Notch activity opposes ras-induced differentiation during the second mitotic wave of the developing Drosophilaeye
© Yang and Baker; licensee BioMed Central Ltd. 2006
Received: 01 September 2005
Accepted: 21 February 2006
Published: 21 February 2006
EGF receptor acts through Ras and the MAPK cascade to trigger differentiation and maintain survival of most of cell types in the Drosophila retina. Cell types are specified sequentially by separate episodes of EGFR activity. All the cell types differentiate in G1 phase of the cell cycle. Before differentiating, many cells pass through the cell cycle in the "Second Mitotic Wave" in response to Notch activity, but no cell fates are specified during the Second Mitotic Wave. It is not known how fate specification is limited to G1-arrested cells.
Competence to differentiate in response to activated RasV12 was diminished during the Second Mitotic Wave accounting for the failure to recruit cell fates from cycling cells. Competence was not restored by blocking cell cycle progression, but was restored by reduced Notch activity.
Competence to differentiate does not depend on cell cycle progression per se, but on the same receptor activity that also induces cell cycle entry. Dual effects of Notch on the cell cycle and on differentiation help ensure that only G1 phase cells undergo fate specification.
EGF receptor acts through Ras and the MAPK cascade to trigger differentiation and maintain survival of most cell types in the Drosophila retina [1–6]. Specification of retinal cells occurs as a 'morphogenetic furrow' spreads across the retinal epithelium from posterior to anterior. Because the morphogenetic furrow progresses, each developing eye imaginal disc displays a series of columns of progressively more mature ommatidia posterior to the morphogenetic furrow, beginning with column 0 within the furrow itself.
Retinal cells are classified into two groups base on cell cycle behaviour. The first five cells are recruited to each ommatidium during a G1 arrest that begins ahead of the morphogenetic furrow, and these five withdraw from the cell cycle permanently. The remaining cells re-enter the cell cycle within the morphogenetic furrow before being recruited to remaining retinal fates post-mitotically, when they are in G1 phase again[8, 9]. The 'Second Mitotic Wave' plays no direct role in specifying or limiting cell fates, but is required to generate adequate numbers of retinal precursor cells[10, 11]. It is not known why differentiation is normally restricted to G1 phase cells, given that eye discs contain cells at other cell cycle stages. It is possible that cell differentiation cannot occur in cells actively progressing through the cell cycle, or in cells not in G1 phase. Otherwise a mechanism is required to account for the inverse relationship between cell cycle progression and differentiation.
How completely can known features of EGFR regulation account for the timing of ommatidial cell recruitment ? One factor might be the distribution of EGFR ligands. If R2, R3, R4, and R5 cells need to produce ligands before further cells are recruited, perhaps this does not happen until column 4. Another explanation might be negative feedback. Perhaps levels of the secreted antagonist Argos need to decay before recruitment can resume. If either explanation were correct, cells should be recruited and differentiate prematurely if the EGFR pathway were activated independent of ligands. In contrast to this prediction, expression of activated RasV12 posterior to the morphogenetic furrow leads to ectopic photoreceptor differentiation only after column 5. Prior to column 5, retinal development looks quite normal (Figure 1A,B). Thus, an additional mechanism may be required to explain the pause in retinal differentiation between columns 1–4.
The correlation between the pause in retinal specification and the Second Mitotic Wave suggests that cell cycle progression might be incompatible with cell fate specification. However, evidence from several mutant genotypes indicates that differentiation can also occur in G2 phase, although it is not certain that such differentiation is normal[9, 19]. If G1 arrest is not a prerequisite for fate specification, another mechanism must explain why only G1 phase cells are normally selected.
We have investigated why Ras activation posterior to the furrow does not make cells differentiate until after column 5. The experiments indicate that after columns 0–1, cells show reduced competence to differentiate in response to Ras until about column 5. We report that progression through the cell cycle is not the cause, however. Instead we find that Notch signaling activity is partly responsible for preventing differentiation in response to Ras. Based on recent findings that Notch signaling is also essential for S-phase entry in the SMW[20, 21], we propose that, in normal development, G1 phase cells differentiate because the Notch activity that promotes cell cycle entry also interferes with differentiation.
Reduced competence to differentiate during the Second Mitotic Wave
The GMR-GAL4 driver drives transcription of UAS-trangenes in all eye disc cells posterior to the morphogenetic furrow[1, 22]. When GMR-GAL4 drives expression of the activated RasV12, essentially all retinal cells differentiated as photoreceptor neurons, and expressed the neuronal marker ELAV(Figure 1A,B). Ubiquitous neural differentiation became apparent around column 6–7, but the pattern and extent of neural differentiation were almost normal earlier, even though GMR-GAL4 driven gene expression is detected from column 1 onwards (our unpublished results). In normal development ELAV protein appeared in R2 and R5 in column 2, indicating a delay of around 2–3 hours between R2/5 specification in column 0–1 and detection of the ELAV protein. The detection of ectopic ELAV expression in column 6–7 suggested that RasV12 was insufficient to recruit ectopic photoreceptor cells earlier than column 5 (Figure 1A,B).
One possible explanation might be that GMR-GAL4 drives UAS-RasV12 expression at a level that is too low to recruit extra photoreceptor cells before column 5. If this were the case, we would expect that higher levels of expression would cause differentiation earlier. To test this we sought to elevate GAL4 activity by raising the temperature. Ras V12 was expressed using the GMR driver at 29°C (Figure 1C). No extra photoreceptor differentiation was observed between columns 1 and 5, although ectopic differentiation still occurred posterior to column 5(Fig. 1C).
RasV12 expression was also increased through use of a distinct GMR-GAL4 insertion (Figure 1D). Previous studies employed a weakly-expressed GMR-GAL4 insertion that does not produce rough eyes when heterozygous. Stronger GMR-GAL4 lines usually have rough eyes in the absence of any UAS transgene, presumably due to 'squelching'(inhibition of genes lacking UAS sites by deprivation of common coactivators by GAL4 ). Using a stronger GMR-GAL4 insertion line, for which a single copy leads to a rough eye, still did not induce ectopic differentiation before column 6 (Fig. 1D).
To test when cells become competent to differentiate in response to RasV12 in a different way, we exposed all cells to Ras activity simultaneously using the heat shock promoter. Induction using a 10 min heat shock of hs-RasV12 had little effect on differentiation until 9 h later, when ectopic differentiation became visible (Figure 1E–F). Ectopic neurons were seen in the posterior of the eye disc, and anterior to the morphogenetic furrow, but not between columns 1–5 (Figure 1E,F). In addition to monitoring ELAV expression, we also assessed 22C10 antigen, with similar results (not shown). Even 14 h after the heat shock, a region of the eye disc continued to develop normally while ectopic neurogenesis occurred both posteriorly and anterior to the morphogenetic furrow (Figure 1G). These results support the notion that a region around the SMW is more resistant to differentiation in response to Ras activity than are other parts of the eye disc.
Cells in columns 1–5 are not completely insensitive, however, because ectopic neurogenesis was seen there when RasV12 was induced to a higher level by longer heatshock (Figure 1H). In addition, expressing Ras V12 under control of the sevenless promoter induces ectopic R7 cells . The Sevenless promoter drives expression at a high level in a dynamic pattern, part of which includes a subset of undifferentiated cells in columns 1–3 ("mystery cells"). We confirmed the observations of Fortini et al that in Sev-RasV12, some ectopic photoreceptors derive from mystery cells in columns 1–3(Fig. 1I). Therefore we conclude that cells require more intense Ras signaling to differentiate in columns 1–5 than at other stages.
Differentiation blocked independent of cell cycle progression
Endogenous Notch activity opposes differentiation
One pathway that could interfere with differentation was Notch signaling. Reduced Notch function leads to ectopic neurogenesis . Some of the ectopic neurogenesis might depend on Notch indirectly, because supernumerary R8 cells develop when Notch is reduced and might recruit excess other photoreceptor cell types. Notch can interfere directly with recruitment of cell types other than R8 when constitutively activated, however, and there is evidence that endogenous Notch may do so also [28, 29].
If Notch prevented photoreceptor differentiation by antagonizing Ras activity, Ras activity should be required for ectopic photoreceptor differentiation when Notch activity was reduced. An alternative was that the normal role of Ras might actually be to block inhibition due to Notch. In this case Ras would be dispensable for photoreceptor differentiation in the absence of N. N ts egfr ts eye discs were examined to distinguish the models. All photoreceptor cells differentiating in N ts egfr ts eye discs at restrictive temperatures also expressed the R8 marker Senseless, indicating that other photoreceptor cell types required EGFR signaling for differentiation, even in the absence of Notch (Fig. 4C). Taken together, these findings indicate that Notch antagonized Ras activity in some cells in columns 0–1. Notch did not seem required to prevent differentiation by cells in columns 2–4, however.
During normal eye development there is a pause in the progressive recruitment of retinal cells. Between columns 1–4, unspecified cells pass through a cell cycle called the Second Mitotic Wave. Because no fates are specified during this period, differentiating retinal cells are normally all in G1 phase. Even activated RasV12 was not sufficient to drive photoreceptor differentiation until after these cells have completed the cell cycle. One hypothesis was that cell cycle progression precludes differentiation.
We found that cell cycle progression was not required to prevent differentiation, because preventing the SMW did not restore competence to differentiate in response to RasV12 (Figure 2). Preventing the SMW also does not affect the amount or timing of differentiation in response to endogenous Ras(Figure 3, 4). Instead reduced competence must in part be due to activity of the receptor protein Notch, because reducing Notch activity increased competence to differentiate in response to Ras (Figures 4,5). In normal development Notch is most critical in column 1, perhaps reflecting declining endogenous Ras activity in columns 2–4. Thus differentiation is limited both by the activity of N and tight regulation of Ras, and perhaps other mechanisms in addition.
The role of Notch in reducing competence to differentiate in response to Ras suggests a mechanism that correlates cell fate specification with cell cycle withdrawal. Recently it was reported that Notch activity is required for cells to enter S phase of the SMW[20, 21]. We propose that Notch opposes differentiation independently of its cell cycle effects, so that the SMW coincides with a pause in differentiation because both are responses to activity of the same receptor. Ras also has cell cycle effects that have been previously noted. Ras activity blocks S phase entry in column 0, and promotes G2/M progression in G2 cells in the SMW. Ras therefore both promotes G1 arrest of differentiating cells, and return to G1 (via mitosis) of cells that receive EGFR signals in G2.
Previously, EGFR activity has been thought to be determined by the sequential expression of ligands and by negative feedback mechanisms. As each photoreceptor cell type begins differentiating, it becomes a source of EGFR ligands and so expands EGFR activity to new cells. Each round of EGFR activation triggers a peak of negative feedback, which rapidly confines the spread of differentiation at each step. Because expression of the Notch ligand Delta is regulated by EGFR[20, 31], Notch activity may be considered a further feedback control on EGFR, acting downstream of Ras. In this view N activity in columns 1–4 is partly a response to earlier EGFR activity in R2-R5 cells, albeit indirectly. Consistent with this, expression of E(spl) bHLH proteins is lost posterior to the morphogenetic furrow in cells mutant for EGFR.
It is important to point out that the model we propose is based on a particular stage of retinal development. Although an inverse correlation between differentiation and proliferation is observed in many developmental events, we do not yet know whether any mechanism links Notch signaling to proliferation in general, although this is one possibility. Even within the retina, Notch later has roles that promote differentiation of R7 and R4 cell types that appear unrelated to cell cycle progression [33–36].
It is probable that cell cycle and cell specification pathways diverge at the level of target genes of the Notch and Ras pathways. Dacapo has been suggested as a component of the G1 arrest program in response to Ras, but even mutating dap and Rbf simultaneously, which permits cells to continue proliferating, does not block differentiation. One target of Ras signaling in R1, R6, and R7 differentiation is Phyllopod. Phyll is not required for R2-5 specification, although it appears to be expressed there and so might act redundantly [37–39]. Notch target genes mediating S-phase entry or antagonizing differentiation of cells other than R8 remain to be identified. One question raised by our present work is how Notch signaling can be epistatic over Ras activity during the SMW, when earlier EGFR is epistatic over N in preventing cell cycle entry by R2,3,4 and R5 cells and promoting their differentiation .
Normal retinal cells always differentiate in G1 phase of the cell, although the retina also contains actively cycling cells. We report that the cycling cells are resistant to Ras-induced fate specification, but not because they are cycling. Instead, the correlation occurs because the SMW occurs during a pause in cell fate specification, maintained in part by the same Notch activity that drives cell cycle entry, so that cells that enter the cell cycle because of N also resist specification.
Metazoan genomes encode many thousands of genes, whose interactions might potentially be very complex. By contrast there appear to be only a limited number of extracellular signaling pathways that are important for development. This constraint may be enough to make it common for correlated developmental processes to be linked through dependence on a shared extracellular signal.
Fixation and immunochemical procedures were as described previously[5, 6]. Fly work was conducted at 25°C except where otherwise indicated in the text. Anti-elav, anti-Cut, anti-cyclin B and mAb22C10 antibodies have been described previously [39, 41–43]. UAS-RasV12, Sev-RasV12, hs-RasV12, UAS-NDN, GMR-p21 and GMR-GAL4 transgenes are all transcriptional fusions of the indicated promoters to the RasV12, N, p21 or GAL4 coding regions. The UAS-NDN line expresses a protein deleted for the intracellular domain . Transgene insertions were heterozygous in all our experiments (the GMR-p21 samples were heterozygous for two independent GMR-p21 insertions) Nts1 and hs-RasV12 flies were obtained from R. Cagan[26, 45]. UAS-RasV12 flies were obtained from F. Karim. Egfrts2 was obtained from K. Moses. Sev-RasV12 was obtained from M. Fortini. GMR-GAL4 flies were obtained from S.L.Zipursky and M. Freeman.
We thank Drs. W. Fu and L. Firth for suggestions, B. Kelley Marcellino for technical assistance, the Developmental Studies Hybridoma Bank at the University of Iowa and Dr. S. Benzer for monoclonal antibodies, and Drs. R. Cagan, M. Fortini, I. Hariharan, F. Karim, A. Marinez-Arias and K. Moses for Drosophila strains. We thank Drs. L. Firth and D. Tyler, and W. Li for comments on the manuscript. This work was funded by grant GM47892 from the NIH. NEB is a Scholar of the Irma T. Hirschl Foundation for Biomedical Sciences.
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