Sex differences in physiology and disease susceptibility are commonly attributed to developmental and/or hormonal factors, but there is increasing realization that cell-intrinsic mechanisms play important and persistent roles1,2. Here we use the Drosophila melanogaster intestine to investigate the nature and importance of cellular sex in an adult somatic organ in vivo. We find that the adult intestinal epithelium is a cellular mosaic of different sex differentiation pathways, and displays extensive sex differences in expression of genes with roles in growth and metabolism. Cell-specific reversals of the sexual identity of adult intestinal stem cells uncovers the key role this identity has in controlling organ size, reproductive plasticity and response to genetically induced tumours. Unlike previous examples of sexually dimorphic somatic stem cell activity, the sex differences in intestinal stem cell behaviour arise from intrinsic mechanisms that control cell cycle duration and involve a new doublesex- and fruitless-independent branch of the sex differentiation pathway downstream of transformer. Together, our findings indicate that the plasticity of an adult somatic organ is reversibly controlled by its sexual identity, imparted by a new mechanism that may be active in more tissues than previously recognized.
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We thank K. Vanezis and L. Game for technical assistance, and C. Gonzalez, T. Carroll and D. Perea for discussions. B. Baker, A. Bardin, A. Baena-Lopez, S. Bray, A. Casali, T. Cline, S. Cohen, D. Eberl, S. Goodwin, G. Jefferis, L. Jones, R. Niwa, B. Prud’homme, I. Salecker, L. Sanchez, C. Thummel, J. Treisman, M. Vidal, D. Yamamoto and L. Zwiebel shared reagents. D. Hadjieconomou, J. Jacobson, G. King and E. Parra-Peralbo provided comments on the manuscript. This work was funded by an ERC Starting Grant to I.M.-A. (ERCStG 310411) and MRC intramural funding. B.H. holds an EMBO long-term fellowship and I.M.-A. is a member of, and is supported by, the EMBO Young Investigator Programme.
The authors declare no competing financial interests.
Extended data figures and tables
a, Number and percentage of genes with sexually dimorphic gene expression, as revealed by RNA-seq transcriptional profiling of virgin male and female dissected midguts (P < 0.05 cutoff). b, Volcano plot displaying all genes with detectable midgut expression. Female/male ratio of gene expression is shown on the x axis (in log2 scale) and significance is displayed on the y axis as the negative logarithm (log10 scale) of the adjusted P value. Genes with significantly upregulated (P < 0.05 cutoff) expression in males and females are coloured in blue and red, respectively. Other genes are displayed in black. Genes with known sex-specific transcription are displayed as red (female-enriched) or blue (male-enriched) open circles. c, d, Comparable analyses for sex-biased isoforms belonging to genes with multiple transcripts. We identifed 714 sex-biased isoforms belonging to a total of 603 genes. Isoforms resulting from known sex-specific alternative splicing are displayed as in panel b. e, Female/male ratios of overall transcript abundance (left graph) and abundance of sex-biased isoforms (right graph) for the members of the Drosophila sex determination pathway as revealed by RNA-seq analysis of the adult midgut. We note a sexual dimorphism in dsx transcript levels. f, Venn diagram illustrating the overlap between the genes showing sex-biased expression (overall transcript abundance, light grey, 1,305 genes) and sex-biased alternative splicing (sex-biased isoforms, dark grey, 603 genes) in the adult midgut. Known members of the sex determination pathway are displayed as examples. g, Heat maps displaying genes with sexually dimorphic expression clustered by enrichment in specific biological processes, as revealed by Gene Ontology enrichment analysis. Genes with sexually dimorphic expression belonging to the top 4 enriched biological processes are shown. h, i, Real-time qRT–PCR data for a subset of genes for which RNA-seq transcriptional profiling experiments revealed sexually dimorphic expression (h) or isoforms (i). RNA was obtained from midguts from virgin male and female samples (same genotypes as for the RNA-seq experiments). For each gene/isoform, expression abundance was arbitrarily set up at 100% for the sex with the highest expression level, and percentage of that expression is displayed for the other sex. See Methods for details and Supplementary Table 1 for a full list of names and quality scores, and Supplementary Information for full genotypes.
Extended Data Figure 2 Cell type-specific expression of sex determinants in the adult intestinal epithelium of virgin flies.
a, In the adult Drosophila midgut, resident stem cells (ISCs) and their postmitotic daughter cells (EBs) maintain the adult intestinal epithelium during normal homeostasis and regenerate it after injury by giving rise to two types of differentiated progeny: ECs and EECs80,81. The posterior midgut area used to visualize and quantify phenotypes is boxed. The following Gal4 drivers were used to label and/or genetically manipulate these four different cell types present in the adult intestinal epithelium: mex1 for ECs, prosv1 for EECs, esg for both ISCs and EBs, and Supressor of Hairless (Su(H)) for EBs alone. b, The canonical sex determination pathway in somatic cells of Drosophila melanogaster, consisting of a cascade of sex-specific alternative splicing events culminating in the production of sex-specific transcription factors encoded by Dsx and FruM. In females, Sex lethal (Sxl) is activated and regulates the splicing of transformer (tra) pre-mRNA, resulting in the production of TraF. TraF regulates the female-specific splicing of dsx pre-mRNA (dsxF) and fru transcript coming from the P1 promoter (fruP1, giving rise to fruM). In males, Sxl is not expressed and no functional Tra is produced, resulting in default splicing of dsx and fru pre-mRNAs, leading to FruM and DsxM proteins, respectively. The resulting male- and female-specific Dsx and Fru isoforms confer sexual identity to the cells in which they are produced. In addition, in females, Sxl represses dosage compensation by inhibiting Msl-2 expression. The tables summarize the cell-specific expression profiles of the sex determinants in adult midguts of virgin males and females, shown in the panels below. c, Sxl protein (in red) is expressed only in female midguts. Co-staining with ISC/EB reporters indicates that Sxl is found esg-positive progenitors (ISCs: GFP-positive and LacZ-negative cells, and EBs: GFP-positive and LacZ-positive cells). It is also expressed in female polyploid ECs (GFP- (in green) and LacZ- (in blue) negative cells). Co-staining with prosV1 reporter indicates that it is also expressed in EECs. d, Msl-2 protein is found in the same cell types only in males (staining is confined to the X chromosome, consistent with the signal observed in non-intestinal tissues82). e, A new reporter of tra promoter activity (tra-LacZ, see Methods for details) is broadly expressed in the epithelium of both male and female midguts, including ISCs and EBs (as revealed by co-staining with esg-Gal4-driven GFP) and ECs (GFP-negative cells with large nuclei). Co-staining with prosV1 reporter indicates that it is also expressed in EECs. f, A dsx-Gal4 reporter (visualized with a GFP reporter that has been false-coloured in red for consistency with the other panels) is active in male and female polyploid ECs (LacZ-negative cells), and is inactive in esg-positive progenitors (LacZ-positive cells, in green). Dsx protein (visualized using a DsxDBD-specific antibody in red) is expressed strongly only in males bot not females, indicating that the sexual dimorphism in dsx transcript levels found in our RNA-seq analyses (Extended Data Fig. 1e) is further enhanced at the protein level. Co-staining of the same antibody with the EC marker mex1-Gal4 confirms expression in ECs. Cytoplasmic dsx-Gal4-driven expression of an mTomato reporter is apparent in ECs (visualized as large cells by co-staining with the membrane-enriched marker Armadillo), but is absent from EECs (as revealed by the gaps in mTomato expression in cells that are labelled with Pros. g, The fruP1-Gal4 reporter (which labels the only sexually dimorphic fru transcript that gives rise to FruM protein) is inactive in both male and female midguts, as revealed by lack of GFP signal (false-coloured in red for consistency with other panels). Consistent with the lack of fruP1-Gal4 expression, a FruM-specific antibody (in red) is not expressed in the male midgut. An independent dsx reporter (dsxΔ2-Gal4) is expressed in polyploid ECs, consistent with the data displayed in f. See Supplementary Information for full genotypes.
Extended Data Figure 3 Sxl controls intrinsic sex differences in adult ISC proliferation independently of dosage compensation.
a, Immunocytochemistry using a Sxl-specific antibody indicates that adult-restricted downregulation of Sxl in intestinal progenitors (ISCs/EBs)—achieved by Gal80TS-controlled expression of a Sxl RNAi transgene—efficiently downregulates Sxl expression in progenitors, but not large polyploid ECs. Conversely, efficient ectopic Sxl protein expression is obtained by expression of a UAS-Sxl transgene in adult ISCs/EBs of male flies. In all panels Sxl antibody is in red; DNA: DAPI, in blue; ISC/EB marker: GFP, in green. b, Quantifications of the number of cells inside control MARCM83 clones, or MARCM clones expressing RNAi transgenes directed against Sxl following DSS treatment. 5 days after clone induction by heat shock, female clones are larger than male clones only when Sxl is present, confirming the cell autonomy of Sxl action. c, Additional controls for Fig. 1a, and confirmation of phenotypes using an independent RNAi transgene. This second RNAi transgene against Sxl (different from the one used in Fig. 1a) reduces the number of pH3-positive cells in DSS-treated female midguts when expressed from esgTS in adults ISCs/EBs, confirming an adult progenitor-specific requirement for Sxl in promoting damage-induced cell divisions in female flies. d, Adult-specific downregulation of Sxl in adult visceral muscle (using the vm driver), trachea (btl-Gal4 and DSRF-Gal4), neurons (nSyb-Gal4, Elav-Gal4), or fat body (stripe-Gal4) does not reduce DSS-induced ISC proliferation in females, By contrast, Sxl downregulation using an ISC/EB driver with suppressed neuronal expression (esg-Gal4 combined with nSyb-Gal80) effectively reduces DSS-induced ISC proliferation in females. Together, these results indicate that Sxl does not control sexually dimorphic DSS-induced ISCs proliferation from non-ISC cells. e, MARCM clones expressing a third RNAi transgene against Sxl (distinct from those used in Fig. 1 and above) are smaller than control clones in females, whereas their size is comparable to that of wild-type or Sxl-RNAi clones in males. This confirms that, during normal homeostasis, female ISCs divide more often than male ISCs because of the cell-autonomous action of Sxl. The graph shows quantifications of the number of cells within each clone 15 days after clone induction by heat shock, and the confocal images show representative clones (labelled in green with GFP) for each genotype. f, Clonal analyses of homeostatic proliferation using the inducible esg flip-out system (which labels progenitors and their progeny generated within a defined temporal window84) in midguts of control males, control females and females in which Sxl downregulation has been confined to adult progenitors. 15 days after induction, the size (assessed as the percentage of GFP-positive area) of control female clones was significantly larger than that of male clones, but both became comparable upon adult-specific Sxl downregulation using Sxl RNAi transgenes. The graph shows area quantifications for each sex/genotype, and the confocal images show representative clones for each genotype. g, Immunohistochemical detection of histone H4 lysine 16 (H4Lys16) acetylation (in red) indicates that adult-specific downregulation of msl-2 in male intestinal progenitors (ISCs/EBs marker: GFP, in green) results in loss of H4Lys16 acetylation of the X chromosome. h, Efficient Msl-2 misexpression in adult female intestinal progenitors (ISCs/EBs marker: GFP, in green) is confirmed by immunocytochemistry using an HA-specific antibody (in red). n denotes the number of guts (c, d, f) or clones (b, e) that were analysed for each genotype. Results were combined from at least two independent experiments. See Supplementary Information for full genotypes.
Extended Data Figure 4 Sexually dimorphic proliferation does not result from sex differences in differentiation.
a, Markers for all four intestinal cell types are still apparent following adult-specific downregulation of Sxl in the intestinal progenitors of females—achieved by Gal80TS-controlled expression of a Sxl RNAi transgene. Indeed, expression of esg-Gal4 (ISC/EBs), Su(H)-LacZ (EBs), Pdm1 (ECs) and Pros (EECs) can be readily detected, suggesting that Sxl downregulation in females (which results in reduced ISC proliferation) does not have a major effect on differentiation. Sxl staining confirms efficient downregulation in ISCs/EBs, but not neighbouring cells. b, The same markers reveal that the differentiation defect resulting from Notch downregulation, previously reported in females, is also apparent in males (note loss of Su(H)-LacZ following Notch downregulation in both males and females), suggesting that sex differences in differentiation do not contribute to the sex differences in susceptibility to Notch-induced tumours. Co-expression of a mitogen (secreted Spitz, sSpi) abrogates the sex differences in tumour susceptibility by efficiently triggering hyperplasia also in males, as revealed by an expanded progenitor (GFP-positive) area in both males and females. The identity of these tumours in males is also comparable to that previously show for Notch tumours in females (consisting of high Pros-positive EEC-like cells and low Pros-positive neoplastic ISC-like cells85. This further suggests that the sex differences in Notch-induced tumour susceptibility do not arise from sexually dimorphic differentiation effects, but result from sex differences in ISC proliferation. See Supplementary Information for full genotypes.
Extended Data Figure 5 tra, but not tra2, controls intrinsic sex differences in adult ISC proliferation.
a, Additional controls for Fig. 2a, and confirmation of phenotypes using independent RNAi transgenes. Two additional RNAi transgenes against tra reduce the number of pH3-positive cells in DSS-treated female, but not male, midguts when expressed from esgTS in adults ISCs/EBs, confirming an adult progenitor-specific requirement for tra in promoting damage-induced cell divisions in female flies. b, tra1 MARCM mutant clones are smaller than control clones in females, whereas their size is comparable to that of wild-type or tra1 clones in males. This confirms that female ISCs divide more often than male ISCs because of the cell-autonomous action of tra. The graph shows quantifications of clone size (in arbitrary units of GFP fluorescence, as described in Methods) 15 days after clone induction by heat shock, and the confocal images show representative clones (labelled in green with GFP) for each genotype. c, Ubiquitous, adult-restricted traF expression from tub-Gal80TS in males increases the number of pH3-positive cells following DSS treatment to levels comparable to those of female flies. d, Re-introduction of this traF transgene specifically in adult ISCs/EBs rescues the reduced, male-like intestinal proliferation (as assessed by the number of pH3-positive cells) of tra null mutant females entirely lacking the tra gene from all their tissues (traKO/tra1) to levels comparable to those of control females. Expression of this transgene in control heterozygous female flies (traKO/+ esgTS>traF) does not significantly increase their proliferation (in fact, it reduces it slightly relative to traKO/+ esgTS> controls, likely as a consequence of its overexpression). e, Clonal analyses of homeostatic proliferation using the inducible esg flip-out system (which labels progenitors and their progeny generated within a defined temporal window84) in midguts of control females and females in which tra downregulation has been confined to adult progenitors. 15 days after induction, the size (assessed as the percentage of GFP-positive area) of control clones is significantly larger than that of tra-RNAi clones. The graph shows area quantifications for each genotype, and the confocal images show representative clones for each genotype. f, Consistent with the tra mutant clonal analysis in Fig. 2c, quantifications of clone size (number of cells per clone) reveal that MARCM clones in which tra has been downregulated are smaller than control clones only in females. Their size is comparable to that of wild-type or tra-downregulated mutant clones in males. The confocal images show representative clones (labelled in green with GFP) for each genotype in females. g, qRT–PCR quantifications of relative abundance of traF, dsxF, dsxM and Yp1 transcripts in adult-specific tra2 mutants (tra2B/ts1 grown at permissive temperatures, then switched to the restrictive temperature 4 days after eclosion and transcriptionally profiled following 10 additional days at the restrictive temperature) and controls (tra2B/+). In tra2 mutant females, dsxF is lost, dsxM is upregulated to levels comparable to those of control males and Yp1 (a DsxF target) is lost (to levels also comparable to those of males). tra mutants (traDf(3L)st-j7/KO) were also used as a positive control. n denotes the number of guts (a, c, d, e) or clones (b, f) that were analysed for each genotype. Results were combined from at least two independent experiments. See Supplementary Information for full genotypes.
Extended Data Figure 6 dsx- and fruM-independent control of sexually dimorphic proliferation in adult intestinal stem cells.
a, Adult-restricted downregulation of dsx (achieved by co-expression of a dsx-RNAi transgene and Dicer-2 (Dcr-2) in ISCs/EBs) has no effect on the compensatory ISC proliferation observed upon DSS treatment in either males or females. dsxF expression in the same conditions does not increase ISC proliferation in either males or females. b, dsxF expression does not rescue the reduced proliferation resulting from tra downregulation in males. Representative images for each genotype are shown in both a and b (DNA: DAPI, in blue; ISC/EB marker: GFP, in green). c, The size of dsx null mutant (dsx1) MARCM clones (quantified in arbitrary units of GFP fluorescence as described in Methods) is comparable to that of controls in both sexes 15 days after clone induction by heat shock. Confocal images show representative clones (labelled in green with GFP) for each genotype. d, Quantifications of clone size in control and dsx null mutant (dsx1) MARCM clones in the midguts of DSS-treated males and females. 5 days after clone induction by heat shock, there are no significant differences in clone size (quantified in arbitrary units of GFP fluorescence as described in Methods) between control and mutants clones in either males or females. Confocal images show representative clones (labelled in green with GFP) for each genotype. e, An RNAi transgene against fru does not reduce the number of pH3-positive cells in DSS-treated midguts when expressed from esgTS in the adult ISCs/EBs of either males or females. Confocal images show that number of intestinal progenitors (esg-positive cells in green) is also unaffected by this manipulation. f, Quantifications of the number of pH3-positive cells upon DSS treatment indicates that the sexual dimorphism in ISC proliferation is unaffected in females with forced fruM expression (fruM/fru4–40) or in males with forced fruF expression (fruF/fru4–40). g, ISC proliferation is unaffected in the migduts of DSS-treated males and females entirely lacking dsx (dsx∆/dsx1), or producing only DsxF (dsx∆/dsx11) or DsxM (dsx∆/dsxD). ISC proliferation is also unaffected in dsx, fruM double null mutant males and females (dsx∆,Df(3R)Exel6179/dsx1, fruP1.LexA), and in dsx null mutants in which fruM is ectopically produced in females (dsx∆,Df(3R)Exel6179/dsx1, fru∆tra). n denotes the number of guts (a, b, e, f, g) or clones (c, d) that were analysed for each genotype. Results were combined from at least two independent experiments. See Supplementary Information for full genotypes.
a, Scatter plot of all 1,346 genes with tra-dependent expression in the adult fly midgut. For each gene, control female/tra null mutant female (Df(3L)st-j7/traKO) fold differences in transcript abundance (x axis, log2 scale) are plotted against tra mutant female with feminized ISCs (adult-restricted rescue of traF in ISCs/EBs)/tra mutant female fold differences (y axis, log2 scale). Genes with tra-sensitive expression and significantly repressed by traF in ISC/EBs (P < 0.05 cutoff) are therefore found in the left-bottom quadrant and are displayed in blue, whereas those significantly activated by traF are found in the top-right quadrant and are displayed in red. Genes with tra-dependent transcription, independent of the action of traF in intestinal precursors are displayed in black. b, Comparable analysis of tra-dependent alternative splicing. c, tra expression in adult ISCs affects splicing of 38 transcripts by at least 5 different mechanisms. The outcome of each of the alternative splicing mechanisms is shown in yellow for a representative gene. d, Adult-restricted downregulation (RNAi lines) or misexpression (UAS lines) of tra targets in adult ISCs/EBs by means of esg-Gal4, tubGal80TS. Genes normally repressed in female progenitors in a traF-dependent manner were downregulated in males (top row) and/or misexpressed in females (bottom row). Genes upregulated in female progenitors in a traF-dependent manner were downregulated in females (bottom row). Adult-restricted downregulation of Idgf1 and Spn88Eb reduces the number of mitoses (pH3-positive cells) in DSS-treated females. Conversely, rdo misexpression inhibits DSS-induced ISC proliferation in females. Adult-restricted downregulation of other traF targets in the same conditions does not affect ISC proliferation in either males or females. e, Male controls for Fig. 3c. In contrast to their effects on females, adult ISC/EB-restricted misexpression of rdo or downregulation of Idgf1 and Spn88Eb does not reduce the percentage of midgut area covered by esg-positive cells in DSS-treated males (DNA: DAPI, in blue; ISC/EB marker: GFP, in green). n denotes the number of guts (d) that were analysed for each genotype. Results were combined from at least two independent experiments. See Supplementary Information for full genotypes.
Extended Data Figure 8 Effects of the sexual identity of adult ISCs on midgut size and reproductive plasticity.
a, The number of cells in the R3a-b and R4a midgut regions, defined by expression of Cut and MvlNP2375 respectively (as described in ref. 86), is higher in females, and can be significantly reduced in females to numbers comparable to those found in males after 20 (but not 3) days of adult-specific downregulation of tra in intestinal progenitors (achieved by esgTS-driven tra downregulation initiated after the phase of midgut post-eclosion growth, see Methods for details). No effects are apparent following downregulation in males. Representative images of these midgut regions (labelled in red with Cut or in green with MvlNP2375,esgTS-driven GFP) are shown to the right for each genotype. b, Adult ISC/EB-specific tra downregulation does not affect the number of ISCs (esg-positive, Su(H)-negative cells) in either males or females, but strongly reduces EB (esg-positive, Su(H)-positive cells) production in females. c, d, Quantifications as in a and b for midguts with adult-specific downregulation of Sxl in intestinal progenitors. c, Reduced number of cells in the R4a midgut region (top graph) and total midgut length (bottom graph) in female flies following 20 days of adult-specific and cell-autonomous masculinization of their intestinal progenitors (achieved by-down regulation of Sxl over 20 days with esg-Gal4). The same manipulation has no discernible effects in males. d, The same genetic manipulation does not affect the number of ISCs (esg-positive, Su(H)-negative cells) in either males or females, but strongly reduces EB (esg-positive, Su(H)-positive cells) production in females. e, The number of EBs (esg- and Su(H)-positive cells, bottom graph), but not ISCs (esg-positive only cells, top graph) is higher in control female flies 3 days after mating. Adult ISC/EB-specific tra downregulation abrogates the postmating increase in EBs in females without affecting EB number in males, or ISC number in males or females. f, Adult-specific Sxl downregulation in intestinal progenitors leads to a small, but significant, reduction in egg production. An unrelated manipulation that also reduces ISC proliferation by inducing differentiation of ISCs (esgTS>Notchintra, images to the right of the graph and ref. 87) also results in reduced egg production, whereas downregulation of Dsx (which does not control sex differences in progenitor proliferation) has no such effect. It should, however, be noted that esg-Gal4 is expressed in a subset of cells in the ovary niche21. Hence, the possibility that these cells contribute to the observed phenotype cannot entirely be ruled out. Images to the right show loss of intestinal progenitor cell makers esg-Gal4 and Su(H)-LacZ following expression of Notchintra in adult intestinal progenitors, indicative of loss of progenitor identity. n denotes the number of guts (a, c), ISCs/EBs (b, d, e) or female flies (f) that were analysed for each genotype. Results were combined from at least two independent experiments. See Supplementary Information for full genotypes.
Extended Data Figure 9 Effects of the sexual identity of adult ISCs on the susceptibility to genetically induced tumours.
a, The number of mitoses in Apc-ras mutant clones is larger than that of control clones in both sexes, but it is higher and dependent on Sxl in females. b, The size of Delta (Dl, the Notch ligand) null mutant (DlRevF10) MARCM clones is larger than that of control clones in both sexes, but female mutant clones are larger than male mutant clones. The graph shows quantifications of the number of cells within each clone 15 days after clone induction by heat shock, and the confocal images show representative clones (labelled in green with GFP) for each genotype. c, In tra ‘female’ mutant flies (traKO and traKO/Df(3L)st-j7) reduced Notch signalling in intestinal progenitors fails to induce the hyperplasia (quantified by the number of pH3 cells) normally observed in control females. d, Following 15 days of adult-specific downregulation of Notch (N) in intestinal progenitors, hyperplasia (quantified by the number of pH3-positive cells and also shown in representative images) is observed in female, but not male midguts. Adult-specific and cell-autonomous reversal of ISC/EB female identity—achieved by esgTS-driven downregulation of Sxl—fully prevents the hyperplasia induced by Notch downregulation in females, but has no effects on males. Confocal images show intestinal progenitor coverage of representative midgut portions for each genotype (DNA: DAPI, in blue; ISC/EB marker: GFP, in green). e, pH3 quantifications show a comparable effect for independent RNAi transgenes against Sxl and Notch. f, Adult-specific downregulation of Notch (N) signalling by ectopic expression of the downstream Notch signalling antagonist Hairless (H)38 leads to hyperplasia (quantified by the number of pH3-positive cells and also shown in representative images) in female, but not male midguts. Adult-specific and cell-autonomous reversal of ISC/EB female identity—achieved by esgTS-driven downregulation of Sxl—fully prevents the hyperplasia induced by Hairless overexpression in females, but has no effects on males. Confocal images show intestinal progenitor coverage of representative midgut portions for each genotype (DNA: DAPI, in blue; ISC/EB marker: GFP, in green). g, The number of pH3-positive cells 15 days after Notch downregulation in adult intestinal progenitors of double null mutant flies lacking dsx and fruM (dsx∆,Df(3R)Exel6179/dsx1, fruP1.LexA) is comparable to that of controls in both males and female flies. Like control flies, it is significantly higher in female flies. Virgin flies were used in all these experiments. n denotes the number of guts (a, c, d, e, f, g) or clones (b) that were analysed for each genotype. Results were combined from at least two independent experiments. See Supplementary Information for full genotypes.
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Hudry, B., Khadayate, S. & Miguel-Aliaga, I. The sexual identity of adult intestinal stem cells controls organ size and plasticity. Nature 530, 344–348 (2016). https://doi.org/10.1038/nature16953
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