Table 1).Most N 55e11 /+ females (82%) have wings with notches located at the distal tip of the wing blade (weak phenotype), while in the presence of tna 1 (N 55e11 /+; tna 1 / +), the flies show extensive notches located mainly along the posterior wing margin with strong (74%) or weak (7%) expressivity.Individuals with the other tested tna alleles also show the notched-wing phenotype with different penetrance and expressivity (Table 1).N 55e11 /+; tna 1 /+ mutant flies present a strong notched-wing phenotype, as Figure 1.Genetic interaction of tna with Notch and wg expression in the wing disc.(A) Schemes of wg expression domains in the wing disc (green, upper panel) and their developmental fate in an adult wing (bottom panel).(B) Adult wings with N and/or tna mutant genotypes.Penetrance and expressivity of the notchedwing phenotype are classified as weak or strong when a single or several notches, respectively, are present in a wing margin.Quantification of each class is shown in Table 1.(C) Wingless signal in wing discs of N and/or tna mutant genotypes.Note that Wingless is further reduced at the D/V boundary domain in N 55e11 /+; tna 1 /+ wing discs (solid arrowhead, magnified in the right panels).(D) Quantification of Wingless in wing discs of the indicated genotypes (see Sup. Fig. 4B).Student's t-test was performed for signal intensity in each bin (P < 0.05*).
www.nature.com/scientificreports/ the more evident loss-of-function phenotype of N, suggesting that TnaA is required for activities of the Notch pathway related to the formation of the wing dorso-ventral boundary.
We also tested the genetic interaction between tna and Su(H) by combining the loss-of-function Su(H) 116 and the alleles tna 1 and tna EY22929 .We found that wing-notching in transheterozygote Su(H)/+; tna/+ individuals increases slightly with respect to notched wings of individuals carrying only the Su(H) 1 allele (16% for Su(H) 1 /+; tna 1 /+, 8% for Su(H) 1 /+; tna EY22929 /+ compared to 3% for Su(H) 1 /+ individuals) (Table 1 and Sup.Fig. 2A) 17 .Thus, there is a genetic interaction between tna and Su(H) although it is not as strong as the one found in N 55e11 /+; tna/+ individuals (Fig. 1B and Table 1).
Since wg expression is controlled by the Notch pathway at the D/V boundary 4,5 , we evaluated the Wingless protein level in wing discs of N 55e11 /+; tna 1 /+ flies.We found that the level of Wingless decreases, in correlation with the observed phenotypes in adult wings (Fig. 1C).Although the Wingless level at the D/V boundary is intact in discs from tna 1 /+ individuals, it is reduced in a few cells at the center of the D/V boundary in discs of N 55e11 /+ genotype.The latter phenotype is enhanced in N 55e11 /+; tna 1 /+ animals (Fig. 1C) and in all combinations of tna alleles tested (Table 1).Quantification of this phenotype is presented in Fig. 1D and Sup.Fig. 4A.
To further test this finding, we asked whether the Wingless protein level decreased in tna 1 clones (Sup.Fig. 3) that cross the D/V boundary since the expression of wg is controlled by NICD in this region 4,5 .In fact, we found that this is the case (Fig. 2A).Consistently, quantification of the Wingless signal is reduced almost 50% in these tna − clones (Fig. 2B), and adult wings derived from these wing discs present notches (Sup Fig. 2B).
Next, we directed the expression of an epitope-tagged version of TnaA 123 that we will name from now on TnaA-Flag, to the D/V boundary.As wild-type TnaA, TnaA-Flag is nuclear (Sup.Fig. 1B), binds to the same bands in polytene chromosomes (Sup.Fig. 1C), and, albeit partially, complements the lethality of tna − individuals (see "Methods").We found that in the presence of TnaA-Flag, Wingless show a two-fold increase along the D/V boundary (Fig. 2C,D and Sup.Fig. 4B), in contrast to the Wingless decrease found in this domain in tna − clones (Fig. 2B), further supporting the notion that TnaA regulates wg expression.
We also analyzed the effect of TnaA-Flag presence at the D/V boundary on the levels of Cut whose expression is controlled by NICD in this region 5 (Fig. 3A).We observed that Cut diminishes considerably at the D/V boundary of these wing discs (Fig. 3A,C, and Sup.Fig. 4B) that develop into defective adult wings (Sup.Fig. 2C).These results are similar to those observed by others in Su(H) mutant individuals 18,19 , suggesting a functional relationship between tna and Su(H).
Next, we tested whether TnaA directly affects Notch-mediated transcriptional activation.We measured GFP expression in flies bearing a Notch pathway reporter construct NRE-GFP (Notch Responsive Element, NRE) 20 .We found that in the presence of TnaA-Flag, the expression of NRE-GFP is substantially reduced, indicating that TnaA interferes with the CSL complex-mediated activation of the NRE-GFP reporter in this specific region of the wing disc (Fig. 3B,C).
We conclude from the loss-of-function experiments that tna is interacting with the Notch pathway to control the level of Wingless at the D/V boundary domain of the wing disc.In addition, the positive and negative effects of TnaA-Flag on wg and ct, respectively, agree with the reported formation of Su(H)-CSL activating and repressor complexes on the promoters of these genes under Su(H) overexpression 18,19 (see "Discussion").
TnaA modulates the expression of wg in the IR domain of the wing disc.We previously established that tna genetically interacts with the Notch pathway to control the level of Wingless protein at the D/V boundary.Next, we knocked-down TnaA (a decrease of approximately 70% with respect to the wild-type level), Table 1.tna interacts genetically with N and Su(H).a N 55e11 /FM0 female virgins were crossed with males carrying different tna alleles.b Number of individuals with the notched-wing phenotype.Penetrance and expressivity of the notched-wing phenotype are classified as weak or strong when a single or several notches, respectively, are present in a wing margin (see Fig. 1B).The percentages are indicated in parentheses.The results are a compilation of F1 of at least four independent crosses.Statistical significance in each case was determined with x 2 (P < 0.05) as stated in "Methods".by expressing a tna RNAi (tna JF02536 , 13,21 ) in the anterior compartment of the wing disc (Sup.Fig. 5) and assessed Wingless levels in their different expression domains (IR and D/V boundary) in this compartment.In this otherwise wild-type background, we did not observe any Wingless fluctuation in any of the evaluated regions, compared to the correspondent regions at the posterior compartment that are expressing wild-type TnaA levels (Sup.Fig. 5).We reasoned that the TnaA knockdown level reached by the expression of tna JF02536 RNAi may not be enough to knock down the robust Wingless expression in the different regions of the disc.We hypothesized that TnaA may act on a particular wg-regulatory element.wg has several embryonic and larval enhancers.One of the larval enhancers is the wing disc IR enhancer (IRE), located about 9 kb upstream the wg promoter 10 .We chose to test the TnaA requirements for the function of this enhancer in an IRE sensitized background.We used a line that carries the wg spd-fg allele, which is a small deletion that removes the IRE region.Wing discs where the deletion is homozygous lack wg expression at the IR while the one at the D/V boundary remains unchanged 10 .When the IRE is haploinsufficient, the Wingless signal looks normal in the IR and in the D/V (Fig. 4A, wg spd-fg / +).The quantification of the Wingless and TnaA signals in each of these regions is shown in Fig. 4B.In contrast, when TnaA is knocked down in the anterior compartment of the wing disc (wg spd-fg /+, ci > tna JF02536 ), there is a decrease in the Wingless signal in the anterior half of the IR (Fig. 4A, wg spd-fg /+, ci > tna JF02536 ).An internal control of this experiment is the normal Wingless signal observed in the posterior IR region where tna JF02536 is not expressed.Moreover, in this wg spd-fg /+ background, Wingless is not reduced at the D/V boundary as expected, since the IRE does not control the wg expression in this domain.The quantification of the TnaA and Wingless levels in these discs is shown in Fig. 4B.
To complement these data, we directed tna-Flag expression to the anteroposterior (A/P) margin of the wing disc (Fig. 4C,D).In this case, we did observe TnaA-Flag effects on wg expression at both the D/V boundary and the IR (Fig. 4C, open and solid arrows, and quantification of the Wingless signal for each region in Fig. 4D and Sup.Fig. 4C).In response to TnaA-Flag, wg expression increases at the D/V boundary (Fig. 4C, open arrowhead).At the IR, wg expression is also increased, and its expression domain is expanded (Fig. 4C solid arrows).Adult wings derived from these discs show defects along the A/P boundary, including the hinge (Sup.Fig. 2D).
directed by a well characterized early enhancer 27 .In early third instar larvae, the expression of wg is detectable in the D/V boundary and the IR 7,27 (Fig. 5A).We investigated whether TnaA acts at a specific time of larval wing disc development.For this goal, we used the TARGET system, which inactivates the GAL4 repressor (GAL80ts) with temperature shifts 28 .We applied temperature shifts to inactivate GAL80ts at specific times along the development of the wing discs.This allowed us to accurately control the induction of tna-Flag expression in the MS1096-GAL4 driver pattern between second and third instar larval stages (72 h AEL) 29,30 (Fig. 5A, see "Methods").We found that as a result of tna-Flag expression since the first instar larval stage (36 h AEL), there is a strong expansion of the IR towards the pouch (Fig. 5A,B).At the third instar larval stage (90 h AEL), induction of tna-Flag expression causes a milder expansion of the IR domain than the one observed when induced at an earlier developmental stage (Fig. 5B, solid arrow).
We also studied whether cells in different regions of the wing disc could induce wg expression in response to TnaA dose.To approach this question, we induced clones expressing tna-Flag on the entire disc at 82 h AEL using the FLP-out technique (Fig. 5C and "Methods").As previously shown, there is an expansion of the IR towards the pouch or the hinge when clones locate at/or near the IR (Fig. 5C, solid arrowheads).We also noticed that these cells rapidly increase the Wingless level in response to TnaA-Flag since the clones were induced only 24 h before dissection.In contrast, clones far from the IR, in other regions of the wing disc, such as the notum or ventral pouch (Fig. 5C empty arrowhead), do not show almost any increase in the level of Wingless.This indicates that proximity to the IR domain is important for the regulation of wg transcription mediated by TnaA.
These results show that TnaA-Flag can activate the expression of wg in the IR even before this domain is resolved in early to mid-third instar larvae.This TnaA-Flag effect is milder but is still observed when its expression is induced after the IR formation.Moreover, TnaA-Flag can rapidly increase wg expression, particularly in cells at or near the IR, with expansion of this domain.Altogether these results suggest that regulatory regions that modulate wg expression in the IR are available and highly sensitive to TnaA doses in specific stages of larval development.TnaA directly affects wg transcription at the IR.We followed the expression of the wg-lacZ reporter 22 at the IR in wing discs where tna-Flag expression was directed to the dorsal hinge with the MS1096-GAL4 driver 23 .This allowed us to monitor the expansion of the IR domain on the dorsal side of the wing disc, leaving the ventral side as an internal control (Fig. 6A,B).We found that under this condition, the expression of tna-Flag increases wg transcription (Fig. 6C).This causes a strong expansion of the dorsal IR domain towards the pouch, making it hard to distinguish it from the D/V boundary.As tna-Flag is not expressed in this region, the ventral IR looks normal (Fig. 6C).We also corroborated that both the A/P and D/V boundary domains remained intact in these wing discs, by monitoring the expression of dpp-lacZ 24 and Dll-lacZ 25 , respectively (Fig. 6D,E).These results reinforce the notion that TnaA specifically influences the transcription of wg at the IR domain.
The wg locus has several enhancers that control its expression in different regions or stages of development.Imaginal wg enhancers include the IRE that controls wg expression in the IR domain of wing and haltere discs 10 , and the VDE which controls the antero-ventral wg expression in leg and eye-antennal discs 8 (Fig. 7A).When the expression of TnaA is knocked down, the Wingless signal decreases in the IR in wing discs that harbor only one functional copy of the IRE (wg spd-fg /+, Fig. 4), suggesting that TnaA is involved in the regulation of wg expression through this enhancer.
To further test the idea that TnaA acts on specific regulatory regions of wg to modulate wg transcription in the IR domain, we expressed tna-Flag on T3 leg and wing discs using the rn-GAL4 driver 31 , and we compared the effect of TnaA-Flag on wg expression in both types of discs (Fig. 7B).We found that in the presence of TnaA-Flag, the Wingless level increases significantly at the wing (Fig. 7B, left), where the IRE and the putative D/V enhancers are active.In contrast, in the T3 leg discs, where wg expression is driven by the VDE 8 , the Wingless level is not altered or expanded (Fig. 7B, right), suggesting that TnaA influences specifically the IRE and not the VDE.
Then, we investigated whether TnaA and TnaA-Flag are present in the IRE in the chromatin of the larval wing discs.To determine this, we performed ChIP-qPCR assays of both proteins in the wg IRE and VDE enhancers (Fig. 7C).Chromatin from wing discs with wild-type TnaA or TnaA-Flag driven by MS1096 genotypes was immunoprecipitated with anti-TnaA TAIL (Sup.Fig. 1D) or anti-FLAG antibodies, respectively.The presence of TnaA in both enhancers was evaluated by qPCR amplification with the appropriate oligonucleotides (Fig. 7A).We found that both TnaA and TnaA-Flag are enriched in the IRE compared to their mock fractions (see "Methods")..Note that the ventral wg IR domain is not affected since the driver is not active in this region.(D) The D/V boundary followed by the Dll-lacZ reporter 25 .(E) The A/P boundary followed by the expression of dpp-lacZ 24 .

Discussion
In this work, we found that TnaA modulates the expression of wg at the D/V boundary and the IR domains in the wing disc.At the D/V boundary domain, TnaA modulates wg expression interacting with the Notch pathway, and at the IR domain, it promotes wg transcription probably through its specific binding to the wg IRE.
Several pieces of evidence in this work indicate that TnaA is involved in the transcription of Notch target genes expressed in the D/V boundary.TnaA plays a role in the transcriptional activation of wg in the D/V boundary domain mediated by CSL, the effector complex of the Notch pathway.The CSL complex consists of NICD, Mam, and Su(H).According to models based on genetic and biochemical data, NICD acts as a permissive signal (e.g., wg transcription), alleviating the repression imposed by corepressors bound to Su(H), while in others (e.g., ct and NRE-GFP transcription), NICD acts as an instructive signal by directly recruiting transcription factors to activate gene expression 32 .In this model, overexpression of Su(H) reduces ct expression, presumably because excessive Su(H) can titrate available NICD as well as any co-repressors 18,19 .ChIP-seq analyses 33 and studies on protein-enhancer dynamics 34,35 showed that NICD binding has different effects on the dwell time of CSL subunits in regulatory regions and on transcriptional outcomes depending on enhancer priming and the chromatin landscape.
Our data suggest that TnaA may facilitate the formation of CSL complexes at their dedicated promoters.Loss of TnaA decreases the Wingless signal in the D/V boundary in tna clones and enhances the decrease in wg caused by mutations in Su(H) or NICD 4,5 .Conversely, TnaA-Flag increases wg expression and reduces ct and NRE-GFP (Fig. 3), in a behavior similar to that found in wing discs with misexpression of Su(H).
Although the precise mechanism of the TnaA function remains elusive, these results fit the interpretation that TnaA is acting in the same direction as the CSL activator complex to facilitate wg expression in this region.Moreover, it is likely that TnaA could be involved in the regulation of the dynamics of CSL complexes or in the chromatin landscape around its target genes.TnaA also modulates the expression of wg in the IR (Figs. 4, 5, 6).The loss of TnaA diminishes the Wingless signal specifically in the IR in wg spd-fg /+ wing discs that are haploinsufficient for the wg IR enhancer 10 (Fig. 4a).In contrast, TnaA-Flag rapidly increases the Wingless signal at the IR, particularly before the wg IR domain is resolved in early to mid-third instar larvae.Its effect is milder after the IR formation.These results suggest that at least some regulatory regions that modulate wg expression in the IR are available and highly sensitive to TnaA doses throughout the development of the wing disc and may reflect the intrinsic ability of TnaA to interact with transcriptional activators and/or to find or influence chromatin changes to make its target regions available for preparation (as for enhancer priming), activation, or maintenance of wg expression in the TnaA is nuclear in all cells of the wing disc (this work, and 14 ).However, it modulates specifically the expression of wg at the D/V boundary and the IR domains.This indicates that TnaA is not promiscuous and that it probably targets regulatory elements of wg that are functional only in specific regions within the wing disc.The complex spatial pattern of wg in the wing disc is regulated through multiple regulatory regions.The broad band enhancer at the notum of the wing disc and the VDE ventral disc enhancer are very close to each other and together with the IRE are accurately located 5,8 .Furthermore, enhancers that specify wings and respond to damage have recently been located close to each other 27 .In contrast, the location of the D/V boundary enhancer that is controlled by the Notch pathway 4,5 is not known.
We found that TnaA and TnaA-Flag are in the IRE (Fig. 7C), influencing the expression of wg.To the best of our knowledge, there is not yet a compilation of which proteins are in this enhancer under wild-type conditions when the enhancer is primed, active, or inactive.Good candidates are key factors for the initiation and establishment of wg expression in the IR domain.These are Nubbin, Rotund, Vestigial, and Scalloped 7,36,37 .Until now, there is little evidence supporting the direct binding of any of these proteins to the IRE and it will be important to determine whether any of them collaborate with TnaA.
The precise location of the Notch-responsive D/V boundary enhancer remains unknown, making it difficult to test whether TnaA binds to it.However, a region located at or near the IRE may mediate Notch regulation of wg.Under conditions with ubiquitous activation of the Notch pathway, NICD and Su(H) are in a region that includes the IRE and an IRE-GFP reporter construct responds to Notch activation 33,38 .When Su(H) is overexpressed, there is an increase in wg expression in the IR 18 .This evidence indicates that there is a Notch-responsive region at or near the IRE that could mediate the Notch regulation of wg at the D/V boundary.According to this, TnaA would modulate the expression of wg in the IR and in the D/V boundary domains by binding to a single region that comprises the IRE and, at least partially, the putative D/V boundary enhancer in the wing disc.Nevertheless, our own data show that there is no change in the Notch-regulated D/V wg expression in animals with a reduced dose of tna upon IRE haploinsufficiency (Fig. 4).Altogether, these data leave open the possibilities that the Notch-responsive regulatory region is not affected by the deletion harbored by the wg spd-flag allele or that it is located elsewhere.
We do not know whether TnaA is in the IRE in all cells of the wing disc or only in cells of the IR since our ChIP-qPCR experiments were carried out with chromatin from whole discs (Fig. 7C).In the wing disc, the IRE should only be active in the stripe of cells that form the IR (and probably in the ones that form the D/V boundary), but it is not known in which activity state the IRE is in other nuclei outside these wg expression domains.
Finally, it is interesting to discuss the role of TnaA in the function of the wg IRE and the D/V enhancers.TnaA is a putative SUMO E3 ligase whose targets could be protein factors recruited to the enhancer and/or histones in particular nucleosomes, histone modifiers, or chromatin remodelers surrounding it.In fact, TnaA has been implicated in the SUMOylation of subunits of the BRAHMA complex 12,14 .The BRAHMA complex has already been implicated in Notch signaling in Drosophila and vertebrates [39][40][41] .
Complexes recruited in enhancers must be very dynamic to respond to signaling at dedicated locations.The study of the mechanisms that help chromatin render a functional environment for the action of these complexes is of particular interest.SUMOylation can modify the activity, location and/or interaction of nuclear target proteins (reviewed in 11 ), and TnaA has two domains that are relevant in this context 12,14 .One is the 300 aminoacidic XSPRING domain with a signature zinc finger of a kind of SUMO E3 ligases and a glutamine-rich region that can help recruit transcription-related factors that also have glutamine-rich regions 42 .Although the specific role of TnaA in wg transcription is not clear, one possibility is that it helps one or more regulatory factors to facilitate their exchange on enhancers such as the wg IRE at the wing disc.
Our data suggest that TnaA is an enhancer-specific factor of wg, modulating only the wg D/V and IR enhancer(s) of the wing imaginal disc.We do not know whether this effect is caused by the interaction of TnaA with a factor that is common to both enhancers or whether they bind to different proteins.Furthermore, if the wg IRE is subjected to the same kind of dynamics discovered for the CSL enhancers, TnaA may play a role in the mechanisms that determine the timing and exchange of the proteins recruited to switch the enhancer to its active or inactive forms.It remains a challenge to determine, in the tightly regulated multiple-tier network of wing disc proliferation and patterning processes, the different elements that help TnaA find, engage and exert its function at specific target genes in different wing disc domains.This will be important in understanding the role of TnaA in this context and in a genome-wide perspective.

Methods
Ethics statement.Drosophila melanogaster handling was approved by the Instituto de Biotecnología, UNAM, Bioethics Committee, Permit Number 359, which follows NOM-062 animal welfare Mexican law.No other animals were used in this study.All efforts were made to minimize animal suffering.Flies were sacrificed by CO2 euthanasia.
Fly strains, growth, and genetic procedures.The lesions of N, Su(H), wg, tna alleles, lacZ reporters for some genes, and GAL4 driver lines used in this work are, unless otherwise noted, described in Flybase 43 .The mutant alleles of tna used in this work are shown in Sup.Fig. 1A.Briefly, tna 1 , tna 5 are dominant negative and null EMS-derived alleles, respectively.tna EY22929 is a hypomorphic P{EPgy2} element insertion-derived allele 44 .These three alleles are described in 13 .tna MI01482 is a MiMIC element insertion-derived allele 45 .tna knockdown was achieved by expressing interference RNA (RNAi) from the tna JF02536 line from Perrimon's pVALIUM10derived TRiP collection 21 , using different drivers.The efficacy of tna knockdown of this line (tna JF02536 ) was previously characterized 13 .
The reporter construct NRE-GFP (Notch Responsive Element, NRE) has three Grainy Head (Grh) binding sites, followed by two pairs of Su(H)-binding sites from the Enhancer of split m8 [E(spl)m8] gene which is regulated by Notch as an instructive signal 20 .
The wg spd-fg allele is a small deletion that removes the IRE region that, hence, lacks wg expression at the IR but the one at the D/V boundary appears to remain unaltered 10 .
Fly culture and crosses were performed according to standard procedures.Flies were raised in yeast-molasses media at 25 °C unless otherwise noted.
Notched-wing phenotypes were scored in adult animals with tna mutant alleles under a Notch loss-offunction genetic background.Penetrance and expressivity of the notched-wing phenotype were classified as weak or strong depending on the presence of single or several notches respectively in a wing margin (see Fig. 1B and Table 1).Adult wings were dissected in 70% ethanol, mounted onto slides in isopropanol, and immediately imaged with an Amscope UCMOS05100 camera attached to a Nikkon Eclipse E600 microscope.The statistical significance of the Notch loss-of-function phenotypes was determined using a t-test (P < 0.05) in animals obtained from at least three independent crosses for each genotype.
tna 1 homozygous clones were generated by homologous recombination using Ubx-FLP 46 as described in 13 .Clones expressing tna-Flag were generated with the FLP-out technique 47 .To remove the stop cassette in hs-FLP, UAS-mCD8::GFP; UAS-tna-Flag/+; Act5C-STOP-GAL4 larvae, we induced a heat-shock in these animals at 82 h AEL in a water-bath for 15 min at 35 °C.In both cases, the wing imaginal discs were dissected from wandering third instar larvae at 96 h AEL and immunostained as described in the following section.
To induce the expression of tna-Flag at different stages of development, we used the Temporal and Regional Gene Expression Targeting (TARGET) system 28 .MS1096-GAL4, UAS-GFP; UAS-tna-Flag/+; tub-GAL80 ts /+ animals were grown at 18 °C and then shifted to 29 °C at 36, 60 and 90 h AEL.Temperature changes were applied at least 12 h before and after the appearance Wingless in the pouch (48 h AEL) and IR (72 h AEL).Wing discs were dissected at around 96 h AEL and tna-Flag expression was corroborated by immunostaining with anti-TnaA TAIL antibody (1:250, see ahead).The results were compared with the ones obtained with flies without induction (grown at 18 °C) or with full induction (grown at 29 °C).
Characterization of epitope-tagged TnaA-Flag Drosophila transgenic lines.TnaA-Flag is a tagged version of TnaA 123 from the Iso1 strain, which is the main nuclear isoform derived from the tna locus 13,14 .The FLAG epitope (DYKDDDDK) was inserted into the carboxy-termini of TnaA 123 , precisely after the last amino acid (Asp1109).The correct tagging was confirmed by DNA sequencing of the construct.The epitopetagged TnaA version was subcloned in the pUAST plasmid, where its expression is controlled by the GAL4-UAS system 48 .The correct molecular weight of TnaA-Flag was confirmed by Western analysis of soluble protein extracts from wing discs using the anti-TnaA XSPRING antibody (Sup.Fig. 1E).
Independent transgenic yw; UAS-tna-Flag lines were obtained, and the different insertions of the transgene (w + ) were mapped to different Drosophila chromosomes with subsequent balancing using classical genetic techniques.The TnaA-Flag protein from several transgenic lines, expressed with different strong and weak drivers, was tested for complementation of lethality caused by heteroallelic tna mutant alleles.It partially rescues adult viability (2% of the expected progeny), probably due to incorrect time/space dosages of the TnaA-Flag version in the whole fly.TnaA-Flag, as the wild-type form, is nuclear in imaginal discs, as corroborated by immunostaining of imaginal discs of third instar larvae with the anti-Flag antibody (Sup.Fig. 1B).TnaA-Flag binds to the same polytene bands as wild-type TnaA 123 bands (Sup.Fig. 1C).

TnaA antibodies and Western blot analyses.
To detect TnaA in this work, we used affinity purified anti-TnaA XSPRING and anti-TnaA TAIL antibodies.Briefly, antibodies were raised in rabbits against different regions of the TnaA 123 isoform encoded by the tna-RD transcript (Sup.Fig. 1D), identified and sequenced by 49 , and reported by Flybase 49 .The anti-TnaA XSPRING is described in Rosales-Vega et al. 13 , and the anti-TnaA TAIL was raised against the 21-mer DVDPMEILSYLDPQPDLNTPPS peptide (aminoacids 1070-1091 of TnaA 123 ) by ProSci, Inc.Both antibodies were affinity-purified from total sera.Western blot analyses of TnaA and actin in soluble protein extracts from wing discs (Sup.Fig. 1E) were performed in duplicate from two different biological replicates with soluble protein extracts from 30 wing discs of each genotype with the appropriate antibodies and were performed as specified in 13 .The membrane chemiluminescence imaging was acquired using a BioRad ChemiDoc imaging system.The raw images were not processed in any manner, and the average level of the normalized signal intensity of the indicated bands with respect to the wild-type levels (dashed line), is represented as bars with standard deviation in Sup.Fig. 1E.These proteins were detected with anti-TnaA XSPRING and mouse anti-Actin (JLA20, Developmental Studies Hybridoma Bank) antibodies, used at 1:250 and 1:3000 dilutions, respectively.Secondary antibodies used were anti-rabbit HRP goat IgG (H + L) (62-6129), and anti-mouse HRP goat IgG/IgA/IgM (H + L) (A106868) (Invitrogen) used both, at 1:5000 dilutions.
Quantification of signal intensity in confocal images.The presence of Wingless, Cut, and NRE-GFP was quantified using the plot profile tool from Fiji (ImageJ) v. 1.0.The mean grey value was used as a measure of the intensity of the signal in rectangular areas and its average value was obtained with measurements of at least six wing discs of each genotype.Statistical analyses of differences in signal intensity, were performed using Student's t-test (with P-values ≤ 0.05*).
To measure the differences in wg expression in the genetic interaction between tna and N, we measured the intensity of the signal in ten bins of 20 µm in width around the center of the wing disc (Sup.Fig. 4A).To measure changes in the levels of Wingless, Cut, and NRE-GFP in C96 > tna-Flag wing discs, we normalized the signal intensity values by subtracting the signal intensity in TnaA-Flag (+) cells from that in TnaA-Flag (−) cells.(Sup.Fig. 4B).To quantify changes in wg expression in ptc > tna-Flag wing discs, we applied the same normalization procedure as in Sup.Fig. 4. The signal intensity was quantified in the pouch, IR, and D/V (Sup.Fig. 4C).

ChIP-qPCR analyses. Chromatin immunoprecipitation was performed on 60 wing imaginal discs from
OreR wandering third instar larvae per biological sample as described in 57 with minor changes.IgA-and IgGcoupled Dynabeads (Invitrogen), were used in a 1:1 ratio for chromatin immunoprecipitation in place of protein A or G agarose/salmon sperm DNA beads.Immunoprecipitations were performed with irrelevant antibodies that do not bind nuclear proteins and serve as Mock samples (rabbit IgG, Invitrogen #02-6102, and mouse IgG, Invitrogen #02-6502), or with 5 µg of affinity purified anti-TnaA TAIL .Three biological samples were obtained in each case and quantitative PCR (qPCR) reactions with the appropriate oligonucleotides were performed to amplify the selected IRE or VDE regions (indicated in Fig. 7).The experiments were carried out with three replicates of each biological sample.
qPCR reactions of different wg regions immunoprecipitated with the anti-TnaA TAIL antibody were performed as described by 58 , in a Lightcycler 480 Real-time PCR system (Roche Applied Science) using the Maxima SYBR Green/Rox qPCR Master Mix (2X) (Thermo Scientific).The wg regions targeted for qPCR amplification are shown in Fig. 7. Oligonucleotide sequences to amplify a 128-bp region within the IRE are Fwd 5′-AAA GTT ATG GGC CTC CGT CT-3′ and Rev 5′-CTG GCC GAA GAG AAG TCA TC-3′, and those used to amplify a 149-bp region of the VDE, used as a negative control, are Fwd 5′-GGA CTG GAG TGG ACG GAT TT-3′ and Rev 5′-CCT AAT TCA CGC GCC AAA GT-3′.The quantification of TnaA by ChIP-qPCR on wg IRE in wing discs was calculated as fold enrichment over background signal and is the average of three independent biological samples with three replicates each.Statistical analyses of differential accumulation of TnaA between samples were performed using Student's t test, P-values ≤ 0.05.

Figure 2 .
Figure 2. Wingless at the D/V boundary in tna-deficient and tna-Flag expressing wing discs.(A) Wingless signal in tna 1 clones (non-GFP cells) induced in the D/V boundary with Ubx-FLP 46 .Dashed squares in the images in the upper panel indicate the amplified region in the lower panel.(B) Quantification of the intensity of the Wingless signal at the D/V boundary in tna + and tna − cells (C) Wingless signal in tna-Flag expressing discs at the D/V boundary driven by the C96-GAL4 driver 59 .The discs were immunostained for TnaA and Wingless with the corresponding antibodies ("Methods").(D) Quantification of Wingless in tna + and tna − cells as indicated in Sup.Fig. 4B.Student's t-test was performed for the intensity of the signal in (B) and (D) (P < 0.01**).

Figure 3 .
Figure 3. Cut and NRE-GFP signal in wing discs expressing tna-Flag along the D/V boundary.The expression of tna-Flag was driven to the D/V boundary with C96-GAL4 59 .(A) TnaA and Cut signals on C96-GAL4 wing discs (upper panel), or in C96 > tna-Flag wing discs (lower panel).(B) TnaA and NRE-GFP signals in wing discs of genotypes as in (A).Note the reduction of Cut and NRE-GFP signals along the D/V boundary domain (C) Quantification of Cut and NRE-GFP in the D/V boundary of wing discs of the indicated genotypes (n ≥ 5 discs).See also Sup.Fig. 4B.Student's t-test was performed for signal intensity in each case (P < 0.0001****).

Figure 4 .
Figure 4. Effect of the dosage of TnaA on wg expression in the IR (A) The Wingless signal in the IR decreases when TnaA is knocked down in wg spd-fg /+ wing discs.Immunostainings of TnaA and Wingless in wing discs of the indicated genotypes.TnaA was knocked down in the anterior compartment with the expression of the tna JF25036 RNAi driven by the ci-GAL4 in wg spd-fg /+ discs (wg spd-fg /+; ci > RNAi-tna JF02536 ).The dashed rectangles (right upper panels) show the amplified region (right lower panels) where the A/P margin is indicated.(B) The wg spd-fg allele is a small deletion that removes the IRE region (upper diagram) and directs the expression of wg to the IR (green), but not to the D/V boundary (grey).Quantification of TnaA and Wingless A/P signal ratio in the D/V boundary and IR in discs with the indicated genotypes (lower panel).(C) TnaA and Wingless signals in wing discs that express tna-Flag at the anteroposterior margin driven by ptc-GAL4 60 that is active since the early second instar stage 61 .The IR (white arrows) and the D/V boundary (empty arrowhead) regions on the A/P axis are indicated (D) Quantification of the Wingless signal in the pouch, D/V and IR in ptc > tna-Flag wing discs (n ≥ 6 discs).See also Sup. Figure 4C.Student's t-test was performed for signal intensity in (B) and (D) in each case (P < 0.05*, P < 0.01**, P < 0.001***).

Figure 5 .
Figure 5.The TnaA-Flag effect depends on its timing of appearance and proximity to the IR during larval development.(A) Developmental timeline (E, Embryo, L1-L3 larval stages) according to hours after egg laying (h AEL).The time when the expression of wg is resolved in the D/V and IR domains (green arrowheads), and the temperature shift times applied to inactivate Gal80ts to allow expression of MS1096 > tna-Flag at the dorsal hinge (pink arrowheads) are indicated.(B) TnaA and Wingless distribution in wing discs expressing tna-Flag at specific times from 36 to 90 h AEL.Note the expansion of the Wingless signal from the IR (white arrow) but not from the D/V boundary domain (empty arrowhead).(C) Expression of wg in TnaA-Flag clones in different regions of the wing disc.TnaA and Wingless immunostainings are indicated, and merged images are shown (right panels).Images from two discs show a TnaA-Flag clone at the IR (upper panel) or near the IR (middle and lower panels).A TnaA-Flag clone in the pouch does not cause an induction of wg expression (middle panel, empty arrowhead).TnaA-Flag clones at/or adjacent to the wg IR domain present the induction of wg expression (middle and lower panels, solid arrowheads).Dashed squares (middle panel) indicate the region amplified in the lower panel.

Figure 6 .
Figure 6.TnaA-Flag transcriptional effect on wg expression in the IR.The expression of tna-Flag was driven to the dorsal hinge with MS1096-GAL4 23 .(A) Scheme of the expression domain of MS1096 > tna-Flag (magenta) and the wg expression pattern (green) in a wing imaginal disc.Under this condition, the expression of tna-Flag overlaps only with the wg IR dorsal side and not with the ventral side, which could be used as a control in the same disc.(B) MS1096 > GFP wing discs showing GFP expression on the dorsal hinge (left), Wingless signal (middle) and merged image (right).(C-E) MS1096-GAL4 and MS1096 > tna-Flag wing discs, immunostained for TnaA (magenta) or LacZ (green).(C) Expression of the transcriptional reporter wg-lacZ62 .Note that the ventral wg IR domain is not affected since the driver is not active in this region.(D) The D/V boundary followed by the Dll-lacZ reporter25 .(E) The A/P boundary followed by the expression of dpp-lacZ24 .

Figure 7 .
Figure 7. TnaA and TnaA-Flag are in the IRE in the wing disc.(A) Scheme of the wg locus showing the IRE and VDE that control wg expression in the wing and T3 leg discs (upper panel).The localization of the regions used (green lines) to evaluate the presence of TnaA by ChIP-qPCR with the anti-TnaA TAIL antibody is indicated.(B) TnaA and Wingless immunostainings of the rn-GAL4 and rn > tna-Flag wing and T3 leg discs (upper and lower panels, respectively).The expression of tna-Flag was directed to the distal part of the discs with rn-GAL4 which is active since the late second instar stage 31 .Note that the TnaA-Flag wing disc shows expansion of the IR domain (green) that is correlating with the presence of TnaA in the IRE in the wing discs.In contrast, the morphology and the Wingless expression pattern are normal in the TnaA-Flag T3 leg disc, where the IRE is not active.(C) TnaA ChIP-qPCRs of the wg IRE and VDE in chromatin from wild type wing discs (left).The presence of TnaA-Flag in the IRE was determined by ChIP-qPCR with a FLAG antibody in MS1096 > tna-Flag discs (right).qPCR reactions with immunoprecipitated DNA samples with anti-TnaA TAIL , anti-FLAG, or with irrelevant antibodies (rabbit and mouse IgG for TnaA and TnaA-Flag, respectively; see "Methods") were performed with the indicated primer sets to amplify the selected IRE or VDE regions indicated in (A) (black vertical lines).Results are shown as fold enrichment over the background signals.Student's t-test was performed on qPCR enrichments in the regions tested (P < 0.001***).